Literature DB >> 12625413

Pituitary adenomas in adolescent patients with multiple endocrine neoplasia type 1.

Ako Oiwa1, Akihiro Sakurai, Yoshihiko Sato, Takahiro Sakuma, Koh Yamashita, Miyuki Katai, Toru Aizawa, Kiyoshi Hashizume.   

Abstract

Two juvenile patients with multiple endocrine neoplasia type 1 (MEN1) who developed pituitary adenomas are reported. The first case, a 14-year-old girl, developed prolactinoma and manifested delayed puberty and growth arrest. The second case, a 16-year-old boy, was asymptomatic and a pituitary adenoma accompanied by mild elevation of PRL and GH was identified through family screening. His growth and pubertal development was not impaired. Medication with bromocriptine was started for both cases with good therapeutic responses. These cases emphasize relevance of early screening of endocrine disorders for members of families with MEN1.

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Year:  2002        PMID: 12625413     DOI: 10.1507/endocrj.49.635

Source DB:  PubMed          Journal:  Endocr J        ISSN: 0918-8959            Impact factor:   2.349


  2 in total

1.  An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and protein.

Authors:  L Drori-Herishanu; A Horvath; M Nesterova; Y Patronas; M Lodish; E Bimpaki; N Patronas; S Agarwal; R Salvatori; M Martari; V Mericq; C A Stratakis
Journal:  Horm Metab Res       Date:  2009-04-23       Impact factor: 2.936

2.  Editorial: Early Genetic and Clinical Diagnosis in MEN1.

Authors:  Delmar M Lourenço; Wouter W de Herder
Journal:  Front Endocrinol (Lausanne)       Date:  2020-04-15       Impact factor: 5.555

  2 in total

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