File:Case 117 118-pres1-1.jpg

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Case_117_118-pres1-1.jpg ‎(134 × 131 pixels, file size: 44 KB, MIME type: image/jpeg)

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Multiple endocrine neoplasia, Type IIB (MEN-IIB) in 14-year-old boy

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.
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Source http://cnx.org/content/m14901/latest/
Author Herbert L. Fred, MD, Hendrik A. van Dijk
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current15:03, 13 December 2007Thumbnail for version as of 15:03, 13 December 2007134 × 131 (44 KB)Filip em (talk | contribs){{Information |Description=Multiple endocrine neoplasia, Type IIB (MEN-IIB) in 14-year-old boy An inherited, autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, and mucosal neuromas, associated at times with prognath

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