Familial autoimmune myasthenia gravis and thymoma: Occurrence in two brothers

Robert M. Pascuzzi, Angelo Sermas, Lawrence H. Phillips, T. R. Johns

Research output: Contribution to journalArticle

13 Scopus citations

Abstract

At ages 31 and 42 years, two brothers presented with clinical, pharmacologic, electrophysiologic, and immunologic characteristics of autoimmune myasthenia gravis. At thymectomy, both had histologic findings of epithelial thymoma. HLA analysis revealed A2, A3, B7, and B39 antigens in one patient and A3, A24, B7, and B40 antigens in the other. Familial myasthenia gravis with thymoma has not been described previously. Familial thymoma has been rarely reported, but never with myasthenia gravis.

Original languageEnglish (US)
Pages (from-to)423-427
Number of pages5
JournalNeurology
Volume36
Issue number3
StatePublished - Mar 1986
Externally publishedYes

ASJC Scopus subject areas

  • Clinical Neurology

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    Pascuzzi, R. M., Sermas, A., Phillips, L. H., & Johns, T. R. (1986). Familial autoimmune myasthenia gravis and thymoma: Occurrence in two brothers. Neurology, 36(3), 423-427.