European Journal of Pediatric Surgery Reports最新文献_第8页

Fatal Course of a Male Newborn with Double Duodenal Atresia. 1例男婴双十二指肠闭锁的死亡过程。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-02-07 DOI: 10.1055/s-0039-3400488

Ahmed Elrouby, Ahmed Koraitim

引用次数: 1

Removal of Ingested Magnetic Bodies via Laparoscopic Appendectomy. 通过腹腔镜阑尾切除术清除摄入的磁性体。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-10-21 DOI: 10.1055/s-0040-1714669

Vojtech Dotlacil, Barbora Frybova, Martin Vyhnanek, Lubos Zeman, Michal Rygl

{"title":"Removal of Ingested Magnetic Bodies via Laparoscopic Appendectomy.","authors":"Vojtech Dotlacil, Barbora Frybova, Martin Vyhnanek, Lubos Zeman, Michal Rygl","doi":"10.1055/s-0040-1714669","DOIUrl":"10.1055/s-0040-1714669","url":null,"abstract":"Ingestion of a foreign body is a frequent diagnosis in the pediatric population. In a small percentage of cases, foreign bodies themselves are strong magnets, and swallowing of multiple magnetic bodies can lead to serious complications in the gastrointestinal tract. Two consecutive case reports of patients who swallowed two magnetic beads are presented. In both cases, the abdominal radiograph described two magnets in contact, one in the area of the left hypochondrium and one in the right hypogastrium. Attempts of endoscopic localization and removal were unsuccessful. Due to the failure of magnet progression, laparoscopic revision of the abdominal cavity was indicated in both patients on the 25th and 4th day after swallowing. Using the magnetic forces between the magnets and the laparoscopic instruments, the foreign bodies were localized in the appendix of the first patient and in the cecum of the other one. The magnets were extracted together with the removal of the appendix in both patients. This is one of the first articles describing the successful extraction of foreign magnetic bodies from the gastrointestinal tract via laparoscopic appendectomy.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"8 1","pages":"e68-e70"},"PeriodicalIF":0.6,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577785/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38527196","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

Urothelial Papilloma of the Urinary Bladder in Children: Report of Two Cases. 儿童膀胱尿路上皮乳头状瘤:附2例报告。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-04-23 DOI: 10.1055/s-0040-1705154

Kata Davidovics, Sandor Davidovics, Andras Farkas, Noemi Benedek, Tamas Tornoczki, Daniel Kardos, Anna Davidovics, Peter Vajda

{"title":"Urothelial Papilloma of the Urinary Bladder in Children: Report of Two Cases.","authors":"Kata Davidovics, Sandor Davidovics, Andras Farkas, Noemi Benedek, Tamas Tornoczki, Daniel Kardos, Anna Davidovics, Peter Vajda","doi":"10.1055/s-0040-1705154","DOIUrl":"https://doi.org/10.1055/s-0040-1705154","url":null,"abstract":"Urothelial neoplasms of the bladder (UNB) are considerably rare throughout the pediatric population. UNB develops from the urothelial tissue in the form of a benign disease, generally favoring a successful prognosis in the majority of cases. The authors present the diagnosis and treatment regarding two medical case reports in which urothelial papilloma was diagnosed and effectively treated. Case 1 : A 15-year-old male patient was presented to our clinic complaining of a painless yet distinctive, macroscopic form of hematuria. Following a routine examination, which included ultrasound (US) and intravenous pyelography, the urethrocystoscopy revealed an intravesical solitary lesion positioned in the vicinity of the left ureteral orifice. Additionally, histology confirmed urothelial papilloma. During the follow-up, laboratory, urinary control tests, and US results all proved negative. Case 2 : A 13-year-old male patient was admitted to our clinic and examined, in regard to complaints associated with recurrent abdominal pain. The pathology was discovered incidentally on abdominal US. Preoperative US and magnetic resonance imaging (MRI) studies ensued, resulting in a scheduled MRI, followed by urethrocystoscopy, which confirmed an intravesical solitary lesion positioned near the right ureteral orifice. Histology revealed urothelial papilloma. During the follow-up control cystoscopy, one resection was repeated due to the presence of a residual tumor. Today, 10 years since the presence of uroepithelial papilloma, both patients are asymptomatic and tumor-free. If there is likely suspicion of recurrence, cystoscopy is recommended.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"8 1","pages":"e23-e26"},"PeriodicalIF":0.6,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0040-1705154","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38054701","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

Clinical Quiz: Reconstructive Strategies in a 5-Month-Old Infant with a Cloaca. 临床测验:5个月大婴儿的泄殖腔重建策略。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-07-12 DOI: 10.1055/s-0040-1713136

