ArticleThe Pan African medical journal2019
Adrenal myelolipoma: from tumorigenesis to management.
Article in The Pan African medical journal, 2019. 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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Who cites it
4 citing papers in PubMed, 9 citations in OpenAlex.
- A rare case of non-functional adrenal myelolipoma associated with hypertension: a case report and literature review.International journal of surgery case reports · 2026Article
- Too Massive and Too Atypical to Be Benign: The Unexpected Face of a Giant Adrenal Myelolipoma.Cureus · 2026Article
- Case report: Adrenal myelolipoma resected by laparoscopic surgery.Frontiers in oncology · 2022Article
- Teratoma of the adrenal gland: clinical experience and literature review.Gland surgery · 2020Article
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Authors and funding
10 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Adrenal myelolipoma (MLS) is a rare, benign and non-functional neoplasm, composed of adipose tissue and myeloid. We report a rare case of adrenal myelolipoma of a 20-year-old female revealed with chronic abdominal pain. Computed tomography (CT) scan of the abdomen guided diagnosis and surgical resection was performed given symptomatic and bulky mass. Histological examination confirmed the diagnosis. At 18 months after the surgery, the patient had no evidence of recurrence. The diagnosis of MLS is radiological. Therapeutic abstention is the rule for a small, asymptomatic tumor. The surgical removal is indicated when it is bulky (exceeds 7cm), symptomatic or hormonal activity.
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