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原发性肺淋巴瘤的临床与误诊分析:一项回顾性研究。

Clinical and misdiagnosed analysis of primary pulmonary lymphoma: a retrospective study.

机构信息

The First Affiliated Hospital of Wenzhou Medical University & Key Laboratory of Heart and Lung, Zhejiang, 325035, China.

Wenzhou Medical University, Zhejiang, 325035, China.

出版信息

BMC Cancer. 2018 Mar 12;18(1):281. doi: 10.1186/s12885-018-4184-1.

Abstract

BACKGROUND

The primary pulmonary lymphoma (PPL), with a low incidence, was highly misdiagnosed in clinic. The present study analyzes the clinical features, laboratory and imaging data, pathologic characteristics, and summarizes misdiagnosis reasons of PPL cases, aims to provide a better understanding and increase the accuracy of early diagnosis and minimize the misdiagnosis of PPL.

METHODS

The clinical data of 19 cases were collected from the first affiliated hospital of Wenzhou medical university (PRC) from April 2010 to May 2016. All cases were confirmed by pathology. The process of misdiagnosis was described. This study retrospectively analyzed the incidence, clinical presentation, laboratory examination, Chest CT scan and diagnosis of the cases.

RESULTS

The symptoms of the 19 cases were dyspnea, fever, hemoptysis, chest pain or physical findings without obvious symptoms. Five patients were pneumonia-like, nine patients had lung single nodule or mass and four patients got pleural effusion, which were reported by computed tomography (HRCT) scan. There were 2 cases of Hodgkin lymphoma (HL), and 17 cases of non-Hodgkin lymphoma (NHL). In NHL cases, 12 cases were confirmed mucosa associated lymphoid tissue B lymphoma type, 3 cases were confirmed diffuse large B-cell lymphoma, angioimmunoblastic T-cell lymphoma and ALK positive anaplastic large cell lymphoma were one case separately. Clinical and imaging manifestation of PPL is untypical, but there are still some hints: 1) Fuzzy shadow at the edge of lung mass with air bronchogram; 2) Lung mass shadow stable for a long time; 3) Pneumonia-like changing without infections clinical and lab manifestation. Thirteen patients (68.4%) were misdiagnosed as pneumonia, lung cancer and tuberculosis initially. The term between initial diagnosis and final diagnosis lasted for half a month up to 2 years, with median time of 6 months. Two cases were misdiagnosed as tuberculosis. One case was misdiagnosed as small cell lung cancer.

CONCLUSION

Clinical and imaging manifestation of PPL is untypical. Biopsies should be taken actively if the imaging findings don't match the symptoms or the anti-infection treatments to "lung infection" don't work. Accurate diagnosis requires adequate tissue sampling with appropriate ancillary pathologic studies. If clinical manifestation and the diagnosis don't match, repeated biopsy should be ordered.

摘要

背景

原发性肺淋巴瘤(PPL)发病率低,临床上误诊率高。本研究分析了 PPL 病例的临床特征、实验室和影像学数据、病理特征,并总结了误诊原因,旨在提高对该病的认识,提高早期诊断的准确性,减少误诊。

方法

收集 2010 年 4 月至 2016 年 5 月温州医科大学附属第一医院 19 例患者的临床资料,均经病理证实。描述误诊过程。本研究回顾性分析了病例的发病率、临床表现、实验室检查、胸部 CT 扫描和诊断。

结果

19 例患者的症状为呼吸困难、发热、咯血、胸痛或无明显症状的体格检查。5 例为肺炎样,9 例为肺部单个结节或肿块,4 例为胸腔积液,均为高分辨率 CT(HRCT)扫描报告。2 例为霍奇金淋巴瘤(HL),17 例为非霍奇金淋巴瘤(NHL)。在 NHL 病例中,12 例为黏膜相关淋巴组织 B 细胞淋巴瘤型,3 例为弥漫性大 B 细胞淋巴瘤,血管免疫母细胞性 T 细胞淋巴瘤和 ALK 阳性间变性大细胞淋巴瘤各 1 例。PPL 的临床和影像学表现不典型,但仍有一些提示:1)肺肿块边缘模糊影伴空气支气管征;2)肺肿块影长期稳定;3)无感染性临床和实验室表现的肺炎样改变。13 例(68.4%)患者最初误诊为肺炎、肺癌和肺结核。从最初诊断到最终诊断的时间间隔为半个月至 2 年,中位数为 6 个月。2 例误诊为肺结核,1 例误诊为小细胞肺癌。

结论

PPL 的临床和影像学表现不典型。如果影像学检查结果与症状不符或抗感染治疗无效,应积极进行活检。准确的诊断需要充分的组织取样和适当的辅助病理研究。如果临床表现和诊断不相符,应重复进行活检。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcf2/5848441/264ca11e6659/12885_2018_4184_Fig1_HTML.jpg

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