Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4143178 | Anales de Pediatría | 2009 | 4 Pages |
Abstract
Malignant thymoma is a very rare neoplasm in paediatric patients; it is usually associated with para-neoplastic syndromes, the most frequent is myasthenia gravis; some haematological abnormalities may also be present, such as pure red cell aplasia or aplastic anaemia. We report a 12-year-old boy suffering from a very large thymoma, treated with multiple chemotherapy, and who developed a severe aplastic anaemia after surgery. He had a poor response to immunosuppressive treatment and later developed massive pulmonary bleeding as a complication.
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Authors
O.M. Escobosa Sánchez, A. Herrero Hernández, T. Acha GarcÃa,