首页 > 最新文献

Cocuk Cerrahisi Dergisi最新文献

英文 中文
Dünya Çocuk Cerrahlarının Sünnette EMLA® Krem ile Oluşturulan Lokal Anestezi Hakkındaki Görüşleri Nedir? EMLA世界儿童外科® 用乳膏创造的局部麻醉有哪些会议?
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.70845
Mustafa Akman
{"title":"Dünya Çocuk Cerrahlarının Sünnette EMLA® Krem ile Oluşturulan Lokal Anestezi Hakkındaki Görüşleri Nedir?","authors":"Mustafa Akman","doi":"10.5222/jtaps.2021.70845","DOIUrl":"https://doi.org/10.5222/jtaps.2021.70845","url":null,"abstract":"","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70852109","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
Congenital Bronchobiliary Fistula in Association with Multiple Other Congenital Anomalies: Case Report 先天性支气管胆管瘘合并其他多种先天性畸形:1例报告
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.82712
Mirzaman Hüseyinov, Ali Ekber Hakalmaz
Congenital bronchobiliary fistula (CBBF) is a rare anomaly in which a fistulous opening exists between the biliary tract and the tracheobronchial tree. CBBF may be accompanied by many congenital anomalies, with biliary system anomalies being the most common. CBBF was also reported to be associated with esophageal atresia in one case and right diaphragmatic hernia in another case. However, as far as we have known, CBBF case accompanied by multiple congenital anomalies has not been reported previously. In this article, we firstly present a case of a neonatal CBBF, incidentally diagnosed intraoperatively, accompanied by multiple congenital anomalies, including congenital diaphragmatic hernia. Secondly, we present our conclusions and updates about CBBF based on what we have learned from both our case and the literature.
先天性支气管胆道瘘(CBBF)是一种罕见的异常,在胆道和气管支气管树之间存在瘘口。CBBF可能伴有许多先天性异常,以胆道系统异常最为常见。据报道,CBBF还与1例食管闭锁和1例右侧膈疝有关。然而,据我们所知,CBBF合并多发性先天性异常的病例此前未见报道。在这篇文章中,我们首先报告了一例新生儿CBBF,术中偶然诊断,伴有多种先天性异常,包括先天性膈疝。其次,根据我们从案例和文献中学到的知识,我们提出了关于CBBF的结论和更新。
{"title":"Congenital Bronchobiliary Fistula in Association with Multiple Other Congenital Anomalies: Case Report","authors":"Mirzaman Hüseyinov, Ali Ekber Hakalmaz","doi":"10.5222/jtaps.2021.82712","DOIUrl":"https://doi.org/10.5222/jtaps.2021.82712","url":null,"abstract":"Congenital bronchobiliary fistula (CBBF) is a rare anomaly in which a fistulous opening exists between the biliary tract and the tracheobronchial tree. CBBF may be accompanied by many congenital anomalies, with biliary system anomalies being the most common. CBBF was also reported to be associated with esophageal atresia in one case and right diaphragmatic hernia in another case. However, as far as we have known, CBBF case accompanied by multiple congenital anomalies has not been reported previously. In this article, we firstly present a case of a neonatal CBBF, incidentally diagnosed intraoperatively, accompanied by multiple congenital anomalies, including congenital diaphragmatic hernia. Secondly, we present our conclusions and updates about CBBF based on what we have learned from both our case and the literature.","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70852382","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
Results of Crystalized Phenol Application in the Treatment of Pilonidal Sinus Disease in Children: Our Single Center Experience 结晶苯酚应用于儿童毛窦疾病治疗的结果:我们的单中心经验
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.96636
Yusuf Atakan Baltrak, Seniha Esin Söğüt, Onursal Varlıklı
Objective: The debate about the etiology of Pilonidal Sinus Disease (PSD) continues over whether the disease is congenital or acquired. After determining the etiologic factora, new pilonidal sinus treatment methods have been developed. Method: The 6-month follow-up results of patients who were treated with crystallized phenol (CF) application with the diagnosis of PSD between March 2020 and August 2020 in the Pediatric Surgery Clinic were retrospectively analyzed. The patients were evaluated by age, height, weight, gender, body mass index, number of sinus mouths, sinus mouth width, sacral cupping distance and cyst diameter by imaging method and pilonidal sinus area measurement. After three consecutive weeks of CF administration, a two-week break was given. Every three weeks of treatment was considered as one treatment cycle. CF treatment was considered unsuccessful for patients whose pilonidal sinus cavity was not closed at the end of three cycles and the complaint of discharge persisted. Results: During the study period, 21 patients with PSH and a maximum of three sinus orifices were treated with CF in our clinic. Including 15 (71.4%) male and 6 (18.6%) female cases. The median age of the patients was 16 (14-17.5) years. In two patients (9.5%) who received three cycles of treatment, the treatment was considered as CF treatment failure because of the persistence of discharge complaints, and surgical treatment was planned for the patient. In the findings obtained as a result of the follow-up of the patients, it was observed that three patients (14.2%) had temporary painless transient dermatitis during follow-up due to phenol applied. Conclusion: The application of CF in the PSD treatment in pediatric age group should be considered as an acceptable method that can be easily applied by any surgeon with its short hospital stay, its applicability under local anesthesia in outpatient clinic conditions, low postoperative complications, high success rates, and low cost.
