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Primary Cutaneous T-Cell/Histiocyte-Rich B-Cell Lymphoma: A Case Report and Literature Review.原发性皮肤T细胞/组织细胞丰富的B细胞淋巴瘤:一例报告及文献综述
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Cutaneous primary B-cell lymphomas: from diagnosis to treatment.皮肤原发性B细胞淋巴瘤:从诊断到治疗
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Primary cutaneous B-cell lymphoma with abundant reactive gamma/delta T-cells within the skin lesion and peripheral blood.原发性皮肤B细胞淋巴瘤,皮肤病变及外周血中存在大量反应性γ/δ T细胞。
Int J Clin Exp Pathol. 2014 Feb 15;7(3):1193-9. eCollection 2014.

α-2a干扰素治疗原发性富含T细胞的B细胞淋巴瘤获得完全缓解

Complete response of a primary cutaneous T-cell-rich B cell lymphoma treated with interferon alpha2a.

作者信息

Wollina U

机构信息

Department of Dermatology, Friedrich Schiller University of Jena, Germany.

出版信息

J Cancer Res Clin Oncol. 1998;124(2):127-9. doi: 10.1007/s004320050144.

DOI:10.1007/s004320050144
PMID:9654196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12201678/
Abstract

Primary B cell lymphomas of the skin are rare disorders and therapy is not yet standardized. A 45-year-old male patient presented 4 years after surgical removal of a subcutaneous tumour of the leg. On examination a reddish nodular tumour was found in the same region. The biopsy revealed a T-cell-rich primary B cell lymphoma of the skin. Interferon alpha2a was given perilesionally at a dosage of 9 MU three times a week. The treatment was well tolerated, had no severe side-effects and induced a complete remission, both clinically and histologically, during a 12-months course.

摘要

皮肤原发性B细胞淋巴瘤是罕见疾病,治疗尚未标准化。一名45岁男性患者在腿部皮下肿瘤手术切除4年后就诊。检查发现同一区域有一个红色结节状肿瘤。活检显示为皮肤富含T细胞的原发性B细胞淋巴瘤。在病灶周围给予α2a干扰素,剂量为9 MU,每周3次。治疗耐受性良好,无严重副作用,在12个月的疗程中临床和组织学上均诱导完全缓解。