ArticleInternational journal of clinical and experimental pathology2019
Ectopic thymoma: report of 2 cases and review of the literature.
Article in International journal of clinical and experimental pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 7 citations in OpenAlex.
- Ectopic Cervical Thymoma with Myasthenia Gravis and Pure Red Cell Aplasia: A Case Report.Surgical case reports · 2026Article
- Article
- Article
- Ectopic cervical thymoma in myasthenia gravis: a case report.BMC neurology · 2024Article
- Incidental finding of an ectopic b2 thymoma attached to the pericardium.Journal of surgical case reports · 2024Article
- Metastatic Ectopic Thymoma of the Neck without Mediastinal Involvement.Iranian journal of otorhinolaryngology · 2022Article
- An ectopic thymoma arising in the middle mediastinum that was difficult to distinguish from a lymph node metastasis.Surgical case reports · 2021Article
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In this report, we present two cases of ectopic thymoma, aiming to explore the clinicopathologic features, diagnosis, and differential diagnosis of ectopic thymoma. Case 1 was a female 56-years-old. For 6 months' time, there was no obvious cause of cough, expectoration, chest tightness, or asthma with chest pain. PET-CT showed a right middle lung and lower lung mass with increased FDG metabolism. Postoperative pathology was diagnosed as right middle and lower lung ectopic thymoma, type B2, invading the chest wall. Case 2 was a male of 54-years-old. By physical examination the right chest cavity had a mass present for 1 week and he was admitted to hospital. Postoperative pathology was diagnosed as right thoracic ectopic thymoma, type AB. No recurrence has been found to in the follow-up of these two patients. In conclusion, ectopic thymoma occurs outside the anterior mediastinum. It is rare, the clinical symptoms are not typical, and pre-operative diagnosis is difficult. It is easily misdiagnosed as other diseases. Surgical treatment is the best method. According to the pathologic type and invasion of the tumor, radiotherapy may be considered.
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31933830PMC6949883W3007832794What OpenQuestion holds
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