Victoria A Lane, Marc A Levitt

引用次数: 1

Complete Resection of a Large Mediastinal Calcifying Fibrous Tumor. 纵隔钙化纤维性大肿瘤的完全切除。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-07-12 DOI: 10.1055/s-0040-1713135

Géraldine L P Bono, Markus Lehner, Freimut H Schilling, Nikolai Stahr, Miriam Nowack, Philipp O Szavay

{"title":"Complete Resection of a Large Mediastinal Calcifying Fibrous Tumor.","authors":"Géraldine L P Bono, Markus Lehner, Freimut H Schilling, Nikolai Stahr, Miriam Nowack, Philipp O Szavay","doi":"10.1055/s-0040-1713135","DOIUrl":"10.1055/s-0040-1713135","url":null,"abstract":"Calcifying fibrous tumor (CFT) is a benign tumor entity which can present in a variety of different sites. Till date, eight cases with a mediastinal manifestation have been published in literature. Surgical removal is the treatment of choice for this often incidentally detected tumor. Surgery of thoracic CFT may be challenging due to its localization within the mediastinum. A 10-year old boy with a right-sided thoracic pectus carinatum-like deformity was referred for further evaluation, incidentally, revealing a mediastinal mass in computed tomography (CT). Laboratory results were all within normal range. Magnetic resonance imaging (MRI) showed a large tumor in the upper anterior mediastinum suggesting expansive but not infiltrative character. The tumor was displacing surrounding structures like the heart and the diaphragm. Lower venous stasis with dilation of the inferior cava vein could be demonstrated. The tumor was considered to be of benign dignity and surgical removal was indicated. Complete tumor resection could be achieved through a sternotomy approach, along with thymectomy. A partial resection of both the pericardium and diaphragm was required due to adhesion with soft tissue at those sites. The specimen's size was 320 mm × 145 mm × 100 mm, histologically confirmed as CFT. The patient showed no residual tumor at 3- and 9-month follow-up. This case is a report on a large mediastinal CFT which underwent successful complete surgical removal. Following tumor resection, prognosis is considered to be good; however, key issue is complete resection to avoid local tumor recurrence.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"8 1","pages":"e48-e51"},"PeriodicalIF":0.6,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0040-1713135","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38261298","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

Laparoscopic Management of Mechanical Small Bowel Obstruction Secondary to Meckel's Diverticulum with a Double Basis. A Rare Anatomic Presentation. 双基性梅克尔憩室继发机械性小肠梗阻的腹腔镜治疗。罕见的解剖表现。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-11-23 DOI: 10.1055/s-0040-1713902

Aurora Mariani, Mohammed Siddiqui, Nicolas Boulard, Dominique Berrebi, Arnaud Bonnard

{"title":"Laparoscopic Management of Mechanical Small Bowel Obstruction Secondary to Meckel's Diverticulum with a Double Basis. A Rare Anatomic Presentation.","authors":"Aurora Mariani, Mohammed Siddiqui, Nicolas Boulard, Dominique Berrebi, Arnaud Bonnard","doi":"10.1055/s-0040-1713902","DOIUrl":"https://doi.org/10.1055/s-0040-1713902","url":null,"abstract":"Meckel's diverticulum (MD) is the most common congenital abnormality of the gastrointestinal tract. Intestinal occlusion due to MD is a commonly observed consequence of intussusception or volvulus. Here, we report a case of an 11-year-old boy who presented to the emergency department with acute abdominal pain, bilious vomiting, and abdominal rebound tenderness. Computed tomography scan concluded a diagnosis of intestinal occlusion with no apparent cause. The patient was submitted to diagnostic laparoscopy, and mechanical occlusion by the permeable Meckel with double base was identified. A diverticulectomy by staplers was performed, and occlusion was alleviated. MD is a rare disease (for only 0.3-2.9% of the general population), and only 4.2 to 9% of patients diagnosed with MD have associated complications. MD can be a large base or a narrow base, with a mesodiverticular band but the diverticulum is usually a blind recess. In our case, the tube connected two intestinal segments. To the best of our knowledge, we have reported the first case of an MD-like permeable tube with a double basis.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"8 1","pages":"e59-e61"},"PeriodicalIF":0.6,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0040-1713902","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38306894","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

Sirolimus: A Rescue Drug to Control Complications of Extensive Venous Malformation. 西罗莫司：一种控制广泛性静脉畸形并发症的抢救药物。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-12-15 DOI: 10.1055/s-0040-1716895

Mohamed Aly Abdelbaky, Iman Ahmed Ragab, Amr AbdelHamid AbouZeid, Shaimaa Abdelsattar Mohammad, Mohamed Moussa Dahab, Mohammed Elsherbeny, Hatem Abdelkader Safaan

