Literature DB >> 12109276

[Hypophyseal incidentaloma in a patient with autosomal dominant polycystic kidney disease].

R Fajfr1, B Müller, P Diem.   

Abstract

The prevalence of incidentally discovered lesions within the pituitary (pituitary incidentalomas) is about 10%. The most common form of sellar mass are clinically nonfunctioning adenomas (less than 10 mm); functioning adenomas, however, are rare. Incidentally discovered pituitary microadenomas causing growth hormone hypersecretion are uncommon. In addition, the association of autosomal dominant polycystic kidney disease with acromegaly is exceptional and has not yet been reported to our knowledge.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12109276     DOI: 10.1024/0369-8394.91.25.1123

Source DB:  PubMed          Journal:  Praxis (Bern 1994)        ISSN: 1661-8157


  2 in total

1.  Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation.

Authors:  Luis V Syro; Jamie L Sundsbak; Bernd W Scheithauer; Rodrigo A Toledo; Mauricio Camargo; Christina M Heyer; Tomoko Sekiya; Humberto Uribe; Jorge I Escobar; Martin Vasquez; Fabio Rotondo; Sergio P A Toledo; Kalman Kovacs; Eva Horvath; Dusica Babovic-Vuksanovic; Peter C Harris
Journal:  Pituitary       Date:  2012-09       Impact factor: 4.107

2.  A RARE CASE OF ACROMEGALY AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE: CASE REPORT AND BRIEF REVIEW OF LITERATURE.

Authors:  Swayamsidha Mangaraj; Debasish Patro; Arun Kumar Choudhury; Anoj Kumar Baliarsinha
Journal:  AACE Clin Case Rep       Date:  2019-06-07
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.