Daar Ghania, Küpeli Serhan, Yalçin Bilgehan, Kesik Vural, Orhan Diclehan, Büyükpamukçu Münevver
Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Pediatr Hematol Oncol. 2010 Oct;27(7):558-63. doi: 10.3109/08880018.2010.493575.
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.
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。