AssessmentsMultiple endocrine neoplasia: Pathology review
USMLE® Step 1 style questions USMLE
A 34-year-old woman comes to the office complaining of consistent diarrhea for the last 2 months. The patient has experienced watery, tea-colored diarrhea that happens even when she has not eaten anything. She denies any associated abdominal pain or difficulty swallowing. The patient feels fatigued and weak with muscle cramps which she attributes to being dehydrated. Medical history includes hyperparathyroidism and nephrolithiasis. The patient’s temperature is 37.0°C (98.6°F), pulse is 100/min, respirations are 20/min, and blood pressure is 100/60 mmHg. Physical examination shows dry mucous membranes and decreased skin turgor without abdominal tenderness. Laboratory tests show the following:
|Parathyroid hormone||350 pg/mL|
Which of the following is the most likely mechanism of this patient’s symptoms?
Content Reviewers:Yifan Xiao, MD
Two individuals came in for genetic testing based on recommendations from their primary care physicians.
The first one is 24 year old Kurt, who was previously diagnosed with Zollinger-Ellison syndrome and also has an adenoma in one of his parathyroid glands.
On the clinical examination, doctors observed that he has gynecomastia.
His mother also has parathyroid adenomas.
Her father has recently been diagnosed with thyroid medullary cancer.
Although their presentation and family history differ, both people have multiple endocrine neoplasias, or MEN for short.
These are a group of inherited diseases which cause tumors to grow in the endocrine glands of the body.
The endocrine glands affected in multiple endocrine neoplasia are the pituitary gland, thyroid gland, parathyroid glands, adrenal glands, and the pancreas.
So in multiple endocrine neoplasias, there are tumors that form in these glands that lead to overproduction of hormones.
Multiple endocrine neoplasias are caused by genetic mutations in one of two genes: either MEN1 or RET, which codes for receptor tyrosine kinase.
For your exams, remember that both of these genes have a dominant inheritance pattern, so only one copy of the mutated gene is needed to get the disease.
Okay, let’s start with the MEN1 gene that is found on chromosome 11 and codes for a tumor suppressor protein called menin, which - under normal circumstances - stops a cell from dividing uncontrollably.
MEN1 mutations cause MEN type 1.
For your tests, you absolutely have to know that there are three types of tumors associated with MEN type 1: parathyroid, pancreatic, and pituitary.
The clinical manifestations of hypercalcemia can be recalled by the mnemonic: “Stones, bones, groans, and moans”.
Stones refers to the calcium kidney stones.
Bones refers to bone pain that results from the increased resorption of bone in hyperparathyroidism.
Groans refers to the abdominal complications in hypercalcemia:including peptic ulcer disease, pancreatitis, and constipation.
Lastly, moans refers to the psychiatric symptoms of hypercalcemia, such as altered mental status and psychosis.
Pancreatic tumors cause problems based on the type of hormone they produce.
The first one is Zollinger-Ellison syndrome, where there’s one or more tiny tumors in the pancreas or the upper part of the small intestine.
These tumors, called gastrinomas, produce gastrin which increases the amount of hydrochloric acid in the stomach and can cause peptic ulcers, abdominal pain, and vomiting.
Insulinomas cause hypoglycemia, which is suggested by the Whipple’s triad.
This includes symptoms of hypoglycemia such as hunger or dizziness, low glucose levels at the time of the symptoms, and finally, relief of symptoms when glucose is given.
On the other hand, glucagonomas cause hyperglycemia, but glucagonomas are pretty rare.
The pituitary gland develops benign tumors called adenomas which usually make an excess amount of at least one of the many hormones produced there.
The next most common hormone being overproduced is growth hormone, which has different effects depending on the age.
In children, growth hormone causes gigantism , meaning they’ll get really tall.
In adults, growth hormone causes acromegaly where they have enlarged hands and feet, a large forehead, and a prominent jaw.
Sometimes, with MEN type 1, there can also be facial angiofibromas, which are benign tumors that consist of blood vessels and connective tissue.
They appear as small, reddish papules that don’t regress.
Next, there can also be collagenomas, which are caused by the proliferation of normal collagen fibers.
They are also benign and appear like multiple, skin-colored or hypopigmented nodules on the face, neck, trunk and upper limbs.
Finally, meningiomas can also appear.
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- "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
- "Zollinger Ellison Syndrome in a Patient with Multiple Endocrine Neoplasia Type 1: A Classic Presentation" Case Reports in Gastrointestinal Medicine (2019)
- "Update on multiple endocrine neoplasia Type 1 and 2" La Presse Médicale (2018)
- "Multiple Endocrine Neoplasia" Surgical Oncology Clinics of North America (2015)
- "Williams Textbook of Endocrinology" Elsevier (2019)