Endocrinology8-2 Flashcards
Light microscopy of a liver biopsy shows: (1) spotty hepatocyte necrosis & (2) inflammatory cell infiltration. The sample was taken from a patient who had just returned from a trip to Mexico. What is the most likely diagnosis?
Hepatitis A
Hallmarks of acute viral Hepatitis: (1) hepatocye injury/”ballooning degeneration” (2) hepatocyte death/”bridging necrosis”
Recent travel to an endemic country + histological signs of acute viral hepatitis=Hep A
What serum molecule(s) is believed to increase insulin resistance in overweight individuals?
- Free fatty acids (FFA)
- Triglycerides (TG)
List two common causes of hyperosmotic volume contraction.
- diabetes insipidus
- profuse sweating
Preferred acute treatment for diabetic ketoacidosis.
Regular insulin IV
Diagnosis:
Your patient has N/V & abdominal pain. He is found to be hypotensive and tachycardic on physical exam. Urine analysis indicates ketones and glucose in the urine.
Diabetic ketoacidosis
This patient most likely has T1DM. Acute treatment is regular insulin.
Diagnosis:
Glucagonoma
Markedly elevated glucagon levels
Diagnosis:
Your patient is a 50-year-old male with a 6 month history of decreased libido and headaches. PE reveals: (1) bitermporal hemaniopsia & (2) ophthalmoplegia.
pituitary apoplexy (pituitary hemorrhage)
Often associated with a pre-existing adenoma (Prolactinoma: suggested by the headaches and decreased libido). The patients are a great risk for cardiovascular collapse due to adrenocortical deficiency. Treatement: glucocorticoids
Clinical Manifestation:
Glucagonoma
- Necrolytic migratory erythema: coalescing erythematous lesions, with bronze indurations in the center
- Diabetes mellitus
- Anemia
Diagnosis:
Fine-needle aspiration cytology shows: (1) Numerous intranuclear inclusion bodies (2) intranuclear grooves & (3) cells with large nuclei and sparse, finely dispersed chromatin.
Papillary carcinoma
Papillary carcinoma is the most common type of thyroid cancer. Psammoma bodies may aslo be detected.
Name that Drug!
Rapid-acting insulins (15 minutes until peak)
Short-acting insulin (30 minutes until peak)
intermediate acting insulin (4-12 hours until peak)
Long acting insulin (3-9 hours until peak)
insulin analog (No peak; lasts 24 hours)
Rapid-acting insulins: (1) Aspart (2) lispro (3) glulisine
Short-acting insulin: Regular insulin
Intermediate acting insulin: NPH
Long acting insulin: Detemir
Insulin analog: Glargine
What is the most common genotype that causes Klinefelter syndrome?
47XXY
46XY/47XXY mosaicism & 48XXXY are possible but less common.
Clinical Manifestation:
Klinefelter Syndrome
- Primary testicular failure: (1) Small, firm testes, (2) azoospermia, (3)infertility, (4) testosterone deficiency, (5) increased FSH and LH (6) cryptorchidism
- Eunuchoid body habitus: tall, sparse facial and body hair, gynecomastia, decreased muscle mass
- Intellectual disability: most are mild or normal, my have psychosocial abnormalities (i.e. lack of insight, poor judgement)
Age range at which a diagnosis of Klinefelter Syndrome is often made
Teenage years
Pathogenesis:
Klinefelter Syndrome
meiotic non-disjunction during meiosis I
Pathogenesis:
Secondary hyperparathyroidism due to ESRD
- Renal dysfunction prevents the production of 1,25 vitamin D (active form)
- In the absence of active vitamin D, the serum Ca2+ is low
- In response to low serum Ca2+, PTH levels increase