European Journal of Pediatric Surgery Reports最新文献_第6页

Endoscopic Treatment of a Severe Vaginal Stenosis Following Battery Insertion in an 11-Year-Old Girl. 内窥镜治疗11岁女童电池插入后严重阴道狭窄。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-09-19 eCollection Date: 2022-01-01 DOI: 10.1055/a-1920-5849

Riccardo Guanà, Andrea Carpino, Giuseppe Garbagni, Cecilia Morchio, Salvatore Garofalo, Alessandro Pane, Federico Scottoni, Elisa Zambaiti, Giulia Perucca, Elena Madonia, Fabrizio Gennari

{"title":"Endoscopic Treatment of a Severe Vaginal Stenosis Following Battery Insertion in an 11-Year-Old Girl.","authors":"Riccardo Guanà, Andrea Carpino, Giuseppe Garbagni, Cecilia Morchio, Salvatore Garofalo, Alessandro Pane, Federico Scottoni, Elisa Zambaiti, Giulia Perucca, Elena Madonia, Fabrizio Gennari","doi":"10.1055/a-1920-5849","DOIUrl":"https://doi.org/10.1055/a-1920-5849","url":null,"abstract":"Acquired vaginal strictures are rare entities in children. As a result, they are generally difficult to manage and tend to recur despite appropriate initial therapy. This case study reports the staged management of vaginal stenosis following the insertion of a button battery. In this case, an 11-year-old girl experienced at 4 years old a battery insertion in the vaginal canal by her neighbor's son, who was 6-year-old at the time. Two weeks from insertion, the parents noted the foreign body discharge spontaneously. The girl had not complained of any symptoms at the time and had been asymptomatic for many years. In November 2020, she came to the emergency department reporting cramping abdominal pain accompanied by mucopurulent discharge. An abdominal ultrasound showed the presence of hematometrocolpos, and a vaginal stenosis dilation under general anesthesia was performed the following day. After 3 weeks, the stenosis was still present, preventing the passage of Hegar number 4. The girl was subjected to a vaginoscopic stenosis resection utilizing a monopolar hook passed through an operative channel. A Bakri catheter filled with 120 mL of water was left in place. After 10 days, the girl was discharged home with the Bakri inserted. Two weeks after discharge, she was reevaluated in the outpatient setting, where the Bakri was removed with no signs of residual stenosis. Acquired vaginal stenosis could be demanding to treat, particularly with the sole conservative approach. A first-line option can be the Hegar dilation. The endoscopic approach can be a second-line, minimally invasive treatment, but long-term outcomes are difficult to predict.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":" ","pages":"e135-e140"},"PeriodicalIF":0.6,"publicationDate":"2022-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484869/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33467997","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: 1

Esophageal Perforation into the Pericardium in a 3-Year-Old Child with Esophageal Stricture: A Rare Complication Following Esophageal Dilatation. 食管穿孔进入心包的3岁儿童食管狭窄:一个罕见的并发症后食管扩张。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-09-02 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1756207

Abdulrahman Nasser, Raif Nassir, Muhammad Younas Awan, Mohammad Anas AlShawa, Zakaria Habib

{"title":"Esophageal Perforation into the Pericardium in a 3-Year-Old Child with Esophageal Stricture: A Rare Complication Following Esophageal Dilatation.","authors":"Abdulrahman Nasser, Raif Nassir, Muhammad Younas Awan, Mohammad Anas AlShawa, Zakaria Habib","doi":"10.1055/s-0042-1756207","DOIUrl":"https://doi.org/10.1055/s-0042-1756207","url":null,"abstract":"Perforation of the esophagus during dilatation is a rare complication that might cause mortality. We present the report of a 3-year-old girl who was diagnosed with B cell acute lymphoblastic leukemia at 17 months of age. She experienced a complicated clinical course after chemotherapy was initiated, which included mucositis and acute pericarditis. She later developed an acquired esophageal stricture and tracheoesophageal fistula, which were managed with resection and primary anastomosis when she was in remission. Postoperatively, the patient developed a leak, which was treated conservatively. She subsequently developed a stricture that was treated successfully. On the fourth dilatation attempt and after she was sent home, she presented with persistent vomiting and low-grade fever and became vitally unstable on the same day, after stabilization, upper gastroenterology contrast revealed contrast filling the pericardium. She was managed conservatively with close observation and serial echocardiograms and then discharged home on day 18 in good condition after complete resolution of the pericardial effusion.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":" ","pages":"e131-e134"},"PeriodicalIF":0.6,"publicationDate":"2022-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9439882/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40348912","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: 2

