Congenital Jejunal Web with Central Aperture in Children: Report of Two Cases of Delayed Diagnosis and Management [0.03%]
儿童先天性空回肠隔膜致肠梗阻2例报告及诊治分析
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 ...
A Case Report of a Syndromic Triad of Persistent Urogenital Sinus, Herlyn-Werner-Wunderlich Syndrome, and Prune Belly Syndrome in a Neonate [0.03%]
新生儿尿道窦畸形、Herlyn-Werner-Wunderlich综合征及 prune belly 综合征三联征的病例报告
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-...
Fibrous Hamartoma of Infancy of the Arm Mimicking a Vascular Malformation: A Diagnostic Pitfall [0.03%]
易误诊为血管畸形的婴儿肢体纤维性错构瘤一例
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...
Waugh's Syndrome: A Case Report and Literature Review of Intussusception and Malrotation [0.03%]
瓦氏综合征的病例报告及肠套叠和肠道位置异常的文献回顾
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...
Inhaled Indocyanine Green Negative-contrast Fluorescence-guided Surgery for Pulmonary Metastasectomy [0.03%]
用于肺转移瘤切除的负对比荧光引导手术中吲哚菁绿雾化应用研究
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...
Umbilical Cord Hernia and Meckel's Diverticulum: Beware of the Umbilical Clamping! [0.03%]
脐疝和梅克尔憩室：注意脐带夹闭！
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...
Unveiling a Unique Posterior Cloaca Variant: Expanding the Spectrum [0.03%]
揭开一种独特的后尿道瓣膜变异类型：扩大临床谱系认知范围
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...
Nabila Bouzakri,Ann-Kathrin Lederer,Julia I Staubitz-Vernazza et al.
Nabila Bouzakri et al.
This case report describes the recurrence of an immature thyroid infiltrating teratoma in a female infant. Initially treated surgically for a cervical mass, the teratoma recurred, requiring further intervention. The case highlights the impo...
Erratum: Erratum: Corrections to Two Articles in European Journal of Pediatric Surgery Reports , Volume 13, Issue 1 [0.03%]
纠错：欧洲儿科手术报告杂志第13卷，第1期的两篇文章的更正 ошибки：应为“欧洲儿科外科报告杂志第13卷，第1期的两篇文章的勘误”
[This corrects the article DOI: 10.1055/a-2692-6661.][This corrects the article DOI: 10.1055/a-2699-8104.]. The Author(s). This is an open access article...
Kaposiform Hemangioendothelioma with Kasabach-Merritt Phenomenon in a Neonate: A Case Report [0.03%]
新生儿Kasabach-Merritt现象伴发卡波西样血管内皮瘤1例报告
Yuyang Zheng,Rongjie Wu,Qilin Chen et al.
Yuyang Zheng et al.
Background: Kaposiform hemangioendothelioma (KHE) is a rare, aggressive vascular tumor frequently complicated by Kasabach-Merritt phenomenon (KMP), a life-threatening consumptive coagulopathy. Neonatal KHE-KMP management ...