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

Porous Ceramic Sternal Prosthesis Implantation in a 13-Year-Old Patient Presenting with Metastatic Ewing's Sarcoma. 多孔陶瓷胸骨假体植入术治疗一例13岁转移性尤文氏肉瘤。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-15 eCollection Date: 2022-01-01 DOI: 10.1055/s-0041-1740328

Nicolas Mainard, Dyuti Sharma, Damien Fron, Aurélie Mezel, Federico Canavese, Michel Bonnevalle, Eric Nectoux

{"title":"Porous Ceramic Sternal Prosthesis Implantation in a 13-Year-Old Patient Presenting with Metastatic Ewing's Sarcoma.","authors":"Nicolas Mainard, Dyuti Sharma, Damien Fron, Aurélie Mezel, Federico Canavese, Michel Bonnevalle, Eric Nectoux","doi":"10.1055/s-0041-1740328","DOIUrl":"https://doi.org/10.1055/s-0041-1740328","url":null,"abstract":"Ewing's sarcoma is the second most frequent primary malignant bone tumor in adolescents and young adults. Locations on the thoracic wall represent up to 20% of primary and secondary locations. We present the case of a 13-year-old patient treated with the use of a radiolucency porous bioceramic prosthesis as a sternal replacement for a wide tumor resection in an oncologic context. Focal radiation therapy was not possible due to the high risk of severe myocardial injuries caused by the sternal location of the tumor. The sternum CERAMIL® (I.CERAM, Limoges, France), in porous alumina (Al 2 O 3 ) has already been implanted into adults in sternal replacement during its invasion by a tumor or its infectious destruction. There were no complication concerning the surgery. The last follow-up at 2 years postoperatively reveals a satisfactory clinical situation with any functional thoracic complaint and nor any functional respiratory symptoms. The porous alumina sternal prosthesis offers a reliable alternative for sternal replacement indications for children in an oncologic context.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":" ","pages":"e1-e5"},"PeriodicalIF":0.6,"publicationDate":"2022-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761061/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39695778","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

Battery Ingestion with Colonic Perforation after Colostomy Closure in a Toddler 幼儿结肠造口术后电池误食并结肠穿孔

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0041-1741558

Annamarie C. Lukish, V. Pat, Anisha M. Apte, M. Levitt

{"title":"Battery Ingestion with Colonic Perforation after Colostomy Closure in a Toddler","authors":"Annamarie C. Lukish, V. Pat, Anisha M. Apte, M. Levitt","doi":"10.1055/s-0041-1741558","DOIUrl":"https://doi.org/10.1055/s-0041-1741558","url":null,"abstract":"Disc and button battery ingestion in children is common. In fact, data reports a dramatic increase in battery ingestion during the coronavirus disease 2019 pandemic likely as a result of increased household population density and electronic product utilization. These batteries often remain lodged in the esophagus causing potentially devastating complications if they are not removed urgently. Batteries that are passed beyond the esophagus usually do not cause any complications. We present the case of a 15-month-old male who underwent a colostomy takedown 2 months following a posterior sagittal anorectoplasty for imperforate anus. He recovered quickly, was advanced on his diet, and was discharged to home on postoperative day 3. On postoperative day 5 following the stoma closure, he presented with an acute abdomen, pneumoperitoneum and an abdominal X-ray that revealed a 21 mm disc battery in the left lower quadrant. He underwent exploration and the battery was found perforating the anastomosis. There was significant fibropurulent exudate and inflammation. The battery was removed, the anastomosis was excised, and a colostomy with Hartman's pouch was performed. The toddler recovered uneventfully. This case offers an opportunity to discuss the concerns of battery ingestion and postoperative care following intestinal surgery in children. We could find no other similar reports in the world's literature of a disrupted colonic anastomosis due to battery ingestion.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"10 1","pages":"e41 - e44"},"PeriodicalIF":0.6,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44409231","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

Ventrally Fused Conjoined Twins (Omphaloischiopagus): A Roadmap to Successful Separation 腹侧融合连体双胞胎:成功分离的路线图

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0042-1743579

A. AbouZeid, S. Mohammad, A. Radwan, L. Eldieb, Y. El-Gendy, H. Ibrahim, A. Amer, T. Shabana, H. Elzahaby, A. Elbarbary, M. Saleh, T. Abdelaziz, S. Elbeshry, S. Abdel-Hay, A. El-Ghoneimi, Ahmad Zaki