Erratum to: Emergency Separation of Extreme VLBW Omphalopagus Twins: Case Report. 紧急分离极端VLBW脐裂双胞胎:病例报告。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-08-23 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1755532

Waleed Burhamah, Amar Alnaqi, Yaqoub Jafar, Esmaeel Taqi

引用次数: 0

Co-injection of Bile and Indocyanine Green for Detecting Pancreaticobiliary Maljunction of Choledochal Cyst. 胆胆与吲哚菁绿联合注射检测胆总管囊肿胰胆管畸形。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-08-23 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1747913

Shun Onishi, Koji Yamada, Masakazu Murakami, Chihiro Kedoin, Mitsuru Muto, Satoshi Ieiri

{"title":"Co-injection of Bile and Indocyanine Green for Detecting Pancreaticobiliary Maljunction of Choledochal Cyst.","authors":"Shun Onishi, Koji Yamada, Masakazu Murakami, Chihiro Kedoin, Mitsuru Muto, Satoshi Ieiri","doi":"10.1055/s-0042-1747913","DOIUrl":"https://doi.org/10.1055/s-0042-1747913","url":null,"abstract":"The usage of near-infrared (NIR) fluorescence imaging with indocyanine green (ICG) has gained popularity in many procedures in pediatric surgery. ICG generates fluorescent light only when it combines with a protein. We herein report a novel technique for detecting pancreaticobiliary maljunction (PBMJ) with co-injection of bile and ICG in laparoscopic choledochal cyst resection and hepaticojejunostomy for a pediatric patient. A 4-year-old girl presented with abdominal pain and intermittent vomiting. Enhanced computed tomography and magnetic resonance cholangiopancreatography showed a 17-mm type Ia choledochal cyst. Definitive PBMJ was not detected preoperatively. Laparoscopic choledochal cyst resection and hepaticojejunostomy were performed using five ports. A percutaneous silicon catheter was inserted into the gallbladder, and bile juice was aspirated. The amylase level of the bile juice was over 3 × 105 IU/L. The aspirated bile juice and ICG were mixed and co-injected into the gallbladder through the catheter. ICG combined with protein in bile juice and generated fluorescent light. Dilated common bile duct and pancreas were detected by NIR fluorescence imaging. This imaging technique was helpful for detecting the dissection margin of the distal side of the choledochal cyst inside the pancreatic tissue and preventing injury of the pancreatic tissue. This is the first case of ICG application for laparoscopic choledochal cyst resection in a pediatric patient. After resection of the choledochal cyst, laparoscopic hepaticojejunostomy was completely performed. Our technique is a safe and low-invasive method of detecting and excising the distal side of the cyst without a risk of radiography and residual bile duct.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":" ","pages":"e127-e130"},"PeriodicalIF":0.6,"publicationDate":"2022-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9398574/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33437819","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: 1

Complete Colonic Duplication and Perineal Fistula: Transanal Mucosectomy of the Ectopic Rectum. 完全结肠复制和会阴瘘:经肛门粘膜切除术治疗异位直肠。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-08-16 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1750028

Johannes W Duess, Peter Zimmermann, Franz W Hirsch, Daniel Graefe, Martin Lacher, Jan-Hendrik Gosemann

