ArticleMedicine2017
Case report of a bilateral adrenal myelolipoma associated with Cushing disease.
Article in Medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 11 citations in OpenAlex.
- Who and how to screen for endogenous hypercortisolism in adrenal and pituitary incidentaloma.Journal of endocrinological investigation · 2025Review
- Laparoscopic resection of giant adrenal myelolipoma: A case report with review of literature.Radiology case reports · 2024Article
- Management of bilateral adrenal myelolipoma without endocrine disorder: About a rare case report.Urology case reports · 2021Article
- Multiple enlarging hepatic and retroperitoneal myelolipomas in the setting of Cushing disease.BMJ case reports · 2021Article
- Adrenal myelolipoma: from tumorigenesis to management.The Pan African medical journal · 2019Article
- Giant Bilateral Adrenal Myelolipoma: Case Report.Indian journal of endocrinology and metabolismArticle
- Radiological concern for liposarcoma unmasked as extra-adrenal myelolipoma: A case report.Medicine internationalArticle
Corrections and comments
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Authors and funding
9 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
rationaleAdrenal myelolipomas are rare benign tumors, composed of a variable mixture of mature adipose tissue and hematopoietic tissue. These tumors are frequently detected incidentally and are usually asymptomatic, and hormonally inactive. PATIENT CONCERNS: During a routine health checkup, a 52-year-old man was found to have a tumor on the bilateral adrenal glands. Abdominal computed tomography revealed a well-defined, heterogeneously enhanced bilateral adrenal mass, suggesting a myelolipoma. DIAGNOSES: The hormonal evaluation revealed adrenocorticotropic hormone (ACTH) dependent Cushing syndrome.
interventionsThe patient underwent left adrenalectomy, and transsphenoidal resection of a pituitary mass. The final diagnosis was adrenal myelolipoma associated with Cushing disease. OUTCOMES: Growth of right adrenal myelolipoma was detected during the 7-year follow-up. There were enhancing pituitary lesions in repeat magnetic resonance imaging of the sellar region, which implies persistent or recurrent pituitary adenoma. This case reinforces relationship between Cushing disease and adrenal myelolipoma. LESSONS: To the best of our knowledge, this is the first reported pathologically confirmed bilateral adrenal myelolipoma associated with Cushing disease. This report supports the idea that ACTH is associated with the development of adrenal myelolipoma.
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