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CD3 +、CD56 +、CD4 -、CD8 -、CD20 -、CD30 -外周T细胞非霍奇金淋巴瘤：一例罕见病例报告

CD3+, CD56+, CD4-, CD8-, CD20-, CD30- Peripheral T-Cell Non-Hodgkin's Lymphoma: A Rare Case Report.

作者信息

Jagati Ashish, Shah Bela J, Tibrewal Sonal, Gajjar Trusha

机构信息

Department of Skin and VD, B.J. Medical College and Civil Hospital, Ahmedabad, Gujarat, India.

出版信息

Indian J Dermatol. 2017 Mar-Apr;62(2):200-202. doi: 10.4103/ijd.IJD_440_16.

DOI:10.4103/ijd.IJD_440_16
PMID:28400642
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5363146/
Abstract

Cutaneous T-cell lymphoma (CTCL) commonly presents as mycosis fungoides or Sezary syndrome, both having CD4 positivity. A subset of CTCL which lacks CD4 surface marker is classified as cutaneous γ and δ-T-cell lymphoma (CGD-TCL). Because of its rarity and inability to study large number of patients, the impact of immunophenotype on the clinical outcome of primary CTCL in patients is limited. We report a case of primary CGD-TCL in a 71-year-old male because of this rarity and to emphasize its aggressive nature.

摘要

皮肤T细胞淋巴瘤（CTCL）通常表现为蕈样肉芽肿或塞扎里综合征，两者均为CD4阳性。缺乏CD4表面标志物的CTCL子集被归类为皮肤γ和δ-T细胞淋巴瘤（CGD-TCL）。由于其罕见性以及无法研究大量患者，免疫表型对原发性CTCL患者临床结局的影响有限。鉴于这种罕见性，我们报告了一例71岁男性原发性CGD-TCL病例，以强调其侵袭性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/99008c355904/IJD-62-200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/d78cc7160431/IJD-62-200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/564b7c1b63de/IJD-62-200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/31afdc9a69fb/IJD-62-200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/99008c355904/IJD-62-200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/d78cc7160431/IJD-62-200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/564b7c1b63de/IJD-62-200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/31afdc9a69fb/IJD-62-200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/5363146/99008c355904/IJD-62-200-g004.jpg

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Cutaneous gamma/delta T-cell lymphoma.皮肤 γ/δ T 细胞淋巴瘤。
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