Fu Michele Y, O'Neill Robert, Silverstone Elizabeth J, Yates Deborah H
University of New South Wales Faculty of Medicine, Sydney, New South Wales, Australia.
St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.
BMJ Case Rep. 2024 Dec 4;17(12):e259587. doi: 10.1136/bcr-2023-259587.
Mucosa-associated lymphoid tissue (MALT) lymphoma is a rare form of B-cell lymphoma which can potentially affect the stomach, spleen, salivary glands, skin, lungs, orbit, and, rarely, the thymus. Patients with Sjögren's syndrome (SjS) are at a 15-20 times increased risk of developing lymphoma compared to the general population.Here, we present a case of primary thymic MALT lymphoma and associated diffuse cystic lung disease, incidentally identified on routine chest imaging. Thymic MALT lymphoma has to date been reported primarily in women of Chinese origin, mainly without cystic lung disease. Diffuse cystic lung disease is well documented in women with SjS and the differential diagnoses also include lymphangioleiomyomatosis, which occurs almost exclusively in women.In the case presented, CT and positron emission tomography-CT showed a large hypermetabolic anterior mediastinal mass, as well as multiple thin-walled bilateral pulmonary cysts of widely varying sizes, without abnormal uptake. The patient was largely asymptomatic. Lung function testing, however, revealed restriction rather than obstruction, which is unusual in diffuse cystic lung disease. Biopsy of the mediastinal mass confirmed thymic MALT lymphoma which was treated medically with resultant improved lung function. This case highlights the association between SjS and MALT lymphoma, illustrates features which enable distinction between different causes of cystic lung disease in SjS, and comments on the multiplicity of SjS-related lung manifestations.
黏膜相关淋巴组织(MALT)淋巴瘤是一种罕见的B细胞淋巴瘤,可能累及胃、脾、唾液腺、皮肤、肺、眼眶,罕见情况下累及胸腺。与普通人群相比,干燥综合征(SjS)患者发生淋巴瘤的风险增加15至20倍。在此,我们报告一例原发性胸腺MALT淋巴瘤及相关弥漫性囊性肺疾病,该病例在常规胸部影像学检查中偶然发现。迄今为止,胸腺MALT淋巴瘤主要报道于华裔女性,主要无囊性肺疾病。弥漫性囊性肺疾病在SjS女性中已有充分记录,鉴别诊断还包括几乎仅发生于女性的淋巴管平滑肌瘤病。在本病例中,CT和正电子发射断层扫描-CT显示前纵隔有一个大的高代谢肿块,以及双侧多个大小差异很大的薄壁肺囊肿,无异常摄取。患者基本无症状。然而,肺功能测试显示为限制性而非阻塞性,这在弥漫性囊性肺疾病中并不常见。纵隔肿块活检确诊为胸腺MALT淋巴瘤,经药物治疗后肺功能改善。本病例突出了SjS与MALT淋巴瘤之间的关联,阐明了有助于区分SjS中囊性肺疾病不同病因的特征,并对SjS相关肺部表现的多样性进行了评论。