Kurihara K, Sakai H, Hashimoto N
J Oral Pathol. 1984 Dec;13(6):640-9. doi: 10.1111/j.1600-0714.1984.tb01466.x.
Two cases of oral B-lymphomas with numerous Russell body-like inclusions are described. One occurred primarily in the hard palate of a 59-year-old female with Sjögren's syndrome, and was diagnosed as lymphoplasmacytoid immunocytoma by Kiel's classification. The other occurred secondarily in the buccal mucosa of a 44-year-old female whose first affected site was orbital soft tissues, and was diagnosed as extramedullary plasmacytoma. The diagnostic problems and the nature of the Russell body-like inclusions are discussed based on the immunoperoxidase (PAP) method and electron microscopic study. The first patient is well without recurrence 19 months after surgery, while the second patient developed extramedullary plasmacytoma in the abdomen 5 months after surgery for the buccal plasmacytoma.
本文描述了两例伴有大量Russell小体样包涵体的口腔B淋巴瘤。其中一例主要发生在一名患有干燥综合征的59岁女性的硬腭,根据基尔分类法诊断为淋巴浆细胞样免疫细胞瘤。另一例继发于一名44岁女性的颊黏膜,其首发受累部位为眼眶软组织,诊断为髓外浆细胞瘤。基于免疫过氧化物酶(PAP)法和电子显微镜研究,对诊断问题及Russell小体样包涵体的性质进行了讨论。首例患者术后19个月情况良好,无复发;而第二例患者在颊部浆细胞瘤手术后5个月,腹部出现了髓外浆细胞瘤。