莱姆病患者弥散性边缘带淋巴瘤1例报告。

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2025-01-08 eCollection Date: 2025-01-01 DOI:10.1159/000543348
Dorit Kraft Weisbjerg, Sigurdur Skarphedinsson, Nanna Skaarup Andersen, Louise Kristensen, Thomas Stauffer Larsen, Fredrikke Christie Knudtzen
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引用次数: 0

摘要

莱姆病与淋巴瘤,特别是皮肤淋巴瘤有关。文献关于抗生素治疗皮肤边缘区淋巴瘤(MZLs)的个体莱姆病是矛盾的。我们报告一位被诊断为莱姆病神经螺旋体病(LNB)和弥散性MZL的患者。病例介绍:一名67岁男性,因神经性疼痛6周,夜间加重,头痛,体重减轻5公斤而就诊。在症状出现前两周,他在左腹股沟有蜱虫叮咬,随后没有皮疹。腰椎穿刺显示单核细胞增多和脑脊液蛋白升高。患者入院并开始服用头孢曲松。伯氏疏螺旋体鞘内试验显示鞘内产生伯氏疏螺旋体抗体,并改为强力霉素治疗,总治疗时间为21天。PET/CT显示淋巴结肿大,FDG摄取增加。病理检查脑脊液显示62%的克隆B细胞-与低级别B细胞淋巴瘤相容。骨髓及腹股沟淋巴结检查证实弥散性MZL。8周后的对照腰椎穿刺显示细胞增多和克隆B细胞减少。在20个月后的最后一次随访中,他仍然无症状,不需要抗肿瘤治疗。结论:据我们所知,这是第一例LNB合并非皮肤b细胞淋巴瘤单独使用抗生素治疗并缓解的病例。对伯氏疏螺旋体阳性淋巴瘤的抗生素治疗尚未进行高证据研究设计的调查,因此鼓励临床医生发表与此相关的阳性和阴性结果。我们相信这个病例为莱姆病患者淋巴瘤的诊断和治疗带来了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disseminated Marginal Zone Lymphoma in a Patient with Lyme Neuroborreliosis: A Case Report.

Introduction: Lyme borreliosis has been associated with lymphoma, particularly cutaneous lymphomas. The literature is conflicted regarding the effect of antibiotic therapy in cutaneous marginal zone lymphomas (MZLs) in individuals with Lyme borreliosis. We present a patient diagnosed with Lyme neuroborreliosis (LNB) and disseminated MZL.

Case presentation: A 67-year-old man was seen due to 6 weeks of neuropathic pain with nightly worsening, headache, and 5 kg weight loss. Two weeks prior to symptom debut, he had a tick bite in the left groin, no subsequent rash. A lumbar puncture revealed mononuclear pleocytosis and elevated CSF protein. The patient was admitted and started on ceftriaxone. The Borrelia burgdorferi intrathecal test showed intrathecally produced Borrelia antibodies, and treatment was changed to doxycycline with a total treatment duration of 21 days. A PET/CT revealed enlarged lymph nodes with increased FDG uptake. On pathological examination, the CSF showed 62% clonal B cells - compatible with low-grade B-cell lymphoma. Examination of bone marrow and an inguinal lymph node confirmed disseminated MZL. A control lumbar puncture 8 weeks later showed declining pleocytosis and clonal B cells. At last follow-up 20 months later, he was still asymptomatic and had not required antineoplastic treatment.

Conclusion: To our knowledge, this is the first published case of LNB with non-cutaneous B-cell lymphoma treated and remitting on antibiotics alone. Antibiotic treatment for Borrelia-positive lymphomas has yet to be investigated with high-evidence study designs, so clinicians are encouraged to publish both positive and negative findings relevant to this. We believe this case brings new perspectives to future diagnosis and treatment of lymphomas in patients with verified Lyme borreliosis.

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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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