一名青少年的骨孤立性浆细胞瘤。
Solitary plasmocytoma of bone in an adolescent.
作者信息
Bertoni-Salateo R, de Camargo B, Soares F, Chojniak R, Penna V
机构信息
Department of Pediatric Oncology, Hospital do Cancer--A. C. Camargo, Sao Paulo, Brazil.
出版信息
J Pediatr Hematol Oncol. 1998 Nov-Dec;20(6):574-6.
PURPOSE
To describe an adolescent with solitary plasmocytoma of bone and compare the pathologic and radiographic findings with osteomyelitis.
PATIENT AND METHODS
A 17-year-old girl had a 3-year history of swelling of the right tibia, local pain, and hyperemia.
RESULTS
Initial biopsy was interpreted as osteomyelitis. The lesion was rebiopsied 3 years later and showed a plasma cell neoplasm. A review of the first biopsy confirmed a similar histologic picture.
CONCLUSION
Although solitary plasmocytoma of bone is a rare neoplasm in adolescence, it must be considered in the differential diagnosis of chronic osteomyelitis.
目的
描述一名患有骨孤立性浆细胞瘤的青少年，并将其病理和影像学表现与骨髓炎进行比较。
患者与方法
一名17岁女孩有右侧胫骨肿胀、局部疼痛和充血3年病史。
结果
初次活检被诊断为骨髓炎。3年后对病变进行再次活检，显示为浆细胞瘤。对初次活检的复查证实了相似的组织学表现。
结论
尽管骨孤立性浆细胞瘤在青少年中是一种罕见的肿瘤，但在慢性骨髓炎的鉴别诊断中必须考虑到它。
Zotero 插件