ArticleJournal of surgical case reports2024
An imaging and diagnostic conundrum-the adrenal haemangioma.
Article in Journal of surgical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed.
- A 20.1 kg adrenal cavernous haemangioma presenting as a giant retroperitoneal mass: diagnostic difficulties and operative strategy - a case report.BMC surgery · 2026Article
- A case of incidental adrenal capillary hemangioma after a partial nephrectomy for renal clear cell carcinoma.Radiology case reports · 2025Article
- Adrenal cavernous hemangioma misdiagnosed as pheochromocytoma: a case report.Urology case reports · 2025Article
- Incidental Adrenal Hemangioma: A Diagnostic and Management Challenge.JCEM case reports · 2025Article
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6 authors.
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Abstract
The adrenal haemangioma, a rare benign vascular tumour, is increasingly detected through abdominal imaging. Just over 70 surgical cases have been reported since 1955. Their potential large size and overlapping imaging features with adrenocortical carcinoma poses a diagnostic challenge. Adrenalectomy is often needed for a definitive diagnosis due to inconclusive imaging. We report the case of a 61-year-old female presenting with an incidental finding of a right-sided 9.5-cm adrenal mass on imaging. Due to the risk of adrenocortical carcinoma with inconclusive imaging findings, an open right adrenalectomy was performed. The patient was discharged after 6 days with no complications. Post-surgical histopathology confirmed a diagnosis of adrenal haemangioma with a secondary adrenal pseudocyst. The presence of an adrenal incidentaloma with discordant radiological features proves to be a diagnostic conundrum. Therefore, in the setting of contradictory radiology and concerning mass size, we recommend adrenalectomy for definitive diagnosis of an adrenal haemangioma.
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