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人类 T 细胞淋巴病毒-1 相关成人 T 细胞白血病/淋巴瘤的皮肤表现:一项单中心回顾性研究。

Cutaneous manifestations of human T-cell lymphotrophic virus type-1-associated adult T-cell leukemia/lymphoma: a single-center, retrospective study.

机构信息

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Dermatopathology Service, Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

J Am Acad Dermatol. 2015 Feb;72(2):293-301. doi: 10.1016/j.jaad.2014.10.006. Epub 2014 Nov 8.

Abstract

BACKGROUND

Limited data exist regarding cutaneous involvement of adult T-cell leukemia/lymphoma (ATLL), particularly in the United States.

OBJECTIVE

We sought to characterize clinical and histopathologic features of ATLL in patients with skin involvement.

METHODS

We retrospectively identified patients with ATLL from a single institution given a diagnosis during a 15-year period (1998-2013). Patients were categorized by the Shimoyama classification and stratified into skin-first, skin-second, and skin-uninvolved courses.

RESULTS

The study population included 17 skin-first, 8 skin-second, and 29 skin-uninvolved cases. Skin-first patients (6 acute, 1 lymphoma, 4 chronic, 6 smoldering) were overwhelmingly of Caribbean origin (94%). They had longer median symptom duration (11.9 vs 1.9 months, P < .001) and overall survival (26.7 vs 10.0 months, P < .001) compared with skin-second/skin-uninvolved patients. Cutaneous lesion morphology at diagnosis included nodulotumoral (35%), multipapular (24%), plaques (24%), patches (12%), and erythroderma (6%). After initial skin biopsy, 14 of 17 received a non-ATLL diagnosis, most commonly mycosis fungoides (47%). Notable histopathologic findings from 43 biopsy specimens included greater than or equal to 20:1 CD4:CD8 ratio (79%), angiocentrism (78%), CD25(+) (71%), large cell morphology (70%), CD30(+) (68%), epidermal infiltration of atypical lymphocytes (67%) forming large Pautrier-like microabscesses (55%), and folliculotropism (65%).

LIMITATIONS

This was a retrospective, single-center, tertiary referral center study with small sample size.

CONCLUSION

Skin-first patients with ATLL in the United States are diagnostically challenging. Familiarity with clinicopathologic features may aid in diagnosis.

摘要

背景

成人 T 细胞白血病/淋巴瘤(ATLL)的皮肤受累情况数据有限,尤其是在美国。

目的

我们旨在描述皮肤受累的 ATLL 患者的临床和组织病理学特征。

方法

我们从一个机构回顾性地确定了在 15 年期间(1998-2013 年)被诊断为 ATLL 的患者。患者根据 Shimoyama 分类进行分类,并分为皮肤首发、皮肤次发和皮肤无累及三种类型。

结果

研究人群包括 17 例皮肤首发、8 例皮肤次发和 29 例皮肤无累及病例。皮肤首发患者(6 例急性、1 例淋巴瘤、4 例慢性、6 例冒烟型)绝大多数来自加勒比地区(94%)。与皮肤次发/皮肤无累及患者相比,他们的中位症状持续时间更长(11.9 个月 vs. 1.9 个月,P<.001)和总生存期更长(26.7 个月 vs. 10.0 个月,P<.001)。诊断时的皮肤病变形态包括结节性肿瘤样(35%)、多斑丘疹样(24%)、斑块样(24%)、斑片状(12%)和红皮病样(6%)。在初始皮肤活检后,17 例中的 14 例接受了非 ATLL 诊断,最常见的是蕈样真菌病(47%)。从 43 份活检标本中发现的显著组织病理学特征包括≥20:1 的 CD4:CD8 比值(79%)、血管中心性(78%)、CD25+(71%)、大细胞形态(70%)、CD30+(68%)、不典型淋巴细胞在表皮中的浸润形成大的 Pautrier 样微脓肿(55%)和滤泡嗜性(65%)。

局限性

这是一项回顾性的、单中心的、三级转诊中心研究,样本量小。

结论

美国的皮肤首发 ATLL 患者具有诊断挑战性。熟悉临床病理特征可能有助于诊断。

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