CD5+原发性皮肤弥漫性大B细胞淋巴瘤,腿型,表现为无症状结节。

IF 1.1 Q4 HEMATOLOGY Hematology Reports Pub Date : 2023-09-01 DOI:10.3390/hematolrep15030053
Amy Xiao, Colleen J Beatty, Sonal Choudhary, Oleg E Akilov
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引用次数: 0

摘要

原发性皮肤弥漫性大B细胞淋巴瘤,腿型(PCDLBCL-LT),是一种罕见的原发性皮淋巴瘤的侵袭性变体,通常表达B细胞以及MUM1/IRF4、BCL2和FOXP1,而BCL6可能存在或检测不到。我们报告了一例CD5+PCDLBCL-LT,表现为左大腿中部6毫米的粉红色蓝色结节,与基底细胞癌有关。组织学检查显示,大的非典型CD5+、CD20+BCL2+、BCL6+、MUM-1+和Cyclin-D1+淋巴细胞在皮内增殖,呈结节状、弥漫性间质和血管周围分布。由于患者出现小的单个结节,因此避免了多药剂化疗的全身治疗,而是开始了利妥昔单抗的局部电子束放射治疗,实现了完全缓解。PCDLBCL-LT的早期鉴定是最大治疗效益和预后的关键;在评估老年患者下肢的单个小结节时,重要的是要考虑PCDLBCL-LT的差异。
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CD5+ Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type, Presenting as an Asymptomatic Nodule.

Primary cutaneous diffuse large B-cell lymphoma, leg type (PCDLBCL-LT), is a rare and aggressive variant of primary cutaneous lymphoma that typically expresses B cells as well as MUM1/IRF4, BCL2, and FOXP1, whereas BCL6 may be present or undetectable. We present a case of CD5+ PCDLBCL-LT presenting as a 6 mm pink-bluish nodule on the mid-left thigh, which was concerning for basal cell carcinoma. The histological examination reveals the presence of an intradermal proliferation of large, atypical CD5+, CD20+ BCL2+, BCL6+, MUM-1+, and Cyclin-D1+ lymphocytes in a nodular, diffuse interstitial and perivascular distribution. Because the patient presented with a small, single nodule, the systemic treatment of multiagent chemotherapy was avoided and localized electron beam radiation therapy with rituximab was initiated instead, achieving complete response. Early identification of PCDLBCL-LT is key for maximal therapeutic benefit and prognosis; it is important to consider PCDLBCL-LT on the differential when evaluating small, single nodules on the lower extremities of elderly patients.

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来源期刊
Hematology Reports
Hematology Reports HEMATOLOGY-
CiteScore
0.90
自引率
0.00%
发文量
47
审稿时长
10 weeks
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