Wang Yanchao, Han Jun, Zhang Fantao, Wang Zhaoyu, Zhao Dahai, Wang Xuan, Wu Ningxin, Lu Rongjian, Wu Chongchong, Gao Jie, Pan Lei, Xue Xinying
Department of CT/MRI Center, People's Hospital of Wuwei city, Gansu, China.
Department of Radiology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.
J Int Med Res. 2020 Apr;48(4):300060519879854. doi: 10.1177/0300060519879854. Epub 2019 Dec 27.
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.
The medical records of 22 patients pathologically diagnosed with PPL were retrospectively analyzed.
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.
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.
本研究旨在比较原发性肺淋巴瘤(PPL)的影像学特征和病理表现,探讨其发生发展的可能机制,总结其影像学特征,提高诊断准确性。
回顾性分析22例经病理诊断为PPL患者的病历资料。
胸部计算机断层扫描(CT)显示肺部单发或多发结节及肿块,沿支气管血管束分布的斑片状模糊影或实变影,纵隔或肺门淋巴结无明显肿大。22例PPL经支气管活检、CT引导下穿刺活检及术后病理均诊断为非霍奇金淋巴瘤(NHL)。多数(16例)为黏膜相关淋巴组织边缘区B细胞淋巴瘤(MALT)。12例病变内可见空气支气管征,13例表现为边界不清的病变伴磨玻璃样毛刷状改变。
PPL是一种罕见的肺部肿瘤,多数为NHL的一种亚型MALT淋巴瘤。胸部CT有助于诊断该病。正电子发射断层显像(PET)/CT对评估病变及患者全身状况具有重要临床价值。对于具有特征性CT及PET/CT表现且临床症状较轻的患者,应考虑PPL的可能,并尽早治疗。