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Lisewski, D., Ryan, S., Lim, E.M., Frost, F. and Nguyen, H. (2006) Concomitant compostite adrenal phoechromocytoma, multipte gastric stromal tumours and pseudohermaphrodism in a patient with von Recklinghausen’s disease. International Seminars in Surgical Oncology, 3, 11. doi:10.1186/1477-7800-3-11

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• TITLE: Concurrence of composite adrenal pheochromocytoma-ganglioneuroma and renal pelvic cancer: A case report

  AUTHORS: Kuniyasu Muraoka, Masashi Honda, Bunya Kawamoto, Seiya Inoue, Katsuya Hikita, Nobuyuki Hinata, Atushi Takenaka

  KEYWORDS: Pheochromocytoma; Ganglioneuroma; Renal Pelvic Cancer

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.2 No.1, March 25, 2013

  ABSTRACT: Embryologically, chromaffin cells of the pheo-chromocytoma and ganglion cells of the ganglioneuroma are both derived from neural crest cells. Composite pheochromocytoma-ganglioneuroma (Pheo-GN) in a single adrenal gland is very rare. A case report of a patient with composite Pheo-GN of the adrenal gland and renal pelvic cancer is presented. Laparoscopic left adrenalectomy, nephroureterectomy and para-aortic lymphadenectomy were performed. This represents the first report of simultaneous surgical treatment for composite Pheo-GN and renal pelvic cancer.