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ALK 阳性原发性皮肤间变大细胞淋巴瘤:一例报告及文献复习。

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

机构信息

Dermatology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center and Weill Cornell Medicine, New York, NY, USA.

Department of Dermatology, University of Alabama, Birmingham, AL, USA.

出版信息

Int J Dermatol. 2018 May;57(5):515-520. doi: 10.1111/ijd.13804. Epub 2017 Oct 23.

Abstract

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.

摘要

皮肤局限型间变大细胞淋巴瘤(ALCL)是一种独特的疾病,被指定为原发性皮肤 ALCL(pcALCL)。与系统性 ALCL(sALCL)相比,它具有惰性病程和明显更好的预后。皮肤 ALCL 病变中表达的间变性淋巴瘤激酶(ALK)经典地被认为是 sALCL 累及皮肤的标志物。然而,最近报道的 ALK 阳性 pcALCL 患者对这一概念提出了挑战,并引发了预后和治疗方面的难题。在此,我们报告了一例 45 岁女性的 ALK 阳性 pcALCL,该患者接受了局部放疗。我们回顾了文献中以前报道的病例,以更好地描述这种罕见的变体。总体而言,ALK 阳性 pcALCL 的皮肤复发率、全身播散率和疾病相关死亡率与以前报道的 pcALCL 无差异。ALK 阳性 pcALCL 在儿童中发病年龄更年轻,疾病病程更好,与成年人相比,皮肤复发率和进展为全身疾病的发生率较低。我们得出结论,ALK 阳性在皮肤 ALCL 中不一定意味着系统性疾病。ALK 阳性 pcALCL 具有极好的预后,应通过切除和/或放疗进行治疗。然而,患者必须接受密切的长期随访,因为可能会出现复发和进展为系统性疾病。

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