IMR Press / EJGO / Volume 28 / Issue 6 / pii/2007215

European Journal of Gynaecological Oncology (EJGO) is published by IMR Press from Volume 40 Issue 1 (2019). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with S.O.G.

Open Access Case Report

A rare case of extra-adrenal pheochromocytoma masquerading as an ovarian mass treated by laparoscopic surgery

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1 Department of Surgical Oncology, Scientific Institute for Research and Treatment of Cancer “Giovanni Paolo II”, Bari, Italy
2 Department of Pathology, Scientific Institute for Research and Treatment of Cancer “Giovanni Paolo II”, Bari, Italy
3 Department of Anesthesiology, Scientific Institute for Research and Treatment of Cancer “Giovanni Paolo II”, Bari, Italy
4 Department of Gynecological Oncology, Scientific Institute for Research and Treatment of Cancer “Giovanni Paolo II”, Bari, Italy
Eur. J. Gynaecol. Oncol. 2007, 28(6), 491–496;
Published: 10 December 2007
Abstract

Background. Extra-adrenal pheochromocytoma, or paraganglioma, is a rare tumour arising from paraganglion chromaffin cells of the sympathetic nervous system. In adults, pheochromocytomas are often called the "10% tumor" because approximately 10% occur above the diaphragm, 10% of intraabdominal pheochromocytomas are extra-adrenal, 10% are bilateral, 10% are multiple, 10% are familial, 10% are malignant, and 10% recur postoperatively. In children, instead, this tumor occurs in ectopic sites in 30-40% of the cases. This paper reports the successful laparoscopic resection of an extra-adrenal pheochromocytoma, simulating an ovarian tumor, combined with a laparoscopic cholecystectomy for gallstones. Case report: The case of a 48-year-old woman affected by an extra-adrenal pheochromocytoma that had been unsuspected for a long time is presented. The patient had some clinical symptoms that had been taken for a climacteric syndrome given her premenopausal age. The atypical and rare location of the pheochromocytoma (parauterine) had contributed to misdiagnosing it as an ovarian tumor. Laparoscopic surgery was chosen for the removal of the tumor because it is a safe technique requiring a shorter hospital stay; a concomitant cholecystectomy was performed due to the presence of gallstones. Conclusion. Surgical resection is the only treatment option for extra-adrenal pheochromocytomas. With adequate preoperative adrenergic receptor blockers and vascular filling, the laparoscopic approach appears to be a valid alternative to open surgery for paragangliomas. Gynecologists should consider the possibility, although rare, of an extra-adrenal pheocromocytoma when preparing to surgically remove a pelvic mass.

Keywords
Pheochromocytoma
Paraganglioma
Laparoscopic surgery
Catecholamines
Pelvic mass
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