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Question 1
Correct
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A 38-year-old woman is diagnosed with hyperthyroidism and started on carbimazole. What is the mechanism of action of this medication?
Your Answer: Prevents iodination of the tyrosine residue on thyroglobulin
Explanation:Carbimazole is a medication used to treat thyrotoxicosis, a condition where the thyroid gland produces too much thyroid hormone. It is usually given in high doses for six weeks until the patient’s thyroid hormone levels become normal, after which the dosage is reduced. The drug works by blocking thyroid peroxidase, an enzyme that is responsible for coupling and iodinating the tyrosine residues on thyroglobulin, which ultimately leads to a reduction in thyroid hormone production. In contrast, propylthiouracil has a dual mechanism of action, inhibiting both thyroid peroxidase and 5′-deiodinase, which reduces the peripheral conversion of T4 to T3.
However, carbimazole is not without its adverse effects. One of the most serious side effects is agranulocytosis, a condition where the body’s white blood cell count drops significantly, making the patient more susceptible to infections. Additionally, carbimazole can cross the placenta and affect the developing fetus, although it may be used in low doses during pregnancy under close medical supervision. Overall, carbimazole is an effective medication for managing thyrotoxicosis, but its potential side effects should be carefully monitored.
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This question is part of the following fields:
- Endocrine System
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Question 2
Incorrect
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A 60-year-old male presents with increasing fatigue.
Three months ago, he was diagnosed with bronchial carcinoma and has undergone chemotherapy. Upon admission, his electrolyte levels were measured as follows:
- Sodium: 118 mmol/L (137-144)
- Potassium: 3.5 mmol/L (3.5-4.9)
- Urea: 3.2 mmol/L (2.5-7.5)
- Creatinine: 65 µmol/L (60-110)
What would be the most appropriate initial investigation for this patient?Your Answer: Serum ADH concentration
Correct Answer: Urine osmolality and sodium concentration
Explanation:Hyponatraemia in Bronchial Carcinoma Patients
Hyponatraemia is a common condition in patients with bronchial carcinoma. It is characterized by a marked decrease in sodium levels, which appears to be dilutional based on other test results that fall within the lower end of the normal range. The most likely cause of this condition is the syndrome of inappropriate ADH secretion (SIADH), which occurs when the tumour produces ADH in an ectopic manner. However, the diagnosis of SIADH is one of exclusion, and other possibilities such as hypoadrenalism due to metastatic disease to the adrenals should also be considered.
To determine the cause of hyponatraemia, initial tests such as urine sodium and osmolality are recommended. These tests can help rule out other possible causes and confirm the diagnosis of SIADH. Treatment for this condition typically involves fluid restriction. It is important to note that measuring ADH concentrations is not a reliable diagnostic tool as it is not widely available and does not provide any useful information.
In summary, hyponatraemia is a common condition in bronchial carcinoma patients, and SIADH is the most likely cause. Initial tests such as urine sodium and osmolality can help confirm the diagnosis, and treatment involves fluid restriction.
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This question is part of the following fields:
- Endocrine System
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Question 3
Correct
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A 58-year-old woman arrives at the emergency department complaining of persistent nausea and vomiting for the past 4 days. Despite taking cyclizine and metoclopramide, she has not experienced any relief. The patient is currently under palliative care for lung cancer with cerebral metastases.
Upon consultation with the palliative care team, it is decided to administer a steroid with potent glucocorticoid activity and minimal mineralocorticoid activity.
What medication is the patient expected to receive?Your Answer: Dexamethasone
Explanation:Dexamethasone is the most suitable example of a steroid that has very high glucocorticoid activity and minimal mineralocorticoid activity among the given options.
Corticosteroids are commonly prescribed medications that can be taken orally or intravenously, or applied topically. They mimic the effects of natural steroids in the body and can be used to replace or supplement them. However, the use of corticosteroids is limited by their numerous side effects, which are more common with prolonged and systemic use. These side effects can affect various systems in the body, including the endocrine, musculoskeletal, gastrointestinal, ophthalmic, and psychiatric systems. Some of the most common side effects include impaired glucose regulation, weight gain, osteoporosis, and increased susceptibility to infections. Patients on long-term corticosteroids should have their doses adjusted during intercurrent illness, and the medication should not be abruptly withdrawn to avoid an Addisonian crisis. Gradual withdrawal is recommended for patients who have received high doses or prolonged treatment.
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This question is part of the following fields:
- Endocrine System
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Question 4
Correct
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Which one of the following is not associated with excessive glucocorticoids?
Your Answer: Hyponatraemia
Explanation:Excessive levels of glucocorticoids can lead to various negative consequences such as skin thinning, osteonecrosis, and osteoporosis. Steroids can cause the body to retain sodium and water, while also resulting in potassium loss and potentially leading to hypokalaemic alkalosis.
Cortisol: Functions and Regulation
Cortisol is a hormone produced in the zona fasciculata of the adrenal cortex. It plays a crucial role in various bodily functions and is essential for life. Cortisol increases blood pressure by up-regulating alpha-1 receptors on arterioles, allowing for a normal response to angiotensin II and catecholamines. However, it inhibits bone formation by decreasing osteoblasts, type 1 collagen, and absorption of calcium from the gut, while increasing osteoclastic activity. Cortisol also increases insulin resistance and metabolism by increasing gluconeogenesis, lipolysis, and proteolysis. It inhibits inflammatory and immune responses, but maintains the function of skeletal and cardiac muscle.
The regulation of cortisol secretion is controlled by the hypothalamic-pituitary-adrenal (HPA) axis. The pituitary gland secretes adrenocorticotropic hormone (ACTH), which stimulates the adrenal cortex to produce cortisol. The hypothalamus releases corticotrophin-releasing hormone (CRH), which stimulates the pituitary gland to release ACTH. Stress can also increase cortisol secretion.
Excess cortisol in the body can lead to Cushing’s syndrome, which can cause a range of symptoms such as weight gain, muscle weakness, and high blood pressure. Understanding the functions and regulation of cortisol is important for maintaining overall health and preventing hormonal imbalances.
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This question is part of the following fields:
- Endocrine System
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Question 5
Correct
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Sam, a 75-year-old man, presents to the GP with a complaint of breast growth that has developed rapidly over the past 3 months. Sam insists that he has no trouble with sexual function. He has recently been diagnosed with a heart problem and is taking multiple medications for it, although he cannot recall their names. Other than that, he claims to be in good health. Upon examination, all of Sam's vital signs are within normal limits. After measuring his height and weight, his body mass index is calculated to be 24 kg/m². Each breast is approximately 10 cm in diameter, with large nipples and tenderness but no pain. Moderate cardiomegaly and a 3rd heart sound are noted during chest assessment. No abnormalities are found during an abdominal examination. Pitting edema is present up to his mid calf. Based on the history and examination, what is the most probable cause of Sam's gynaecomastia?
