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Virginie Audard

Publications and source records attributed to Virginie Audard.

4 recordsLinked to original sources

[A large para-renal PEComa].

We report the case of a 45-year-old man with a voluminous para-renal mass. The tumor was composed of epithelioid or spindle-shaped eosinophilic and clear cells with some atypia and an elevated mitotic count. The immunohistochemical study was positive for anti-HMB45 antibodies and anti-actin-antibodies and negative for epithelial markers and PS100 antibodies. The diagnosis of epithelioid AML (PEComa) was established. Two years later, recurrence was observed with a voluminous mass in the left upper quadrant of the abdomen, with high cellular density and the same immunohistochemical features. This tumor belongs to the PEComa and is not easy to diagnose clinically and morphologically. The immunohistochemical phenotype is characteristic. AML are usually benign but some epithelioid AMLS outcome can be unfavorable with metastatic dissemination. Criteria of malignancy are not clearly defined in the literature. This case shows that the mitotic count and the tumor size are probably important.

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[Misleading Kaposi's sarcoma: usefulness of anti HHV-8 immunostaining].

We report two cases of early Kaposi's sarcoma illustrating the risk of misdiagnosis. Both lesions showed histological features and clinical aspects that mimicked lymphangioendothelioma. The diagnosis of lymphangioma-like Kaposi's sarcoma was not made until a few years later, after the lesions had become more extensive and bilateral. Because of this evolution which is uncommon for a lymphangioendothelioma, immunohistochemical staining with anti-HHV8 antibody was done, and was positive in successive biopsies of our two patients. These results reveal that these vascular lesions had been Kaposi's sarcomas of the lymphangioma-like type since the beginning. In conclusion, it seems essential to search for HHV8 within endothelial cells of any vascular lesion mimicking lymphangioendothelioma or any other vascular proliferation difficult to classify. These results lead us to question whether lymphangioendothelioma is a real entity.

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