European Journal of Pediatric Surgery Reports最新文献

Congenital Jejunal Web with Central Aperture in Children: Report of Two Cases of Delayed Diagnosis and Management. 儿童先天性空肠网伴中心孔：2例延迟诊断及治疗报告。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2026-04-02 eCollection Date: 2026-01-01 DOI: 10.1055/a-2839-6197

Umama Huq, Md Hasanuzzaman, Sadruddin Al Masud, Kaniz Hasina, Zobaer Hassan Chowdhury

引用次数: 0

A Case Report of a Syndromic Triad of Persistent Urogenital Sinus, Herlyn-Werner-Wunderlich Syndrome, and Prune Belly Syndrome in a Neonate. 新生儿持续性泌尿生殖窦综合征、Herlyn-Werner-Wunderlich综合征、Prune Belly综合征三联征1例报告。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2026-02-24 eCollection Date: 2026-01-01 DOI: 10.1055/a-2806-3084

Elena Grömping, Johanna Hagens, Hans C Schmidt, Katharina Wenke, Christian Tomuschat, Konrad Reinshagen

{"title":"A Case Report of a Syndromic Triad of Persistent Urogenital Sinus, Herlyn-Werner-Wunderlich Syndrome, and Prune Belly Syndrome in a Neonate.","authors":"Elena Grömping, Johanna Hagens, Hans C Schmidt, Katharina Wenke, Christian Tomuschat, Konrad Reinshagen","doi":"10.1055/a-2806-3084","DOIUrl":"https://doi.org/10.1055/a-2806-3084","url":null,"abstract":"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-like syndrome, combined with severe bilateral cystic dysplastic kidneys and complex urinary obstruction.Case report: A female infant was born at 34 3/7 weeks' gestation via cesarean section due to prenatal detection of hydrops fetalis and massive urinary ascites. Prenatal ultrasound had shown oligohydramnios, ascites, megacystis, and hydrocolpos. Postnatally, urinary ascites, a persistent urogenital sinus, severe upper urinary tract dilation, bilateral dysplastic kidneys, and an obstructive vaginal septum were confirmed. Management included staged urinary drainage, vaginal septum incision, intensive respiratory and renal support, and multidisciplinary care.Conclusion: This unique combination of anomalies presents significant diagnostic and therapeutic challenges. Early recognition and individualized multidisciplinary management are essential to improve postnatal outcomes and guide long-term planning in such cases.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"14 1","pages":"e17-e21"},"PeriodicalIF":0.7,"publicationDate":"2026-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12932032/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147310260","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Fibrous Hamartoma of Infancy of the Arm Mimicking a Vascular Malformation: A Diagnostic Pitfall. 模仿血管畸形的婴儿期手臂纤维错构瘤：一个诊断缺陷。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2026-01-31 eCollection Date: 2026-01-01 DOI: 10.1055/a-2790-2093

Layth J M Saada, Malak Ismael Marei, Izzeddin A Bakri, Jamil Saada

{"title":"Fibrous Hamartoma of Infancy of the Arm Mimicking a Vascular Malformation: A Diagnostic Pitfall.","authors":"Layth J M Saada, Malak Ismael Marei, Izzeddin A Bakri, Jamil Saada","doi":"10.1055/a-2790-2093","DOIUrl":"10.1055/a-2790-2093","url":null,"abstract":"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 tissue neoplasms.Case presentation: A 7-month-old male presented with a rapidly enlarging, firm, non-pulsatile subcutaneous mass involving the anterior aspect of almost the entire right arm. MRI suggested a low-flow vascular malformation; however, due to clinical concern for alternative pathology and the lesion's benign appearance, large size, superficial location, and resectability, complete excision was performed. Histopathology revealed the characteristic triphasic pattern confirming fibrous hamartoma of infancy. The patient recovered well with no recurrence at 3-month follow-up.Conclusion: This case highlights the diagnostic pitfalls of FHI, which may closely mimic vascular anomalies on imaging, and underscores the importance of surgical excision for both definitive diagnosis and curative treatment. To our knowledge, this represents the first reported case of FHI from Palestine.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"14 1","pages":"e9-e16"},"PeriodicalIF":0.7,"publicationDate":"2026-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12860553/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146107928","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Waugh's Syndrome: A Case Report and Literature Review of Intussusception and Malrotation. 沃氏综合征：肠套叠及旋转不良1例报告及文献复习。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2026-01-27 eCollection Date: 2026-01-01 DOI: 10.1055/a-2781-7827