{"title":"Ventrally Fused Conjoined Twins (Omphaloischiopagus): A Roadmap to Successful Separation","authors":"A. AbouZeid, S. Mohammad, A. Radwan, L. Eldieb, Y. El-Gendy, H. Ibrahim, A. Amer, T. Shabana, H. Elzahaby, A. Elbarbary, M. Saleh, T. Abdelaziz, S. Elbeshry, S. Abdel-Hay, A. El-Ghoneimi, Ahmad Zaki","doi":"10.1055/s-0042-1743579","DOIUrl":"https://doi.org/10.1055/s-0042-1743579","url":null,"abstract":"Conjoined twining is one of the most fascinating and challenging situations which a pediatric surgeon may face in his career. Only few surgeons may have the opportunity to share in separation of such cases. In this report, we aim to share our experience with the successful separation of ventrally fused male conjoined twins (omphaloischiopagus). The case was thoroughly studied via preoperative cross-sectional imaging modalities (magnetic resonance imaging [MRI] and computed tomography [CT] angiography), complemented by data obtained from reviewing similar cases in the literature. A clear delineation of the complex anatomy was achieved preoperatively which proved to be well consistent with the operative findings. A detailed description of the operative procedure to divide/redistribute the shared abdominal/pelvic organs between both twins is provided. To the best of our knowledge, this is the first report to describe the detailed and unique internal anatomy of a common central phallus associating ischiopagus conjoined twins. The penis was centrally located in the perineum in between both twins with an open urethral plate. This common phallus had a peculiar configuration with four crura anchoring ischial bones of both twins together.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"10 1","pages":"e53 - e62"},"PeriodicalIF":0.6,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45641090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

Clinical Quiz—Newborn Female with an Anorectal Malformation and a Gynecological Abnormality 临床测验-新生儿肛门直肠畸形和妇科异常

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0041-1741508

Anisha M. Apte, Allison Mayhew, E. McKenna, V. Gomez-Lobo, M. Levitt

引用次数: 0

Tubular Duplication of the Esophagus in a Newborn, Treated by Thoracoscopy 胸腔镜治疗新生儿食管管状重复畸形1例

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0042-1742594

I. Khvorostov, A. Gusev, A. Alkhasov, S. Yatsyk, E. D'yakonova

引用次数: 3

Intraneural Ganglion of the Peroneal Nerve—A Rare Cause of Pediatric Peroneal Nerve Palsy: A Case Report 腓骨神经神经内神经节——小儿腓骨神经麻痹的罕见病因1例

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0042-1742608

F. Bucher, Vincent Maerz, D. Obed, P. M. Vogt, B. Weyand

{"title":"Intraneural Ganglion of the Peroneal Nerve—A Rare Cause of Pediatric Peroneal Nerve Palsy: A Case Report","authors":"F. Bucher, Vincent Maerz, D. Obed, P. M. Vogt, B. Weyand","doi":"10.1055/s-0042-1742608","DOIUrl":"https://doi.org/10.1055/s-0042-1742608","url":null,"abstract":"Intraneural ganglia are benign mucinous cysts located within the epineurium of a peripheral nerve. The pathogenesis and formation of intraneural ganglia are controversial. The main theories described in the literature are of degenerative, synovial or de novo occurrence. We present the case of a 14-year-old boy who presented in our outpatient clinic with a complaint of interdigital neuralgia between hallux and second toe, as well as left foot drop. MRI examination showed a hyperintense cystic distension of the common peroneal nerve measuring 130 mm × 5 mm extending from the poplitea to the anterior compartment of the leg. We performed microscopic decompression and neurolysis surgery. The cyst showed a sac-like distension at its distal end with connection to the tibiofibular joint and was resected. After 8 weeks, postoperatively, the boy claimed to be pain-free and slight recovery of the superficial peroneal nerve was noticed. At 6 months postoperative, the patient showed a continuous improvement of motor function, demonstrating foot eversion with 3/5 muscle strength and foot extension with 2/5 muscle strength. Intraneural ganglia reported for pediatric patients represent a very rare entity. To the best of our knowledge, less than 15 cases have been described within the English-speaking literature.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"10 1","pages":"e33 - e36"},"PeriodicalIF":0.6,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41460321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 3

Bilateral Native Kidney Papillary Renal Cell Carcinomas in a 11-Year-Old Renal Transplant Patient. 11岁儿童肾移植患者双侧原生肾乳头状肾细胞癌。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0042-1759546

Çiğdem Ulukaya Durakbaşa, Deniz Ugurlu, Sabriye Gulcin Bozbeyoglu, Sinem Aydoner, Hatice Seneldir, Mehmet Onur Candir, Cengiz Candan, Atilla Gemici