目的:关于毛窦病(PSD)的病因是先天性的还是后天的争论仍在继续。在确定病因后,新的治疗方法被开发出来。方法:回顾性分析2020年3月至2020年8月在小儿外科诊所接受结晶苯酚(CF)应用治疗并诊断为PSD的患者6个月随访结果。以年龄、身高、体重、性别、体质指数、窦口数、窦口宽度、骶骨拔罐距离、囊肿直径为评价指标,采用影像学方法和测毛窦面积。连续三周服用CF后,休息两周。每三周治疗一次为一个治疗周期。对于在三个周期结束时仍未关闭毛窦腔且持续出现出院症状的患者,认为CF治疗不成功。结果:研究期间,21例PSH患者(最多3个窦口)接受CF治疗。其中男性15例(71.4%),女性6例(18.6%)。患者的中位年龄为16岁(14-17.5岁)。2例(9.5%)患者接受了3个周期的治疗,由于出院主诉持续存在,认为CF治疗失败,并计划对患者进行手术治疗。在对患者的随访中,有3例患者(14.2%)在随访期间因使用苯酚而出现暂时性无痛性短暂性皮炎。结论:CF在小儿年龄段PSD治疗中应用,住院时间短,门诊局麻条件下适用,术后并发症少,成功率高,费用低,是任何外科医生都可以接受的治疗方法。
{"title":"Results of Crystalized Phenol Application in the Treatment of Pilonidal Sinus Disease in Children: Our Single Center Experience","authors":"Yusuf Atakan Baltrak, Seniha Esin Söğüt, Onursal Varlıklı","doi":"10.5222/jtaps.2021.96636","DOIUrl":"https://doi.org/10.5222/jtaps.2021.96636","url":null,"abstract":"Objective: The debate about the etiology of Pilonidal Sinus Disease (PSD) continues over whether the disease is congenital or acquired. After determining the etiologic factora, new pilonidal sinus treatment methods have been developed. Method: The 6-month follow-up results of patients who were treated with crystallized phenol (CF) application with the diagnosis of PSD between March 2020 and August 2020 in the Pediatric Surgery Clinic were retrospectively analyzed. The patients were evaluated by age, height, weight, gender, body mass index, number of sinus mouths, sinus mouth width, sacral cupping distance and cyst diameter by imaging method and pilonidal sinus area measurement. After three consecutive weeks of CF administration, a two-week break was given. Every three weeks of treatment was considered as one treatment cycle. CF treatment was considered unsuccessful for patients whose pilonidal sinus cavity was not closed at the end of three cycles and the complaint of discharge persisted. Results: During the study period, 21 patients with PSH and a maximum of three sinus orifices were treated with CF in our clinic. Including 15 (71.4%) male and 6 (18.6%) female cases. The median age of the patients was 16 (14-17.5) years. In two patients (9.5%) who received three cycles of treatment, the treatment was considered as CF treatment failure because of the persistence of discharge complaints, and surgical treatment was planned for the patient. In the findings obtained as a result of the follow-up of the patients, it was observed that three patients (14.2%) had temporary painless transient dermatitis during follow-up due to phenol applied. Conclusion: The application of CF in the PSD treatment in pediatric age group should be considered as an acceptable method that can be easily applied by any surgeon with its short hospital stay, its applicability under local anesthesia in outpatient clinic conditions, low postoperative complications, high success rates, and low cost.","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70852136","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
Congenital Duodenal Obstruction: Evaluation of 68 Cases 先天性十二指肠梗阻68例分析
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.70846
Emel Colak, A. Celayir
INTRODUCTION: Congenital duodenal obstruction, which is one of the most common causes of intestinal obstruction in neonates, gain importance in terms of associated anomalies. In this study, we aimed to review our experience with congenital duodenal obstruction cases operated in our clinic while evaluating the results of these patients. METHODS: All hospital records of neonates with congenital duodenal obstruction which had operated in our department between 2004 and 2017 were reviewed retrospectively. Patients were evaluated according to their demographic features, clinical presentations, associated anomalies, treatments and outcomes. RESULTS: During 13 years, 68 newborns (36 males, 32 females) with congenital duodenal