Your Answer: Digoxin
Explanation:Digoxin is the correct answer as it can lead to drug-induced gynaecomastia. Sam is likely taking digoxin due to his heart failure, and this medication has a side effect of causing breast tissue growth in men. This is thought to occur because digoxin has a similar structure to oestrogen and can directly stimulate oestrogen receptors.
While cirrhosis can also cause gynaecomastia, it is unlikely in this case as there are no signs or symptoms of liver disease. Cirrhosis typically causes gynaecomastia due to the liver’s reduced ability to clear oestrogens from the bloodstream.
Obesity is not the correct answer as Sam is not obese, with a BMI of 24 kg/m². However, obesity is a common cause of gynaecomastia as excess fat can be distributed to the breasts and result in increased aromatisation of androgens to oestrogens.
An oestrogen-secreting tumour is not the correct answer as there is no evidence in Sam’s history or examination to suggest he has one, although these tumours can cause gynaecomastia in men.
Understanding Gynaecomastia: Causes and Drug Triggers
Gynaecomastia is a condition characterized by the abnormal growth of breast tissue in males, often caused by an increased ratio of oestrogen to androgen. It is important to distinguish the causes of gynaecomastia from those of galactorrhoea, which is caused by the actions of prolactin on breast tissue.
Physiological changes during puberty can lead to gynaecomastia, but it can also be caused by syndromes with androgen deficiency such as Kallmann and Klinefelter’s, testicular failure due to mumps, liver disease, testicular cancer, and hyperthyroidism. Additionally, haemodialysis and ectopic tumour secretion can also trigger gynaecomastia.
Drug-induced gynaecomastia is also a common cause, with spironolactone being the most frequent trigger. Other drugs that can cause gynaecomastia include cimetidine, digoxin, cannabis, finasteride, GnRH agonists like goserelin and buserelin, oestrogens, and anabolic steroids. However, it is important to note that very rare drug causes of gynaecomastia include tricyclics, isoniazid, calcium channel blockers, heroin, busulfan, and methyldopa.
In summary, understanding the causes and drug triggers of gynaecomastia is crucial in diagnosing and treating this condition.
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This question is part of the following fields:
- Endocrine System
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Question 6
Incorrect
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A 14-year-old boy is brought to the clinic by his mother due to concerns about his height compared to other boys his age. The boy also shares that he often receives comments about his appearance, with some likening him to a toy doll. What can be inferred about the pattern of hormone release that he may be lacking?
Your Answer: Released diurnally
Correct Answer: It is released in a pulsatile manner
Explanation:The doll-like appearance of the boy in his presentation suggests that he may be suffering from growth hormone deficiency, which can cause short stature, forehead prominence, and maxillary hypoplasia. The hypothalamus controls the release of growth hormone through the pulsatile release of growth hormone releasing hormone. Therefore, measuring GHRH levels is not a useful method for investigating growth hormone deficiency.
Understanding Growth Hormone and Its Functions
Growth hormone (GH) is a hormone produced by the somatotroph cells in the anterior pituitary gland. It plays a crucial role in postnatal growth and development, as well as in regulating protein, lipid, and carbohydrate metabolism. GH acts on a transmembrane receptor for growth factor, leading to receptor dimerization and direct or indirect effects on tissues via insulin-like growth factor 1 (IGF-1), which is primarily secreted by the liver.
GH secretion is regulated by various factors, including growth hormone releasing hormone (GHRH), fasting, exercise, and sleep. Conversely, glucose and somatostatin can decrease GH secretion. Disorders associated with GH include acromegaly, which results from excess GH, and GH deficiency, which can lead to short stature.
In summary, GH is a vital hormone that plays a significant role in growth and metabolism. Understanding its functions and regulation can help in the diagnosis and treatment of GH-related disorders.
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This question is part of the following fields:
- Endocrine System
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Question 7
Incorrect
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A 27-year-old man presents to the consultant's office with complaints of increased thirst and frequent urination for the past month. He has a history of physical injuries due to a motor vehicle accident that occurred 4 months ago. The patient is currently not on any medications and is in good health. Urinalysis reveals a decreased sodium concentration and urine osmolarity of 90 mOsm/L. What renal tubular changes would be anticipated in this patient due to his current condition?
Your Answer: Decreased activity of K+/H+ exchanger in the collecting ducts
Correct Answer: Decreased expression of aquaporin-2 channels in the collecting ducts
Explanation:The insertion of aquaporin-2 channels by antidiuretic hormone promotes water reabsorption, which is compromised in central diabetes insipidus (DI) caused by physical trauma to the pituitary gland. Symptoms include increased thirst, polydipsia, and polyuria, with urinalysis showing decreased urine osmolality and sodium concentration. Aldosterone regulates epithelial sodium channel (ENaC) and K+/H+ exchanger, while angiotensin II regulates Na+/H+ exchanger in proximal tubules. Loop diuretics decrease activity of Na-K-Cl cotransporter in the loops of Henle. However, none of these are relevant to this patient’s presentation.
Understanding Antidiuretic Hormone (ADH)
Antidiuretic hormone (ADH) is a hormone that is produced in the supraoptic nuclei of the hypothalamus and released by the posterior pituitary gland. Its primary function is to conserve body water by promoting water reabsorption in the collecting ducts of the kidneys through the insertion of aquaporin-2 channels.
ADH secretion is regulated by various factors. An increase in extracellular fluid osmolality, a decrease in volume or pressure, and the presence of angiotensin II can all increase ADH secretion. Conversely, a decrease in extracellular fluid osmolality, an increase in volume, a decrease in temperature, or the absence of ADH can decrease its secretion.
Diabetes insipidus (DI) is a condition that occurs when there is either a deficiency of ADH (cranial DI) or an insensitivity to ADH (nephrogenic DI). Cranial DI can be treated with desmopressin, which is an analog of ADH.
Overall, understanding the role of ADH in regulating water balance in the body is crucial for maintaining proper hydration and preventing conditions like DI.
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This question is part of the following fields:
- Endocrine System
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Question 8
Incorrect
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A 50-year-old woman has just had a thyroidectomy to treat medullary thyroid cancer. What is the clinical tumor marker used to screen for recurrence?
Your Answer: Free T4
Correct Answer: Calcitonin
Explanation:Calcitonin is used in clinical practice to detect recurrence of medullary thyroid cancer. Thyroid function tests are not used for diagnosis or follow-up of malignancies. However, regular monitoring of TSH levels may be necessary for patients taking thyroxine.
