Multiple endocrine neoplasia (MEN) type 2B is the rarest and most aggressive form of MEN syndrome. MEN 2B patients manifest characteristic oral and facial features besides the neural crest cell-derived tumors, including medullary carcinoma, pheochromocytoma, mucosal neuroma, and ganglioneuromatosis of the gut. We report a case of MEN 2B diagnosed on the basis of the warning signs of mucosal neuroma and multiple neural hyperplasias in the maxillary bone resected during orthognathic surgery. A subsequent systemic examination under the pathologic diagnosis of neural lesions revealed medullary thyroid carcinoma, megacolon, thickened corneal nerves, and RET gene mutation, thus verifying the diagnosis of MEN 2B. An immunohistochemical study revealed an increased number of unmyelinated Schwann cells in the hyperplastic nerves. We suggest that intraosseous neural hyperplasia is a specific finding of the MEN 2B syndrome in addition to the known oral and facial manifestations.
Keyphrases
- middle aged
- case report
- end stage renal disease
- squamous cell carcinoma
- ejection fraction
- lymph node
- newly diagnosed
- bone mineral density
- minimally invasive
- single cell
- acute coronary syndrome
- peritoneal dialysis
- induced apoptosis
- oxidative stress
- neoadjuvant chemotherapy
- coronary artery bypass
- percutaneous coronary intervention
- bone loss
- signaling pathway
- postmenopausal women
- cell cycle arrest
- wound healing
- bone regeneration