ArticleSurgical case reports2019
Primary thymic MALT lymphoma in a patient with Sjögren's syndrome and multiple lung cysts: a case report.
Article in Surgical case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 6 citations in OpenAlex.
- Molecular pathology assists the diagnosis of lymphoepithelial sialadenitis, Sjögren's syndrome and extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue.Journal of dental sciences · 2024Article
- A systematic review and meta-analysis of thymic mucosa-associated lymphoid tissue lymphoma.Journal of thoracic disease · 2022Article
- Incidence, mortality, and survival analyses of patients with thymic lymphoma.Frontiers in oncology · 2022Article
- [Clinicopathological analysis of mucosa associated lymphoid tissue lymphoma secondary to Sjögren' s syndrome in salivary gland].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2020Article
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Authors and funding
5 authors at 1 institution in 1 country.
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Abstract
backgroundThymic mucosa-associated lymphoid tissue (MALT) lymphoma is rare and also known for its association with autoimmune diseases, especially Sjögren's syndrome (SjS), which could affect the systemic organs, and pulmonary involvement often reveals multiple lung cysts. CASE PRESENTATION: A 40-year-old woman presented with an anterior mediastinal mass and multiple lung cysts on computed tomography. We suspected thymoma concomitant with lymphangioleiomyomatosis and performed a total thymectomy and wedge resection of the lung as a surgical biopsy. The histopathological diagnosis of the mediastinal mass was a MALT lymphoma, and there were no specific findings in the lung specimen. She had a history of SjS, which had been overlooked during the initial work-up.
conclusionsA history of SjS should raise suspicion of a MALT lymphoma for the differential diagnosis of an anterior mediastinal mass. A precise history taking is crucial for the correct diagnosis, and we could have avoided a lung resection in our case.
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