Thyroid cancer rarely causes hyperthyroidism or hypothyroidism as it does not usually secrete thyroid hormones. The most common type of thyroid cancer is papillary carcinoma, which is often found in young females and has an excellent prognosis. Follicular carcinoma is less common, while medullary carcinoma is a cancer of the parafollicular cells that secrete calcitonin and is associated with multiple endocrine neoplasia type 2. Anaplastic carcinoma is rare and not responsive to treatment, causing pressure symptoms. Lymphoma is also rare and associated with Hashimoto’s thyroiditis.
Management of papillary and follicular cancer involves a total thyroidectomy followed by radioiodine to kill residual cells. Yearly thyroglobulin levels are monitored to detect early recurrent disease. Papillary carcinoma usually contains a mixture of papillary and colloid filled follicles, while follicular adenoma presents as a solitary thyroid nodule and malignancy can only be excluded on formal histological assessment. Follicular carcinoma may appear macroscopically encapsulated, but microscopically capsular invasion is seen. Medullary carcinoma is associated with raised serum calcitonin levels and familial genetic disease in up to 20% of cases. Anaplastic carcinoma is most common in elderly females and is treated by resection where possible, with palliation achieved through isthmusectomy and radiotherapy. Chemotherapy is ineffective.
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This question is part of the following fields:
- Endocrine System
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Question 9
Incorrect
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A 19-year-old man was recently admitted to hospital with invasive meningococcal disease. He has no other medical history but is now complaining of extreme fatigue, light-headedness and rapid weight loss. He has also noticed his skin appears much more tanned than usual. His BP is 98/60 mmHg. Capillary glucose is found to be 2.2 mmol/L.
Hb 135 g/L Male: (130 - 180)
Platelets 280 * 109/L (150 - 400)
WBC 5.5 * 109/L (4.0 - 11.0)
Na+ 128 mmol/L (135 - 145)
K+ 5.8 mmol/L (3.5 - 5.0)
Bicarbonate 19 mmol/L (22 - 29)
Urea 8.0 mmol/L (2.0 - 7.0)
Creatinine 125 µmol/L (55 - 120)
What is the most likely cause of his symptoms?Your Answer:
Correct Answer: Waterhouse-Friedrichsen syndrome
Explanation:Understanding Waterhouse-Friderichsen Syndrome
Waterhouse-Friderichsen syndrome is a condition that occurs when the adrenal glands fail due to a previous adrenal haemorrhage caused by a severe bacterial infection. The most common cause of this condition is Neisseria meningitidis, but it can also be caused by other bacteria such as Haemophilus influenzae, Pseudomonas aeruginosa, Escherichia coli, and Streptococcus pneumoniae.
The symptoms of Waterhouse-Friderichsen syndrome are similar to those of hypoadrenalism, including lethargy, weakness, anorexia, nausea and vomiting, and weight loss. Other symptoms may include hyperpigmentation, especially in the palmar creases, vitiligo, and loss of pubic hair in women. In severe cases, a crisis may occur, which can lead to collapse, shock, and pyrexia.
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This question is part of the following fields:
- Endocrine System
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Question 10
Incorrect
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A 50-year-old man comes to the clinic complaining of gynaecomastia. He is currently undergoing treatment for heart failure and gastro-oesophageal reflux. Which medication that he is taking is the most probable cause of his gynaecomastia?
Your Answer:
Correct Answer: Spironolactone
Explanation:Medications Associated with Gynaecomastia
Gynaecomastia, the enlargement of male breast tissue, can be caused by various medications. Spironolactone, ciclosporin, cimetidine, and omeprazole are some of the drugs that have been associated with this condition. Ramipril has also been linked to gynaecomastia, but it is a rare occurrence.
Aside from these medications, other drugs that can cause gynaecomastia include digoxin, LHRH analogues, cimetidine, and finasteride. It is important to note that not all individuals who take these medications will develop gynaecomastia, and the risk may vary depending on the dosage and duration of treatment.
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This question is part of the following fields:
- Endocrine System
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Question 11
Incorrect
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A 43-year-old woman with a history of severe ulcerative colitis (UC) presents to the emergency department with her fourth acute flare in the past 6 months. She has a past medical history of recreational drug use and depression. The patient is given IV hydrocortisone and appears to be responding well. She is discharged after a day of observation with a 7-day course of prednisolone, but the consultant is considering long-term steroid therapy due to the severity of her condition. Which of the following is associated with long-term steroid use?
Your Answer:
Correct Answer: Increased risk of mania
Explanation:Long-term use of steroids can lead to a higher risk of psychiatric disorders such as depression, mania, psychosis, and insomnia. This risk is even greater if the patient has a history of recreational drug use or mental disorders. While proximal myopathy is a known adverse effect of long-term steroid use, distal myopathy is not commonly observed. However, some studies have reported it as a rare and uncommon adverse effect. Steroids are also known to increase appetite, leading to weight gain, making the last two options incorrect.
Corticosteroids are commonly prescribed medications that can be taken orally or intravenously, or applied topically. They mimic the effects of natural steroids in the body and can be used to replace or supplement them. However, the use of corticosteroids is limited by their numerous side effects, which are more common with prolonged and systemic use. These side effects can affect various systems in the body, including the endocrine, musculoskeletal, gastrointestinal, ophthalmic, and psychiatric systems. Some of the most common side effects include impaired glucose regulation, weight gain, osteoporosis, and increased susceptibility to infections. Patients on long-term corticosteroids should have their doses adjusted during intercurrent illness, and the medication should not be abruptly withdrawn to avoid an Addisonian crisis. Gradual withdrawal is recommended for patients who have received high doses or prolonged treatment.
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This question is part of the following fields:
- Endocrine System
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Question 12
Incorrect
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A 42-year-old woman visits her GP complaining of chest pain. She has a history of hypertension and is currently taking metformin for diabetes. The GP observes that her BMI is 45. What is a possible complication of the metabolic syndrome in this case?
Your Answer:
Correct Answer: Ischemic stroke
Explanation:Metabolic syndrome is a group of risk factors for cardiovascular disease that are caused by insulin resistance and central obesity.
Obesity is associated with higher rates of illness and death, as well as decreased productivity and functioning, increased healthcare expenses, and social and economic discrimination.
The consequences of obesity include strokes, type 2 diabetes, heart disease, certain cancers (such as breast, colon, and endometrial), polycystic ovarian syndrome, obstructive sleep apnea, fatty liver, gallstones, and mental health issues.
The Physiology of Obesity: Leptin and Ghrelin
Leptin is a hormone produced by adipose tissue that plays a crucial role in regulating body weight. It acts on the hypothalamus, specifically on the satiety centers, to decrease appetite and induce feelings of fullness. In cases of obesity, where there is an excess of adipose tissue, leptin levels are high. Leptin also stimulates the release of melanocyte-stimulating hormone (MSH) and corticotrophin-releasing hormone (CRH), which further contribute to the regulation of appetite. On the other hand, low levels of leptin stimulate the release of neuropeptide Y (NPY), which increases appetite.
