一例偶然出现在伤口清创样本中的具有γ-δ表型的 CD4+ T 细胞淋巴瘤。

Paige E Adams, Vida Ehyayee, Aadil Ahmed
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引用次数: 0

摘要

我们报告了一名 85 岁男性患者的病史,他患有严重的银屑病,大腿伤口在 9 个月内缓慢扩大。患者曾因骨髓炎接受过截肢治疗。组织样本的组织学检查显示,伤口出现大面积溃疡,大面积坏死延伸至皮下。标本边缘还发现皮下脂肪组织中有由非典型细胞组成的结节状淋巴浸润。这些细胞只有 CD3、CD4 和 T 细胞受体 (TCR) δ 染色阳性。肿瘤细胞的 Ki-67 增殖指数约为 70%。肿瘤细胞的CD30、CD8、CD56、TCR BF1、颗粒酶、TIA1、CD123和Epstein-Barr编码区(EBER)染色均为阴性。诊断结果为γ-δT细胞淋巴瘤。进一步的影像学检查显示患者有区域性淋巴结肿大。患者开始接受迷你CHOP和filgrastim治疗,但在确诊后1个月内死亡。这是一例有趣的γ-δT 细胞淋巴瘤病例,是在慢性伤口上偶然诊断出来的。此外,它还表现出 CD4+、CD8- 表型,这在γ-delta 表型的 T 细胞淋巴瘤中极为罕见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of CD4+ T-Cell Lymphoma With Gamma-Delta Phenotype, Incidentally Manifesting in a Wound Debridement Sample.
We report an 85-year-old male patient with a medical history significant for psoriasis who presented with a thigh wound that expanded slowly over the course of 9 months. The patient was previously treated with amputation of hand digits for osteomyelitis. Histologic examination of the tissue sample revealed a broad ulceration with large areas of necrosis extending into the subcutis. The edge of the specimen also revealed a nodular lymphoid infiltrate in the subcutaneous adipose tissue composed of atypical cells. These cells were only positive for CD3, CD4, and T-cell receptor (TCR) delta stains . The Ki-67 proliferation index of tumor cells was about 70%. The tumor cells were negative for CD30, CD8, CD56, TCR BF1, granzyme, TIA1, CD123, and Epstein-Barr encoding region (EBER)-ish stains. A diagnosis of gamma-delta T-cell lymphoma was made. Further imaging showed regional lymphadenopathy. The patient was started on mini-CHOP and filgrastim; however, the patient died within 1 month after the diagnosis. This is an interesting case of gamma-delta T-cell lymphoma that was incidentally diagnosed on a chronic wound. In addition, it showed a CD4+, CD8- phenotype that is exceedingly rare for T-cell lymphomas with gamma-delta phenotype.
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