Gao Zirui, Xu Qianxi, Chen Xue, Mao Dandan, Zhang Jianzhong, Jin Jiang
Department of Dermatology, Peking University People's Hospital, Beijing, People's Republic of China.
Clin Cosmet Investig Dermatol. 2022 May 30;15:975-979. doi: 10.2147/CCID.S366789. eCollection 2022.
Rhupus syndrome, as an overlap syndrome of rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE), is relatively rare because of their substantially different immunopathological mechanisms. Herein, we report the first case of primary cutaneous anaplastic large cell lymphoma (PC-ALCL) in a patient with rhupus syndrome and Sjogren's syndrome and review the relevant literature. A 52-year-old Chinese woman with a history of rhupus syndrome and Sjogren's syndrome was treated with methotrexate, who developed gradually increasing nodules on the waist. Histopathological studies showed that the dermis and subcutaneous tissue were infiltrated with medium-to-large, atypical lymphocytes with the oval nucleus. The tumor cells showed CD3-, CD4-, CD8-, CD30+, LCA+, and EBV-encoded RNA (EBER) in situ hybridization (ISH) was positive. Therefore, the patient was diagnosed with PC-ALCL. Both immune disorders and EBV infection may be related to the onset of PL-ALCL, and further studies are needed to clarify the pathogenesis.
类风湿性红斑综合征作为类风湿性关节炎(RA)和系统性红斑狼疮(SLE)的重叠综合征,由于其免疫病理机制存在显著差异,相对较为罕见。在此,我们报告首例患有类风湿性红斑综合征和干燥综合征的原发性皮肤间变性大细胞淋巴瘤(PC-ALCL)患者,并对相关文献进行综述。一名有类风湿性红斑综合征和干燥综合征病史的52岁中国女性接受甲氨蝶呤治疗,其腰部逐渐出现增大的结节。组织病理学研究显示,真皮和皮下组织浸润有中等至大型、具有椭圆形核的非典型淋巴细胞。肿瘤细胞显示CD3-、CD4-、CD8-、CD30+、LCA+,且EB病毒编码RNA(EBER)原位杂交(ISH)呈阳性。因此,该患者被诊断为PC-ALCL。免疫紊乱和EB病毒感染可能均与原发性皮肤间变性大细胞淋巴瘤的发病有关,尚需进一步研究以阐明其发病机制。