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Hepatic angiomyolipoma: A case report and literature review
INTRODUCTION: Hepatic angiomyolipoma (HAML) is a rare mesenchymal liver tumour which belongs to the family of perivascular epithelioid cell tumours (PEComas). It is typically composed of blood vessels, smooth muscle, and adipose cells, and shows strong immunoreactivity for HMB-45. PRESENTATION OF TH...
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| Yayımlandı: | Int J Surg Case Rep |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Elsevier
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7683232/ https://ncbi.nlm.nih.gov/pubmed/33212308 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijscr.2020.11.045 |
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