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Adrenal angiomyolipoma: A case report and review of literature

Angiomyolipoma (AML) is a rare mesenchymal tumour arising from perivascular epithelioid cells. It is most commonly seen in kidney, but rarely AML can arise in extra renal sites. Adrenal AML is a very rare clinical entity, and very few cases have been reported so far. We present our experience with a...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Goswami, Amit, Sharma, Anil, Khullar, Rajesh, Soni, Vandana, Baijal, Manish, Chowbey, Pradeep
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Medknow Publications & Media Pvt Ltd 2014
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4204268/
https://ncbi.nlm.nih.gov/pubmed/25336825
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0972-9941.141531
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