Key result
Surgical management of rare primary adrenal incidentalomas, including angiosarcoma and diffuse B-cell lymphoma, resulted in disease-free survival at 6 months to 3 years of follow-up.
Why the study?
Rare histopathological findings in incidentally detected adrenal tumors are uncommon, prompting the need to identify their clinical characteristics, management, and post-treatment outcomes.
Population
Two patients with rare primary adrenal tumors initially diagnosed as incidentalomas
Design
Case report
Authors
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Rare adrenal incidentalomas extend the differential in imaging-detected masses; leaves open standardized management and outcomes data.
Case Report (n=2)
No
Rare primary adrenal tumors such as angiosarcoma and lymphoma can present as incidentalomas and be successfully managed with adrenalectomy and appropriate adjuvant therapy.
Elbaset et al. (2020) conducted a case report in Adrenal incidentalomas (n=2). Adrenalectomy was evaluated on Clinical outcome after treatment. Surgical management of rare primary adrenal incidentalomas, including angiosarcoma and diffuse B-cell lymphoma, resulted in disease-free survival at 6 months to 3 years of follow-up.
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