obstruction were operated. The mean gestational age was 35.7±3.1weeks (28-44weeks), the mean birth weight was 2477±651.5 gram (1100–4100 gram) and 46 (67.7%) of them were premature. Associated abnormalities were detected in 37 neonates (54.4%); 16 of them (23.5%) had congenital cardiac malformations, and 13 of them (19.1%) had Down Syndrome. In neonates with associated abnormalities; the avarage period to start enteral feeding was 9.5±5.8 days (4-37days) and the mean hospitalization period was 25.6±26.2days (9-140days). These values were found 7.6±3.2 days (4-20days) and 17.5±13.7days (8-80days) respectively for the patients having no associated anomalies. Postoperative complications such as ileus, septicemia and nutritional intolerance were seen in 17 patients (25%); 3 of them (4.4%) need re-operation. While 63 patients (92.6%) were discharged on average 21.4±22 days (8-140 days); due to septicemia and severe congenital cardiac malformations 5 patients (7.4%) were died in 27.2±14.1 days (11-43days) postoperatively. The rate of septicemia was statistically significantly higher in patients with excitus than the ones who were discharged (p<0.001). DISCUSSION AND CONCLUSION: The presence of associated abnormalities in patients with congenital duodenal obstruction increases the risk of morbidity and mortality. Septicemia and severe congenital cardiac malformations adversely affect prognosis.
简介:先天性十二指肠梗阻是新生儿肠梗阻最常见的原因之一,在相关异常方面受到重视。在这项研究中,我们的目的是回顾我们的经验,先天性十二指肠梗阻的情况下,在我们的诊所进行手术,并评估这些患者的结果。方法:回顾性分析2004 ~ 2017年在我科手术治疗的先天性十二指肠梗阻新生儿的住院记录。根据患者的人口学特征、临床表现、相关异常、治疗和结果对患者进行评估。结果:13年来共收治新生儿先天性十二指肠梗阻68例(男36例,女32例)。平均胎龄为35.7±3.1周(28 ~ 44周),平均出生体重为2477±651.5克(1100 ~ 4100克),早产46例(67.7%)。相关异常37例(54.4%);其中先天性心脏畸形16例(23.5%),唐氏综合征13例(19.1%)。伴有相关异常的新生儿;平均开始肠内喂养时间为9.5±5.8天(4 ~ 37天),平均住院时间为25.6±26.2天(9 ~ 140天)。无相关异常的患者分别为7.6±3.2天(4 ~ 20天)和17.5±13.7天(8 ~ 80天)。术后并发症如肠梗阻、败血症和营养不耐受17例(25%);其中3例(4.4%)需再次手术。63例(92.6%)平均出院21.4±22天(8 ~ 140天);因败血症及严重先天性心脏畸形死亡5例(7.4%),死亡时间为术后27.2±14.1天(11 ~ 43天)。兴奋期患者败血症发生率明显高于出院期患者(p<0.001)。讨论与结论:先天性十二指肠梗阻患者的相关异常增加了发病率和死亡率的风险。败血症和严重的先天性心脏畸形对预后有不利影响。
{"title":"Congenital Duodenal Obstruction: Evaluation of 68 Cases","authors":"Emel Colak, A. Celayir","doi":"10.5222/jtaps.2021.70846","DOIUrl":"https://doi.org/10.5222/jtaps.2021.70846","url":null,"abstract":"INTRODUCTION: Congenital duodenal obstruction, which is one of the most common causes of intestinal obstruction in neonates, gain importance in terms of associated anomalies. In this study, we aimed to review our experience with congenital duodenal obstruction cases operated in our clinic while evaluating the results of these patients. METHODS: All hospital records of neonates with congenital duodenal obstruction which had operated in our department between 2004 and 2017 were reviewed retrospectively. Patients were evaluated according to their demographic features, clinical presentations, associated anomalies, treatments and outcomes. RESULTS: During 13 years, 68 newborns (36 males, 32 females) with congenital duodenal obstruction were operated. The mean gestational age was 35.7±3.1weeks (28-44weeks), the mean birth weight was 2477±651.5 gram (1100–4100 gram) and 46 (67.7%) of them were premature. Associated abnormalities were detected in 37 neonates (54.4%); 16 of them (23.5%) had congenital cardiac malformations, and 13 of them (19.1%) had Down Syndrome. In neonates with associated abnormalities; the avarage period to start enteral feeding was 9.5±5.8 days (4-37days) and the mean hospitalization period was 25.6±26.2days (9-140days). These values were found 7.6±3.2 days (4-20days) and 17.5±13.7days (8-80days) respectively for the patients having no associated anomalies. Postoperative complications such as ileus, septicemia and nutritional intolerance were seen in 17 patients (25%); 3 of them (4.4%) need re-operation. While 63 patients (92.6%) were discharged on average 21.4±22 days (8-140 days); due to septicemia and severe congenital cardiac malformations 5 patients (7.4%) were died in 27.2±14.1 days (11-43days) postoperatively. The rate of septicemia was statistically significantly higher in patients with excitus than the ones who were discharged (p<0.001). DISCUSSION AND CONCLUSION: The presence of associated abnormalities in patients with congenital duodenal obstruction increases the risk of morbidity and mortality. Septicemia and severe congenital cardiac malformations adversely affect prognosis.","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70852286","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
Childhood Ruptured Pulmonary Hydatid Cysts 儿童肺包虫病破裂
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.60437
V. Avcı, Kemal Ayengin, Mehmet Göksu
{"title":"Childhood Ruptured Pulmonary Hydatid Cysts","authors":"V. Avcı, Kemal Ayengin, Mehmet Göksu","doi":"10.5222/jtaps.2021.60437","DOIUrl":"https://doi.org/10.5222/jtaps.2021.60437","url":null,"abstract":"","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70852311","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
Childhood And Adolescent Period Breast Cancer 儿童和青少年时期乳腺癌
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.08216
A. Gül, D. Aygin
Objective: Breast cancer is a global public health problem which draws attention with the gradual increase in morbidity and mortality rates. Unlike adults, breast cancers in children and adolescents are rarely seen. Since the risk factors are not well defined, cancer findings are mixed with other disease findings and follow-up/treatment processes differ. As a result, childhood/adolescent breast cancers are ignored. It is stated that the prognosis of childhood and adolescent breast cancers is not good, although they are seen in a limited number of patients, the mortality rate is high and it significantly affects the life of the patient and his/her family. The main aim of this compilation is to examine the literature on the pediatric and adolescent breast cancers and the treatment process. Its secondary purpose is to increase the awareness of health professionals and the society and help to create a guideline in this regard to pediatric surgeons, and nurses. Methods: We identified 24 case reports comprising the data of 24 cases of childhood or adolescent breast cancers that were reported between 2000 and 2018. Results: Twenty-four cases (10 males, 14 females) published about breast cancer in children and adolescents were reached. Pathologies of the patients with a mean age of 12.19±4.13 have been reported as secretory carcinoma (70.8%), infiltrative secretory carcinoma (8.3%), malignant phyllodes tumor (8.3%), pleomorphic carcinoma (4.2%), invasive ductal carcinoma (4.2%), secretory adenocarcinoma (4.2%). Modified radical mastectomy was performed in 26.31% of patients with secretory carcinoma, mastectomy in 52.63%, breast-conserving surgery in 10.53%, and wide local excision in 10.53%. While 33.3% of the patients received adjuvant chemotherapy, 29.2% were given radiotherapy. Two patients had recurrence after surgery (3-17 months; median: 10 months). Three patients died due to postoperative metastases. Conclusion: Breast malignancies are relatively rare in the pediatric and adolescent period. However, mortality rates are quite significant contrary to what’s believed. In these patients, difficulties in diagnosing the disease may affect the treatment process negatively. While there isn’t a consensus about the treatment of the disease, the authors reported a wide range of treatments with different combinations of radiotherapy, chemotherapy, breast-conserving surgery, modified radical mastectomy and radical mastectomy.
