Dagdas Simten, Ozet Gulsum, Alanoglu Guchan, Ayli Meltem, Gokmen Akoz Ayla, Erekul Selim
Department of Hematology, Ankara Numune Hospital, Ankara, Turkey.
Acta Haematol. 2006;116(3):198-202. doi: 10.1159/000094681.
A 42-year-old woman was diagnosed with myelodysplastic syndrome with fibrosis that developed bilaterally, cervical lymphadenopathy and cutaneous infiltration by trilineage extramedullary hematopoiesis after granulocyte colony-stimulating factor therapy because of severe neutropenia. Hepatosplenomegaly was not observed during her follow-up. Extramedullary hematopoiesis disappeared after growth factor therapy was stopped. Although the neutropenia was alleviated by growth factor administration, the appearance of an unusual involvement of extramedullary hematopoiesis should be kept in mind.
一名42岁女性被诊断为伴有纤维化的骨髓增生异常综合征,该疾病双侧发展,在因严重中性粒细胞减少接受粒细胞集落刺激因子治疗后出现双侧颈部淋巴结病和三系髓外造血的皮肤浸润。随访期间未观察到肝脾肿大。停止生长因子治疗后,髓外造血消失。虽然生长因子给药缓解了中性粒细胞减少,但应牢记出现不寻常的髓外造血受累情况。