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Juarez, D., Brown, R.W., Ostrowski, M., Reardon, M.J., Lechago, J. and Truong, L.D. (1999) Pheochromocytoma associated with neuroendocrine carcinoma. A new type of composite pheochromocytoma. Archives of Pathology & Laboratory Medicine, 123, 1274-1279.

has been cited by the following article:

• 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.