耐人寻味的皮下结节——惊恐发作的泛膜炎

S. Jagadeesan, Radhika Krishna, M. Eapen
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引用次数: 0

摘要

一个13岁的男孩在过去的6个月里表现出身体上多次短暂的无痛性肿胀。病变将持续6-8周,并自行消退,留下变色和改变的皮肤质地。临床检查显示左臂上有一个2 × 2厘米的单一柔软、无痛的可移动结节,同时在手臂、大腿和躯干上有多个离散的清晰的炎症后低色素斑块和色素沉着的鳞状丘疹。皮肤活检显示由淋巴样细胞、组织细胞和浆细胞组成的小叶性潘膜炎,淋巴样细胞包围脂肪细胞,提示细胞吞噬性组织细胞潘膜炎。免疫组化示CD3、CD5、CD7、CD8阳性,CD20阴性,CD4、CD56、Ki67 - 75 ~ 80%, CD68突出组织细胞,C30阴性。正电子发射断层扫描-磁共振成像显示全身有多个氟脱氧葡萄糖(FDG)结节,腋窝和腹股沟淋巴结有少量氟脱氧葡萄糖结节。最终诊断为皮下绒毛炎样t细胞淋巴瘤。我们的病人开始口服强的松龙和环孢素逐渐减少剂量,之后病变明显改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intriguing Subcutaneous Nodules – A Panic-Stricken Panniculitis
A 13-year-old boy presented with multiple transient painless swellings over the body for the past 6 months. Lesions would persist for 6–8 weeks and spontaneously resolve leaving behind discolouration and altered skin texture. Clinical examination revealed a single soft, non-tender mobile nodule of 2 × 2 cm over left arm, along with multiple discrete well defined post-inflammatory hypopigmented patches with hyperpigmented scaly papules over the arms, thighs and trunk. Skin biopsy showed lobular panniculitis composed of lymphoid cells, histiocytes and plasma cells with characteristic rimming of fat cells by lymphoid cells suggestive of cytophagic histiocytic panniculitis. Immunohistochemistry showed positive CD3, CD5, CD7 and CD8, negative CD20, CD4, CD56, Ki67 – 75–80%, CD68 highlighting the histiocytes and C30 negative. Positron emission tomography–magnetic resonance imaging showed multiple fluorodeoxyglucose (FDG) avid cutaneous and subcutaneous nodules throughout the body and minimally FDG avid axillary and inguinal lymph nodes. Thereby, a final diagnosis of subcutaneous panniculitis like T-cell lymphoma was concluded. Our patient was started on tapering dose of oral prednisolone and cyclosporine, following which the lesions significantly improved.
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