European Journal of Pediatric Surgery Reports最新文献_第10页

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

IF 0.6

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

Resection of an Extraovarian Noniuteinized Thecoma in a 14-Year-Old Girl 14岁女孩卵巢外非卵泡化囊肿的切除

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0042-1742712

O. Aubert, R. Wachowiak, C. Roth, A. K. Höhn, M. Lacher, S. Mayer

{"title":"Resection of an Extraovarian Noniuteinized Thecoma in a 14-Year-Old Girl","authors":"O. Aubert, R. Wachowiak, C. Roth, A. K. Höhn, M. Lacher, S. Mayer","doi":"10.1055/s-0042-1742712","DOIUrl":"https://doi.org/10.1055/s-0042-1742712","url":null,"abstract":"Thecomas are rare benign sex cord-stromal tumors that account for less than 1% of all ovarian tumors. They usually affect postmenopausal women and become symptomatic with abnormal bleeding. In adolescents, less than 10 cases have been reported so far, mainly with symptoms of hormonal disbalance. Extraovarian thecomas represent an even rarer entity, with only two cases described so far, none of them in the pediatric population. We report the case of a 14-year-old girl who presented with sudden-onset abdominal pain, dysuria, and fever, as well as highly elevated serum inflammation parameters. Ultrasound and magnetic resonance imaging (MRI) revealed a large, inhomogeneous pelvic mass (16 cm × 9 cm × 13 cm) with indistinct margins, suggestive of an infiltrative malignant teratoma or sarcoma. Laparoscopy confirmed a large mass of unknown origin. In contrast to the infiltrative character seen on preoperative MRI, the tumor could be easily exteriorized and resected after conversion to laparotomy. Ovaries, fallopian tubes, and uterus remained unaffected. Histopathology revealed a benign nonluteinized thecoma. The postoperative course and 19-month follow-up were uneventful.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"10 1","pages":"e37 - e40"},"PeriodicalIF":0.6,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48199458","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

When to Suspect DRUJ's Instability in Children? Case Report of a Rare Presentation of Distal Forearm Fractures 何时怀疑儿童DRUJ不稳定？罕见前臂远端骨折病例报告

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2022-01-01 DOI: 10.1055/s-0042-1748317

C. Saugy, A. Bregou

引用次数: 0

Communicating Bronchopulmonary Foregut Malformation Type IB: Diagnostic and Surgical Challenges. 交通性支气管肺前肠畸形IB型:诊断和手术挑战。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2021-12-13 eCollection Date: 2021-01-01 DOI: 10.1055/s-0041-1740321

Bhushanrao Jadhav, Ranjithatharsini Vaseeharan, Prabhu Sekaran, Semiu Eniola Folaranmi, Karim Awad

{"title":"Communicating Bronchopulmonary Foregut Malformation Type IB: Diagnostic and Surgical Challenges.","authors":"Bhushanrao Jadhav, Ranjithatharsini Vaseeharan, Prabhu Sekaran, Semiu Eniola Folaranmi, Karim Awad","doi":"10.1055/s-0041-1740321","DOIUrl":"https://doi.org/10.1055/s-0041-1740321","url":null,"abstract":"Communicating bronchopulmonary foregut malformations (CBPFM) are extremely rare. We present a complex case of type IB CBPFM with esophageal atresia and distal tracheoesophageal fistula (EA/TOF), duodenal atresia/annular pancreas (DA/AP), and intestinal malrotation who underwent primary repair for EA/TOF on day 3. Bilious aspirates on day 8 prompted an upper gastrointestinal (GI) contrast revealing a duodenal obstruction and communication between the right lung lower lobe and the esophagus (T8-T9 level). DA/AP and malrotation were repaired by a gastrojejunostomy and Ladd's procedure. A repeat contrast swallow identified a 2nd communication from the esophagus into the right lower lobe (T5-T6 level) raising the suspicion of a recurrent TOF. Computed tomography (CT) thorax confirmed above findings with an anomalous blood supply to right lung. An exploratory thoracotomy identified a three-lobed lung. However, the lower lobe was enlarged and connected in two separate locations to the esophagus. The child recovered after the disconnection of the esophageal connections and partial right lower lobectomy. CBPFM are extremely rare anomalies requiring a high index of suspicion, use of an upper GI contrast series, and CT scans for diagnosis. The treatment of choice is resection of the affected lung and disconnection of the esophageal communications.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"9 1","pages":"e80-e83"},"PeriodicalIF":0.6,"publicationDate":"2021-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668381/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39732857","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: 3

Hemi-Clamshell Approach for Fetal Lung Interstitial Tumor Resection in a Neonate: A Case Report. 半翻盖入路切除新生儿肺间质瘤1例。

IF 0.6

European Journal of Pediatric Surgery Reports Pub Date : 2021-11-24 eCollection Date: 2021-01-01 DOI: 10.1055/s-0041-1735807

Yasuhiro Kuroda, Hiroaki Fukuzawa, Insu Kawahara, Keiichi Morita

{"title":"Hemi-Clamshell Approach for Fetal Lung Interstitial Tumor Resection in a Neonate: A Case Report.","authors":"Yasuhiro Kuroda, Hiroaki Fukuzawa, Insu Kawahara, Keiichi Morita","doi":"10.1055/s-0041-1735807","DOIUrl":"https://doi.org/10.1055/s-0041-1735807","url":null,"abstract":"Fetal lung interstitial tumor (FLIT) is a rare primary lung mass in neonates. Classical incisions, such as posterolateral thoracotomy or median sternotomy, do not provide optimal exposure of the operative field for the resection of pediatric thoracic giant tumors. Herein, we report a rare case of a FLIT in a full-term male neonate, with complete resection achieved using a hemi-clamshell approach, which provided the required visualization of the operative field. The neonate was transferred to our hospital because of mild respiratory distress, which developed 18-hour after normal vaginal delivery. A mass in his right chest, without a midline shift, was observed on chest radiographs. Computed tomography showed a well-circumscribed solid anterior cervicothoracic mass, with a uniform density and no apparent cysts, diagnosed as a primary thoracic giant tumor. Once the patient was clinically stabilized, we proceeded with right upper lobectomy, using a hemi-clamshell approach, full sternotomy, and anterolateral thoracotomy, on postnatal day 22. Histopathologic examination revealed an 8.5 × 6.5 × 4.0 cm solid mass within the right upper lobe, which was diagnosed as a FLIT. His postoperative recovery was uneventful. The patient was followed up for 1 year, with no complaints or symptoms and no postoperative shoulder dysfunction. Gross total resection of primary thoracic giant tumors can be accomplished in neonates with optimal exposure of the chest cavity using a hemi-clamshell approach.","PeriodicalId":43204,"journal":{"name":"European Journal of Pediatric Surgery Reports","volume":"9 1","pages":"e72-e75"},"PeriodicalIF":0.6,"publicationDate":"2021-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612870/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39947958","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