Multiple Mucosal Neuromata with Endocrine Tumors Syndrome (Multiple Mucosal Neuromas, Pheochromocytoma, and Medullary Thyroid Carcinoma Syndrome)
General: Pheochromocytoma can be inherited and found in combination with neurofibromatosis and other brain tumors (meningioma, spongioblastoma, ependymoma, astrocytoma, cerebellar hemangioblastoma), multiple mucosal neuromas, and medullary carcinoma of the thyroid.
Ocular: Conjunctival neuromas; multiple, white, myelinated nerve fibers in corneal stroma arising at limbus with anastomoses in center of cornea.
Clinical: Neuromas of lips or anterior portion of tongue or, more rarely, of buccal, gingival, or laryngeal mucosa; hypertension; flushing; weakness; sweating; palpitations; headaches.
Burgdorf W. Letter: multiple mucosal neuroma syndrome. Arch Dermatol 1975; 111:931.
Paloyan E, et al. familial pheochromocytoma, medullary thyroid carcinoma and parathyroid adenomas. JAMA 1970; 214:1443.
Williams ED, Pollock DJ. Multiple mucosal neuromata with endocrine tumors: a syndrome allied to von Recklinghausen's disease. J Pathol Bacteriol 1966; 91:71.
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