Mário Rui Correia, Ana Isabel Barros, Jorge Cagigal, Joana Sinde, Catarina Sousa-Lopes, Maria Luísa Gaspar, Helena M Silva, Hélder Morgado, José Banquart-Leitão

{"title":"Waugh's Syndrome: A Case Report and Literature Review of Intussusception and Malrotation.","authors":"Mário Rui Correia, Ana Isabel Barros, Jorge Cagigal, Joana Sinde, Catarina Sousa-Lopes, Maria Luísa Gaspar, Helena M Silva, Hélder Morgado, José Banquart-Leitão","doi":"10.1055/a-2781-7827","DOIUrl":"https://doi.org/10.1055/a-2781-7827","url":null,"abstract":"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 conditions and the frequent success of non-operative reduction of intussusception, which often results in underdiagnosis of malrotation. We present a case of a 6-month-old boy who developed recurrent vomiting, feeding intolerance, and failure to thrive. Ultrasound imaging revealed ileocolic intussusception and a mobile cecum. Laparoscopy confirmed malrotation, and the patient underwent manual reduction of intussusception, followed by Ladd procedure. The child had an uneventful postoperative recovery without complications. Early diagnosis of Waugh's syndrome requires a high index of suspicion, particularly in recurrent obstructive symptoms where malrotation may be present. Enhanced imaging techniques can facilitate prompt diagnosis and guide appropriate surgical intervention, preventing complications. Clinicians should maintain a high degree of suspicion for Waugh's syndrome to ensure timely and effective intervention.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"14 1","pages":"e5-e8"},"PeriodicalIF":0.7,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12846850/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146094617","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Inhaled Indocyanine Green Negative-contrast Fluorescence-guided Surgery for Pulmonary Metastasectomy. 吸入吲哚菁绿阴性对比荧光引导肺转移瘤切除术。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2026-01-24 eCollection Date: 2026-01-01 DOI: 10.1055/a-2780-3527

Ángel Javier Gallego Fernández, Jose Andrés Moreno Delgado, Juan Francisco Navarro Pardo, Eloísa Diaz Moreno, Cristina Palomares Garzón, Ricardo Fernandez-Valadés

{"title":"Inhaled Indocyanine Green Negative-contrast Fluorescence-guided Surgery for Pulmonary Metastasectomy.","authors":"Ángel Javier Gallego Fernández, Jose Andrés Moreno Delgado, Juan Francisco Navarro Pardo, Eloísa Diaz Moreno, Cristina Palomares Garzón, Ricardo Fernandez-Valadés","doi":"10.1055/a-2780-3527","DOIUrl":"10.1055/a-2780-3527","url":null,"abstract":"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 intravenously. We present a case of inhaled indocyanine green use for the identification and resection of pulmonary metastatic nodules. A 12-year-old female patient with a history of sternal Ewing sarcoma with bone and pulmonary metastases was treated with chemotherapy, proton therapy, partial sternal and costal cartilage resection, and reconstruction with mesh and absorbable plates. She later developed pulmonary relapse, with two subpleural metastases identified in segments 6 and 9 of the right lung. After initiating chemotherapy, thoracoscopic surgery was planned to resect the nodules. Before surgery, nebulization of indocyanine green was performed via an endotracheal tube at 0.2 mg/kg using an inhalation chamber for 5 minutes at 6 liters per minute. During surgery, fluorescence was observed in the insufflated lung parenchyma, allowing for clear differentiation of metastatic nodules from peripheral fibrotic or inflammatory tissue and enabling a safe wedge resection of both lesions. The postoperative period was uneventful, and the patient is currently completing postoperative chemotherapy cycles.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"14 1","pages":"e1-e4"},"PeriodicalIF":0.7,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12831635/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146054154","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Umbilical Cord Hernia and Meckel's Diverticulum: Beware of the Umbilical Clamping! 脐带疝和梅克尔憩室：当心脐带夹紧！

