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ALK阴性系统型间变性大细胞淋巴瘤累及皮肤1例

A case of ALK negative systemic anaplastic large cell lymphoma with cutaneous involvement
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摘要 报告ALK阴性系统型间变性大细胞淋巴瘤累及皮肤1例。患者男,38岁。因全身丘疹、结节4个月,加重伴发热7天就诊。皮肤专科检查:面颈部、躯干及四肢见散在分布数个紫红色丘疹、结节,大小不等,最大直径3 cm,边界清,部分丘疹破溃后溢脓,愈后遗留色素减退性疤痕。右颏下、锁骨上、双侧腹股沟可触及多发性皮下包块,最大直径3 cm,界尚清,无压痛,活动度可。全身PET-CT示:全身多处局部皮肤增厚代谢活跃,多发淋巴结代谢活跃,广泛骨病灶代谢活跃,考虑恶性病变。左颈部皮损病理检查:真皮血管,汗腺小皮神经周围淋巴组织细胞、嗜中性白细胞和嗜酸性白细胞浸润,少许细胞有异型性,抗酸染色(-),PAS(-)。免疫组化:CD30、CD3、CD4均(+),TIA-1、CD8、CD20均(+-),CD79a、CD56、ALK均(-)。左颈部淋巴结病理检查:镜下见多形大细胞与大量炎症细胞混杂浸润,细胞体积较大,具有明显异型性。免疫组化:CD30、CD2、CD43均(+),CD20、CD3、CD15、CK、ALK均(-),Ki-67(+约30%~40%)。病理诊断:ALK阴性间变性大细胞淋巴瘤。诊断:ALK阴性系统型间变性大细胞淋巴瘤Ⅲ期B型(累及皮肤)。
出处 《皮肤性病诊疗学杂志》 2018年第5期280-283,共4页 Journal of Diagnosis and Therapy on Dermato-venereology
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