A case of cutaneous variant of intravascular large B-cell lymphoma in which dermoscopy revealed telangiectasias associated with erythematous induration

IF 2.3 Q2 DERMATOLOGY Dermatology Reports Pub Date : 2023-09-13 DOI:10.4081/dr.2023.9731
Shigeru Koizumi, Yaei Togawa, Yuka Saeki, Ryo Shimizu, Michiyo Nakano
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Abstract

Intravascular large B-cell lymphoma (IVLBCL) is a rare type of extranodal, diffuse, large B-cell lymphoma characterized by the selective growth of lymphoma cells within the lumen of small blood vessels, with no lymphadenopathy or masses. Herein, we report a cutaneous variant of IVLBCL that is rare in Asia. A healthy 73-year-old Japanese woman presented to our hospital with painful erythematous indurations and telangiectasia of the lower extremities, which was confirmed on dermoscopy. Physical examination revealed no systemic involvement, and laboratory parameters were within normal ranges. No abnormal FDG uptake was detected on 18FDG-PET/CT. Histopathological examination revealed proliferation and dilatation of blood vessels in the subcutis layer, occluded by CD20-positive atypical lymphoid cells. Thus, the patient was diagnosed with a cutaneous variant of IVLBCL without systemic symptoms. In conclusion, it is important to confirm telangiectasia using dermoscopy and perform skin biopsies in patients presenting with sudden-onset erythematous induration.
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皮肤变异体血管内大b细胞淋巴瘤病例,皮肤镜检查显示毛细血管扩张伴红斑硬化
血管内大b细胞淋巴瘤(IVLBCL)是一种罕见的结外弥漫性大b细胞淋巴瘤,其特征是淋巴瘤细胞在小血管腔内选择性生长,无淋巴结病变或肿块。在此,我们报告一种在亚洲罕见的IVLBCL的皮肤变异。一名73岁的健康日本女性以下肢疼痛的红斑性硬化和毛细血管扩张就诊于我院,经皮肤镜检查证实。体格检查未发现全身受累,实验室参数在正常范围内。18FDG-PET/CT未见FDG摄取异常。组织病理学检查显示皮下血管增生和扩张,被cd20阳性的非典型淋巴样细胞所阻塞。因此,该患者被诊断为无全身症状的IVLBCL皮肤变异型。总之,在出现突发性红斑性硬结的患者中,重要的是通过皮肤镜检查和皮肤活检来确认毛细血管扩张。
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来源期刊
Dermatology Reports
Dermatology Reports DERMATOLOGY-
CiteScore
1.40
自引率
0.00%
发文量
74
审稿时长
10 weeks
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