Fine-needle aspiration can be utilized for the diagnosis of primary epithelioid angiosarcoma of the adrenal gland, a rare condition associated with poor clinical outcomes.
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FNA with IHC may support diagnosis of rare adrenal epithelioid angiosarcoma; leaves open whether earlier detection alters its dismal prognosis.
Primary epithelioid angiosarcoma of the adrenal gland is extremely rare. Only 37 cases have been reported in the scientific literature.Here we describe the case of a 55-year-old woman affected by metastatic angiosarcoma in the right adrenal gland, who died few days after the histological diagnosis made by fine-needle aspiration (FNA). This is the second case of primary epithelioid angiosarcoma diagnosed by FNA among scientific articles published in English in PubMed. Microscopically, the tumor showed a predominant epithelioid differentiation, thus making the diagnostic process more difficult than usual. Immunohistochemical examination revealed positive reactivity for cytokeratin, CD31, and CD34. The literature shows that epithelioid adrenal angiosarcoma has poor clinical outcome, especially when metastatic at presentation.
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Torelli et al. (2017) studied this question.
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