Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia · 2018
[Hepatic epithelioid angiomyolipoma/PEComa and focal nodular hyperplasia in a patient with a previous history of cutaneous melanoma].
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Machado Isidro, Marhuenda Ana, Trallero Marta, Caballero María, Santos Jesús, Cruz Julia, Estevan Rafael
Аннотация
Hepatic perivascular epithelioid cell tumors (PEComas) are uncommon mesenchymal neoplasms. PEComas concurrent with other hepatic lesions is a very rare occurrence, with only two previously reported cases. We report a primary hepatic PEComa associated with focal nodular hyperplasia in a patient with a previous history of cutaneous melanoma. Diagnostic imaging studies suggested a hepatic adenoma and the patient underwent a segmentectomy. The tumor was mainly composed of epithelioid cells, adipose tissue and smooth muscle fibers intermixed with blood vessels. The neoplastic cells were diffusely immunoreactive for HMB-45, Melan-A and smooth muscle actin, but not for Hepatocyte, S100, MITF or BRAF. Molecular studies were negative for BRAFV600 mutation. The final diagnosis was hepatic epithelioid angiomyolipoma/PEComa. The differential diagnosis of hepatic PEComa is discussed.
Предметные рубрики MeSH
AdenomaAdultAngiomyolipomaBiomarkers, TumorDiagnosis, DifferentialFemaleFocal Nodular HyperplasiaGastrointestinal Stromal TumorsHumansLiver NeoplasmsMagnetic Resonance ImagingMelanomaMutationNeoplasm ProteinsNeoplasms, Second PrimaryPerivascular Epithelioid Cell NeoplasmsProto-Oncogene Proteins B-rafSkin NeoplasmsCutaneous Malignant Melanoma