{"title":"Complete Colonic Duplication and Perineal Fistula: Transanal Mucosectomy of the Ectopic Rectum.","authors":"Johannes W Duess, Peter Zimmermann, Franz W Hirsch, Daniel Graefe, Martin Lacher, Jan-Hendrik Gosemann","doi":"10.1055/s-0042-1750028","DOIUrl":"https://doi.org/10.1055/s-0042-1750028","url":null,"abstract":"Background Colonic duplication may present in different anatomic variants. The surgical approach towards these anomalies can be challenging and has implications for subsequent future continence. Case Description We report on a 1-year-old girl with congenital heart defect and pacemaker who was referred to us with an anorectal malformation. The patient was stooling from both an anus and a perineal fistula. Examination under anesthesia revealed an orthotopic and age-appropriate sized anus with surrounding sphincter and a second rectal lumen ending as a perineal fistula. A computed tomography and contrast enema indicated colonic duplication. Exploratory laparotomy showed a duplicated terminal ileum leading to two ceca and appendices, which joined to a duplicated colon with a septum and common mesentery. At the rectosigmoid junction, one part of the duplication ended as a perineal fistula, the second one led to the (orthotope) anus. The common colonic wall was divided using a stapler. The rectal duplication leading to the perineal fistula was not completely resected but treated by mucosectomy only (Soave plane) leaving its muscular cuff in place. Finally, an ileostomy was created. The postoperative course was uneventful. A contrast enema prior to ostomy takedown demonstrated a well-configurated colon and rectum without stenosis or impaction. The girl is currently continent with a complete resolution of her constipation. Conclusion In cases of complete colonic duplication division of the common wall is simple and safe. Mucosectomy of the ectopic rectum limits pelvic dissection and preserves the entire muscular wall of the duplicated orthotope rectum.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":" ","pages":"e102-e106"},"PeriodicalIF":0.6,"publicationDate":"2022-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9381363/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40628727","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

A Rare Case of Colonic Triplication with Associated Imperforate Anus in a Newborn Male. 新生儿男性结肠三分症合并肛门闭锁一例。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-08-16 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1750318

Elise McKenna, Christina Ho, Andrea Badillo, Gustavo Villalona, Marc A Levitt

引用次数: 1

COVID-19-Related Intestinal Ischemia in A 7-Year Old Boy. 一名7岁男孩与covid -19相关的肠道缺血

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-08-16 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1755721

Balázs Fadgyas, Gábor István Garai, János Schnur, Viktória Irén Kiss, Viktória Vass, Enikő Mátyus, György Balázs, Tamas Cserni

引用次数: 2

Transanal Mesenteric Resection in Hirschsprung's Disease Using ICG under Concept of NOTES Technique. 在NOTES技术概念下应用ICG经肛门肠系膜切除先天性巨结肠。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-08-16 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1751051

Mitsuru Muto, Shun Onishi, Masakazu Murakami, Keisuke Yano, Toshio Harumatsu, Satoshi Ieiri

引用次数: 0

Osteoid Osteoma of the Coracoid Process Presenting as Adhesive Capsulitis in a 10-Year-Old Male: A Case Report. 10岁男性冠突骨样骨瘤表现为粘连性囊炎1例。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-07-27 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1751241

Anthony Mancuso, Amy Singleton, Hadeel Abaza, Michael Albert, Jeffrey Mikutis

引用次数: 0

Cloaca-Like Anomalies in the Male: A Report on Two Cases. 男性阴囊样畸形2例报告。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-07-27 eCollection Date: 2022-01-01 DOI: 10.1055/s-0042-1750409

Amr AbdelHamid AbouZeid, Shaimaa Abdelsattar Mohammad, Marco Rady Sos, Nader Nassef Guirguis, Heba A Mahmoud, Manal El-Mahdy

{"title":"Cloaca-Like Anomalies in the Male: A Report on Two Cases.","authors":"Amr AbdelHamid AbouZeid, Shaimaa Abdelsattar Mohammad, Marco Rady Sos, Nader Nassef Guirguis, Heba A Mahmoud, Manal El-Mahdy","doi":"10.1055/s-0042-1750409","DOIUrl":"https://doi.org/10.1055/s-0042-1750409","url":null,"abstract":"\"Cloaca\" is a term used to describe an anomaly in the female where a single orifice is located in the perineum draining both urogenital and gastrointestinal tracts. Few reports used the same term \"cloaca\" to describe the counterpart anomaly in the male. We present two \"male\" cases of anorectal anomalies associated with significant penile deformity (caudally displaced penis) that were managed during the period between January 2010 and September 2021. Characteristically, both cases had a single \"central\" perineal orifice. The latter was located anterior to the predestined site of the normal anus and just beneath a caudally positioned hypospadiac phallus. The caudal displacement of the penis was strikingly obvious by the presence of severe form of penoscrotal transposition. Both cases were associated with a perineal swelling (hamartoma) just beside the central perineal orifice. The urethra was very short (like that in the female), besides the single perineal orifice, which makes the presentation very similar to cloacal anomalies.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":" ","pages":"e93-e97"},"PeriodicalIF":0.6,"publicationDate":"2022-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329137/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40573385","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