Primary Cutaneous Anaplastic Large-Cell Lymphoma

IF 1.6 Q3 DERMATOLOGY
Dermatopathology Pub Date : 2019-06-26 DOI:10.1159/000500259
N. Moodley, Patiswa Nombona, A. Mosam
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引用次数: 8

Abstract

A 35-year-old male presented with a 6-month history of asymptomatic, generalised, self-healing lesions. On clinical examination, there were diffuse, ulcerated, necrotic papules and nodules with lymphoedema of the face. Histology sections confirmed atypical lymphoid-type cells which appeared round-to-oval with irregular nuclei (horseshoe-shaped). Immunohistochemistry stains were positive for CD30, CD3, and epithelial membrane antigen. The features were in keeping with an anaplastic large-cell lymphoma, T cell type. This transformed into a systemic variant of the disease after the patient had completed chemotherapy.
原发性皮肤变性大细胞淋巴瘤
一名35岁男性,有6个月的无症状、全身性、自愈性病变史。临床检查可见面部弥漫性、溃疡性、坏死性丘疹、结节伴淋巴水肿。组织学切片证实非典型淋巴型细胞,呈圆形至椭圆形,细胞核不规则(马蹄形)。免疫组化染色CD30、CD3和上皮膜抗原阳性。特征与间变性大细胞淋巴瘤,T细胞型一致。在患者完成化疗后,这转化为疾病的系统性变体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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