BENIGN INTRACRANIAL HYPERTENSION AND PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
- 1 January 1986
- journal article
- research article
- Vol. 142 (10) , 782-785
Abstract
A 35 year-old caucasian man suffered from paroxysmal nocturnal haemoglobinuria (PNH) or Marchiafava-Micheli''s disease diagnosed in 1976 and complicated by several thrombotic episodes. He developed a benign intracranial hypertension. A digitalized intravenous angiography showed occlusion of both lateral sinuses. Partial improvement followed lombo-peritoneal shunting and steroid therapy. Cerebral venous thrombosis is a well-known complication of PNH but only a few cases have been radiologically and/or pathologically proven. It usually involves the superior longitudinal sinus and/or cortical veins resulting in hemorrhagic infarction of poor outcome. Benign intracranial hypertension due to a venous occlusion is rate. In 3 published cases, as in our own, the neurologic outcome was good. Steroid therapy seems useful. The risks of anticoagulant therapy are discussed.This publication has 4 references indexed in Scilit:
- Paroxysmal Nocturnal HaemoglobinuriaActa Haematologica, 1984
- Pseudotumor CerebriAnnals of Internal Medicine, 1982
- Mechanism of complement-mediated activation of human blood platelets in vitro: comparison of normal and paroxysmal nocturnal hemoglobinuria platelets.Journal of Clinical Investigation, 1977
- EFFECT OF HEPARIN ON COMPLEMENT ACTIVATION AND LYSIS OF PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (PNH) RED-CELLS1977