Ghrelin, on the other hand, is a hormone that stimulates hunger. It is mainly produced by the P/D1 cells lining the fundus of the stomach and epsilon cells of the pancreas. Ghrelin levels increase before meals, signaling the body to prepare for food intake, and decrease after meals, indicating that the body has received enough nutrients.
In summary, the balance between leptin and ghrelin plays a crucial role in regulating appetite and body weight. In cases of obesity, there is an imbalance in this system, with high levels of leptin and potentially disrupted ghrelin signaling, leading to increased appetite and weight gain.
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This question is part of the following fields:
- Endocrine System
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Question 13
Incorrect
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A 34-year-old male presents with tingling in his thumb, index, and middle finger, along with complaints of excessive fatigue and snoring. Upon examination, he displays a prominent brow ridge and significant facial changes over time. Following blood tests and an MRI scan, the patient is prescribed octreotide. What is the mechanism of action of this medication?
Your Answer:
Correct Answer: Somatostatin analogue
Explanation:Acromegaly is a condition that results from excessive growth hormone production. The release of growth hormone is directly inhibited by somatostatin, which is why somatostatin analogues are used to treat acromegaly.
To answer the question, one must first recognize the symptoms of acromegaly, such as carpal tunnel syndrome, sleep apnea, and changes in facial features over time. The second part of the question involves identifying octreotide as a somatostatin analogue commonly used to treat acromegaly.
While dopamine agonists were previously used to treat acromegaly, they are no longer preferred due to the availability of more effective treatments. Dopamine antagonists have never been used to treat acromegaly. Pegvisomant is an example of a growth hormone antagonist, but antagonists for insulin growth factor-1 release have not yet been developed.
Acromegaly is a condition that can be managed through various treatment options. The first-line treatment for the majority of patients is trans-sphenoidal surgery. However, if the pituitary tumour is inoperable or surgery is unsuccessful, medication may be indicated. One such medication is a somatostatin analogue, which directly inhibits the release of growth hormone. Octreotide is an example of this medication and is effective in 50-70% of patients. Another medication is pegvisomant, which is a GH receptor antagonist that prevents dimerization of the GH receptor. It is administered once daily subcutaneously and is very effective, decreasing IGF-1 levels in 90% of patients to normal. However, it does not reduce tumour volume, so surgery is still needed if there is a mass effect. Dopamine agonists, such as bromocriptine, were the first effective medical treatment for acromegaly but are now superseded by somatostatin analogues and are only effective in a minority of patients. External irradiation may be used for older patients or following failed surgical/medical treatment.
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This question is part of the following fields:
- Endocrine System
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Question 14
Incorrect
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Which one of the following does not trigger insulin secretion?
Your Answer:
Correct Answer: Atenolol
Explanation:The release of insulin is prevented by beta blockers.
Factors that trigger insulin release include glucose, amino acids, vagal cholinergic stimulation, secretin/gastrin/CCK, fatty acids, and beta adrenergic drugs.
Insulin is a hormone produced by the pancreas that plays a crucial role in regulating the metabolism of carbohydrates and fats in the body. It works by causing cells in the liver, muscles, and fat tissue to absorb glucose from the bloodstream, which is then stored as glycogen in the liver and muscles or as triglycerides in fat cells. The human insulin protein is made up of 51 amino acids and is a dimer of an A-chain and a B-chain linked together by disulfide bonds. Pro-insulin is first formed in the rough endoplasmic reticulum of pancreatic beta cells and then cleaved to form insulin and C-peptide. Insulin is stored in secretory granules and released in response to high levels of glucose in the blood. In addition to its role in glucose metabolism, insulin also inhibits lipolysis, reduces muscle protein loss, and increases cellular uptake of potassium through stimulation of the Na+/K+ ATPase pump.
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This question is part of the following fields:
- Endocrine System
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Question 15
Incorrect
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A 25-year-old female visits her GP complaining of chronic thirst, polyuria, and nocturia that have persisted for 2 months. She has a medical history of premenstrual dysphoric disorder diagnosed 3 years ago. After a series of tests, the patient is diagnosed with primary polydipsia. What results are expected from her water deprivation test?
Your Answer:
Correct Answer: High urine osmolality after both fluid deprivation and desmopressin
Explanation:The patient has primary polydipsia, a psychogenic disorder causing excessive drinking despite being hydrated. Urine osmolality is high after both fluid deprivation and desmopressin, as the patient still produces and responds to ADH. Low urine osmolality after both fluid deprivation and desmopressin is typical of nephrogenic DI, while low urine osmolality after fluid deprivation but high after desmopressin is typical of cranial DI. Low urine osmolality after desmopressin and low urine osmolality after fluid deprivation but normal after desmopressin are not commonly seen with any pathological state.
The water deprivation test is a diagnostic tool used to assess patients with polydipsia, or excessive thirst. During the test, the patient is instructed to refrain from drinking water, and their bladder is emptied. Hourly measurements of urine and plasma osmolalities are taken to monitor changes in the body’s fluid balance. The results of the test can help identify the underlying cause of the patient’s polydipsia. Normal results show a high urine osmolality after the administration of DDAVP, while psychogenic polydipsia is characterized by a low urine osmolality. Cranial DI and nephrogenic DI are both associated with high plasma osmolalities and low urine osmolalities.
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This question is part of the following fields:
- Endocrine System
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Question 16
Incorrect
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Mr. Smith is a 54-year-old man who visits your GP clinic for his annual review of his type 2 diabetes. He informs you that he has been managing it through diet for a few years, but lately, he has gained some weight. His latest HbA1C reading is 9.8% (normal range 3.7-5.0%). You suggest continuous dietary advice and prescribe metformin to regulate his blood glucose levels. Which of the following statements about metformin is accurate?
Your Answer:
Correct Answer: It decreases hepatic gluconeogenesis
Explanation:While some diabetic treatments such as insulin and sulfonylureas can lead to weight gain, metformin is not associated with this side effect. Metformin functions by enhancing insulin sensitivity and reducing hepatic gluconeogenesis, without directly impacting insulin secretion from pancreatic beta cells, thus it does not cause significant hypoglycemia. Ghrelin, a hormone that controls appetite, is not influenced by any diabetic medications.
Understanding Diabetes Mellitus: A Basic Overview
Diabetes mellitus is a chronic condition characterized by abnormally raised levels of blood glucose. It is one of the most common conditions encountered in clinical practice and represents a significant burden on the health systems of the developed world. The management of diabetes mellitus is crucial as untreated type 1 diabetes would usually result in death. Poorly treated type 1 diabetes mellitus can still result in significant morbidity and mortality. The main focus of diabetes management now is reducing the incidence of macrovascular and microvascular complications.
