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Idiopathic portal hypertension during a catastrophic attack in a patient with primary antiphospholipid syndrome
M A Cikrikcioglu1, H Erkal, M Hursitoglu
1Vakif Gureba Training and Research Hospital, Fatih, Istanbul, Turkey. malicikrikcioglu@yahoo.com
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.
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.
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