Article ID Journal Published Year Pages File Type
3290149 Gastroentérologie Clinique et Biologique 2010 4 Pages PDF
Abstract

SummaryBackgroundSecondary polycythemia is a rare condition, which is usually associated to neoplasia or chronic pulmonary disorders.Case reportA 41-year-old man man with no history of liver disease was admitted for erythrocytosis. The paraclinical investigations revealed an increased erythropoietin level in the serum and a voluminous hepatic tumor but its identification was unclear. A liver resection was performed and the histopathological examination concluded that the tumor was a giant cavernous haemangioma with extensive myxoid changes. After surgical resection of the haemangioma, normal haemoglobin and serum erythropoietin were obtained without any further treatment.ConclusionLiver haemangioma must be included in rare cause of secondary polycythemia, and surgical resection of the haemangioma should be considered as the standard to induce complete remission.

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