There are different types of diabetes mellitus, including type 1 diabetes mellitus, type 2 diabetes mellitus, prediabetes, gestational diabetes, maturity onset diabetes of the young, latent autoimmune diabetes of adults, and other types. The presentation of diabetes mellitus depends on the type, with type 1 diabetes mellitus often presenting with weight loss, polydipsia, polyuria, and diabetic ketoacidosis. On the other hand, type 2 diabetes mellitus is often picked up incidentally on routine blood tests and presents with polydipsia and polyuria.
There are four main ways to check blood glucose, including a finger-prick bedside glucose monitor, a one-off blood glucose, a HbA1c, and a glucose tolerance test. The diagnostic criteria are determined by WHO, with a fasting glucose greater than or equal to 7.0 mmol/l and random glucose greater than or equal to 11.1 mmol/l being diagnostic of diabetes mellitus. Management of diabetes mellitus involves drug therapy to normalize blood glucose levels, monitoring for and treating any complications related to diabetes, and modifying any other risk factors for other conditions such as cardiovascular disease. The first-line drug for the vast majority of patients with type 2 diabetes mellitus is metformin, with second-line drugs including sulfonylureas, gliptins, and pioglitazone. Insulin is used if oral medication is not controlling the blood glucose to a sufficient degree.
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This question is part of the following fields:
- Endocrine System
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Question 17
Incorrect
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A 39-year-old male presents to an endocrine clinic with acromegaly caused by a growth hormone-secreting tumor. The patient is prescribed Octreotide, a somatostatin analogue, to suppress growth hormone release.
What additional hormonal effects can be attributed to somatostatin?Your Answer:
Correct Answer: Decreases secretion of glucagon
Explanation:Somatostatin has an inhibitory effect on the secretion of glucagon, but it does not affect the secretion of estrogen. It also decreases the secretion of insulin, and overproduction of somatostatin can lead to diabetes mellitus. Additionally, somatostatin reduces the secretion of gastrin, which in turn decreases the production of gastric acid by parietal cells. It also decreases the secretion of thyroid stimulating hormone (TSH), resulting in a decrease in the production of thyroxine in the thyroid.
Somatostatin: The Inhibitor Hormone
Somatostatin, also known as growth hormone inhibiting hormone (GHIH), is a hormone produced by delta cells found in the pancreas, pylorus, and duodenum. Its main function is to inhibit the secretion of growth hormone, insulin, and glucagon. It also decreases acid and pepsin secretion, as well as pancreatic enzyme secretion. Additionally, somatostatin inhibits the trophic effects of gastrin and stimulates gastric mucous production.
Somatostatin analogs are commonly used in the management of acromegaly, a condition characterized by excessive growth hormone secretion. These analogs work by inhibiting growth hormone secretion, thereby reducing the symptoms associated with acromegaly.
The secretion of somatostatin is regulated by various factors. Its secretion increases in response to fat, bile salts, and glucose in the intestinal lumen, as well as glucagon. On the other hand, insulin decreases the secretion of somatostatin.
In summary, somatostatin plays a crucial role in regulating the secretion of various hormones and enzymes in the body. Its inhibitory effects on growth hormone, insulin, and glucagon make it an important hormone in the management of certain medical conditions.
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This question is part of the following fields:
- Endocrine System
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Question 18
Incorrect
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A 45-year-old male is recovering from trans-sphenoidal surgery for a non-functioning pituitary adenoma. He reports excessive thirst and increased water intake to the doctors during the ward round, four days after the surgery. The patient's fluid chart shows a urine output of 7 litres in the past 24 hours, and his blood glucose level is 5.2mmol/L. To confirm the diagnosis, the doctors plan to conduct a water-deprivation test and a vasopressin test.
What are the expected results of the urine osmolality investigations, given the likely diagnosis?Your Answer:
Correct Answer: After fluid deprivation, low; after desmopressin, high
Explanation:The patient has developed cranial diabetes insipidus after pituitary surgery. Water deprivation testing showed low urine osmolality after fluid deprivation and high urine osmolality after desmopressin administration. This condition can also be caused by head trauma or occur idiopathically. Water deprivation testing can also be useful for investigating psychogenic polydipsia. Nephrogenic diabetes insipidus is the other main cause, where the kidneys cannot properly respond to vasopressin.
The water deprivation test is a diagnostic tool used to assess patients with polydipsia, or excessive thirst. During the test, the patient is instructed to refrain from drinking water, and their bladder is emptied. Hourly measurements of urine and plasma osmolalities are taken to monitor changes in the body’s fluid balance. The results of the test can help identify the underlying cause of the patient’s polydipsia. Normal results show a high urine osmolality after the administration of DDAVP, while psychogenic polydipsia is characterized by a low urine osmolality. Cranial DI and nephrogenic DI are both associated with high plasma osmolalities and low urine osmolalities.
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This question is part of the following fields:
- Endocrine System
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Question 19
Incorrect
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A 49-year-old man visits the clinic with complaints of muscle cramps and constipation that have been present for a week. He appears to be in good health otherwise. Upon conducting a serum potassium test, you discover that his levels are below the normal range. Your next step is to determine the underlying cause of his hypokalaemia. Which of the following medical conditions is commonly linked to low potassium levels?
Your Answer:
Correct Answer: Cushing's syndrome
Explanation:Cushing’s syndrome is the correct answer as it causes excess cortisol which can exhibit mineralocorticoid activity and lead to hypokalaemia. The kidneys play a major role in maintaining potassium balance, but other factors such as insulin, catecholamines, and aldosterone also influence potassium levels. The other options listed (congenital adrenal hypoplasia, Addison’s, rhabdomyolysis, metabolic acidosis) all cause hyperkalaemia. Addison’s disease and adrenal hypoplasia result in mineralocorticoid deficiency, leading to hyperkalaemia. Acidosis and rhabdomyolysis also cause hyperkalaemia. Symptoms of hypokalaemia include fatigue, muscle weakness, myalgia, muscle cramps, constipation, hyporeflexia, and rarely paralysis.
Causes of Cushing’s Syndrome
Cushing’s syndrome is a condition that can be caused by both endogenous and exogenous factors. However, it is important to note that exogenous causes, such as the use of glucocorticoid therapy, are more common than endogenous ones. The condition can be classified into two categories: ACTH dependent and ACTH independent causes.
ACTH dependent causes of Cushing’s syndrome include Cushing’s disease, which is caused by a pituitary tumor secreting ACTH and producing adrenal hyperplasia. Ectopic ACTH production, which is caused by small cell lung cancer, is another ACTH dependent cause. On the other hand, ACTH independent causes include iatrogenic factors such as steroid use, adrenal adenoma, adrenal carcinoma, Carney complex, and micronodular adrenal dysplasia.