目的:乳腺癌是一个全球性的公共卫生问题,随着发病率和死亡率的逐渐上升,它引起了人们的关注。与成人不同,儿童和青少年很少患乳腺癌。由于危险因素没有很好地定义,癌症的发现与其他疾病的发现是混合的,随访/治疗过程也不同。因此,儿童/青少年乳腺癌被忽视了。据指出,儿童和青少年乳腺癌的预后并不好,尽管在少数患者中发现,但死亡率很高,严重影响患者及其家人的生活。本汇编的主要目的是检查关于儿童和青少年乳腺癌和治疗过程的文献。其次要目的是提高卫生专业人员和社会的认识,并帮助建立儿科外科医生和护士在这方面的指导方针。方法:我们确定了24例病例报告,其中包括2000年至2018年报告的24例儿童或青少年乳腺癌的数据。结果:共收集到24例儿童及青少年乳腺癌病例,其中男10例,女14例。患者的平均年龄为12.19±4.13岁,病理表现为分泌性癌(70.8%)、浸润性分泌性癌(8.3%)、恶性叶状瘤(8.3%)、多形性癌(4.2%)、浸润性导管癌(4.2%)、分泌性腺癌(4.2%)。分泌性癌患者行改良根治术占26.31%,乳房切除术占52.63%,保乳手术占10.53%,广泛局部切除占10.53%。33.3%的患者接受了辅助化疗,29.2%的患者接受了放疗。术后复发2例(3 ~ 17个月);中位数:10个月)。3例患者因术后转移而死亡。结论:乳腺恶性肿瘤在儿童和青少年时期相对少见。然而,死亡率与人们所认为的相反。在这些患者中,诊断疾病的困难可能会对治疗过程产生负面影响。虽然对该疾病的治疗方法尚无共识,但作者报告了多种治疗方法,包括放疗、化疗、保乳手术、改良乳房根治术和乳房根治术的不同组合。
{"title":"Childhood And Adolescent Period Breast Cancer","authors":"A. Gül, D. Aygin","doi":"10.5222/jtaps.2021.08216","DOIUrl":"https://doi.org/10.5222/jtaps.2021.08216","url":null,"abstract":"Objective: Breast cancer is a global public health problem which draws attention with the gradual increase in morbidity and mortality rates. Unlike adults, breast cancers in children and adolescents are rarely seen. Since the risk factors are not well defined, cancer findings are mixed with other disease findings and follow-up/treatment processes differ. As a result, childhood/adolescent breast cancers are ignored. It is stated that the prognosis of childhood and adolescent breast cancers is not good, although they are seen in a limited number of patients, the mortality rate is high and it significantly affects the life of the patient and his/her family. The main aim of this compilation is to examine the literature on the pediatric and adolescent breast cancers and the treatment process. Its secondary purpose is to increase the awareness of health professionals and the society and help to create a guideline in this regard to pediatric surgeons, and nurses. Methods: We identified 24 case reports comprising the data of 24 cases of childhood or adolescent breast cancers that were reported between 2000 and 2018. Results: Twenty-four cases (10 males, 14 females) published about breast cancer in children and adolescents were reached. Pathologies of the patients with a mean age of 12.19±4.13 have been reported as secretory carcinoma (70.8%), infiltrative secretory carcinoma (8.3%), malignant phyllodes tumor (8.3%), pleomorphic carcinoma (4.2%), invasive ductal carcinoma (4.2%), secretory adenocarcinoma (4.2%). Modified radical mastectomy was performed in 26.31% of patients with secretory carcinoma, mastectomy in 52.63%, breast-conserving surgery in 10.53%, and wide local excision in 10.53%. While 33.3% of the patients received adjuvant chemotherapy, 29.2% were given radiotherapy. Two patients had recurrence after surgery (3-17 months; median: 10 months). Three patients died due to postoperative metastases. Conclusion: Breast malignancies are relatively rare in the pediatric and adolescent period. However, mortality rates are quite significant contrary to what’s believed. In these patients, difficulties in diagnosing the disease may affect the treatment process negatively. While there isn’t a consensus about the treatment of the disease, the authors reported a wide range of treatments with different combinations of radiotherapy, chemotherapy, breast-conserving surgery, modified radical mastectomy and radical mastectomy.","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70851470","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
Orthopaedic Management of Bladder Exstrophy 膀胱外翻的骨科治疗
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.25986
R. Özer
Bladder exstrophy is an embryologic malformation that affects urogenital and skeletal systems. Non-operative treatment of this rare problem is impossible. Urogenital reconstructions can be facilitated by orthopedic procedures. These reconstructions can be performed in a single stage as a complete repair or multi-stage approaches. The goal of the treatment is closure of the bladder and abdominal wall for the achievement of continence, preservation of renal functions, and cosmetic and functional reconstruction of genital organs. Orthopedic procedures are performed to decrease the tension that complicates the bladder and abdominal wall closure by approximating the pubic rami to achieve a secure closure and a low recurrence rate. Surgical interventions consist of the approximation of the pubic rami with different materials such as suture materials and plaque or the application of different osteotomy types such as posterior iliac, anterior pelvic (pubic), diagonal iliac, horizontal iliac and posterior pelvic resection osteotomies. The age of the patient, the amount of pubic diastasis and history of previous operations that the patient has undergone should be considered during the operation planning. Pubic rami can be approximated without performing pelvic osteotomy in patients who are operated within the first 72 hours after birth. But, osteotomy is required in children older than 2 years of age with severe pubic diastasis, concomitant cloacal exstrophy and unsuccessful operation history. The surgical team should have enough knowledge and experience to perform different osteotomy types in case of need to combine anterior and posterior iliac osteotomies. With these multidisciplinary approaches, much more successful outcomes could be achieved.
