Laparoscopic Adrenalectomy for Pheochromocytoma

Dawn E. Jaroszewski, Deron J. Tessier, Richard T. Schlinkert, Clive S. Grant, Geoffrey B. Thompson, Jon A. Van Heerden, David R. Farley, Stephen L. Smith, Ronald A. Hinder

Research output: Contribution to journalArticlepeer-review

58 Scopus citations

Abstract

Objective: To determine the safety and results of laparoscopic resection of benign pheochromocytomas. Patients and Methods: We retrospectively reviewed the medical charts of all patients who underwent laparoscopic adrenalectomy for benign pheochromocytomas at all 3 Mayo Clinic sites between January 1, 1992, and December 31, 2001. Demographics, comorbidities, clinical presentation, imaging studies, biochemical findings, operative intervention, and outcome were examined. Long-term follow-up was obtained via chart review and/or by direct telephone contact with the patient or a relative. Results: Twenty-four women and 23 men with a mean age of 53.1 years (range, 16-81 years) underwent attempted laparoscopic resection of pheochromocytomas. In 5 patients, the procedure was converted to open laparotomy because of bleeding (2), inadequate exposure (2), and adhesions (1). The mean tumor size was 4.3 cm. The mean operative time (181.8 vs 1403 minutes; P=.03), mean hospital stay (6.00 vs 2.64 days; P<.001), and mean blood loss (340 mL vs 80 mL; P<.001) were greater in patients who underwent open laparotomy vs those who underwent laparoscopic resection. All specimens were classified as benign. The mean follow-up was 41 months (range, 10-89 months). No patients experienced a recurrence or developed metastatic disease. Conclusions: In light of surgical and anesthesia expertise, laparoscopic resection of benign pheochromocytomas is safe and effective with resultant short hospital stays. A low threshold to convert to an open procedure reduces operative times and decreases potentially serious complications. Although there have been no recurrences to date, long-term follow-up is required for all patients, especially those with hereditary forms of pheochromocytomas.

Original languageEnglish (US)
Pages (from-to)1501-1504
Number of pages4
JournalMayo Clinic proceedings
Volume78
Issue number12
DOIs
StatePublished - Dec 2003

ASJC Scopus subject areas

  • Medicine(all)

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