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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Chronic liver disease in a patient with sickle cell anemia
Nurten Akyürek Savafi1, Sabiye Akbulut, Tankut Köseoglu
1Departments of Gastroenterology, Ankara Numune Training and Research Hospital, Ankara, Turkey. nakyurek2000@yahoo.com
Abstract:
Various disorders of the hepatobiliary system can occur due to sickling in patients with sickle cell anemia. Pathology and frequency of these disorders are not clearly known. Liver biopsies of these patients show erythrocytosis, erythrophagocytosis, sinusoidal dilatation and hyperplasia in Kupffer cells. We present a 21-year-old male patient diagnosed with sickle cell anemia who developed chronic liver disease, together with a review of the literature.
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