| Literature DB >> 21299166 |
M A Cikrikcioglu1, H Erkal, M Hursitoglu, A Karadag, E Gundogan, S M Kayacan, T Tukek.
Abstract
A 43-year old male patient with hyponatremic hypertensive syndrome was diagnosed as catastrophic primary antiphospholipid syndrome (PAPS). He subsequently developed hepatosplenomegaly. The patient also carried thrombophilia- and haemochromatosis-associated gene mutations. Further investigations upon persistence of splenomegaly indicated development of idiopathic portal hypertension.Entities:
Mesh:
Year: 2010 PMID: 21299166
Source DB: PubMed Journal: Acta Gastroenterol Belg ISSN: 1784-3227 Impact factor: 1.316