[原发性皮肤间变性大细胞淋巴瘤：1例报告]

[Primary cutaneous anaplastic large cell lymphoma: Report of one case].

作者信息

Navarrete-Dechent Cristián, Molgó Montserrat, Sandoval-Osses Mauricio, González Sergio

出版信息

Rev Med Chil. 2015 Oct;143(10):1351-5. doi: 10.4067/S0034-98872015001000015.

DOI:10.4067/S0034-98872015001000015

Abstract

Primary cutaneous anaplastic large cell lymphoma (PCALCL) is within the spectrum of cutaneous CD30-positive lymphoproliferative disorders. It presents as localized or multifocal tumors or plaques and carries an excellent long-term prognosis even in cases with regional and/or ipsilateral lymph node involvement or in cases of recurrent disease. We report a 34 year-old female with a thigh lesion. Skin biopsy confirmed the diagnosis of PCALCL. The patient was strictly monitored but no treatment was instituted and the tumor regressed spontaneously. After 24 months of follow-up the patient remains free of disease without new lesions.

摘要

原发性皮肤间变性大细胞淋巴瘤（PCALCL）属于皮肤CD30阳性淋巴增殖性疾病范畴。它表现为局限性或多灶性肿瘤或斑块，即使在出现区域和/或同侧淋巴结受累的病例或复发病例中，也具有良好的长期预后。我们报告一名34岁患有大腿部病变的女性。皮肤活检确诊为PCALCL。该患者受到严格监测，但未进行治疗，肿瘤自行消退。经过24个月的随访，患者无疾病复发且无新病变。