Literature DB >> 8396298

Von Recklinghausen neurofibromatosis and hematologic malignancies: 2 case reports in adulthood.

N Van Baren1, A Issa, A Delannoy.   

Abstract

Von Recklinghausen's neurofibromatosis is a hereditary disease predisposing to distinctive malignant hemopathies. These often develop during early childhood and are characterized by particular cytologic subtypes: juvenile chronic myeloid leukemia, monosomy 7-associated myeloproliferative syndrome and myelomonocytic leukemia. The etiopathologic mechanism underlying this association begins to be elucidated: the neurofibromatosis gene behaves like a tumor suppressor gene; its inactivation by mutation results in activation of the corresponding oncogenes. We report here the cases of two late-aged adults with neurofibromatosis: the first developed acute myelogenous leukemia, the second polycythemia vera. Based on a review of the literature, we suggest that, in opposition to childhood, the association between neurofibromatosis and malignant blood diseases is not demonstrated in adulthood.

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Year:  1993        PMID: 8396298     DOI: 10.1080/17843286.1993.11718304

Source DB:  PubMed          Journal:  Acta Clin Belg        ISSN: 1784-3286            Impact factor:   1.264


  1 in total

1.  A case report of acute myeloid leukemia and neurofibromatosis 1.

Authors:  Chiara Sartor; Cristina Papayannidis; Maria Chiara Abbenante; Antonio Curti; Nicola Polverelli; Emanuela Ottaviani; Ilaria Iacobucci; Viviana Guadagnuolo; Giovanni Martinelli
Journal:  Hematol Rep       Date:  2013-07-03
  1 in total

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