{"title":"Bilateral Native Kidney Papillary Renal Cell Carcinomas in a 11-Year-Old Renal Transplant Patient.","authors":"Çiğdem Ulukaya Durakbaşa, Deniz Ugurlu, Sabriye Gulcin Bozbeyoglu, Sinem Aydoner, Hatice Seneldir, Mehmet Onur Candir, Cengiz Candan, Atilla Gemici","doi":"10.1055/s-0042-1759546","DOIUrl":"https://doi.org/10.1055/s-0042-1759546","url":null,"abstract":"Renal cell carcinomas (RCCs) are the most common renal tumors in adults and are usually sporadic and unilateral. Renal transplant recipients have an increased risk of developing RCC. RCC development after kidney transplantation is very rarely reported in children. We present a 11-year-old boy who had cadaveric kidney transplantation for kidney failure 2 years ago. He was under immunosuppressive therapy and presented with microscopic hematuria. An ultrasound (US) revealed bilateral solid renal masses. Further cross-sectional imaging showed a 60 × 70 × 60-mm right renal mass with claw sign and a 5 × 6 × 6-mm mass in the left renal lower pole. A bilateral radical nephroureterectomy of native kidneys was performed. The pathology revealed bilateral papillary RCC without TFE3 upregulation. The patient was kept on low-dose immunosuppressive therapy in the perioperative period. He received no chemotherapy but a close radiological surveillance was undertaken. He is tumor-free 2 years after the operation. RCC is a rare tumor for children and bilateralism is even rarer. The child had a history of chronic kidney disease, peritoneal dialysis, and immunosuppressive therapy. As there are no standardized protocols regarding imaging in transplanted kidneys routine surveillance, US follow-up should also focus on detecting malignancy.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"10 1","pages":"e160-e163"},"PeriodicalIF":0.6,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719804/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10737933","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

Juvenile Xanthogranuloma as Differential Diagnosis of a Vulvar Mass: A Case Report 幼年黄色肉芽肿作为外阴肿块的鉴别诊断:1例报告

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0042-1743159

I. Bada Bosch, A. Cañizo, M. Campos-Domínguez, J. Ordóñez, M. D. Blanco Verdú, M. Fanjul, L. Pérez-Egido, J. D. de Agustín

引用次数: 0

Hindgut Duplication in an Infant with Omphalocele–Exstrophy–Imperforate Anus–Spinal Defects (OEIS) Complex 婴儿脐膨出-肥大-闭锁肛-脊柱缺陷(OEIS)复合体的后肠复制

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European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0041-1742154

Timothy F. Tirrell, Farokh R. Demehri, C. Lillehei, J. Borer, B. Warf, Belinda H. Dickie

{"title":"Hindgut Duplication in an Infant with Omphalocele–Exstrophy–Imperforate Anus–Spinal Defects (OEIS) Complex","authors":"Timothy F. Tirrell, Farokh R. Demehri, C. Lillehei, J. Borer, B. Warf, Belinda H. Dickie","doi":"10.1055/s-0041-1742154","DOIUrl":"https://doi.org/10.1055/s-0041-1742154","url":null,"abstract":"Introduction The congenital anomaly of omphalocele, cloacal exstrophy, imperforate anus, and spinal abnormalities (OEIS complex) is rare but well recognized. Hindgut duplications are also uncommon and are not known to be associated with OEIS. We describe a neonate with OEIS who was found to have fully duplicated blind-ending hindguts. Case Report A premature infant boy with OEIS underwent first-stage closure on day of life 6, which included excision of the omphalocele sac, separation of the cecal plate and bladder halves, tubularization of the cecal plate, hindgut rescue with end colostomy, and joining of the bladder halves. Cecal plate inspection revealed two hindgut structures that descended distally, one descended midline into the pelvis along the sacrum and the second laterally along the left border of the sacrum. Both lumens connected to the cecal plate and had separate mesenteries. In an effort to maximize the colonic mucosal surface area, the hindgut segments were unified through a side-to-side anastomosis, creating a larger caliber hindgut. The cecal plate was tubularized and an end colostomy was created. Bowel function returned and he was discharged home on full enteral feeds. Discussion This case represents a cooccurrence of two extremely rare and complex congenital anomalies. The decision to unify the distinct hindguts into a single lumen was made in an effort to combine the goals of management for both OEIS and alimentary duplications. The hindgut is abnormal in OEIS and should be assessed carefully during repair.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"10 1","pages":"e45 - e48"},"PeriodicalIF":0.6,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45809248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Thoracoscopic Resection of a Foregut Duplication Cyst with the Use of a 5-mm Stapling Device in an Infant—A Case Report 胸腔镜下5毫米吻合器切除婴儿前肠重复囊肿1例报告

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0042-1742713

M. Da Col, N. Regamey, P. Szavay

引用次数: 1