ArticleInternational journal of surgery case reports2017
Adrenal gland hemangioma: A rare case of the incidentaloma: Case report.
Article in International journal of surgery case reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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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
5 citing papers in PubMed, 12 citations in OpenAlex.
- Adrenal gland haemangioma, a rare entity difficult to differentiate from malignancy.BJR case reports · 2024Article
- Anastomosing haemangioma of adrenal gland: an unusual vascular tumour.BMJ case reports · 2024Article
- Incidental adrenal hemangioma clinically suspicious for malignancy: diagnostic considerations and review of the literature.International journal of clinical and experimental pathology · 2022Article
- Cross-sectional imaging features of unusual adrenal lesions: a radiopathological correlation.Abdominal radiology (New York) · 2021Review
- Adrenal hemangioma: A rare presentation of bleeding incidentaloma: Case report.International journal of surgery case reports · 2020Article
Corrections and comments
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
bakgroundAdrenal glands hemangiomas are rare, benign and non-functional tumors. They are often discovered as incidentalomas either during imaging or autopsies. Nearly 70 cases were reported in the literature. CASE REPORT: We report a case of a non-functional adrenal hemangioma (AH) that was incidentally found on abdominal ultra sonography (US) during the routine control of diabetes of a 58 year-old man. Imaging with US and Computed tomography (CT) showed an heterogeneous and partially calcified 6 cm tumor of the right adrenal gland. The mass was surgically excised and the histological examination concluded to an adrenal haemangioma.
conclusionAlthough rare, AH should be included in the differential diagnosis of the adrenal neoplasmas.
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