膀胱外翻是一种影响泌尿生殖系统和骨骼系统的胚胎畸形。非手术治疗这种罕见的问题是不可能的。泌尿生殖器官的重建可以通过矫形手术进行。这些重建可以作为一个完整的修复或多阶段的方法在一个阶段进行。治疗的目的是闭合膀胱和腹壁,以达到尿失禁,保存肾功能,以及生殖器官的美容和功能重建。骨科手术是通过接近耻骨来减少张力,使膀胱和腹壁闭合变得复杂,从而实现安全闭合和低复发率。手术干预包括用不同的材料(如缝线材料和斑块)逼近耻骨支或应用不同的截骨类型,如髂后、骨盆前(耻骨)、髂斜、髂水平和骨盆后切除术。在手术计划时应考虑患者的年龄、耻骨离断的程度和既往手术史。在出生后72小时内手术的患者可以在不进行骨盆截骨术的情况下接近耻骨支。但是,对于2岁以上的儿童,伴有严重的耻骨移位,并伴有局部腔外翻,且手术史不成功,则需要行截骨术。当需要髂前后联合截骨时,手术团队应具备足够的知识和经验来实施不同的截骨方式。通过这些多学科方法,可以取得更成功的结果。
{"title":"Orthopaedic Management of Bladder Exstrophy","authors":"R. Özer","doi":"10.5222/jtaps.2021.25986","DOIUrl":"https://doi.org/10.5222/jtaps.2021.25986","url":null,"abstract":"Bladder exstrophy is an embryologic malformation that affects urogenital and skeletal systems. Non-operative treatment of this rare problem is impossible. Urogenital reconstructions can be facilitated by orthopedic procedures. These reconstructions can be performed in a single stage as a complete repair or multi-stage approaches. The goal of the treatment is closure of the bladder and abdominal wall for the achievement of continence, preservation of renal functions, and cosmetic and functional reconstruction of genital organs. Orthopedic procedures are performed to decrease the tension that complicates the bladder and abdominal wall closure by approximating the pubic rami to achieve a secure closure and a low recurrence rate. Surgical interventions consist of the approximation of the pubic rami with different materials such as suture materials and plaque or the application of different osteotomy types such as posterior iliac, anterior pelvic (pubic), diagonal iliac, horizontal iliac and posterior pelvic resection osteotomies. The age of the patient, the amount of pubic diastasis and history of previous operations that the patient has undergone should be considered during the operation planning. Pubic rami can be approximated without performing pelvic osteotomy in patients who are operated within the first 72 hours after birth. But, osteotomy is required in children older than 2 years of age with severe pubic diastasis, concomitant cloacal exstrophy and unsuccessful operation history. The surgical team should have enough knowledge and experience to perform different osteotomy types in case of need to combine anterior and posterior iliac osteotomies. With these multidisciplinary approaches, much more successful outcomes could be achieved.","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70851773","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
Effectiveness of Frenotomy in Ankyloglossia Treatment Between 0-1 Years Old 截骨术治疗0 ~ 1岁婴幼儿强直性咬合的疗效
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.37530
Fatih Akova
Objective: The aim of this study is to present the frenotomy technique in cases of ankyloglossia (tongue-tie), which is diagnosed and treated in the first year of life. Patients were operated by a single surgeon. Method: Cases of ankyloglossia operated at Biruni University Faculty of Medicine Hospital Pediatric Surgery Clinic Between 2016-2020 were evaluated retrospectively in terms of clinical complaints, age, type of ankyloglossia, surgical technique, indications and results of surgery. Results: Frenotomy was performed in 56 patients including 47 boys (84%) and 9 girls (16%), between the ages of 0-1. Average age of the patients was 93 days (1-360). Patients were divided into two groups as Group 1 (n: 40: 0-90 days old) and Group 2 (n: 16: 90-360 days old). Patients were admitted with complaints of having difficulty in sucking the mother’s breast, not being able to take their tongue out, feeding with a bottle, pain at the nipple and not being able to grasp the breast. No additional intervention was required for bleeding in Group 1, and in 12 (75%) patients in Group 2 bleeding control was achieved using bipolar cautery. During follow-up, significant improvement was obtained in all patients who had difficulty in sucking and gripping the nipple. Improvement was observed in 15 of 25 patients with nipple pain. Conclusion: Frenotomy is an easily applied surgical procedure with minimal complications. Additional application may be required for bleeding control in infants older than 3 months. It should be considered that the probability of recurrence may depend on the type, intervention used and thickness of the frenulum, and phrenotomy may not be sufficient. The improvement in breast feeding function of Frenotomy may provide a significant improvement in the complaints of nipple pain, and may contribute to the emotional attachment between the mother and her baby. Randomized controlled trials are required to determine the effects of phrenotomy.
