Moran C A, Suster S, Fishback N, Koss M N
Department of Pulmonary and Mediastinal Pathology, Armed Forces Institute of Pathology, Washington, DC, USA.
Mod Pathol. 1995 Apr;8(3):249-51.
We present four cases of extramedullary hematopoiesis occurring in the posterior mediastinum. The patients are two women and two men between the ages of 20 and 87 years. Two patients presented with a history of thalassemia, and one had a history of anemia of undetermined etiology. One patient was asymptomatic, and the posterior mediastinal mass was detected during a routine chest radiographs. Surgical resection of the mass was performed in one patient, whereas a biopsy was performed in the other three. Histologically, all the cases showed the typical features of extramedullary hematopoiesis, namely the presence of numerous lymphocytes admixed with megakaryocytes and red cell precursors. Follow-up information ranging from 2 mo to 3 years showed that all patients are alive and well.
我们报告4例发生于后纵隔的髓外造血病例。患者为2名女性和2名男性,年龄在20至87岁之间。2例患者有地中海贫血病史,1例有病因不明的贫血病史。1例患者无症状,后纵隔肿块在常规胸部X线检查时被发现。1例患者进行了肿块手术切除,另外3例进行了活检。组织学上,所有病例均显示髓外造血的典型特征,即存在大量淋巴细胞,并混有巨核细胞和红细胞前体。随访信息从2个月至3年不等,显示所有患者均存活且状况良好。