Population
9 patients with adrenal epithelioid angiosarcomas (AEA), median age 60 (range 45-85 years), 5 men and 4 women.
Design
Case_series
Follow-up
up to 13 years
Authors
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Long-term survival possible after resection of adrenal epithelioid angiosarcoma; leaves open identification of prognostic factors and adjuvant strategies.
Adrenal epithelioid angiosarcomas are rare, aggressive neoplasms where surgical resection is the primary treatment, though metastasis and mortality remain significant.
Wenig et al. (1994) studied this question.
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