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印度多方面成人T细胞白血病/淋巴瘤:病例系列

Multifaceted adult T-cell leukemia/lymphoma in India: a case series.

作者信息

Khader Anza, Shaan Mohamed, Balakrishnan Sunitha, Ambooken Betsy, Muhammed Kunnummel, Rajan Uma

机构信息

Department of Dermatology, Government Medical College, Calicut, Kerala, India.

Department of Medicine, Government Medical College, Calicut, Kerala, India.

出版信息

Indian J Dermatol. 2015 Jan-Feb;60(1):103. doi: 10.4103/0019-5154.147846.

Abstract

BACKGROUND

Adult T-cell leukemia/lymphoma (ATL) is caused by human T-cell lymphotropic virus type-1 (HTLV-1). India is considered as a nonendemic region for HTLV-1. Recent upsurge of cases have been noted in southern parts of India.

AIMS AND OBJECTIVES

The objective was to describe skin manifestations in various types of ATL.

MATERIALS AND METHODS

Clinical examination, blood investigations, skin biopsies, lymph node biopsies, and immunohistochemistry were performed in five patients. Flow cytometry was performed in two cases.

RESULTS

Serological testing was positive for HTLV-1 in all patients. All patients presented with skin lesions. Rare presentations of molluscum contagiosum like papules, purpuric macules and plaques, hypopigmented macules and verrucous papules were seen. Dermatophytic infections occurred in two patients. Mucosal lesion was seen in one patient. Histological features include dermal lymphoid infiltrate with or without epidermotropism. Presence of epidermotropism did not correlate with the severity of disease. All patients except one succumbed to illness within few months to 1 year period.

CONCLUSIONS

ATL manifest in myriad presentations and skin lesions are often the earliest manifestation. Cutaneous manifestations of ATL vary from subtle hypopigmented macules to florid nodular lesions, and HTLV-1 screening need to be carried out in all doubtful cases.

摘要

背景

成人T细胞白血病/淋巴瘤(ATL)由1型人类嗜T细胞病毒(HTLV-1)引起。印度被认为是HTLV-1的非流行地区。最近在印度南部发现病例有所增加。

目的

描述不同类型ATL的皮肤表现。

材料与方法

对5例患者进行了临床检查、血液检查、皮肤活检、淋巴结活检和免疫组化。2例患者进行了流式细胞术检查。

结果

所有患者HTLV-1血清学检测均为阳性。所有患者均有皮肤病变。可见传染性软疣样丘疹、紫癜性斑疹和斑块、色素减退斑和疣状丘疹等罕见表现。2例患者发生皮肤癣菌感染。1例患者出现黏膜病变。组织学特征包括真皮淋巴细胞浸润,伴或不伴亲表皮现象。亲表皮现象的存在与疾病严重程度无关。除1例患者外,所有患者均在数月至1年内死亡。

结论

ATL有多种表现形式,皮肤病变往往是最早的表现。ATL的皮肤表现从细微的色素减退斑到明显的结节性病变不等,所有可疑病例均需进行HTLV-1筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d6f/4318027/1d9af2226d6b/IJD-60-103c-g001.jpg

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