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.
J Am Acad Dermatol. 2015 Feb;72(2):293-301. doi: 10.1016/j.jaad.2014.10.006. Epub 2014 Nov 8.
Limited data exist regarding cutaneous involvement of adult T-cell leukemia/lymphoma (ATLL), particularly in the United States.
We sought to characterize clinical and histopathologic features of ATLL in patients with skin involvement.
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.
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%).
This was a retrospective, single-center, tertiary referral center study with small sample size.
Skin-first patients with ATLL in the United States are diagnostically challenging. Familiarity with clinicopathologic features may aid in diagnosis.
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。
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。
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。
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%)。
这是一项回顾性的、单中心的、三级转诊中心研究,样本量小。
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。