Laparoscopic adrenalectomy for pheochromocytoma

被引:47
作者
Jaroszewski, DE
Tessier, DJ
Schlinkert, RT
Grant, CS
Thompson, GB
van Heerden, JA
Farley, DR
Smith, SL
Hinder, RA
机构
[1] Mayo Clin, Dept Surg, Scottsdale, AZ 85259 USA
[2] Mayo Clin, Dept Surg, Rochester, MN USA
关键词
D O I
10.4065/78.12.1501
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. Longterm 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 140.5 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.
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页码:1501 / 1504
页数:4
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