Acta gastro-enterologica Belgica, cilt.73, sa.4, ss.521-6, 2010 (SCI-Expanded)
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. (Acta gastroenterol. belg., 2010, 73, 521-526).