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Background: Adrenalectomy for pheochromocytoma (PHEO) is challenging because of the high risk of intraoperative hemodynamic instability (HDI). This study aimed to compare the incidence and risk factors of intraoperative HDI between laparoscopic left adrenalectomy (LLA) and laparoscopic right adrenalectomy (LRA).
Methods: We retrospectively analyzed two hundred and seventy-one patients aged > 18 years with unilateral benign PHEO of any size who underwent transperitoneal laparoscopic adrenalectomy at our hospitals between September 2016 and September 2023. Patients were divided into LRA (N = 122) and LLA (N = 149) groups. Univariate and multivariate logistic regression analyses were used to predict intraoperative HDI. In multivariate analysis for the prediction of HDI, right-sided PHEO, PHEO size, preoperative comorbidities, and preoperative systolic blood pressure were included.
Results: Intraoperative HDI was significantly higher in the LRA group than in the LLA (27% vs. 9.4%, p < 0.001). In the multivariate regression analysis, right-sided tumours showed a higher risk of intraoperative HDI (odds ratio [OR] 5.625, 95% confidence interval [CI], 1.147-27.577, p = 0.033). The tumor size (OR 11.019, 95% CI 3.996-30.38, p < 0.001), presence of preoperative comorbidities [diabetes mellitus, hypertension, and coronary heart disease] (OR 7.918, 95% CI 1.323-47.412, p = 0.023), and preoperative systolic blood pressure (OR 1.265, 95% CI 1.07-1.495, p = 0.006) were associated with a higher risk of HDI in both LRA and LLA, with no superiority of one side over the other.
Conclusion: LRA was associated with a significantly higher intraoperative HDI than LLA. Right-sided PHEO was a risk factor for intraoperative HDI.
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http://dx.doi.org/10.1007/s00464-024-10974-w | DOI Listing |
Eur J Endocrinol
September 2025
Endocrinology & Nutrition Department. Hospital Universitario Ramón y Cajal Madrid, Spain & Instituto de Investigación Biomédica Ramón y Cajal (IRYCIS), Madrid, Spain.
Objective: The indication for laparoscopic partial adrenalectomy (LPA) in patients with primary aldosteronism due to aldosterone-producing adenoma (APA) remains controversial. This study aimed to determine the functional and surgical outcomes of LPA in this context.
Methods: This is a systematic review and meta-analysis.
Int J Urol
September 2025
Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.
Objectives: This study aimed to compare the perioperative outcomes of robotic adrenalectomy (RA) and laparoscopic adrenalectomy (LA) at Kobe University Hospital. We evaluated operation time, blood loss, complication rates, and hospital length of stay (LOS), as well as factors influencing operation time.
Methods: We reviewed data from patients who underwent RA or LA at Kobe University Hospital between April 2020 and June 2024.
Endocrinol Diabetes Metab Case Rep
July 2025
Division of Endocrinology and Metabolism, Albany Medical College, Albany, New York, USA.
Summary: Pheochromocytomas are rare neuroendocrine tumors derived from adrenal chromaffin cells that result in hyperactivity of the sympathetic nervous system. We present the case of a patient with biochemical evidence of pheochromocytoma, but surgical pathology revealed absence of tumor. This is an 80-year-old female with a past medical history of metastatic follicular lymphoma and hypertension with an incidental 1.
View Article and Find Full Text PDFUpdates Surg
August 2025
Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Here, we present the case of a 27-year-old male with a known history of Von Hippel Lindau (vHL) syndrome who was found to have a recurrent paraganglioma in the retrocaval space after laparoscopic right partial adrenalectomy at age 16. He was referred for consideration of a minimally invasive approach to resection. This is particularly important in vHL patients as they are at a high risk of recurrence and need for additional surgical interventions over the course of their lifetime.
View Article and Find Full Text PDFUpdates Surg
August 2025
Endocrinology Department, Medical Center "Manufactura Clinic", Khodosivka, Kiev Region, Ukraine.
Primary Bilateral Macronodular Adrenal Hyperplasia (PBMAH) is considered a rare cause of Cushing syndrome (CS). Despite progress in understanding the pathogenesis, clinical evaluation of the disease and optimal treatment remain relevant. Data were retrieved from institutional/hospital databases.
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