Zhao Melissa
University of California San Diego School of Medicine, La Jolla, CA, USA.
Case Rep Med. 2016;2016:6853936. doi: 10.1155/2016/6853936. Epub 2016 Dec 19.
. Systemic lupus erythematosus (SLE) is a chronic, inflammatory, connective tissue disease that commonly affects the joints and a variety of organs due to an overactivation of the body's immune system. There is wide heterogeneity in presentation of SLE patients, including lung, central nervous system, skin, kidney, and hematologic manifestations. . We report a case of atypical manifestation of SLE in a 53-year-old man who presented with neutropenic fever. Physical findings of interest included oral ulcers on the lower lip, a malar-like rash across the bridge of the nose, and a discoid-like rash on extensor surfaces of the elbows and knees. Labs include ANC <100, weakly positive anti-dsDNA, negative ANA, ferritin 1237 ng/mL, low C3/C4, and positive direct Coombs' test. A thorough workup for infection and hematologic malignancy was negative. Two days after initiation of therapy with 25 mg IV solumedrol twice a day, the patient's daily fevers resolved. ANC drastically improved to 2000 after two weeks of steroid treatment. He was later found to have a high titer of anti-neutrophil antibodies. . Autoimmune leukopenia is a common presentation in SLE, occurring in 50-60% of patients. Severe autoimmune neutropenia is uncommon and may correlate with high anti-neutrophil antibody activity despite a negative ANA. As neutropenia is usually mild, there are currently no guidelines for therapy. For our patient, we started him on low dose IV solumedrol and found that he responded drastically to treatment. Given strongly positive nonspecific anti-neutrophil antibodies in the setting of a negative ANA noted in our patient, it is likely that there are other currently unknown antibodies associated with SLE which may correlate strongly with autoimmune neutropenia.
系统性红斑狼疮(SLE)是一种慢性炎症性结缔组织病,由于机体免疫系统过度激活,常累及关节和多种器官。SLE患者的临床表现具有广泛的异质性,包括肺部、中枢神经系统、皮肤、肾脏和血液系统表现。我们报告一例53岁男性SLE非典型表现病例,该患者以中性粒细胞减少性发热为表现。相关体格检查发现包括下唇口腔溃疡、鼻梁处类似蝶形的皮疹以及肘部和膝部伸侧类似盘状的皮疹。实验室检查结果包括中性粒细胞绝对值(ANC)<100、抗双链DNA弱阳性、抗核抗体(ANA)阴性、铁蛋白1237 ng/mL、补体C3/C4降低以及直接抗人球蛋白试验阳性。针对感染和血液系统恶性肿瘤的全面检查均为阴性。每天两次静脉注射25 mg甲泼尼龙治疗两天后,患者的每日发热症状消退。类固醇治疗两周后,ANC大幅改善至2000。后来发现他有高滴度的抗中性粒细胞抗体。自身免疫性白细胞减少是SLE的常见表现,见于50% - 60%的患者。严重的自身免疫性中性粒细胞减少并不常见,尽管ANA阴性,但可能与高抗中性粒细胞抗体活性相关。由于中性粒细胞减少通常较轻,目前尚无治疗指南。对于我们的患者,我们开始给予低剂量静脉注射甲泼尼龙治疗,发现他对治疗反应显著。鉴于我们的患者在ANA阴性的情况下非特异性抗中性粒细胞抗体呈强阳性,很可能存在其他目前未知的与SLE相关的抗体,这些抗体可能与自身免疫性中性粒细胞减少密切相关。