Narimatsu Hiroto, Morishita Yoshihisa, Shimada Kazuyuki, Ozeki Kazutaka, Kohno Akio, Kato Yukio, Nagasaka Tetsuro
Department of Hematology and Oncology, JA Aichi Showa Hospital Aichi.
Intern Med. 2003 Apr;42(4):354-7. doi: 10.2169/internalmedicine.42.354.
An 80-year-old woman was diagnosed with primary cutaneous B cell lymphoma. She had multifocal cutaneous tumors, but no nodal lymphadenopathy or bone marrow involvement. Histopathological examination of a biopsy specimen showed diffuse large B cell lymphoma without a bcl-2 expression. Complete resolution of hypercalcemia and disappearance of tumors were achieved with CHOP therapy, but a rapidly progressive skin lesion was observed soon after the completion of the therapy. The clinical manifestation of primary cutaneous diffuse large B cell lymphoma is diverse and the treatment strategy is not entirely clarified. This case represents another example of this rare lymphoma.
一名80岁女性被诊断为原发性皮肤B细胞淋巴瘤。她有多发性皮肤肿瘤,但无淋巴结肿大或骨髓受累。活检标本的组织病理学检查显示为弥漫性大B细胞淋巴瘤,无bcl-2表达。CHOP治疗使高钙血症完全缓解,肿瘤消失,但治疗结束后不久观察到皮肤病变迅速进展。原发性皮肤弥漫性大B细胞淋巴瘤的临床表现多样,治疗策略尚未完全明确。该病例是这种罕见淋巴瘤的又一实例。