File:Case 117 118-pres1-2.jpg
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Multiple endocrine neoplasia, Type IIB (MEN-IIB) in 23-year-old woman An inherited, autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, and mucosal neuromas, associated at times with prognathism, puffy lips, and bony abnormalities. Both of these patients had surgically treated medullary thyroid carcinoma, neuromas of the tongue and lips, and prognathism. Neither, however, had any evidence, as yet, of adrenal disease. |
| Date | |
| Source | http://cnx.org/content/m14901/latest/ |
| Author | Herbert L. Fred, MD, Hendrik A. van Dijk |
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| current | 15:04, 13 December 2007 | | 145 × 131 (36 KB) | Filip em (talk | contribs) | {{Information |Description=Multiple endocrine neoplasia, Type IIB (MEN-IIB) in 23-year-old woman An inherited, autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, and mucosal neuromas, associated at times with progna |
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