目的:本研究的目的是介绍在一岁前诊断和治疗的强直性咬合(舌结)病例的截骨术。病人由一名外科医生进行手术。方法:回顾性分析2016-2020年在比鲁尼大学医学院附属附属医院小儿外科门诊接受手术的患者的临床主诉、年龄、类型、手术手法、适应证及手术效果。结果:56例患者行截骨术,其中男孩47例(84%),女孩9例(16%),年龄0 ~ 1岁。患者平均年龄93天(1 ~ 360)。患者分为两组:1组(n: 40: 0 ~ 90 d)和2组(n: 16: 90 ~ 360 d)。入院的病人抱怨吮吸母亲的乳房有困难,不能把舌头伸出来,用奶瓶喂养,乳头疼痛,不能抓住乳房。第1组的出血不需要额外的干预,第2组的12例(75%)患者通过双极烧灼实现了出血控制。在随访中,所有有吮吸和抓握乳头困难的患者均有显著改善。25例乳头疼痛患者中有15例得到改善。结论:截骨术是一种简单易行、并发症少的手术方法。3个月以上的婴儿出血控制可能需要额外的应用。应考虑到复发的可能性可能取决于类型,使用的干预措施和系带的厚度,而颅静脉切开术可能是不够的。乳房切开术对母乳喂养功能的改善可能会显著改善乳头疼痛的抱怨,并可能有助于母亲与婴儿之间的情感依恋。需要随机对照试验来确定颅静脉切开术的效果。
{"title":"Effectiveness of Frenotomy in Ankyloglossia Treatment Between 0-1 Years Old","authors":"Fatih Akova","doi":"10.5222/jtaps.2021.37530","DOIUrl":"https://doi.org/10.5222/jtaps.2021.37530","url":null,"abstract":"Objective: The aim of this study is to present the frenotomy technique in cases of ankyloglossia (tongue-tie), which is diagnosed and treated in the first year of life. Patients were operated by a single surgeon. Method: Cases of ankyloglossia operated at Biruni University Faculty of Medicine Hospital Pediatric Surgery Clinic Between 2016-2020 were evaluated retrospectively in terms of clinical complaints, age, type of ankyloglossia, surgical technique, indications and results of surgery. Results: Frenotomy was performed in 56 patients including 47 boys (84%) and 9 girls (16%), between the ages of 0-1. Average age of the patients was 93 days (1-360). Patients were divided into two groups as Group 1 (n: 40: 0-90 days old) and Group 2 (n: 16: 90-360 days old). Patients were admitted with complaints of having difficulty in sucking the mother’s breast, not being able to take their tongue out, feeding with a bottle, pain at the nipple and not being able to grasp the breast. No additional intervention was required for bleeding in Group 1, and in 12 (75%) patients in Group 2 bleeding control was achieved using bipolar cautery. During follow-up, significant improvement was obtained in all patients who had difficulty in sucking and gripping the nipple. Improvement was observed in 15 of 25 patients with nipple pain. Conclusion: Frenotomy is an easily applied surgical procedure with minimal complications. Additional application may be required for bleeding control in infants older than 3 months. It should be considered that the probability of recurrence may depend on the type, intervention used and thickness of the frenulum, and phrenotomy may not be sufficient. The improvement in breast feeding function of Frenotomy may provide a significant improvement in the complaints of nipple pain, and may contribute to the emotional attachment between the mother and her baby. Randomized controlled trials are required to determine the effects of phrenotomy.","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70851486","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
Hydrosalpinx in adolescent girls: What did two cases teach? 青春期女孩输卵管积水:两个病例告诉我们什么?
