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原发性皮肤间变性大细胞淋巴瘤

Primary cutaneous anaplastic large cell lymphoma.

作者信息

Daar Ghania, Küpeli Serhan, Yalçin Bilgehan, Kesik Vural, Orhan Diclehan, Büyükpamukçu Münevver

机构信息

Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

出版信息

Pediatr Hematol Oncol. 2010 Oct;27(7):558-63. doi: 10.3109/08880018.2010.493575.

Abstract

Anaplastic large cell lymphoma (ALCL) is characterized by proliferation of anaplastic large CD 30+ T-cell lymphoid cells with abundant cytoplasm. Primary cutaneous ALCL is a rare form of ALCL, usually seen in elderly patients. In this report, the authors present an unusual case of 15-year-old boy with a solitary left ear lobe mass, previously reported as keratoacanthoma which was later histopathologically and immunohistochemically diagnosed as T-cell phenotype, anaplastic lymphoma kinase (ALK)-negative primary cutaneous anaplastic large cell lymphoma. The patient's response to chemotherapy was good and he is receiving the continuation phases of his chemotherapy.

摘要

间变性大细胞淋巴瘤(ALCL)的特征是具有丰富细胞质的间变性大的CD 30 + T细胞样淋巴细胞增殖。原发性皮肤ALCL是ALCL的一种罕见形式,通常见于老年患者。在本报告中,作者介绍了一例不寻常的病例,一名15岁男孩,左耳叶有一个孤立肿块,此前报告为角化棘皮瘤,后来经组织病理学和免疫组织化学诊断为T细胞表型、间变性淋巴瘤激酶(ALK)阴性的原发性皮肤间变性大细胞淋巴瘤。该患者对化疗反应良好,目前正在接受化疗的延续阶段治疗。

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