{"title":"Sirolimus: A Rescue Drug to Control Complications of Extensive Venous Malformation.","authors":"Mohamed Aly Abdelbaky, Iman Ahmed Ragab, Amr AbdelHamid AbouZeid, Shaimaa Abdelsattar Mohammad, Mohamed Moussa Dahab, Mohammed Elsherbeny, Hatem Abdelkader Safaan","doi":"10.1055/s-0040-1716895","DOIUrl":"https://doi.org/10.1055/s-0040-1716895","url":null,"abstract":"Abstract Venous malformations represent a major sector of vascular anomalies. Most cases are asymptomatic or subclinical; however, large extensive lesions can cause severe disability and sometimes mortality. In this report, we present a successful case of sirolimus treatment in managing an extensive venous malformation in the pelvis of a 21-month-old boy who presented with life-threatening complications. With a history dating since the day 2 of life, the patient suffered from chronic bleeding due to scrotal skin ulcerations, in addition to recurrent attacks of severe bleeding per rectum necessitating hospital admission and blood transfusion (three attacks since the age of 7 months). Pelvic magnetic resonance image showed the typical findings of extensive venous malformation involving the pelvis, perineum, scrotum, and extending to the gluteal region. The lesion was seen totally encasing the anorectum with marked thickening of their walls almost occluding their lumen. Oral sirolimus (2 mg/m2) was started with a target blood trough level of 5 to 10 ng/mL. Over a follow-up period of 5 months, there was obvious clinical improvement that included healing of skin lesions (scrotal ulcer) with complete re-epithelialization, absence of bleeding per rectum with improvement of constipation, and rise of hemoglobin level from 7.5 to 11.5 g/dL.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"8 1","pages":"e90-e94"},"PeriodicalIF":0.6,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0040-1716895","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38724770","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: 4

Image of the Month: Enterocolitis Following a Pull-through for Total Colonic Hirschsprung Disease in a 2-Year-Old Boy. 本月图片:一名2岁男孩因完全性结肠巨结肠病进行肠结肠炎手术。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2021-01-09 DOI: 10.1055/s-0040-1721050

Anisha Apte, Elise McKenna, Marc A Levitt

引用次数: 0

Post Circumcision Intraperitoneal Rupture of the Urinary Bladder: A Rare Complication. 包皮环切术后腹腔内膀胱破裂:一种罕见的并发症。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-03-06 DOI: 10.1055/s-0039-1700986

Sherif Abdelmaksoud, Mohammed Albishbishy, Mostafa Elayyouti, Mohamed Zohiri, Adham Elsaied

引用次数: 3

Primary Umbilical Endometriosis in an Adolescent Girl: Unsuspected Pathology. 青春期女孩原发性脐子宫内膜异位症:未预料的病理。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-02-08 DOI: 10.1055/s-0039-1700987

Leel Nellihela, Mudher Al-Adnani, Dorothy Kufeji

{"title":"Primary Umbilical Endometriosis in an Adolescent Girl: Unsuspected Pathology.","authors":"Leel Nellihela, Mudher Al-Adnani, Dorothy Kufeji","doi":"10.1055/s-0039-1700987","DOIUrl":"https://doi.org/10.1055/s-0039-1700987","url":null,"abstract":"Endometriosis affects 7 to 10% of women of reproductive age. Primary umbilical endometriosis (PUE) is even rarer with unclear pathogenesis. We report a case of PUE possibly the youngest patient reported in the literature. A 16-year-old girl of African origin presented with painful umbilical lump for 2 to 3 months duration with background history of precocious puberty, cyclical vomiting, and menorrhagia. Clinical examination showed dark-colored, tender, irreducible umbilical lump. A provisional diagnosis of incarcerated umbilical hernia was made. Abdominal X-ray showed no features of intestinal obstruction. Ultrasound scan of the abdomen showed lump containing heterogeneous echogenic material measuring 2.0 × 1.5cm within the umbilicus with no visible bowel loops or peristalsis. This was reported as consistent with an umbilical hernia with narrow neck possibly containing mesentery or intra-abdominal fat. The patient underwent urgent exploration of umbilicus under general anesthetic. At operation, a dark-colored, firm mass was excised and sent for histology. The underlying fascia and peritoneum were repaired. Histological examination confirmed the excised tissue was endometriosis. Follow-up continues in the endometriosis clinic. Umbilical endometriosis should be considered in differential diagnoses of painful umbilical lesion in adolescent girls and women of reproductive age. Complete excision and histology are highly recommended for obtaining a definitive diagnosis, to exclude malignancy and to prevent recurrence.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"8 1","pages":"e10-e13"},"PeriodicalIF":0.6,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-0039-1700987","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37630803","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: 7