Endocrine Tumors Flashcards

1
Q

Presents with watery diarrhea, flushing, abdominal cramps, wheezing (bronchospasm/ Asthma-like) and murmur (cardiac valvular abnormalities)
± telangiectasias

If untreated complications can lead to:
skin rash, diarrhea, and memory impairement

A

Carcinoid Syndrome
(locations: Small intestine, Lungs, Colon)

Carcinoid cells (endocrine tumor) cause increased production of serotonin from tryptophan (required for niacin), resulting in niacin deficiency (ie, pellagra → dermatitis, diarrhea, and dementia)

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2
Q

Treatment for Carcinoid Syndrome

A

Octreotide (somatostatin analogue) for symptomatic patients
& prior to surgery/anesthesia

Surgery for liver metastases

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3
Q

Elevated 24-hr urinary excretion of 5-HIAA (5-hydroxyindoleacetic acid) is seen in what disorder?

A

Carcinoid Syndrome

(Get CT abd/pelv)

OctreoScan to detect metastases
Echo (if murmur)

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4
Q

Presents with episodic headache, sweating & tachycardia
HTN accompanied by unexplained Hyperglycemia.

Imaging: Adrenal mass

A

Pheochromacytoma

Urine or plasma metanephrine levels
Confirmatory abdominal imaging for ↑ metanephrines

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5
Q

Treatment for Pheochromacytoma (2)

A

alpha blocker before beta blocker

Phenoxybenzamine, Terazosin

Then surgical resection

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6
Q

In pheochromocytoma, Beta-blocker therapy in the absence of (or before) alpha-adrenergic blockade can lead to lethal hypertensive crisis due to _____.

A

unopposed alpha-1 stimulation

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7
Q

In pheochromocytoma, Beta-blocker therapy in the absence of (or before) alpha-adrenergic blockade can lead to lethal ____

A

hypertensive crisis

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8
Q

Presents with watery diarrhea, flushing, lethargy, nausea, muscle weakness/cramps
Labs show:
hypokalemia
hypercalcemia
hyperglycemia
Gastric hypochloremia

Imaging: pancreatic mass

Diagnosis?

A

VIPoma
a pancreatic tumor: pancreatic cells that produce vasoactive intestinal peptide (VIP).

Most patients develop VIPoma syndrome (pancreatic cholera) with watery diarrhea, muscle weakness/cramps (due to hypokalemia), and hypo- or achlorhydria (due to decreased gastric acid secretion).
Stool studies are consistent with secretory diarrhea;
a VIP level >75 pg/mL confirms diagnosis.

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9
Q

Treatment for VIPoma (2)

A

Octreotide (inhibits VIP secretion)
Tumor resection

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10
Q

Hypertensive crises can be triggered by palpation of the tumor on abdominal exam

A

Pheochromacytoma

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11
Q

Treat PHEochromocytoma with PHEnoxybenzamine, but remember that Alpha blockers should be given Ahead and Beta blockers Behind.

A

FYI

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12
Q

Pheochromacytomas are catecholamine-producing tumors arising from chromaffin cells of the adrenal medulla.

catecholamine-surges cause severe hypertension in patients & can be precipitated by ___ , ___, and a number of medications.

A

surgical procedures
induction of anesthesia

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13
Q

Young adult presents with:
Cerebellar & retinal hemangioblastomas
Pheochromocytoma
± Renal cell carcinoma

Diagnosis?

A

Von Hippel-Lindau disease

Surveillance
Eye/retinal exams
Urine metanephrines
MRI of the brain, spine & abdomen

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14
Q

Presents with watery diarrhea, abdominal cramps, worsening painful, pruritic rash, weight loss, and hyperglycemia

A
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15
Q

Presents with watery diarrhea, abdominal cramps, worsening painful, pruritic rash, weight loss, and hyperglycemia

± anemia

Diagnosis?

A

Glucagonoma

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16
Q

Treatment for Glucagonoma?

A

Octreotide (if tumor is inoperable)

17
Q

Presents with Weight loss

Necrolytic migratory erythema erythematous papules that coalesce to form large, indurated plaques with central clearing

Diabetes mellitus/hyperglycemia
Gastrointestinal symptoms (diarrhea, anorexia, abdominal pain)

A

Glucagonoma

18
Q

MEN 1 disordeers

A

Primary hyperparathyroidism (parathyroid adenomas or hyperplasia- Hypercalcemia)

Pituitary tumors (prolactin, visual defects)

Pancreatic tumors (especially gastrinomas)

19
Q

Men 2A disorders

A

Medullary thyroid cancer (↑ calcitonin)

Pheochromocytoma

Primary hyperparathyroidism (hypercalcemia, kidney stones)

20
Q

Men 2B disorders

A

Medullary thyroid cancer (↑ calcitonin)

Pheochromocytoma

Mucosal neuromas/marfanoid habitus

21
Q

Presents in a child with pituitary hormone deficiency sxs (diabetes insipidus, growth failure) and visual field defects.

A

Craniopharyngeoma

bitemporal hemianopsia
suprasellar mass with cysts and/or calcification

22
Q

Patients with a macroprolactinoma (>1 cm) or a symptomatic prolactinoma should be treated with ____ which can lower prolactin levels and reduce tumor size.

A

dopaminergic agonists
(cabergoline, bromocriptine)

23
Q

Exogenous insulin-induced hypoglycemia
High serum insulin levels
___ c-peptide levels

A

low

(High C-peptide levels in insulinoma)