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Angiomyolipoma of the left adrenal gland: a case report and literature review

Angiomyolipoma (AML) is apparent a part of mesenchymal tumor arising from perivascular epithelioid cell origin. AML is formed of blood vessels, spindle and epithelioid cells, and mature adipocytes. Adrenal AML is very rare. Indeed, only 21 cases of adrenal AML have been reported in the English-langu...

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Bibliografski detalji
Izdano u:Gland Surg
Glavni autori: Bai, Yonghua, Li, Lingli, Zhang, Jingjing, Hu, Jie, Yin, Yu, He, Cheng, Liu, Junwei, Liu, Heng
Format: Artigo
Jezik:Inglês
Izdano: AME Publishing Company 2021
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8184383/
https://ncbi.nlm.nih.gov/pubmed/34164328
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/gs-21-244
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