Agrawal Shaily, Jangir Amit K, Yogesh M, Gandhi Rohankumar
Second-Year MBBS Student, Shri MP Shah Medical College, Jamnagar, Gujarat, India.
Department of Community Medicine, Shri MP Shah Medical College, Jamnagar, Gujarat, India.
J Family Med Prim Care. 2024 Nov;13(11):5402-5406. doi: 10.4103/jfmpc.jfmpc_874_24. Epub 2024 Nov 18.
Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by damage to organs and cells, initially mediated by tissue-binding autoantibodies and immune complexes. Lymphomas have been frequently reported, but the association of SLE with acute leukemia is rare and likely coincidental. We report a case of a 40-year-old female admitted for an etiological diagnosis of fever and dyspnea with peripheral edema. She had a history of SLE diagnosed 2 years prior and had been on immunosuppressive therapy since then. Hematological investigations showed leukocytosis, anemia, and thrombocytopenia. Further diagnostic testing could not be done as she passed away 3 days after acute leukemia was diagnosed. This case highlights the challenges of diagnosing hematological malignancies in immunosuppressed SLE patients where symptoms may be obscured.
系统性红斑狼疮(SLE)是一种自身免疫性疾病,其特征是器官和细胞受损,最初由组织结合自身抗体和免疫复合物介导。淋巴瘤已有频繁报道,但SLE与急性白血病的关联罕见且可能是巧合。我们报告一例40岁女性,因发热、呼吸困难伴外周水肿入院进行病因诊断。她有2年前诊断为SLE的病史,此后一直在接受免疫抑制治疗。血液学检查显示白细胞增多、贫血和血小板减少。由于在诊断为急性白血病3天后她去世,无法进行进一步的诊断测试。该病例凸显了在免疫抑制的SLE患者中诊断血液系统恶性肿瘤的挑战,因为症状可能被掩盖。