ArticleUrology case reports2021
Adrenal cavernous Hemangioma;A rare diagnosis of adrenal incidentaloma:A case report, and literature review.
Article in Urology case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.
What it found
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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
4 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.
- The diagnostic dilemma of adrenal vascular tumors: analysis of 21 cases and systematic review of the literature.Endocrine · 2025Pooled it
- A Rare Case of Cavernous Haemangioma of the Adrenal Gland: A Case Report and Review of Literature.Cureus · 2022Article
- Incidental adrenal hemangioma clinically suspicious for malignancy: diagnostic considerations and review of the literature.International journal of clinical and experimental pathology · 2022Article
- Clinical Features and Outcomes of Adrenal Cavernous Hemangioma: A Study of 8 Cases from a Single Center.International journal of endocrinology · 2021Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Adrenal cavernous hemangioma is an extremely rare benign tumor. To date, less than 70 cases have been reported in the literature. In most of the cases, the tumor is hormonally silent, discovered incidentally and the diagnosis is made postoperatively. Pre-operative differentiation between this benign tumor and other malignant adrenal tumors is challenging. In this article we present a case of a non-functioning adrenal incidentaloma that was managed by laparoscopic adrenalectomy. The post-operative histological diagnosis was adrenal cavernous hemangioma.
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