In some cases, a condition called Pseudo-Cushing’s can mimic Cushing’s syndrome. This is often caused by alcohol excess or severe depression and can cause false positive results in dexamethasone suppression tests or 24-hour urinary free cortisol tests. To differentiate between Cushing’s syndrome and Pseudo-Cushing’s, an insulin stress test may be used.
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This question is part of the following fields:
- Endocrine System
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Question 20
Incorrect
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A 33-year-old woman with a history of coeliac disease presents to the emergency department with palpitations, diaphoresis, and tremors. Upon examination, her vital signs reveal a heart rate of 110 bpm and respiratory rate of 24 per min. She displays hand tremors, bulging eyeballs, and diffuse swelling in her neck. Her blood tests show:
TSH 0.1 mU/l
Free T4 32.5 pmol/l
Free T3 12.5 pmol/l
What is the most probable underlying pathophysiology in this patient?Your Answer:
Correct Answer: Antibodies to TSH receptors
Explanation:Graves’ disease is the most probable cause of thyrotoxicosis in a middle-aged woman, particularly if she exhibits exophthalmos. This autoimmune disorder is characterised by the presence of antibodies to the thyroid stimulating hormone (TSH) receptors.
Graves’ Disease: Common Features and Unique Signs
Graves’ disease is the most frequent cause of thyrotoxicosis, which is commonly observed in women aged 30-50 years. The condition presents typical features of thyrotoxicosis, such as weight loss, palpitations, and heat intolerance. However, Graves’ disease also displays specific signs that are not present in other causes of thyrotoxicosis. These include eye signs, such as exophthalmos and ophthalmoplegia, as well as pretibial myxoedema and thyroid acropachy. The latter is a triad of digital clubbing, soft tissue swelling of the hands and feet, and periosteal new bone formation.
Graves’ disease is characterized by the presence of autoantibodies, including TSH receptor stimulating antibodies in 90% of patients and anti-thyroid peroxidase antibodies in 75% of patients. Thyroid scintigraphy reveals a diffuse, homogenous, and increased uptake of radioactive iodine. These features help distinguish Graves’ disease from other causes of thyrotoxicosis and aid in its diagnosis.
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This question is part of the following fields:
- Endocrine System
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Question 21
Incorrect
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A 65-year-old male with a diagnosis of lung cancer presents with fatigue and lightheadedness. Upon examination, the following results are obtained:
Plasma sodium concentration 115 mmol/L (137-144)
Potassium 3.5 mmol/L (3.5-4.9)
Urea 3.2 mmol/L (2.5-7.5)
Creatinine 67 µmol/L (60-110)
What is the probable reason for his symptoms based on these findings?Your Answer:
Correct Answer: Syndrome of inappropriate ADH secretion
Explanation:Syndrome of Inappropriate ADH Secretion
Syndrome of inappropriate ADH secretion (SIADH) is a condition characterized by low levels of sodium in the blood. This is caused by the overproduction of antidiuretic hormone (ADH) by the posterior pituitary gland. Tumors such as bronchial carcinoma can cause the ectopic elaboration of ADH, leading to dilutional hyponatremia. The diagnosis of SIADH is one of exclusion, but it can be supported by a high urine sodium concentration with high urine osmolality.
Hypoadrenalism is less likely to cause hyponatremia, as it is usually associated with hyperkalemia and mild hyperuricemia. On the other hand, diabetes insipidus is a condition where the kidneys are unable to reabsorb water, leading to excessive thirst and urination.
It is important to diagnose and treat SIADH promptly to prevent complications such as seizures, coma, and even death. Treatment options include fluid restriction, medications to block the effects of ADH, and addressing the underlying cause of the condition.
In conclusion, SIADH is a condition that can cause low levels of sodium in the blood due to the overproduction of ADH. It is important to differentiate it from other conditions that can cause hyponatremia and to treat it promptly to prevent complications.
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This question is part of the following fields:
- Endocrine System
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Question 22
Incorrect
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The following results were obtained on a 57-year-old male who complains of fatigue:
Free T4 9.8 pmol/L (9.0-25.0)
TSH 50.02 mU/L (0.27-4.20)
What physical signs would you anticipate during the examination?Your Answer:
Correct Answer: Slow relaxation of tendon jerks
Explanation:Symptoms and Signs of Hypothyroidism
Hypothyroidism is a condition that is characterized by an underactive thyroid gland, which leads to a decrease in the production of thyroid hormones. This condition is associated with several symptoms and signs, including a relative bradycardia, slow relaxation of tendon jerks, pale complexion, thinning of the hair, and weight gain. In severe cases of hypothyroidism, hypothermia may also be present.
A relative bradycardia refers to a slower than normal heart rate, which is a common symptom of hypothyroidism. Additionally, slow relaxation of tendon jerks is another sign of this condition. This refers to a delay in the relaxation of muscles after a reflex is elicited. Other physical signs of hypothyroidism include a pale complexion and thinning of the hair, which can be attributed to a decrease in metabolic activity.
Weight gain is also a common symptom of hypothyroidism, as the decrease in thyroid hormone production can lead to a slower metabolism and decreased energy expenditure. In severe cases of hypothyroidism, hypothermia may also be present, which refers to a body temperature that is lower than normal.
It is important to note that while a thyroid bruit is typical of Graves’ thyrotoxicosis, it is not a common sign of hypothyroidism. Overall, the symptoms and signs of hypothyroidism can vary in severity and may require medical intervention to manage.
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This question is part of the following fields:
- Endocrine System
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Question 23
Incorrect
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A teenage girl and her mother come to the doctor's office with concerns about ambiguous genitalia. After gathering information and conducting various tests, the doctor determines that the cause is congenital adrenal hyperplasia, which is linked to a deficiency in which specific enzyme?
Your Answer:
Correct Answer: 21-hydroxylase
Explanation:Insufficient production of cortisol and compensatory adrenal hyperplasia are the consequences of 21-hydroxylase deficiency. This leads to elevated androgen production and ambiguous genitalia. However, enzymes such as 5-a reductase, aromatase, 17B-HSD, and aldosterone synthase are not involved in this disorder. Other enzymes, including 11-beta hydroxylase and 17-hydroxylase, may also be involved.
Congenital adrenal hyperplasia is a genetic condition that affects the adrenal glands and can result in various symptoms depending on the specific enzyme deficiency. One common form is 21-hydroxylase deficiency, which can cause virilization of female genitalia, precocious puberty in males, and a salt-losing crisis in 60-70% of patients during the first few weeks of life. Another form is 11-beta hydroxylase deficiency, which can also cause virilization and precocious puberty, as well as hypertension and hypokalemia. A third form is 17-hydroxylase deficiency, which typically does not cause virilization in females but can result in intersex characteristics in boys and hypertension.
