Cargando…

Inflammatory myofibroblastic tumor arising from the ascending aorta mimicking a thymoma

An inflammatory myofibroblastic tumor originating from the aorta is extremely rare. Here, we report a case involving a 41-year-old female patient with an aortic inflammatory myofibroblastic tumor. Although preoperative imaging showed a mediastinal mass indicative of invasive thymoma, surgical findin...

Descripción completa

Detalles Bibliográficos
Autores principales: Yun, Ju Sik, Song, Sang Yun, Na, Kook Joo, Kim, Seok, Choi, Yoo Duk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522066/
https://www.ncbi.nlm.nih.gov/pubmed/31641928
http://dx.doi.org/10.1007/s11748-019-01231-2
Descripción
Sumario:An inflammatory myofibroblastic tumor originating from the aorta is extremely rare. Here, we report a case involving a 41-year-old female patient with an aortic inflammatory myofibroblastic tumor. Although preoperative imaging showed a mediastinal mass indicative of invasive thymoma, surgical findings revealed that this mass originated from the aorta. The patient underwent partial resection of the aorta, including the mass with patch angioplasty. Based on the postoperative histological findings, the patient was diagnosed with an aortic inflammatory myofibroblastic tumor and is currently under outpatient follow-up.