ArticleJCEM case reports2025
Incidental Adrenal Hemangioma: A Diagnostic and Management Challenge.
Article in JCEM case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Adrenal hemangioma: A rare incidental tumor managed with laparoscopic partial adrenalectomy.Urology case reports · 2026Article
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Adrenal hemangioma is a rare, benign vascular tumor often discovered incidentally during imaging. Here, we present the case of a 43-year-old male individual who was incidentally found to have a right adrenal mass during evaluation for polycythemia. Initial imaging revealed a 3.1 × 2.3 cm mass. The unenhanced computed tomography (CT) attenuation was 31 Hounsfield units (HU), and the post-contrast attenuation was approximately 61 HU. Hormonal evaluations, including cortisol, dehydroepiandrosterone sulfate (DHEA-S), aldosterone, renin, and metanephrines, were all within normal limits. The patient was managed conservatively, with close follow-up. Over the course of 2 years, the lesion remained stable in size until a sudden increase was noted, reaching 4.3 × 3.3 cm, with magnetic resonance imaging (MRI) revealing necrotic areas and peripheral enhancement. Due to the lesion's rapid growth and indeterminate features, the patient underwent a laparoscopic right adrenalectomy. The histopathological analysis confirmed the diagnosis of a cavernous adrenal hemangioma. This case emphasizes the importance of recognizing adrenal hemangiomas, as they can mimic more aggressive adrenal tumors and require careful monitoring.
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