Overall, congenital adrenal hyperplasia can have significant impacts on a person’s physical development and health, and early diagnosis and treatment are important for managing symptoms and preventing complications.
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This question is part of the following fields:
- Endocrine System
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Question 24
Incorrect
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A 35-year-old woman is referred to the endocrine clinic due to missed periods and lactation. She has also gained weight and experiences vaginal dryness. The endocrinologist decides to measure her prolactin levels. What hormone is responsible for suppressing the release of prolactin from the pituitary gland?
Your Answer:
Correct Answer: Dopamine
Explanation:Dopamine consistently prevents the release of prolactin.
Understanding Prolactin and Its Functions
Prolactin is a hormone that is produced by the anterior pituitary gland. Its primary function is to stimulate breast development and milk production in females. During pregnancy, prolactin levels increase to support the growth and development of the mammary glands. It also plays a role in reducing the pulsatility of gonadotropin-releasing hormone (GnRH) at the hypothalamic level, which can block the action of luteinizing hormone (LH) on the ovaries or testes.
The secretion of prolactin is regulated by dopamine, which constantly inhibits its release. However, certain factors can increase or decrease prolactin secretion. For example, prolactin levels increase during pregnancy, in response to estrogen, and during breastfeeding. Additionally, stress, sleep, and certain drugs like metoclopramide and antipsychotics can also increase prolactin secretion. On the other hand, dopamine and dopaminergic agonists can decrease prolactin secretion.
Overall, understanding the functions and regulation of prolactin is important for reproductive health and lactation.
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This question is part of the following fields:
- Endocrine System
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Question 25
Incorrect
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A 59-year-old man with a known history of type-2 diabetes comes for a check-up. He is currently on metformin only for his diabetes and reports compliance with the prescribed regimen.
His HbA1c is 63 mmol/mol (target = 53mmol/mol) and the patient and clinician agree to initiate a sulfonylurea along with his metformin.
What is the primary mode of action of the new treatment?Your Answer:
Correct Answer: Increases stimulation of insulin secretion by pancreatic B-cells and decreases hepatic clearance of insulin
Explanation:Sulfonylureas are a type of oral hypoglycemic agent that stimulate insulin secretion by pancreatic B-cells and reduce the clearance of insulin by the liver. They are known as insulin secretagogues.
Sulfonylureas are a type of medication used to treat type 2 diabetes mellitus. They work by increasing the amount of insulin produced by the pancreas, but only if the beta cells in the pancreas are functioning properly. Sulfonylureas bind to a specific channel on the cell membrane of pancreatic beta cells, known as the ATP-dependent K+ channel (KATP).
While sulfonylureas can be effective in managing diabetes, they can also cause some adverse effects. The most common side effect is hypoglycemia, which is more likely to occur with long-acting preparations like chlorpropamide. Another common side effect is weight gain. However, there are also rarer side effects that can occur, such as hyponatremia (low sodium levels) due to inappropriate ADH secretion, bone marrow suppression, hepatotoxicity (liver damage), and peripheral neuropathy.
It is important to note that sulfonylureas should not be used during pregnancy or while breastfeeding.
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This question is part of the following fields:
- Endocrine System
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Question 26
Incorrect
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A 20-year-old man was admitted to hospital with a 5 day history of vomiting, fever and chills. He developed a purpuric rash on his lower limbs and abdomen. During examination, the patient was found to have a pulse rate of 100 beats per minute and a systolic blood pressure of 70mmHg. A spinal tap was performed for CSF microscopy and a CT scan revealed adrenal haemorrhage. Based on the CT scan, the doctor suspected Waterhouse-Friderichsen syndrome. What is the most common bacterial cause of this syndrome?
Your Answer:
Correct Answer: Neisseria meningitidis
Explanation:The most frequent cause of Waterhouse-Friderichsen syndrome is Neisseria meningitidis. This syndrome is characterized by adrenal gland failure caused by bleeding into the adrenal gland. Although any organism that can induce disseminated intravascular coagulation can lead to adrenal haemorrhage, neisseria meningitidis is the most common cause and therefore the answer.
Understanding Waterhouse-Friderichsen Syndrome
Waterhouse-Friderichsen syndrome is a condition that occurs when the adrenal glands fail due to a previous adrenal haemorrhage caused by a severe bacterial infection. The most common cause of this condition is Neisseria meningitidis, but it can also be caused by other bacteria such as Haemophilus influenzae, Pseudomonas aeruginosa, Escherichia coli, and Streptococcus pneumoniae.
The symptoms of Waterhouse-Friderichsen syndrome are similar to those of hypoadrenalism, including lethargy, weakness, anorexia, nausea and vomiting, and weight loss. Other symptoms may include hyperpigmentation, especially in the palmar creases, vitiligo, and loss of pubic hair in women. In severe cases, a crisis may occur, which can lead to collapse, shock, and pyrexia.
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This question is part of the following fields:
- Endocrine System
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Question 27
Incorrect
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A 65-year-old man with a history of poorly-controlled type 2 diabetes presents to the emergency department with altered mental status. His daughter reports that he has been complaining of increased thirst and urination over the past few days and has been skipping his insulin injections. On examination, he is dehydrated with a GCS of 3. His vital signs are recorded, and he is intubated and given ventilatory support. An arterial blood gas shows mild metabolic acidosis and his capillary blood glucose is undetectable. What is the next most appropriate step in his treatment?
Your Answer:
Correct Answer: 0.9% sodium chloride
Explanation:In the ABCDE approach, the patient should be promptly given sodium chloride to restore their intravascular volume and maintain circulatory function. However, insulin is not recommended as an initial treatment for HHS. This is because glucose in the intravascular space helps maintain circulating volume, which is crucial for dehydrated patients. Administering insulin before fluid resuscitation can cause a reduction in intravascular volume and worsen hypotension. It may also worsen pre-existing hypokalaemia by driving potassium into the intracellular space. Potassium chloride should be administered only after fluid resuscitation and guided by potassium levels obtained from an arterial blood gas. Thiamine supplementation is not indicated at the moment as urgent resuscitation should be the priority.
Hyperosmolar hyperglycaemic state (HHS) is a serious medical emergency that can be challenging to manage and has a high mortality rate of up to 20%. It is typically seen in elderly patients with type 2 diabetes mellitus (T2DM) and is caused by hyperglycaemia leading to osmotic diuresis, severe dehydration, and electrolyte imbalances. HHS develops gradually over several days, resulting in extreme dehydration and metabolic disturbances. Symptoms include polyuria, polydipsia, lethargy, nausea, vomiting, altered consciousness, and focal neurological deficits. Diagnosis is based on hypovolaemia, marked hyperglycaemia, significantly raised serum osmolarity, and no significant hyperketonaemia or acidosis.
