间变性大细胞淋巴瘤alk阴性:关于一个罕见的儿科病例报告

Louachama Ouidad, Elbaz Meriem, El Houdzi Jamila
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引用次数: 0

摘要

间变性大细胞淋巴瘤(ALCL)在儿童时期罕见,但临床上具有侵袭性。当代世界卫生组织(WHO)对血液恶性肿瘤的分类识别出系统性ALCL的两种不同亚型:间变性淋巴瘤激酶(ALK)阴性和ALK阳性。我们报告一个罕见的儿童皮肤结节显示间变性大细胞淋巴瘤(ALCL) ALK -皮肤,肌肉和神经节。根据who分类,采用综合化疗治疗,疗效良好。ALCL包括几种不同的临床病理实体,具有独特的基因组打印。这种罕见的儿科ALCL观察提出了一个新的病理尚不完全清楚的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anaplastic Large Cell Lymphoma ALK-Negative: About a Rare Pediatric Case Report
Anaplastic Large Cell Lymphomas (ALCL) are rare in childhood but clinically aggressive. The contemporary World Health Organization (WHO) classification of hematologic malignancies recognizes two distinct subtypes of systemic ALCL: Anaplastic Lymphoma Kinase (ALK)-negative, and ALK-positive. We report a rare pediatric observation of cutaneous nodule revealing an Anaplastic Large Cell Lymphoma (ALCL) ALK - cutaneous, muscular and ganglionic. It was classified according to who classification, treated by polychemotherapy with good outcome. ALCL encompasses several distinct clinicopathologic entities with unique genomic under printing. This rare pediatric observation of ALCL presents a new discussion on a pathology still incompletely known.
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