Conn's Syndrome
C. Expansion of his plasma volume (e.g. through putting him on a high salt diet) should be able to suppress his serum aldosterone level
Conn's Syndrome
Conn's Syndrome
- Primary hyperaldosteronism results from autonomous aldosterone secretion, which, in turn, leads to suppression of renin secretion.
- Primary aldosteronism usually occurs in individuals between the ages of 30 and 50 years and accounts for 1% of cases of hypertension.
- Primary hyperaldosteronism is usually associated with hypokalemia; however, more patients with Conn's syndrome are being diagnosed with normal potassium levels.
- Most cases result from a solitary functioning adrenal adenoma (approximately 70%) and idiopathic bilateral hyperplasia (30%).
- Adrenocortical carcinoma and glucocorticoid suppressible hyperaldosteronism are rare, each accounting for less than 1% of cases.
- Patients typically present with hypertension, which is longstanding, moderate to severe, and may be difficult to control despite multiple-drug therapy. Other symptoms include muscle weakness, polydipsia, polyuria, nocturia, headaches, and fatigue. Weakness and fatigue are related to the presence of hypokalemia.
- Hypokalemia is a common finding and hyperaldosteronism must be suspected in any hypertensive patient who presents with coexisting hypokalemia while on diuretic therapy, despite potassium replacements.
- Patients with primary hyperaldosteronism have an elevated plasma aldosterone concentration (PAC) level with a suppressed plasma renin activity (PRA); a PAC:PRA ratio of 25 to 30:1 is strongly suggestive of the diagnosis.
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Subacute granulomatous thyroiditis
THYROIDITIS
- Acute - Bacterial abscess- rare.
- Subacute granulomatous (de Quervain's) thyroiditis. Uncommon. A viral etiology is suspected but not proved. The patient has symmetrical or focal enlargement with a painful and firm gland (hence also known as 'painful thyroiditis'). Transient thyrotoxicosis may be present due to destruction of the thyroid follicles with release of thyroid hormones. Microscopically, the gland shows granulomatous inflammation, histiocytic giant cells, and lymphocytes. It is a self-limiting disease and the patient generally recover after several weeks or months.
- Subacute lymphocytic thyroiditis: Also referred to as "painless", "silent", or "postpartum" thyroiditis. Histologically, it is part of the spectrum of autoimmune thyroditis and the biopsy shows lymphocytic infiltrate but not as striking as in Hashimoto's thyroiditis. Moreover, the autoimmune reactions are inconstant and evanescent. Clinically, it is regarded as a form of "subacute thyroiditis". Fifty percent of these patients will develop transient thyrotoxic symptoms because an excess of preformed hormone leaks from the thyroid gland due to inflammation. New hormone formation is decreased however, owing to the suppression of TSH secretion by the hormone excess. Since the inflammatory disorder is transitory and since stores of preformed hormones are ultimately depleted, the thyrotoxicosis is self-limited and often followed by a transient period of thyroid hormone insufficiency (hypothyroidism). However, a small number of the patients assessed a decade later will show permanent hypothyroidism due to more severe inflammation destroying the thyroid parenchyma.
- Chronic lymphocytic (Hashimoto's) thyroiditis. This is the most common form of thyroiditis. It is an autoimmune disease. Classically, the patient has painless bilateral diffuse enlargement caused by lymphoid infiltration. The serum antimicrosomal antibody titre is elevated. The thyroid follicles undergo destruction and the cytoplasm of the follicular cells undergo eosinophilic change (Hurthle cells). The inflammation may resolve; if not, fibrosis may develop. Patients are euthyroid until the late (fibrotic) stage; then often become hypothyroid (NOTE: Hashimoto's thyroiditis is a frequent cause of hypothyroidism).
- Riedel's Thyroiditis - Very rare disease characterized by dense fibrosis (stony hard gland). It is often associated with idiopathic fibrosis of the mediastinum and retroperitoneum.
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Menningococcemia
The Correct answer is B. 5 year old boy with meningismus, shock and diffuse cutaneous petechial hemorrhages
Menningococcemia --
Menningococcemia --
- intravascular multiplication of N. meningitidis in the blood can result in a petechial rash (minute
hemorrhagic spots the size of a pin that do not blanch when pressed).
- The rash can enlarge if the organisms multiply in the blood to the leading to fulminant meningoccemia (Waterhouse-Friderichsen syndrome--bilateral hemorrhage into the adrenals).
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Waterhouse-Friderichsen Syndrome
The correct answer is B. Massive bilateral adrenal hemorrhage complicating septicemic infection
Waterhouse-Friderichsen Syndrome is massive bilateral adrenal hemorrhage and shock caused by
meningococcal septicemia. Usually fatal.
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Adrenal Cortical Adenoma
The correct answer is E. Commonly show bright-yellow to orange discoloration on cut section
Cortical Adenoma –
Cortical Adenoma –
- Adenomas are circumscribed, discrete tumour. They are usually small, and seldom weigh more than 150 grams.
- Cut surface is bright yellow due to lipid-laden tumour cells.
- Non-functioning adenomas are more common than functioning (hormonally active) adenomas. Most non-functioning adenomas are clinically silent (unless they are large) and are found incidentally at autopsy.
- Functioning cortical adenomas usually hyper-secrete a single hormones, "pure", such as cortisol with resultant.
- Cushing's features or aldosterone with hyperaldosteronism.
- The combined presence of cortisol and androgen or mineralocorticoid excess suggests the possibility that the tumour may be a cortical carcinoma.
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Adrenal Crisis or Insufficiency
B. Hyperkalemia, hypotension, metabolic acidosis and hyponatremia
- Adrenal insufficiency should be suspected in patients with clinical features or disease processes associated
with adrenal dysfunction. These include sepsis, HIV infection, head trauma, bilateral flank pain, and DIC.
- Hypotension that is refractory to fluid and requires vasopressors is a common presentation. One should always suspect adrenal insufficiency in patients with unexplained hyponatremia, hypokalemia, hypoglycemia, or eosinophilia.
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Endocrinology MCQ Answer 077
The Correct Answer is B. Congenital 11-beta hydroxylase deficiency
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Endocrinology MCQ Answer 076
The Correct Answer is A. Congenital 21-hydroxylase deficiency
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Endocrinology MCQ Answer 073
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Endocrinology MCQ Answer 074
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Endocrinology MCQ Answer 071
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Endocrinology MCQ Answer 070
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Endocrinology MCQ Answer 069
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Endocrinology MCQ Answer 068
The Correct Answer is C. Sheets of small spindle cells between islands of amorphous pink material showing apple green birefringence on Congo red staining
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Endocrinology MCQ Answer 067
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Endocrinology MCQ Answer 065
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Endocrinology MCQ Answer 067
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Endocrinology MCQ Answer 066
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Endocrinology MCQ Answer 063
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Endocrinology MCQ Answer 062
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Endocrinology MCQ Answer 061
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Endocrinology MCQ Answer 059
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Endocrinology MCQ Answer 060
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Endocrinology MCQ Answer 058
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Endocrinology MCQ Answer 057
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Endocrinology MCQ Answer 056
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