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秘鲁的原发性肺淋巴瘤。

Primary pulmonary lymphoma in Peru.

作者信息

Requena Elily Dianet Apumayta, Ocrospoma Danery Valdez, Ruiz Jhonatanael Salvador, De la Guerra Pancorvo Alberto, Kajatt Edgar Amorin

机构信息

Surgical Oncology Resident, Instituto Nacional de Enfermedades Neoplásicas, Lima, Perú.

https://orcid.org/0000-0002-1828-7009.

出版信息

Ecancermedicalscience. 2023 Jun 15;17:1559. doi: 10.3332/ecancer.2023.1559. eCollection 2023.

Abstract

OBJECTIVE

To describe the clinical features, imaging, pathology and management of patients with primary pulmonary lymphoma (PPL).

METHODOLOGY

This is a case series study involving a retrospective analysis of 24 patients diagnosed with PPL between the years 2000-2019 at Instituto Nacional de Enfermedades Neoplásicas in Lima, Perú.

RESULTS

73.9% of patients were male. Cough (78.3%) and weight loss (56.5%) were the most frequent clinical features. Dyspnoea and elevated values of DHL and B2 microglobulin were frequently altered in advanced stages. Diffuse large B cell lymphoma (DLBCL) represented 47.8% of the cases and the most common radiologic alterations were a mass (60%) and consolidation with air bronchogram (60%). The most utilised treatment was chemotherapy alone (60%). Three patients received only surgery. Median survival was 30 months. Five overall survival was 45%, and up to 60% in the case of mucosa-associated lymphoid tissue lymphoma.

CONCLUSION

PPL is infrequent. Clinical features are unspecific and the principal finding is a mass, nodule or consolidation with air bronchogram. Definitive diagnosis needs biopsy and immunohistochemistry. There is no standard treatment, it depends on histology type and stage.

摘要

目的

描述原发性肺淋巴瘤(PPL)患者的临床特征、影像学表现、病理及治疗情况。

方法

本病例系列研究对2000年至2019年间在秘鲁利马国家肿瘤研究所诊断为PPL的24例患者进行回顾性分析。

结果

73.9%的患者为男性。咳嗽(78.3%)和体重减轻(56.5%)是最常见的临床特征。晚期患者常出现呼吸困难以及乳酸脱氢酶(DHL)和β2微球蛋白值升高。弥漫性大B细胞淋巴瘤(DLBCL)占病例的47.8%,最常见的影像学改变是肿块(60%)和伴有空气支气管征的实变(60%)。最常用的治疗方法是单纯化疗(60%)。3例患者仅接受了手术。中位生存期为30个月。总体生存率为45%,黏膜相关淋巴组织淋巴瘤患者的生存率高达60%。

结论

PPL较为罕见。临床特征不具特异性,主要表现为肿块、结节或伴有空气支气管征的实变。确诊需要活检和免疫组化。目前尚无标准治疗方案,治疗方案取决于组织学类型和分期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d00c/10310327/33693b26b178/can-17-1559fig1.jpg

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