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Primary Cutaneous Anaplastic Large-Cell Lymphoma

机译:原发性皮肤间变性大细胞淋巴瘤

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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.
机译:一名35岁男性,有6个月无症状,全身性,自愈性病史。临床检查发现,弥漫性,溃疡性坏死性丘疹和结节伴面部淋巴水肿。组织学切片证实非典型淋巴样细胞呈圆形到卵形,核不规则(马蹄形)。免疫组织化学染色对CD30,CD3和上皮膜抗原呈阳性。其特征与间变性大细胞淋巴瘤(T细胞型)一致。患者完成化疗后,这转变为该疾病的全身性变异。

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