Poorly differentiated, ovarian Sertoli-Leydig cell tumor with heterologous rhabdomyosarcoma and glandular elements: Diagnosis and management of a rare neoplasm

Ovarian Sertoli-Leydig cell tumors (SLCT) represent <2% of primary ovarian tumors, which range from benign to malignant; majority of the latter are low-grade. We present the case of a 12-year-old pre-pubertal female with poorly differentiated SLCT and heterologous rhabdomyosarcoma (FIGO stage-IA)...

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Detalles Bibliográficos
Autores principales: Singh, Charanjeet, Ahmad, Sarfraz, Hajjar, Fouad M., Holloway, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005800/
https://www.ncbi.nlm.nih.gov/pubmed/29922708
http://dx.doi.org/10.1016/j.gore.2018.06.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005800/
https://www.ncbi.nlm.nih.gov/pubmed/29922708
http://dx.doi.org/10.1016/j.gore.2018.06.003

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