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首页> 外文期刊>American journal of clinical dermatology >Cutaneous anaplastic large-cell lymphoma should be evaluated for systemic involvement regardless of ALK-1 status: case reports and review of literature.
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Cutaneous anaplastic large-cell lymphoma should be evaluated for systemic involvement regardless of ALK-1 status: case reports and review of literature.

机译:无论ALK-1状态如何,均应评估皮肤间变性间变性大细胞淋巴瘤的系统性受累:病例报告和文献复习。

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摘要

Anaplastic large-cell lymphoma (ALCL) is a lymphoma that expresses CD30. Cutaneous ALCL presents either as primary cutaneous disease or as secondary skin involvement due to the systemic disease. Herein, we describe two patients who presented to dermatology for evaluation of skin lesions diagnosed by non-dermatologists as a cutaneous abscess and lupus erythematosus, respectively. Upon investigation by a team of medical dermatologists and dermatopathologists, systemic ALCL with secondary skin involvement was discovered in both patients. The majority of cases of systemic ALCL with cutaneous involvement express anaplastic lymphoma kinase-1 (ALK-1), and are associated with a more favorable prognosis than ALK-1-negative cases. However, cutaneous ALCL regardless of ALK-1 status may be secondary to systemic lymphoma. This article stresses the importance of dermatologists being aware of the diagnosis of systemic lymphoma based on cutaneous findings, and being aggressive in initiating appropriate diagnostic testing. Primary cutaneous ALCL and systemic ALCL are reviewed.
机译:间变性大细胞淋巴瘤(ALCL)是表达CD30的淋巴瘤。由于全身性疾病,皮肤ALCL表现为原发性皮肤病或继发性皮肤受累。在这里,我们描述了两名患者,他们接受了皮肤病学评估,分别由非皮肤科医生诊断为皮肤脓肿和红斑狼疮。经过医学皮肤科医生和皮肤病理学家团队的调查,在两名患者中均发现了具有继发性皮肤受累的全身性ALCL。系统性ALCL皮肤受累的大多数病例都表达间变性淋巴瘤激酶-1(ALK-1),并且比ALK-1阴性病例的预后更好。但是,无论ALK-1状态如何,皮肤ALCL可能继发于全身淋巴瘤。本文强调了皮肤科医生必须根据皮肤发现认识到系统性淋巴瘤的诊断,并积极开展适当的诊断测试,这一点很重要。回顾了原发性皮肤ALCL和全身性ALCL。

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