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Anterior Mediastinal Leiomyosarcoma: A Case Report and Literature Review

Primary mediastinal sarcomas are extremely rare. Additionally, mediastinal leiomyosarcomas account for approximately 9% of mediastinal sarcoma cases. Until date, only few cases of anterior mediastinal leiomyosarcomas have been reported. Herein, we report a case of an 85-year-old female with an anter...

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Detalles Bibliográficos
Autores principales: Ishikawa, Akira, Kuraoka, Kazuya, Zaitsu, Junichi, Saito, Akihisa, Kamigaichi, Atsushi, Mimura, Takeshi, Yamashita, Yoshinori, Taniyama, Kiyomi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983580/
https://www.ncbi.nlm.nih.gov/pubmed/33776690
http://dx.doi.org/10.1159/000509772
Descripción
Sumario:Primary mediastinal sarcomas are extremely rare. Additionally, mediastinal leiomyosarcomas account for approximately 9% of mediastinal sarcoma cases. Until date, only few cases of anterior mediastinal leiomyosarcomas have been reported. Herein, we report a case of an 85-year-old female with an anterior mediastinal mass of 15 mm. Histological examination revealed spindle tumor cells showing a fascicular growth pattern. Immunohistochemically, the tumor cells were focal positive for desmin, calponin, and α-smooth muscle actin. The pathological diagnosis was leiomyosarcoma. In conclusion, we encountered a case of a very rare leiomyosarcoma that occurred in the anterior mediastinum, and our report may contribute to the understanding of this disease.