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ALK-positive primary cutaneous anaplastic large cell lymphoma: a case report and review of the literature

机译:ALK阳性原发性皮肤间变性大细胞淋巴瘤:1例报道并文献复习

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摘要

Anaplastic large cell lymphoma (ALCL) limited to the skin is a distinct disease that is designated primary cutaneous ALCL (pcALCL). It has an indolent course with a significantly better prognosis compared to systemic ALCL (sALCL). Anaplastic lymphoma kinase (ALK) expression in lesions of cutaneous ALCL is classically considered to be a marker for skin involvement by sALCL. However recent reports of patients with ALK-positive pcALCL challenge this concept and raise prognostic and therapeutic dilemmas. Herein we report a case of ALK-positive pcALCL in a 45 year-old woman who was treated with local radiotherapy. We review previously reported cases in the literature to better characterize this rare variant. Overall the rates of cutaneous recurrence, systemic dissemination and disease related mortality in ALK-positive pcALCL do not differ from those previously reported in pcALCL. ALK-positive pcALCL is diagnosed at younger age and has a better disease course in children compared to adults with lower incidences of skin recurrence and progression to systemic disease. We conclude that ALK-positivity in cutaneous ALCL does not necessarily imply systemic disease. ALK-positive pcALCL has an excellent prognosis and should be treated by excision and/or radiotherapy. However patients must remain under close long-term follow-up as recurrence and progression to systemic disease may occur.
机译:限于皮肤的间变性大细胞淋巴瘤(ALCL)是一种独特的疾病,称为原发性皮肤ALCL(pcALCL)。与系统性ALCL(sALCL)相比,它的病程缓慢,预后明显好转。皮肤ALCL病变中的间变性淋巴瘤激酶(ALK)表达通常被认为是sALCL累及皮肤的标志物。然而,最近关于ALK阳性pcALCL患者的报道挑战了这一概念,并增加了预后和治疗难题。在此,我们报告了一名接受局部放疗的45岁女性中ALK阳性pcALCL的病例。我们回顾了文献中以前报道的病例,以更好地表征这种罕见的变异。总的来说,ALK阳性pcALCL的皮肤复发率,全身性传播率和与疾病相关的死亡率与pcALCL中先前报道的率没有差异。与成年人相比,ALK阳性的pcALCL被诊断为较年轻,并且儿童的病程更好,皮肤复发和发展为全身性疾病的几率较低。我们得出的结论是,皮肤ALCL中的ALK阳性不一定暗示系统性疾病。 ALK阳性的pcALCL预后良好,应通过切除和/或放疗进行治疗。但是,由于复发和发展为全身性疾病,患者必须长期接受密切随访。

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