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系统性红斑狼疮表现为红斑狼疮性肿胀和狼疮性肾炎:一例报告。

Systemic lupus erythematosus presenting as lupus erythematosus tumidus and lupus nephritis: a case report.

机构信息

Department of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.

Kidney Pathology Laboratory LR00SP01, Charles Nicolle Hospital, Tunis, Tunisia.

出版信息

J Med Case Rep. 2023 Jun 14;17(1):242. doi: 10.1186/s13256-023-03981-3.

Abstract

BACKGROUND

Lupus nephritis and lupus erythematosus tumidus (LET) are uncommon manifestations of systemic lupus erythematosus (SLE), and their coexistence as the initial presentation of SLE is exceedingly rare. Here, we report such a case, emphasizing the diagnostic challenges and therapeutic implications of this unusual association.

CASE REPORT

A 38-year-old North African woman presented in Nephrology department with a history of lower extremity edema, fatigue, and weight loss of 3 kg in 4 weeks. Physical examination revealed LET lesions on the chest and the Neck. Laboratory investigations showed lymphopenia, low C3 and C4 complement levels, positive antinuclear antibodies, anti-dsDNA antibodies, and anti-SSA/Ro antibodies. Renal function tests showed normal serum creatinine and nephrotic proteinuria. Renal biopsy revealed Class V lupus nephritis. Skin biopsy confirmed the diagnosis of LET, with the presence of lymphohistiocytic infiltrates and dermal mucin. The patient was diagnosed with SLE based on the 2019 EULAR/ACR criteria and treated with prednisone (1 mg/kg/day) and hydroxychloroquine. She showed significant improvement in her cutaneous and renal symptoms at 6 and 12 months follow-up.

CONCLUSION

The rarity of the coexistence of LET and lupus nephritis as the initial manifestation of SLE, especially in the North African population, underscores the need for further research to elucidate the immunopathogenic mechanisms and prognostic factors associated with this association.

摘要

背景

狼疮肾炎和红斑狼疮性肿胀(LET)是系统性红斑狼疮(SLE)的罕见表现,它们同时作为 SLE 的初始表现极为罕见。在此,我们报告了这样一个病例,强调了这种不常见关联的诊断挑战和治疗意义。

病例报告

一位 38 岁的北非女性因下肢水肿、疲劳和体重在 4 周内减轻 3kg 到肾病科就诊。体格检查显示胸部和颈部有 LET 病变。实验室检查显示淋巴细胞减少、补体 C3 和 C4 水平降低、抗核抗体、抗 dsDNA 抗体和抗 SSA/Ro 抗体阳性。肾功能检查显示血清肌酐正常和肾病蛋白尿。肾活检显示狼疮肾炎 5 型。皮肤活检证实了 LET 的诊断,存在淋巴组织细胞浸润和真皮粘蛋白。根据 2019 年 EULAR/ACR 标准,患者被诊断为 SLE,并接受泼尼松(1mg/kg/天)和羟氯喹治疗。在 6 个月和 12 个月的随访中,她的皮肤和肾脏症状显著改善。

结论

LET 和狼疮肾炎同时作为 SLE 的初始表现极为罕见,尤其是在北非人群中,这突显了需要进一步研究来阐明与这种关联相关的免疫发病机制和预后因素。

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