边缘带淋巴瘤伪装为肿性痤疮酒渣鼻:一个案例研究。

Q3 Medicine
Skin health and disease Pub Date : 2025-04-11 eCollection Date: 2025-06-01 DOI:10.1093/skinhd/vzaf026
Hina S Baloch, Zhenghao Wang, Joy U L Staniforth, Azaharry Yaakub
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引用次数: 0

摘要

边缘带淋巴瘤(MZL)是一种惰性b细胞淋巴瘤,其临床表现具有相当大的异质性。皮肤MZL通常表现为丘疹、斑块或结节,常累及躯干和手臂。罕见的病例MZL表现为痤疮酒渣鼻已被报道;然而,这些主要被报道为肉芽肿性酒糟鼻。MZL的具体证据表现为肿性痤疮酒渣鼻是极其罕见的,并没有很好地记录在医学文献。我们报告一例罕见的原发性全身性结节性MZL与皮肤结节外MZL一起表现,模仿鼻疣性和耳粘膜性痤疮酒渣鼻。84岁白人男性,有13年淋巴结性MZL病史,在积极监测下,表现为耳部和鼻部红斑、肿胀病变。这最初被诊断为痤疮酒渣鼻;然而,常规治疗证明无效,患者被转介进行皮肤病学评估。耳垂皮肤活检显示小淋巴样B细胞弥漫性浸润,CD20、CD79a和BCL2阳性,CD5和CD23阴性,与皮肤MZL一致。进一步影像学显示全身受累,横膈膜上下淋巴结肿大,脾肿大。患者开始接受R-CVP化疗(利妥昔单抗、环磷酰胺、长春新碱和强的松龙),导致皮肤病变和全身性疾病的显着改善。然而,由于化疗不耐受,治疗在四个周期后停止。本病例表现为罕见的MZL,类似肿性痤疮红斑痤疮的特征,尤其是鼻肿和耳肿。与酒渣鼻的相似,特别是肿型亚型,导致最初的误诊和适当治疗的延误。这强调了在非典型或无反应性皮肤病患者中考虑替代诊断的重要性,特别是当常规治疗失败时。早期活检和组织学评估对于确保及时诊断和治疗至关重要,可能会改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Marginal zone lymphoma masquerading as phymatous acne rosacea: a case study.

Marginal zone lymphoma (MZL) is an indolent B-cell lymphoma characterized by considerable heterogeneity in clinical presentation. Cutaneous MZL typically manifests as papules, plaques or nodules, often affecting the trunk and arms. Rare cases of MZL presenting as acne rosacea have been reported; however, these have been primarily reported as granulomatous rosacea. Specific evidence of MZL presenting as phymatous acne rosacea is extremely rare and not well documented in the medical literature. We report a rare case of primary systemic nodal MZL manifesting alongside cutaneous extra-nodal MZL, mimicking rhinophymatous and otophymatous acne rosacea. An 84-year-old White man with a 13-year history of nodal MZL, under active monitoring, presented with erythematous, swollen lesions on the ears and nose. This was initially diagnosed as acne rosacea; however, conventional treatment proved ineffective, and the patient was referred for dermatological evaluation. A skin biopsy from the earlobe revealed a diffuse infiltrate of small lymphoid B cells, positive for CD20, CD79a and BCL2, and negative for CD5 and CD23, consistent with cutaneous MZL. Further imaging revealed systemic involvement, with enlarged lymph nodes above and below the diaphragm and splenomegaly. The patient was started on R-CVP chemotherapy (rituximab, cyclophosphamide, vincristine and prednisolone), leading to significant improvement in both the skin lesions and systemic disease. However, due to chemotherapy intolerance, treatment was discontinued after four cycles. This case highlights a rare presentation of MZL, mimicking the features of phymatous acne rosacea, particularly rhinophyma and otophyma. The resemblance to rosacea, particularly phymatous subtypes, leads to initial misdiagnosis and delays in appropriate treatment. This underlines the importance of considering alternative diagnoses in patients with atypical or nonresponsive dermatological conditions, especially when conventional therapies fail. Early biopsy and histological evaluation are critical for ensuring timely diagnosis and treatment, potentially improving patient outcomes.

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