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原发性肺浆细胞瘤:一例报告。

Primary pulmonary plasmacytoma: A case report.

作者信息

Jin Cong, Yan Lina, Zhang Jing, Cao Lihua, Zhang Dan

机构信息

Department of Respiratory and Critical Care Medicine, The Second Hospital of Dalian Medical University, Dalian, Liaoning Province, China.

出版信息

Medicine (Baltimore). 2024 Dec 20;103(51):e40941. doi: 10.1097/MD.0000000000040941.

Abstract

RATIONALE

Extramedullary plasmacytoma is an extremely rare malignant clonal plasmacytoma, which can occur in any tissue or organ of the body other than bone marrow hematopoietic tissue. Lesions mostly occur in the head and neck or upper respiratory tract, and rarely in the lower respiratory tract. Primary plasmacytoma of the lung, also known as primary pulmonary plasmacytoma (PPP), is rarer and is mainly diagnosed on the basis of the histopathology of biopsy tissue. In this report, we present a case of PPP.

PATIENT CONCERNS

A 65-year-old woman with repeated episodes of cough and sputum for many years was hospitalized for an acute episode of chest pain and shortness of breath. Chest computed tomography revealed bilateral inflammation of multiple lobes, accompanied by slight bronchial dilatation.

DIAGNOSES

The results of pathology of the electronic bronchoscopy sample were different from those of common infections but were consistent with plasmacytoma.

INTERVENTIONS AND OUTCOMES

The patient was discharged after hormone anti-inflammatory therapy. As patients lose contact, further follow-up of the patient was not possible.

LESSONS

PPP is a rare lung tumor, and diagnosis of this lesion on the basis of bronchoscopic biopsy is even rarer. With this case report, we seek to enhance the awareness and understanding of PPP. We recommend that in cases wherein chest imaging findings suggest multiple lung lesions, the possibility of pulmonary plasmacytoma should also be considered, and biopsy should be actively performed to confirm the diagnosis and guide treatment. This report provides valuable insights and guidance for clinicians in the management and diagnosis of patients with PPP.

摘要

原理

髓外浆细胞瘤是一种极为罕见的恶性克隆性浆细胞瘤,可发生于除骨髓造血组织以外的身体任何组织或器官。病变大多发生在头颈部或上呼吸道,很少发生在下呼吸道。肺原发性浆细胞瘤,也称为原发性肺浆细胞瘤(PPP),更为罕见,主要根据活检组织的组织病理学进行诊断。在本报告中,我们介绍了一例PPP病例。

患者情况

一名65岁女性,多年来反复咳嗽、咳痰,因胸痛和气短急性发作入院。胸部计算机断层扫描显示多个肺叶双侧炎症,伴有轻度支气管扩张。

诊断

电子支气管镜检查样本的病理结果与常见感染不同,但与浆细胞瘤一致。

干预措施及结果

患者经激素抗炎治疗后出院。由于患者失去联系,无法对其进行进一步随访。

经验教训

PPP是一种罕见的肺部肿瘤,通过支气管镜活检诊断该病变更为罕见。通过本病例报告,我们旨在提高对PPP的认识和理解。我们建议,在胸部影像学检查结果提示肺部有多个病变的情况下,也应考虑肺浆细胞瘤的可能性,并应积极进行活检以明确诊断并指导治疗。本报告为临床医生管理和诊断PPP患者提供了有价值的见解和指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31c0/11666214/75bcbcd5c49a/medi-103-e40941-g001.jpg

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