A case of multiple endocrine neoplasia type 2B

Jpn J Clin Oncol. 1997 Aug;27(4):268-73. doi: 10.1093/jjco/27.4.268.

Abstract

A sporadic case of multiple endocrine neoplasia type 2B in a twenty-six year old man who manifested medullary thyroid carcinoma, multiple mucosal neuromas of the tongue and a marfanoid habitus is reported. At the time of diagnosis, he also had multiple liver and lung metastases. Genetic analysis of his lymphocytes revealed a point mutation in exon 16 of the RET proto-oncogene. Since multiple endocrine neoplasia type 2B has a relatively poor prognosis because of the occasional aggressive behavior of medullary thyroid carcinoma, the necessity of the genetic diagnosis of multiple endocrine neoplasia in the early stage is suggested.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Carcinoma, Medullary / pathology*
  • Drosophila Proteins*
  • Exons / genetics
  • Fatal Outcome
  • Follow-Up Studies
  • Humans
  • Liver Neoplasms / secondary
  • Lung Neoplasms / secondary
  • Male
  • Marfan Syndrome / pathology
  • Multiple Endocrine Neoplasia Type 2b / genetics
  • Multiple Endocrine Neoplasia Type 2b / pathology*
  • Neuroma / pathology*
  • Point Mutation / genetics
  • Prognosis
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins c-ret
  • Proto-Oncogenes / genetics
  • Receptor Protein-Tyrosine Kinases / genetics
  • Thyroid Neoplasms / pathology*
  • Tongue Neoplasms / pathology*

Substances

  • Drosophila Proteins
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-ret
  • Receptor Protein-Tyrosine Kinases
  • Ret protein, Drosophila