USMLE® Step 1 style questions USMLE
USMLE® Step 2 style questions USMLE
A 25-year-old woman comes to the office because of episodes of headache, diaphoresis, palpitations, and nausea for 2 weeks. These symptoms last for a few minutes before resolving. The most recent episode was yesterday, and she says that her blood pressure was 190/105 mmHg measured with her father's home blood pressure cuff. After extensive work-up, she is diagnosed with a pheochromocytoma in the left adrenal gland. She undergoes an elective removal of the affected gland. During the operation, the surgeon notes that her left adrenal gland does not drain into the left renal vein. Which of the following veins does her left adrenal gland most likely drain into?
In pheochromocytoma, pheo- means dark, chromo- refers to color, cyto- refers to a cell and -oma means tumor. So a pheochromocytoma is a rare adrenal gland tumor where the cells darken when they form tumors.
Now, there are two adrenal glands, one above each kidney, and each one has an outer layer called the cortex and an inner layer called the medulla.
In the medulla, there are cells called chromaffin cells and their job is to make hormones called catecholamines. The catecholamines include epinephrine and norepinephrine - the fight or flight hormones.
The epinephrine and norepinephrine bind to alpha and beta receptors in various tissues throughout our body and cause an increase in cardiac output, increased blood pressure, dilated pupils, increased blood flow to skeletal muscles, and increased blood sugar.
Pheochromocytomas are tumors that form when these chromaffin cells start to divide uncontrollably.
They typically form in one of the adrenal glands, but rarely can be in both and sometimes can even develop in other parts of the body where chromaffin cells are found like the carotid arteries in the neck, the bladder, and the abdominal aorta.
Most pheochromocytomas arise sporadically, but some are associated with an inherited syndrome.
One of these is multiple endocrine neoplasias type 2A and type 2B, where pheochromocytoma is caused by a mutation in the RET gene, which is a protooncogene that encodes for proteins that promote cell growth and division.
When the RET gene mutates, it becomes an oncogene that causes the cells to divide constantly.
A third disease is neurofibromatosis type 1, which is caused by a mutation in the gene NF1 that encodes for another tumor suppressor protein called neurofibromin, and the mechanism here is similar to Von Hippel-Lindau disease.
Once pheochromocytomas develop, they cause problems by releasing too many catecholamines into the blood. The catecholamine release is unregulated and could happen continuously or at random times.
Imagine getting stressed, and then going to the gym, and then indulging in a plate of chocolate and cheese washed down with a glass of wine - a recipe for triggering catecholamine release!
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