ArticleUrology annals2013
Composite pheochromocytoma-ganglioneuroma of the adrenal gland: A case report with immunohistochemical study.
Article in Urology annals, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.
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Who cites it
12 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.
- Composite phaeochromocytomas-a systematic review of published literature.Langenbeck's archives of surgery · 2022Pooled it
- A case report of a composite pheochromocytoma that occurred 13 years after adrenalectomy for pheochromocytoma.Frontiers in oncology · 2026Article
- Adrenocorticotropin-Secreting Pure Adrenal Ganglioneuroma Leading to Cushing Syndrome.JCEM case reports · 2025Article
- Case Report: Composite pheochromocytoma with ganglioneuroma component: A report of three cases.Frontiers in endocrinology · 2022Article
- A Novel MAX Gene Mutation Variant in a Patient With Multiple and "Composite" Neuroendocrine-Neuroblastic Tumors.Frontiers in endocrinology · 2020Article
- Hypertensive retinopathy as the initial presentation of neuroblastoma.American journal of ophthalmology case reports · 2017Article
- A rare and easily misdiagnosed tumor of the urinary bladder: primary composite pheochromocytoma.International journal of clinical and experimental pathology · 2017Article
- Laparoscopic resection of primary adrenal ganglioneuroma: A case report and review of the literature.Oncology letters · 2015Article
- Adrenal Ganglioneuroma Presenting As Left Renal Mass.World journal of oncology · 2014Article
- Composite Pheochromocytoma Presenting as Severe Lactic Acidosis and Back Pain: A Case Report.Indian journal of nephrologyArticle
- Composite Pheochromocytoma: A Rare Form of Tumor.Indian journal of nephrologyArticle
- Expression of Extracellular Signal-regulated Kinase 5 and Ankyrin Repeat Domain 1 in Composite Pheochromocytoma and Ganglioneuroblastoma Detected Incidentally in the Adult Adrenal Gland.Internal medicine (Tokyo, Japan)Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Composite tumors of the adrenal medulla consisting of pheochromocytoma and ganglioneuroma are rare tumors accounting for less than 3% of all sympathoadrenal tumors. These tumors display more than one line of differentiation in which normal and neoplastic chromaffin cells are capable of differentiating into ganglion cells under the influence of nerve growth factors. To the best of our knowledge, we report the second case with a composite tumor of the adrenal medulla in a normotensive patient from India.
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Registered trials
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