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The role of double stenting techniques in distal bifurcation left main (LM) disease has gaining interest over the latest years. We present the 3-year multicentre registry outcomes of dual stenting using ultra-thin strut stents and the Nano-Inverted-T (NIT) technique in complex unprotected true LM bifurcation disease. We analysed the procedural and medical data of consecutive patients enrolled between 1st January 2014 and 1st December 2019 in a multicentre registry for complex LM bifurcation disease treated with the double stenting technique called NIT due contraindications and/ or refusal to surgical treatment. Target lesion failure (TLF) was defined as the composite of cardiovascular death, target-vessel MI (TVMI) and clinically driven target lesion revascularization (TLR). Among two hundred-ninety-five patients (138 males, mean age 70.3 ± 12.8 years), post-operative success was achieved in 100% of cases. Contrast volume, procedural time, and radiation exposure were 139.2 ± 23.4 ml, 15.3 ± 4.9 min, and 1080 ± 1034 cGy/m, respectively. At a mean follow-up of 39.5 ± 0.6 months TLF rate was 6.1% (n = 18) while TLR and cardiovascular mortality rates were 3.0 (n = 9) and 2.6% (n = 8), respectively. Clinically-driven angiographic follow-up was available in 26.4% of patients at a mean time from the procedure of 7.5 ± 0.4 months. Clinically restenosis rate was 3.3%.Revascularization of complex LM bifurcation disease using the NIT double stenting technique resulted feasible and safe with a low incidence of TLF, excellent survival rate and no stent thrombosis.
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http://dx.doi.org/10.1007/s10554-020-02106-x | DOI Listing |
Front Surg
August 2025
Department of General Medicine, Yanbian University Hospital, Yanji, Jilin, China.
The accessory middle cerebral artery (AMCA) refers to the cerebral vascular variation originating from the anterior cerebral artery, passing through the lateral fissure and accompanying the middle cerebral artery (MCA), and participating in the blood supply area of the MCA. Relevant literature reports that the incidence of this variant vessel is 0.3%-2.
View Article and Find Full Text PDFJ Surg Case Rep
September 2025
Department of Urology, The Eighth Clinical Medical College of Guangzhou University of Chinese Medicine, No. 6 of Qinren Road, Foshan 528000, Guangdong, People's Republic of China.
A 55-year-old female presented with left flank pain and ureteral obstruction. Imaging revealed a retroperitoneal mass suspicious for malignancy. Histopathology confirmed an inflammatory myofibroblastic tumor (IMT; anaplastic lymphoma kinase [ALK]-negative, mouse double minute 2 homolog-positive).
View Article and Find Full Text PDFJ Visc Surg
September 2025
Department of Visceral and Digestive Surgery, Timone Hospital, Marseille, France. Electronic address:
Ureteral complications occur rarely during colorectal surgery (0.3 to 1.5%), are mainly diagnosed postoperatively (50-70%), and result in both short- and long-term morbidity.
View Article and Find Full Text PDFJ Surg Case Rep
August 2025
Faculté de Medecine et de Pharmacie de Rabat, Université Mohammed V de Rabat, Avenue Mohammed Belarbi El Alaoui, Souissi, Rabat 10170, Rabat, Morocco.
Congenital ureteral stricture is a rare but important differential diagnosis in antenatal hydronephrosis, often mistaken for ureteropelvic junction obstruction. We report the case of a 5-year-old girl who underwent surgery for suspected ureteropelvic junction obstruction based on imaging findings, including renal ultrasound and scintigraphy. Intraoperatively, the pyeloureteral junction appeared normal, but a proximal ureteral stricture was discovered 4 cm distal to the renal pelvis.
View Article and Find Full Text PDFFront Pharmacol
August 2025
Department of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu, China.
Introduction: Stevens-Johnson syndrome is a rare, severe cutaneous adverse reaction. There is a lack of literature reporting the complications of the bladder and ureter caused by Stevens-Johnson syndrome. In this case, we describe a 10-year-old boy with hydronephrosis and nephrogenic adenoma secondary to Stevens-Johnson syndrome.
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