原发性皮肤cd30阳性大t细胞淋巴瘤1例80岁男性。

ISRN Dermatology Pub Date : 2011-01-01 Epub Date: 2011-03-30 DOI:10.5402/2011/634042
Rehan Hussain, Amir Bajoghli
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引用次数: 2

摘要

原发性皮肤CD30阳性大细胞淋巴瘤(CD30+ PCLCL)是一种罕见的皮肤t细胞淋巴瘤(CTCL)亚型,其表现形式多种多样。我们报告一个病人三个月的历史扩大,外生性肿块和两个较小的卫星病变在左前臂。皮肤活检显示CD30阳性,经过全面的系统评估,诊断为CD30+ PCLCL。当怀疑PCLCL时,重要的是进行CD30类型的免疫组织学研究,并进行彻底的检查以排除全身性LCL。这些措施将减少对CD30+ PCLCL(一种预后良好的惰性疾病)不必要的积极化疗方案的使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary Cutaneous CD30-Positive Large T-Cell Lymphoma in an 80-Year-Old Man: A Case Report.

Primary Cutaneous CD30-Positive Large T-Cell Lymphoma in an 80-Year-Old Man: A Case Report.

Primary Cutaneous CD30-Positive Large T-Cell Lymphoma in an 80-Year-Old Man: A Case Report.

Primary Cutaneous CD30-Positive Large T-Cell Lymphoma in an 80-Year-Old Man: A Case Report.

Primary cutaneous CD30-positive large cell lymphoma (CD30+ PCLCL) is a rare subtype of cutaneous T-cell lymphoma (CTCL) that can present in a variety of ways. We report a patient with a three-month history of an enlarging, exophytic mass with two smaller satellite lesions on the left forearm. Biopsy of the skin stained positive for CD30, and, after thorough systemic evaluation, a diagnosis of CD30+ PCLCL was made. When PCLCL is suspected, it is important to perform immunohistological studies for CD30 types and conduct a thorough workup to rule out systemic LCL. These measures will reduce the use of unnecessarily aggressive chemotherapy regimens for CD30+ PCLCL, an indolent disease with a favorable prognosis.

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