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Rev. med. Chile ; 150(9): 1256-1259, sept. 2022. ilus
Artículo en Español | LILACS | ID: biblio-1431893

RESUMEN

Angiomyolipomas (AML) are mesenchymal tumors belonging to the group of perivascular epithelioid cell tumors, which, rarely, can display a malignant behavior. They are composed of adipose tissue, vessels, and muscle tissue in different proportions, and constitute a differential diagnosis for other focal liver lesions. We report a 34-year-old woman in whom a focal hepatic lesion was discovered incidentally. The pathology report of an ultrasound guided biopsy informed an epithelioid angiomyolipoma, a rare variant of these lesions. During ten years of imaging follow, the size and features of the lesion has not changed. The patient rejected a surgical excision.


Asunto(s)
Humanos , Femenino , Adulto , Angiomiolipoma/cirugía , Angiomiolipoma/diagnóstico por imagen , Neoplasias Hepáticas/cirugía , Neoplasias Hepáticas/diagnóstico por imagen , Ultrasonografía
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