Comparison of radiologic characteristics and pathological presentations of primary pulmonary lymphoma in 22 patients

Author:

Wang Yanchao1,Han Jun2ORCID,Zhang Fantao3,Wang Zhaoyu4,Zhao Dahai5,Wang Xuan6,Wu Ningxin7,Lu Rongjian8,Wu Chongchong9,Gao Jie10,Pan Lei11,Xue Xinying11

Affiliation:

1. Department of CT/MRI Center, People’s Hospital of Wuwei city, Gansu, China

2. Department of Radiology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China

3. Department of Radiology, Shengli Oilfield Central Hospital of Dongying city, Shandong, China

4. Department of Pathology, Zhoushan Hospital, Zhejiang, China

5. Department of Respiratory Medicine, The Second Hospital of Anhui Medical University, Anhui, China

6. Department of Psychiatry, Beijing Huilongguan Hospital, Beijing, China

7. Department of Cadres, 971 Hospital of the Chinese People’s Liberation Army Navy, Beijing, China

8. Department of Stomatology, Chinese PLA 307th Hospital, Beijing, China

9. Department of Radiology, General Hospital of PLA, Beijing, China

10. Department of Pathology, General Hospital of PLA, Beijing, China

11. Department of Respiratory Medicine, Beijing Shijitan Hospital, Capital Medical University, Beijing, China

Abstract

Objective This study was performed to compare the radiologic characteristics and pathological presentations of primary pulmonary lymphoma (PPL), explore the possible mechanism underlying its development, summarize its radiologic characteristics, and improve the accuracy of its diagnosis. Methods The medical records of 22 patients pathologically diagnosed with PPL were retrospectively analyzed. Results Chest computed tomography (CT) demonstrated single or multiple nodules and masses in the lungs, patchy opacities or consolidation along the bronchovascular bundle, and no significantly enlarged mediastinal or hilar lymph nodes. All 22 cases of PPL were classified as non-Hodgkin’s lymphoma (NHL) by transbronchial biopsy, CT-guided needle biopsy, and postoperative pathology. Most (16 cases) were marginal-zone B-cell lymphomas of mucosa-associated lymphoid tissue (MALT). Twelve patients had air bronchograms within the lesion, and 13 showed ill-defined lesions with ground-glass brush-like changes. Conclusion PPL is a rare lung tumor, and most are classified as MALT lymphoma, a subtype of NHL. Chest CT can help to diagnose this disease. Positron emission tomography (PET)/CT is of great clinical value for evaluation of the lesion and patient’s general condition. The possibility of PPL should be considered in patients with characteristic CT and PET/CT findings and mild clinical symptoms, and early treatment should be administered.

Funder

National Natural Science Fund Youth Project

Beijing Outstanding Young Talent Fund

Publisher

SAGE Publications

Subject

Biochemistry, medical,Cell Biology,Biochemistry,General Medicine

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