Key Associations part 3 Flashcards
Congenital adrenal hyperplasia, hypotension
21-hydroxylase deficiency
Hypopituitarism
Pituitary adenoma (usually benign tumor)
Congenital hypothyroidism (cretinism)
Thyroid dysgenesis/dyshormonogenesis, iodine deficiency
Thyroid cancer
Papillary carcinoma (childhood irradiation)
Hypoparathyroidism
Accidental excision during thyroidectomy
1° hyperparathyroidism
Adenomas, hyperplasia, carcinoma
2° hyperparathyroidism
Hypocalcemia of chronic kidney disease
Cushing syndrome
Iatrogenic (from corticosteroid therapy)
Adrenocortical adenoma (secretes excess cortisol)
ACTH-secreting pituitary adenoma (Cushing disease)
Paraneoplastic (due to ACTH secretion by tumors)
1° hyperaldosteronism
Adrenal hyperplasia or adenoma
Tumor of the adrenal medulla (kids)
Neuroblastoma (malignant)
Tumor of the adrenal medulla (adults)
Pheochromocytoma (usually benign)
Refractory peptic ulcers and high gastrin levels
Zollinger-Ellison syndrome (gastrinoma of duodenum or pancreas), associated with MEN1
Esophageal cancer
Squamous cell carcinoma (worldwide); adenocarcinoma (US)
Acute gastric ulcer associated with CNS injury
Cushing ulcer (high intracranial pressure stimulates vagal gastric H+ secretion)
Acute gastric ulcer associated with severe burns
Curling ulcer (greatly reduced plasma volume results in sloughing of gastric mucosa)
Bilateral ovarian metastases from gastric carcinoma
Krukenberg tumor (mucin-secreting signet ring cells)
Chronic atrophic gastritis (autoimmune)
Predisposition to gastric carcinoma (can also cause pernicious anemia)
Alternating areas of transmural inflammation and normal colon
Skip lesions (Crohn disease)
Site of diverticula
Sigmoid colon
Diverticulum in pharynx
Zenker diverticulum (diagnosed by barium swallow)
Hepatocellular carcinoma
HBV (+/– cirrhosis) or other causes of cirrhosis (eg, alcoholic liver disease, hemochromatosis), aflatoxins
Congenital conjugated hyperbilirubinemia (black liver)
Dubin-Johnson syndrome (inability of hepatocytes to secrete conjugated bilirubin into bile)
Hereditary harmless jaundice
Gilbert syndrome (benign congenital unconjugated hyperbilirubinemia)
Wilson disease
Hereditary ATP7B mutation (copper buildup in liver, brain, cornea, kidneys)
Hemochromatosis
Multiple blood transfusions or hereditary HFE mutation (can result in heart failure, “bronze diabetes,” and risk of hepatocellular carcinoma)
Pancreatitis (acute)
Gallstones, alcohol
Pancreatitis (chronic)
Alcohol (adults), cystic fibrosis (kids)