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期刊名:European journal of pediatric surgery reports

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ISSN:2194-7619

e-ISSN:2194-7627

IF/分区:0.5/Q4

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共收录本刊相关文章索引307
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Francesco Fascetti-Leon,Federica Varner,Federica De Corti et al. Francesco Fascetti-Leon et al.
Congenital esophageal stenosis is a rare and heterogenous malformation often associated with esophageal atresia (EA). Failure of conservative endoscopic treatment leads to surgery. Transthoracic approach is rarely advocated due to the perid...
Thilo Stolze,Larissa Seidmann,Asim Zouari et al. Thilo Stolze et al.
Bronchogenic cysts are congenital foregut malformations most often found in the mediastinum or lung parenchyma. Abdominal locations are exceedingly rare and most commonly found in the left retroperitoneum. They may mimic other intra-abdomin...
Abdelrahman S Elnour,Bushara Abdullah,Leena Abdelmagid et al. Abdelrahman S Elnour et al.
Introduction: Epigastric heteropagus twinning is an extremely rare form of asymmetric conjoined twinning, characterized by a parasitic twin attached to the upper abdomen of a structurally normal autosite. ...
Umama Huq,Md Hasanuzzaman,Sadruddin Al Masud et al. Umama Huq et al.
Congenital intestinal web of the jejunum is an exceptionally rare condition. While most intestinal atresias present during the neonatal period, jejunal webs with central apertures can lead to delayed presentations, often causing diagnostic ...
Elena Grömping,Johanna Hagens,Hans C Schmidt et al. Elena Grömping et al.
Background: We present a case of a premature female neonate with a triad of persistent urogenital sinus with urinary ascites, bilateral hydrocolpos in a duplex uterus, and abdominal wall hypoplasia resembling Prune Belly-...
Layth J M Saada,Malak Ismael Marei,Izzeddin A Bakri et al. Layth J M Saada et al.
Background: Fibrous hamartoma of infancy (FHI) is a rare benign soft tissue tumor of early childhood, often misdiagnosed due to its clinical and/or radiological resemblance to vascular malformations or pediatric soft tiss...
Mário Rui Correia,Ana Isabel Barros,Jorge Cagigal et al. Mário Rui Correia et al.
Waugh's syndrome, the rare coexistence of intussusception and intestinal malrotation, has rarely been reported in literature, with fewer than 100 cases described globally. Its diagnosis is challenging due to non-specific symptoms of both co...
Ángel Javier Gallego Fernández,Jose Andrés Moreno Delgado,Juan Francisco Navarro Pardo et al. Ángel Javier Gallego Fernández et al.
Indocyanine green fluorescence (ICG-F)-guided surgery has, in recent years, optimized the precision and safety of surgical procedures. Although its applications are increasingly widespread, in most cases, the dye is administered intravenous...
Taisia Bollettini,Thibault Planchamp,Solène Joseph et al. Taisia Bollettini et al.
Congenital hernia in the umbilical cord is a rare form of ventral abdominal wall defect, which, if not diagnosed, can lead to iatrogenic intestinal injuries due to improper umbilical clamping. We report a case of a newborn referred to our c...
Tarlia Rasa Govender,Emanuele Trovalusci,Andre Theron et al. Tarlia Rasa Govender et al.
A posterior cloacal variant is a congenital malformation where a urogenital sinus terminates anterior to a normally placed anus. These are rare malformations with highly variable anatomy. We report on three cases of a novel phenotype of pos...