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2025-12-06 eCollection Date: 2025-01-01 DOI: 10.1055/a-2747-7295

Taisia Bollettini, Thibault Planchamp, Solène Joseph, Luana Carfagna, Olivier Abbo

引用次数: 0

Unveiling a Unique Posterior Cloaca Variant: Expanding the Spectrum. 揭开一个独特的后泄殖腔变体：扩大光谱。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2025-11-14 eCollection Date: 2025-01-01 DOI: 10.1055/a-2733-3072

Tarlia Rasa Govender, Emanuele Trovalusci, Andre Theron, Chris Westgarth-Taylor, Giulia Brisighelli

引用次数: 0

Recurrence of an Immature Thyroid Infiltrating Teratoma in a Female Infant. 1例女婴未成熟甲状腺浸润性畸胎瘤复发。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2025-11-11 eCollection Date: 2025-01-01 DOI: 10.1055/a-2733-2840

Nabila Bouzakri, Ann-Kathrin Lederer, Julia I Staubitz-Vernazza, Larissa Seidmann, Joachim Pohlenz, Meinolf Siepermann, Thomas J Musholt

引用次数: 0

Erratum: Erratum: Corrections to Two Articles in European Journal of Pediatric Surgery Reports , Volume 13, Issue 1. 勘误：勘误：更正两篇文章在欧洲儿科外科杂志报告，第13卷，第1期。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2025-09-26 eCollection Date: 2025-01-01 DOI: 10.1055/a-2706-9632

引用次数: 0

Kaposiform Hemangioendothelioma with Kasabach-Merritt Phenomenon in a Neonate: A Case Report. 新生儿卡泊样血管内皮瘤伴卡萨巴赫-梅里特现象1例。

IF 0.7

European Journal of Pediatric Surgery Reports Pub Date : 2025-09-19 eCollection Date: 2025-01-01 DOI: 10.1055/a-2699-8104

Yuyang Zheng, Rongjie Wu, Qilin Chen, Shiyu Xiong, Jialu Yun, Wei Peng

{"title":"Kaposiform Hemangioendothelioma with Kasabach-Merritt Phenomenon in a Neonate: A Case Report.","authors":"Yuyang Zheng, Rongjie Wu, Qilin Chen, Shiyu Xiong, Jialu Yun, Wei Peng","doi":"10.1055/a-2699-8104","DOIUrl":"10.1055/a-2699-8104","url":null,"abstract":"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 requires urgent intervention but is complicated by immunosuppression risks, especially in Bacillus Calmette-Guérin (BCG)-vaccinated infants.Methods: A full-term male neonate with prenatal right upper limb thickening presented postnatally with a violaceous, firm mass. Laboratory findings confirmed KMP. Due to recent BCG vaccination, sirolimus was initially withheld. First-line therapies failed, prompting sirolimus initiation on day 3, supplemented by fibrinogen transfusions.Results: Platelets normalized by day 13 (283 × 10 9 /L) with marked tumor regression. Transient fever/diarrhea resolved with supportive care. At discharge (day 27), platelets stabilized (183 × 10 9 /L). Three-month follow-up showed sustained platelet recovery (268-532 × 10 9 /L), near-complete tumor resolution, and age-appropriate development. Prophylactic trimethoprim-sulfamethoxazole prevented infections.Conclusion: Sirolimus is a critical salvage therapy for refractory neonatal KHE-KMP, even in BCG-vaccinated infants. Timely initiation reverses life-threatening coagulopathy and achieves favorable outcomes, necessitating multidisciplinary monitoring to balance immunosuppression risks.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"13 1","pages":"e155-e158"},"PeriodicalIF":0.7,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12449040/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145114556","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0