Fujii H, Seki S, Suyama Y, Shimizu T, Kano T, Yasuda N
Gan No Rinsho. 1983 Apr;29(4):A-22, 342-8.
The case report here was documented clinically, cytologically and histologically over a period of 5 years. A 49-year-old man was admitted to our hospital in September, 1975 because of a painful lump over the sternum and a diagnosis of solitary well-differentiated plasmocytoma (BJ-lambda) was made. The tumor promptly subsided following chemotherapy. In July, 1980 as it had in June, 1979, the sternal tumor relapsed; morphologically it was a poorly differentiated plasmocytoma. It promptly subsided following the start of chemotherapy and/or radiation therapy. In February, 1981, an abdominal tumor and ascites developed, morphologically it was plasma cell sarcoma composed of giant and bizarre tumor cells of plasma cell origin as demonstrated by immunoelectron microscopy. In April, 1981, the patient died of cachexia. At autopsy, multiple tumor formations consisting of giant and bizarre myeloma cells were found in the abdominal cavity, liver, retroperitoneum, diaphragm, left adrenal gland, mediastinum and lymph nodes. There was no infiltration of myeloma cells into bones other than the sternum.
本病例报告历经5年,进行了临床、细胞学及组织学记录。一名49岁男性于1975年9月因胸骨上疼痛性肿块入院,诊断为孤立性高分化浆细胞瘤(BJ-λ)。化疗后肿瘤迅速消退。1980年7月,如同1979年6月一样,胸骨肿瘤复发;形态学上为低分化浆细胞瘤。化疗和/或放疗开始后肿瘤迅速消退。1981年2月,出现腹部肿瘤及腹水,形态学上为浆细胞肉瘤,免疫电子显微镜显示由浆细胞来源的巨大怪异肿瘤细胞组成。1981年4月,患者死于恶病质。尸检时,在腹腔、肝脏、腹膜后、膈肌、左肾上腺、纵隔及淋巴结发现由巨大怪异骨髓瘤细胞组成的多个肿瘤灶。除胸骨外,未见骨髓瘤细胞浸润至其他骨骼。