Hosenpud J D, Thorning D, Greenberg G
Cancer. 1980 Jan 15;45(2):345-8. doi: 10.1002/1097-0142(19800115)45:2<345::aid-cncr2820450225>3.0.co;2-3.
A case report of liposarcoma occurring in a man with probable hereditary multiple lipomata and metastasizing to bone marrow is presented. The neoplasm was studied by light and electron microscopy. The first evidence for metastatic disease was myelophthisic anemia. This unusual clinical occurrence is discussed briefly in conjunction with other neoplasms causing myelophthisis.
本文报告一例发生于一名可能患有遗传性多发性脂肪瘤的男性患者的脂肪肉瘤,并已转移至骨髓。通过光镜和电镜对该肿瘤进行了研究。转移性疾病的首个证据是骨髓痨性贫血。结合其他导致骨髓痨的肿瘤简要讨论了这一不寻常的临床病例。