3例儿童非典型γ - δ阳性t细胞增生伴淋巴样丘疹病的临床特征

IF 0.5
Lachance Madeleine, Ram-Wolff Caroline, Delisle Bernard, Sigg Nina, Bataille Pauline, Bourrat Emmanuelle, Dumont Maëlle, Battesti Gilles, Bozonnat Alizée, Louveau Baptiste, Mourah Samia, Moins-Teisserenc Hélène, Bagot Martine, Lamant Laurence, Croue Anne, Michalak Sophie, BAH Ismael, Kempf Werner, Battistella Maxime, De Masson Adèle
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引用次数: 0

摘要

原发性皮肤γ - δ t细胞淋巴瘤被描述为一种预后不良的侵袭性实体。然而,γ - δ t细胞受体的表达已在各种类型的皮肤淋巴细胞增生中被描述。小儿LyP病例越来越多的认识,但小儿LyP与γ - δ表型很少被描述。我们报告了三名患有惰性γ - δ淋巴细胞增生的儿科患者,其复发缓解过程引起LyP。这三个病例强调TCR在淋巴增生中表达γ - δ并不是γ - δ淋巴瘤的同义词。事实上,这些病例提出了cd30阴性淋巴样丘疹病的儿科变体的问题,其组织学特征是非典型γ - δ阳性t细胞淋巴细胞增殖,并强调了在面对γ - δ淋巴细胞增殖时谨慎的临床组织学相关性,以避免过度治疗的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Atypical Gamma-Delta-Positive T-Cell Lymphoproliferation With Clinical Features of Lymphomatoid Papulosis in Three Children

Atypical Gamma-Delta-Positive T-Cell Lymphoproliferation With Clinical Features of Lymphomatoid Papulosis in Three Children

Primary cutaneous gamma-delta T-cell lymphoma has been described as an aggressive entity with a poor prognosis. However, gamma-delta T-cell receptor expression has been described in various types of skin lymphoproliferations. Paediatric cases of LyP are increasingly recognized, but paediatric LyP with a gamma-delta phenotype have been rarely described. We report three paediatric patients with indolent gamma-delta lymphoproliferation, with a relapsing-remitting course evoking LyP. These three cases emphasize that TCR gamma-delta expression in a lymphoproliferation is not a synonym of gamma-delta lymphoma. Indeed, these cases raise the question of a paediatric variant of CD30-negative lymphomatoid papulosis with histological features of atypical gamma-delta-positive T-cell lymphoproliferation and underline the necessity of cautious clinico-histological correlation when facing a gamma-delta lymphoproliferation to avoid overtreatment.

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