How does multiple mucosal neuroma syndrome typically present? As the name implies, this syndrome is characterized by the development of multiple flesh-colored papules on the tongue, lips, and, occasionally, other mucosal surfaces early in life. These patients have a characteristic appearance with thick prominent lips and a marfanoid habitus. Ninety percent of these patients develop medullary thyroid carcinoma, and half will suffer from pheochromocytoma that is often multifocal and/or bilateral. |
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