Angiomyolipoma and Malignant PEComa: Discussion of Two Rare Adrenal Tumors

Angiomyolipoma and PEComa are rare tumors descending from perivascular epithelial cells (PECs), with distinctive IHC, morphological, and ultrastructural features. The kidney is the most frequent site of origin, but not the only one; however, adrenal gland angiomyolipomas are extremely rare. We descr...

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Detalles Bibliográficos
Autores principales: Kwazneski II, Douglas, Merrill, Megan, Young, Jessica, Sell, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779821/
https://www.ncbi.nlm.nih.gov/pubmed/26998374
http://dx.doi.org/10.1155/2016/5204092

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779821/
https://www.ncbi.nlm.nih.gov/pubmed/26998374
http://dx.doi.org/10.1155/2016/5204092

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