O'Donnell P G, Jackson S A, Tung K T, Hassan B, Wilkins B, Mead G M
Department of Radiology, Royal South Hants Hospital, Southampton, UK.
Clin Radiol. 1998 Apr;53(4):258-63. doi: 10.1016/s0009-9260(98)80123-2.
We review the radiological findings in 13 patients with histologically proven (n = 10) or clinically diagnosed (n = 3) lymphomas arising in mucosa-associated lymphoid tissue (MALT) of the lung. These rare B-cell lymphomas typically follow an indolent course, and many cases are still being incorrectly described in current radiological literature under the term pseudolymphoma. The patients frequently give a history of autoimmune disease involving the affected organ, and involvement of another mucosal site as part of a disseminated MALT lymphoma, is common. The radiographic patterns of pulmonary parenchymal involvement in lung MALT lymphomas have been reviewed, and correlation made with their clinical behaviour.
我们回顾了13例经组织学证实(n = 10)或临床诊断(n = 3)的起源于肺黏膜相关淋巴组织(MALT)的淋巴瘤患者的影像学表现。这些罕见的B细胞淋巴瘤通常病程进展缓慢,在当前的放射学文献中,许多病例仍被错误地描述为假性淋巴瘤。患者常有受累器官自身免疫性疾病史,作为播散性MALT淋巴瘤的一部分,其他黏膜部位受累也很常见。我们回顾了肺MALT淋巴瘤肺实质受累的影像学表现,并将其与临床行为进行了相关性分析。