Endocrine Pathology 2 Flashcards

0
Q

Pseudohypoparathyroidism

A

Unresponsiveness of kidney to PTH
Hypocalcemia, shortened 4th/5th digits
Autosomal dominant
Short stature

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1
Q

Hypoparathyroidism causes

A

Accidental surgical excision of Parathyroid glands or autoimmune destruction
Chvostek sign - tap face, leads to face contraction
Trousseau sign - occlusion of brachial artery with BP cuff

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2
Q

Familial hypocalciuric hypercalcemia

A

Defective calcium sensing receptor of parathyroid cells

PTH cant be suppressed when Ca is high

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3
Q

Primary Hyperparathyroidism

A

Due to parathyroid adenoma or hyperplasia
Increased PTH, Ca, ALP, cAMP, low phosphate
Osteitis fibrosa cystica - cystic bone spaces filled with brown fibrous tissue
Stones, Bones, groans with psychiatric overtones

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4
Q

Secondary and tertiary hyperparathyroidism

A

Secondary - chronic renal failure, low calcium, increased PTH, ALP, PO3-
Tertiary - refractory hyperparathyroidism after kidney replacement PTH is still high and so is Calcium as a result

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5
Q

Diabetes Insipidus

A

Intense thirst and polyuria with inability to concentrate urine due to ADH lack or insensitivity
Central DI tx - intra nasal Desmopressin acetate and hydration
Nephrogenic DI to - HCTZ, indomethacin, amilioride and hydration

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6
Q

SIADH

A

Excess free water retention, euvolemic hyponatremia with urinary Na secretion, urine osmolality greater than serum osmolality
Body response - Low aldosterone which can lead to cerebral edema, seizures
Correct slowly to prevent demyelination syndrome
Tx- fluid restriction, IV hypertonic saline, conivapatan, demeclocycline

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7
Q

Hypopituitarism

A

Sheehan syndrome - ischemic infarction of pituitary
Empty sella syndrome - atrophy or compression of pituitary
Pituitary apoplexy - sudden hemorrhage of pituitary gland
Tx by HRT

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8
Q

Diabetes mellitus acute manifestation

A

Polydypsia, polyuria, polyphagia, weight loss, diabetic keto acidosis in type 1, hyperosmolar coma in type 2.

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9
Q

Diabetic mellitus chronic complications

A

Non enzymatic glycation
- small vessel disease, retinopathy, glaucoma, neuropathy, nephropathy
- large vessel atherosclerosis, CAD, peripheral vascular occlusive disease, gangrene, MI
Osmotic damage
- sorbitol accumulation in organs with aldosterone reductase, neuropathy, cataracts

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10
Q

Diabetes types and diagnosis

A

Type 1 - autoimmune destruction of beta cells, juvenile, not associated with obesity, HLA DR3 and HLA DR4, severe glucose intolerance, high insulin sensitivity, islet leukocyte infiltrate, KETOACIDOSIS

Type 2 - strong genetic predisposition, no HLA association, islet amyloid peptide deposits

Dx - fasting serum glucose, oral glucose tolerance test, HbA1c

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11
Q

Diabetes ketoacidosis, symptoms, labs, complications, tx

A

Due to increased insulin requirements from increased stress
Excess fat breakdown and increased ketogenesis from increased fatty acids ~>ketone bodies (beta hydroxy butyrate >acetoacetate)

Kussmaul respiration, nause/vomiting, abdominal pain, psychosis, fruity breath odor, dehydration

Labs - hyperglycemia, low bicarb, hyperkalemia but total body K depletion

Complications - mucor mycosis, cerebral edema, cardiac arrythmia, HF

Tx - IV Fluids, insulin, K, glucose

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12
Q

Glucagonoma and Insulinoma

A

Glucagonoma- presents with 4Ds Dermatitis, diabetes, DVT, depression
Insulinoma - decreased blood glucose and increased C peptide. Tx is surgery

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13
Q

Carcinoid syndrome

A

Metastatic tumor secreting seretonin , rosettes on histology
Recurrent diarrhea, flushing, asthma, right side valvular disease, 5 HIAA in urine, niacin deficiency
Rule of 1/3 - metastasize, present with secondary malignancy, multiple

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14
Q

Zollinger-Ellison syndrome

A

Gastrin secreting tumor, ulcers, abdominal pain, gastrin remains elevated after secretin administration which should not in healthy patients

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15
Q

Multiple Endocrine Neoplasias (MEN)

A

Autosomal dominant inheritance
MEN 1 - 3 Ps parathyroid, pituitary, pancreas (Zollinger-Ellison, Insulinoma, VIPomas)
MEN 2A - 2 Ps parathyroid, pheochromocytoma + medullary thyroid cancer
MEN 2B - 1 P pheochromocytoma + medullary thyroid cancer + neuroma

MEN 2 A and B associatd with marfanian habitus and RET gene mutation