医学
脂膜炎
病理
淋巴瘤
活检
系统性红斑狼疮
抗核抗体
红斑狼疮
皮肤病科
疾病
抗体
免疫学
自身抗体
作者
Mun Leng Lee,Puo Nen Lim,Jane Colgan,John R. Goodlad
出处
期刊:Case Reports
[BMJ]
日期:2024-06-01
卷期号:17 (6): e255592-e255592
标识
DOI:10.1136/bcr-2023-255592
摘要
A white Caucasian woman in her 30s presented with an indurated lesion on her right upper arm. Panniculitis was clinically suspected. Antinuclear antibody testing was positive but incisional biopsy showed subcutaneous panniculitis-like T-cell lymphoma (SPTCL), although with some unusual features more in keeping with lupus. Initial treatment was with oral prednisolone and radiotherapy but with only partial response. A second biopsy was taken from an area of presumed residual disease. This displayed histological features that were much more typical of lupus erythematosus profundus (LEP) but with tiny foci suggesting concomitant microscopic areas of SPTCL. Immunofluorescence for IgM was positive. This case highlights the rare occurrence of a patient with overlapping clinical and pathological features of SCPTL and LEP. It emphasises the need for close clinicopathological correlation in the workup of patients with suspected panniculitis and the importance of careful pathological examination for features of both diseases.
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