Peripheral T-Cell Lymphoma, Not Otherwise Specified - a case report and short literature review.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Rafael Henriques de Figueiredo, Beatriz Simão Parreira, Pedro Amoroso Canão, Leila Cardoso, Elsa Fonseca, Jorge Almeida
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Abstract

Peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) is the most common subgroup of peripheral T-cell lymphomas (PTCL), and constitutes a diagnosis of exclusion. At presentation, most patients exhibit B symptoms and generalized lymphadenopathy, with or without concomitant extra-nodal involvement. We present a case of a man admitted to the hospital with B symptoms, generalized lymphadenopathy and a pruritic exanthema. Laboratory workup reveled persistent eosinophilia and malignant hypercalcemia. The excisional lymph node biopsy diagnosed PTCL-NOS, and the skin biopsy demonstrated a lichenoid dermatitis, compatible with the presumptive clinical diagnosis of a drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome. The patient was treated with topical betamethasone with good overall response, and initiated the first cycle of chemotherapy before discharge. This case report describes a PTCL-NOS with a concomitant non-lymphoproliferative disease, the challenging diagnostic workup of the two diseases and reinforces the most important features of the lymphoproliferative neoplasm.

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外周t细胞淋巴瘤,无其他特异性- 1例报告和简短的文献回顾。
非特异性外周t细胞淋巴瘤(PTCL- nos)是外周t细胞淋巴瘤(PTCL)最常见的亚群,构成排除诊断。在就诊时,大多数患者表现为B型症状和全身性淋巴结病,伴或不伴淋巴结外受累。我们提出的情况下,一名男子入院与B症状,全身性淋巴结病和瘙痒性湿疹。实验室检查发现持续嗜酸性粒细胞增多和恶性高钙血症。切除淋巴结活检诊断为PTCL-NOS,皮肤活检显示为地衣样皮炎,符合药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)综合征的推定临床诊断。患者局部应用倍他米松治疗,总体疗效良好,出院前开始第一周期化疗。本病例报告描述了PTCL-NOS合并非淋巴细胞增生性疾病,这两种疾病的诊断工作具有挑战性,并强调了淋巴细胞增生性肿瘤的最重要特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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