Literature DB >> 15112914

McCune-Albright syndrome associated with pituitary microadenoma: patient report.

Chun-Jung Chen1, Jah-Yao Liu, Shin-Nan Cheng, Fung-Wei Chang, Yeong-Seng Yuh.   

Abstract

McCune-Albright syndrome (MAS) is a rare disorder characterized by the classic triad of precocious puberty, polyostotic fibrous dysplasia and café-au-lait spots. Additional endocrine abnormalities may also be present, including hyperthyroidism, growth hormone excess and hyperprolactinemia. The most commonly encountered endocrine dysfunction is gonadal hyperfunction. Gonadotropin-independent precocious puberty is typically the initial manifestation of MAS in girls. Ovarian cysts may be detected on pelvic ultrasound. Our patient was also found to have pituitary microadenoma, evidenced by dynamic magnetic resonance imaging.

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Year:  2004        PMID: 15112914     DOI: 10.1515/jpem.2004.17.3.365

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  3 in total

1.  Gastrointestinal polyps in McCune Albright syndrome.

Authors:  Margaret Zacharin; Anurag Bajpai; Chung Wo Chow; Anthony Catto-Smith; Constantine Stratakis; Michelle W Wong; Rodney Scott
Journal:  J Med Genet       Date:  2011-02-28       Impact factor: 6.318

Review 2.  Acromegaly and McCune-Albright syndrome.

Authors:  Sylvie Salenave; Alison M Boyce; Michael T Collins; Philippe Chanson
Journal:  J Clin Endocrinol Metab       Date:  2014-02-11       Impact factor: 5.958

3.  The activating mutation R201C in GNAS promotes intestinal tumourigenesis in Apc(Min/+) mice through activation of Wnt and ERK1/2 MAPK pathways.

Authors:  C H Wilson; R E McIntyre; M J Arends; D J Adams
Journal:  Oncogene       Date:  2010-06-07       Impact factor: 9.867

  3 in total

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