Management of HHS involves fluid replacement with IV 0.9% sodium chloride solution at a rate of 0.5-1 L/hour, depending on clinical assessment. Potassium levels should be monitored and added to fluids as needed. Insulin should not be given unless blood glucose stops falling while giving IV fluids. Patients are at risk of thrombosis due to hyperviscosity, so venous thromboembolism prophylaxis is recommended. Complications of HHS include vascular complications such as myocardial infarction and stroke.
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This question is part of the following fields:
- Endocrine System
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Question 28
Incorrect
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A 36-year-old male visits the GP after being diagnosed with Conn's syndrome, which causes excessive production of aldosterone. How will this affect the balance of sodium and potassium in his blood?
Your Answer:
Correct Answer: Increased sodium, decreased potassium
Explanation:Hypertension, hypernatraemia, and hypokalemia are common symptoms of primary hyperaldosteronism.
The adrenal gland produces aldosterone, which is responsible for regulating potassium levels. Its primary function is to increase sodium absorption and decrease potassium secretion in the distal tubules and collecting duct of the nephron. As a result, sodium levels increase while potassium levels decrease.
Primary hyperaldosteronism is a condition characterized by hypertension, hypokalaemia, and alkalosis. It was previously believed that adrenal adenoma, also known as Conn’s syndrome, was the most common cause of this condition. However, recent studies have shown that bilateral idiopathic adrenal hyperplasia is responsible for up to 70% of cases. It is important to differentiate between the two causes as it determines the appropriate treatment. Adrenal carcinoma is an extremely rare cause of primary hyperaldosteronism.
To diagnose primary hyperaldosteronism, the 2016 Endocrine Society recommends a plasma aldosterone/renin ratio as the first-line investigation. This test should show high aldosterone levels alongside low renin levels due to negative feedback from sodium retention caused by aldosterone. If the results are positive, a high-resolution CT abdomen and adrenal vein sampling are used to differentiate between unilateral and bilateral sources of aldosterone excess. If the CT is normal, adrenal venous sampling (AVS) can be used to distinguish between unilateral adenoma and bilateral hyperplasia.
The management of primary hyperaldosteronism depends on the underlying cause. Adrenal adenoma is treated with surgery, while bilateral adrenocortical hyperplasia is managed with an aldosterone antagonist such as spironolactone. It is important to accurately diagnose and manage primary hyperaldosteronism to prevent complications such as cardiovascular disease and stroke.
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This question is part of the following fields:
- Endocrine System
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Question 29
Incorrect
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A 44-year-old man has been diagnosed with type II diabetes mellitus but cannot tolerate metformin therapy. What is the mechanism of action of alogliptin, which has been prescribed as an alternative?
Your Answer:
Correct Answer: Reduce the peripheral breakdown of incretins
Explanation:Gliptins (DPP-4 inhibitors) work by inhibiting the enzyme DPP-4, which reduces the breakdown of incretin hormones such as GLP-1. This leads to a glucose-dependent increase in insulin secretion and a reduction in glucagon secretion, ultimately regulating glucose homeostasis. However, gliptins do not increase the production of GLP-1, directly stimulate the release of insulin from pancreatic beta cells, inhibit the SGLT2 receptor, or reduce insulin resistance.
Diabetes mellitus is a condition that has seen the development of several drugs in recent years. One hormone that has been the focus of much research is glucagon-like peptide-1 (GLP-1), which is released by the small intestine in response to an oral glucose load. In type 2 diabetes mellitus (T2DM), insulin resistance and insufficient B-cell compensation occur, and the incretin effect, which is largely mediated by GLP-1, is decreased. GLP-1 mimetics, such as exenatide and liraglutide, increase insulin secretion and inhibit glucagon secretion, resulting in weight loss, unlike other medications. They are sometimes used in combination with insulin in T2DM to minimize weight gain. Dipeptidyl peptidase-4 (DPP-4) inhibitors, such as vildagliptin and sitagliptin, increase levels of incretins by decreasing their peripheral breakdown, are taken orally, and do not cause weight gain. Nausea and vomiting are the major adverse effects of GLP-1 mimetics, and the Medicines and Healthcare products Regulatory Agency has issued specific warnings on the use of exenatide, reporting that it has been linked to severe pancreatitis in some patients. NICE guidelines suggest that a DPP-4 inhibitor might be preferable to a thiazolidinedione if further weight gain would cause significant problems, a thiazolidinedione is contraindicated, or the person has had a poor response to a thiazolidinedione.
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This question is part of the following fields:
- Endocrine System
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Question 30
Incorrect
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A 25-year-old woman presents to the endocrinology clinic with a diagnosis of Grave's disease. The diagnosis was made based on her elevated levels of thyroid hormones T3 and T4, as well as symptoms of heat intolerance, weight loss, and tremors. Typically, where are the receptors for thyroid hormones found?
Your Answer:
Correct Answer: Nucleus
Explanation:Thyroid hormones can enter cells through diffusion or carriers. Once inside, they bind to intracellular DNA-binding proteins called thyroid hormone receptors located in the nucleus. This binding forms a complex that attaches to the thyroid hormone responsive element on DNA. The outcome of this process is an increase in mRNA production, protein synthesis, Na/K ATPase, mitochondrial function leading to higher oxygen consumption, and adrenoceptors.
Thyroid disorders are commonly encountered in clinical practice, with hypothyroidism and thyrotoxicosis being the most prevalent. Women are ten times more likely to develop these conditions than men. The thyroid gland is a bi-lobed structure located in the anterior neck and is part of a hypothalamus-pituitary-end organ system that regulates the production of thyroxine and triiodothyronine hormones. These hormones help regulate energy sources, protein synthesis, and the body’s sensitivity to other hormones. Hypothyroidism can be primary or secondary, while thyrotoxicosis is mostly primary. Autoimmunity is the leading cause of thyroid problems in the developed world.
Thyroid disorders can present in various ways, with symptoms often being the opposite depending on whether the thyroid gland is under or overactive. For example, hypothyroidism may result in weight gain, while thyrotoxicosis leads to weight loss. Thyroid function tests are the primary investigation for diagnosing thyroid disorders. These tests primarily look at serum TSH and T4 levels, with T3 being measured in specific cases. TSH levels are more sensitive than T4 levels for monitoring patients with existing thyroid problems.
Treatment for thyroid disorders depends on the cause. Patients with hypothyroidism are given levothyroxine to replace the underlying deficiency. Patients with thyrotoxicosis may be treated with propranolol to control symptoms such as tremors, carbimazole to reduce thyroid hormone production, or radioiodine treatment.
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This question is part of the following fields:
- Endocrine System
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