Background: The application of robotic adrenalectomy (RA) is increasing. However, there is still controversy over whether RA is more feasible than laparoscopic adrenalectomy (LA) for large adrenal tumors (LATs).
Methods: This meta-analysis compares the efficacy and safety of RA versus LA for LATs. A systematic literature search of PubMed, the Cochrane Library, Embase, CNKI, WANFANG database, and other databases (up to December 2024) was performed to identify studies comparing RA and LA. Data were analyzed using the Cochrane Collaboration's Review Manager (RevMan) 5.3 software.
Results: Overall, eight studies with 601 patients were included in the analysis. There were no statistically significant differences between the two groups in operative time (SMD = -0.65, 95% CI -1.48 to 0.18; P = 0.12), transfusion rate (OR = 1.12, 95% CI 0.59 to 2.16; P = 0.73), hemodynamic instability (OR = 0.67, 95% CI 0.23 to 1.92; P = 0.46), postoperative transfer to SICU (OR = 1.26, 95% CI 0.15 to 10.51; P = 0.83). Patients from the RA group could benefit from less occurrence of conversion to open (OR = 0.18, 95% CI 0.05 to 0.59; P = 0.005), lower EBL (SMD = -1.11, 95% CI -1.71 to -0.52; P = 0.0002), quicker time to removal of drainage (SMD = -1.12, 95% CI -2.03 to -0.21; P = 0.02), and shorter length of hospital stay (SMD = -1.61, 95% CI -2.41 to -0.81; P < 0.0001, I = 94%). Meanwhile, it should be noted that the RA group produces higher cost compared to the LA group (SMD = 24.12, 95% CI 12.96 to 35.29; P < 0.0001, I = 99%).
Conclusions: Compared to LA, RA has higher advantages in certain aspects. RA is an effective and safe treatment option for LATs.
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http://dx.doi.org/10.1007/s11255-025-04442-0 | DOI Listing |
J Endocr Soc
March 2025
Division of Endocrinology and Metabolism, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Context: Cells derived from neural crest populate several organs. A particular precursor cell, sympathogonia, gives rise to pheochromoblasts and neuroblasts. Due to common origin, tumors originating from pheochromoblasts, such as pheochromocytoma (PHEO) and paraganglioma (PGL), may rarely coexist with ganglioneuroma (GN).
View Article and Find Full Text PDFInt J Endocrinol Metab
October 2024
Clinic for Endocrine Surgery, University Clinical Centre of Serbia, Belgrade, Serbia.
Introduction: Sertoli cell tumors are rare sex cord-stromal tumors, accounting for less than 1% of primary testicular tumors. They typically arise in the testes and ovaries, with other localizations being uncommon. We present the case of a Sertoli cell tumor in the adrenal gland, which, to our knowledge, is the first reported in the literature.
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March 2025
Department of Urology, Gansu Province Clinical Research Center for Urinary System Disease, Lanzhou University Second Hospital, Cuiying Men 80, Chengguan District, Lanzhou, 730030, Gansu, China.
Background: The application of robotic adrenalectomy (RA) is increasing. However, there is still controversy over whether RA is more feasible than laparoscopic adrenalectomy (LA) for large adrenal tumors (LATs).
Methods: This meta-analysis compares the efficacy and safety of RA versus LA for LATs.
Cureus
March 2025
Department of Cardiovascular Surgery, Japanese Red Cross Society Kyoto Daiichi Hospital, Kyoto, JPN.
Pheochromocytomas present with paroxysmal hypertension due to a sudden release of catecholamines stimulated by radiological contrast media, surgery, or anesthetic agents. This often complicates the maintenance of patient hemodynamics during surgery. A 55-year-old man with a high fever was admitted to a hospital.
View Article and Find Full Text PDFJCEM Case Rep
March 2025
Department of Endocrinology, MKCG Medical College and Hospital, Berhampur, Odisha 760004, India.
Primary pigmented nodular adrenocortical disease (PPNAD) is a rare but important cause of adrenocorticotropic hormone (ACTH)-independent Cushing syndrome (CS). It usually presents as cyclical CS in young adults. Childhood onset of PPNAD is exceedingly rare.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!