Robot-Assisted Laparoscopic Endorectal Pull-Through Combined with Deloyers Turnover in Long-Segment Hirschsprung Disease: A Case Report [0.03%]
机器人辅助腹腔镜内括约肌下拖出术联合Deloyers切开治疗长段型先天性巨结肠症1例报告
Maria Stella Cipriani,Maria G Faticato,Federica Fanti et al.
Maria Stella Cipriani et al.
We report the first documented pediatric case of the Deloyers procedure performed using robotic surgery to treat a female patient with long-segment Hirschsprung disease. A 9-month-old child was diagnosed with long-segment Hirschsprung disea...
Successful Treatment of Concurrent Cholangiohydatidosis with Obstructive Jaundice and Hepatothoracic Transit in a Pediatric Patient [0.03%]
一例合并阻塞性黄疸和肝胸腔交通的胆管囊尾蚴病成功手术治疗报告
Narcis Flavius Tepeneu,Călin Marius Popoiu,Emil Radu Iacob et al.
Narcis Flavius Tepeneu et al.
Concurrent rupture of hepatic hydatid cysts into the biliary tree and into the pleural cavity is a very rare complication in echinococcosis and can pose diagnostic and treatment challenges. We present the case of a 15-year-old female patien...
Stefanie Welke,Ferdinand Kosch,Andreas Müller et al.
Stefanie Welke et al.
A 12-year-old girl presented with inguinal swelling and recurrent groin pain since menarche. Ultrasound showed an inguinally located ovary with normal perfusion. Herniorrhaphy revealed an ectopic inguinal left ovary with fallopian tube and ...
Cloacal Exstrophy Associated with a Hindgut Duplication Anomaly: A Case Report of Challenges in Hindgut Preservation [0.03%]
与后肠重复畸形相关的泄殖腔外翻：一例具有后肠保留挑战的病例报告
Suliaman Alaqeel,Jamila Almaary,Fatmah Alrabodh et al.
Suliaman Alaqeel et al.
Cloacal exstrophy (CE) is a rare condition, and the preservation of a short hindgut is crucial for growth, fluid-electrolyte balance, and bowel management. Herein, we present the case of an infant with concurrent anomalies and the challenge...
Successful Repair of Esophageal Atresia with Tracheoesophageal Fistula and Interrupted Inferior Vena Cava: A Rare Case Report [0.03%]
食管闭锁合并气管食管瘘及下腔静脉间断的成功的修复：一个罕见病例报道
Xiao Long Mu,Junqiu Wang
Xiao Long Mu
Esophageal atresia (EA) with tracheoesophageal fistula (TEF) is a congenital anomaly that can present complex surgical challenges, especially when accompanied by rare vascular conditions like an interrupted inferior vena cava (IVC). The div...
Arterio-Ureteral Fistula as a Long-term Complication Following Retroperitoneal Presacral Ganglioneuroma Resection: Case Report in an Adolescent and Review of the Literature [0.03%]
盆腔外神经纤维瘤切除术后的长期并发症：与动脉的瘘管及文献回顾
Theresa S Haecker,Thomas F Krebs,Regula von Allmen et al.
Theresa S Haecker et al.
Arterio-ureteral fistula (AUF) is a rare condition affecting nearby adult-only patients. Patients usually present with hematuria, often starting as intermittent hematuria which frequently increases, and may lead to hemorrhagic shock. Withou...
Anal Sphincter Reconstruction Using the Posterior Sagittal Approach for Pediatric Perineal Trauma [0.03%]
后矢状入路肛门括约肌修复术治疗儿童会阴部损伤
Julia Ann Ryan,Thomas O Xu,Christina Ho et al.
Julia Ann Ryan et al.
Traumatic perineal injuries are rare but can result in significant morbidity, particularly when the anal sphincter is injured. The management of such injuries in the pediatric population is rarely noted in the literature. We aimed to descri...
Soumitra Saha,Mayank Tripathi,Kumar Vineet et al.
Soumitra Saha et al.
Gastric teratomas are an extremely rare variety of teratomas in children. The aim of our series is to present the natural history and progression of the disease. Retrospective analysis of prospectively maintained data of all the gastric ter...
Transverse Testicular Ectopy and an Incarcerated Inguinal Hernia in a 2-Month-Old Preterm Boy [0.03%]
一例早产儿2月龄睾丸横位并发腹股沟嵌顿疝急诊手术治疗一例
Marcin Lech Kordasz,Michael Nakhleh,Christoph Matissek et al.
Marcin Lech Kordasz et al.
Transverse testicular ectopy (TTE) is a rare anomaly in which both testicles descend through the same inguinal canal. Different variants of this anomaly exist, with the most common presenting as two separate spermatic cords and testicular v...
Lotte Bruyninckx,Paul De Leyn,Dirk Van Raemdonck et al.
Lotte Bruyninckx et al.
An inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal tumor that occurs predominantly in children and young adults. Etiology remains unclear. But based on the frequent detection of chromosomic alterations, especially near the an...