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A rare case of ALK negative CD30+ primary cutaneous anaplastic large cell lymphoma in a young adult

机译:年轻人中ALK阴性CD30 +原发性皮肤间变性大细胞淋巴瘤的罕见病例

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Cutaneous anaplastic large cell lymphoma can present either as a primary disease or as secondary to a pre-existing systemic anaplastic lymphoma. Distinguishing primary cutaneous anaplastic lymphoma (PC-ALCL) from its systemic counterpart requires a complete clinical and laboratory workup. We hereby report a case of PC-ALCL in a young adult, who presented with unusual rapidly progressive ulcerated mass in the neck. Biopsy showed anaplastic large cells, which were strongly positive for CD30 and CD25 but ALK1 gene product was negative. Clinical examination and computed tomography (CT) scan ruled out extracutaneous involvement. Chemotherapy with 6 cycles of CHOP regimen was planned and on follow-up, a complete remission of the lesion was attained.
机译:皮肤间变性间变性大细胞淋巴瘤可作为原发性疾病或继发于系统性间变性间变性淋巴瘤的继发性。要将原发性皮肤间变性淋巴瘤(PC-ALCL)与全身性的区别开来,需要进行完整的临床和实验室检查。我们在此报告一例在年轻人中出现PC-ALCL的病例,该年轻人表现出异常的颈部快速进行性溃疡性肿块。活检显示间变性大细胞,其对CD30和CD25呈强阳性,但ALK1基因产物呈阴性。临床检查和计算机断层扫描(CT)扫描排除了皮肤外累及。计划使用CHOP方案的6个周期的化学疗法,并在随访中实现病灶的完全缓解。

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