Department of Pathology, the Affiliated Taian City Central Hospital of Qingdao University, Tai'an, 271000, China.
Department of Rehabilitation, the Affiliated Taian City Central Hospital of Qingdao University, Tai'an, 271000, China.
World J Surg Oncol. 2023 Jan 23;21(1):20. doi: 10.1186/s12957-023-02904-2.
Mucosa-associated lymphoid tissue (MALT) lymphoma is a common, low-grade, malignant B-cell lymphoma. However, simultaneous MALT lymphoma in the thymus and lung is extremely rare, and concomitant adenocarcinoma of the lung is even rarer. Herein, we report a rare case of a collision tumor in which MALT lymphoma was found in both the thymus and lung with Sjögren's syndrome (SS) and adenocarcinoma in the lung.
A physical examination of a 32-year-old woman revealed an anterior superior mediastinal space-occupying lesion, and chest computed tomography (CT) indicated a nodular ground-glass opacity and irregular mixed-density focus in the right lung. All lung cancer-related tumor biomarkers were within normal ranges. The thymus and part of the lung tissue were surgically resected. The histopathology and molecular examinations confirmed MALT lymphoma of the thymus and lung with lung adenocarcinoma. SS was also diagnosed. No special postoperative treatment was performed for the MALT lymphoma, and the patient underwent immunosuppressive therapy for SS after 4 months of follow-up observation.
MALT lymphoma of the thymus and lung tissues has no specific presentation on imaging and is difficult to differentiate from common malignant tumors, and the definite diagnoses of these tumors are highly dependent on histopathological examination in combination with molecular testing and cytogenetics. SS may be an important potential condition for the occurrence of MALT lymphoma in the thymus and lung. Additional similar cases are needed to clarify the biological pathways and potential molecular mechanisms of rare lymphomas and collision tumors.
黏膜相关淋巴组织(MALT)淋巴瘤是一种常见的低级别恶性 B 细胞淋巴瘤。然而,胸腺和肺部同时发生 MALT 淋巴瘤极其罕见,同时合并肺部腺癌则更为罕见。在此,我们报告一例罕见的碰撞瘤病例,该病例同时在胸腺和肺部发现 MALT 淋巴瘤,且患者合并有干燥综合征(SS)和肺部腺癌。
一名 32 岁女性接受体格检查时发现前上纵隔占位病变,胸部计算机断层扫描(CT)提示右肺结节状磨玻璃样混浊和不规则混合密度灶。所有肺癌相关肿瘤标志物均在正常范围内。行胸腺和部分肺组织切除术。组织病理学和分子检查证实胸腺和肺部为 MALT 淋巴瘤合并肺腺癌,同时诊断为 SS。MALT 淋巴瘤未行特殊的术后治疗,患者在随访观察 4 个月后行 SS 免疫抑制治疗。
胸腺和肺部 MALT 淋巴瘤在影像学上无特异性表现,与常见恶性肿瘤难以区分,这些肿瘤的明确诊断高度依赖于组织病理学检查结合分子检测和细胞遗传学。SS 可能是胸腺和肺部 MALT 淋巴瘤发生的重要潜在条件。需要更多类似的病例来阐明罕见淋巴瘤和碰撞瘤的生物学途径和潜在分子机制。