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.49091
A. Şahin
Hydrosalphinx is the fallopian tubes getting filled with fluid due to their blockage. It usually occurs with obstruction of fallopian tubes after infection in women of sexually active age. The aim of this article is to draw attention to hydrosalpinx in adolescent girls because of two adolescent cases. First case; a cystic lesion of 38x51x76 mm in the right adnexal region was detected in the lower abdominal magnetic resonance imaging of a 13-year-old girl who presented with the complaint of abdominal pain and vomiting. Right tubal torsion and hydrosalpinx were detected during abdominal exploration. The tube was detorsioned and marsupialization was applied to the hydrosalpinx. Second case; a cystic lesion with dimensions of 24x12x35 cm was detected in the abdominal ultrasonography of a 16-year-old girl who presented with the complaint of abdominal pain and a palpable mass. On abdominal exploration, a right hydrosalpinx filling the entire abdomen was detected. Tubal excision was performed. Both cases have not been undergone any intraabdominal surgery previously. Hydrosalpinx is very rare in adolescent girls. Hydrosalpinx also should be considered in lower abdominal pain. Cases should be examined in terms of preventing infertility problems in future carefully, development of adhesion should be curtailed and parents should be informed in detail.
输卵管积水是指输卵管因堵塞而充满液体。它通常发生在性活跃年龄的妇女感染后输卵管梗阻。这篇文章的目的是提请注意输卵管积水在青春期的女孩,因为两个青春期的情况下。第一个案例;13岁女孩,以腹痛和呕吐为主诉,下腹磁共振成像发现右附件区一38x51x76 mm囊性病变。腹部探查时发现右侧输卵管扭转及输卵管积水。对输卵管进行变形和有袋化处理。第二个案例;16岁女孩腹部超声检查发现一囊性病变,尺寸为24x12x35 cm,主诉为腹痛和可触及的肿块。腹部探查发现右侧输卵管积水充满整个腹部。行输卵管切除术。这两个病例以前都没有做过任何腹内手术。输卵管积水在青春期女孩中非常罕见。下腹疼痛时也应考虑输卵管积水。应仔细检查病例,以防止将来出现不孕问题,应减少粘连的发展,并应详细告知父母。
{"title":"Hydrosalpinx in adolescent girls: What did two cases teach?","authors":"A. Şahin","doi":"10.5222/jtaps.2021.49091","DOIUrl":"https://doi.org/10.5222/jtaps.2021.49091","url":null,"abstract":"Hydrosalphinx is the fallopian tubes getting filled with fluid due to their blockage. It usually occurs with obstruction of fallopian tubes after infection in women of sexually active age. The aim of this article is to draw attention to hydrosalpinx in adolescent girls because of two adolescent cases. First case; a cystic lesion of 38x51x76 mm in the right adnexal region was detected in the lower abdominal magnetic resonance imaging of a 13-year-old girl who presented with the complaint of abdominal pain and vomiting. Right tubal torsion and hydrosalpinx were detected during abdominal exploration. The tube was detorsioned and marsupialization was applied to the hydrosalpinx. Second case; a cystic lesion with dimensions of 24x12x35 cm was detected in the abdominal ultrasonography of a 16-year-old girl who presented with the complaint of abdominal pain and a palpable mass. On abdominal exploration, a right hydrosalpinx filling the entire abdomen was detected. Tubal excision was performed. Both cases have not been undergone any intraabdominal surgery previously. Hydrosalpinx is very rare in adolescent girls. Hydrosalpinx also should be considered in lower abdominal pain. Cases should be examined in terms of preventing infertility problems in future carefully, development of adhesion should be curtailed and parents should be informed in detail.","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70851726","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
Retrospective Evaluation of Ultrasound Guided 525 Permanent Tunneled Catheter Placement Procedure in Pediatric Hematology and Oncology Patients 超声引导下525永久隧道置管在儿科血液学和肿瘤学患者中的回顾性评价
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.5222/jtaps.2021.16023
M. Okumuş, U. Alkara, H. Sarbay, A. Atay, B. Malbora
{"title":"Retrospective Evaluation of Ultrasound Guided 525 Permanent Tunneled Catheter Placement Procedure in Pediatric Hematology and Oncology Patients","authors":"M. Okumuş, U. Alkara, H. Sarbay, A. Atay, B. Malbora","doi":"10.5222/jtaps.2021.16023","DOIUrl":"https://doi.org/10.5222/jtaps.2021.16023","url":null,"abstract":"","PeriodicalId":35435,"journal":{"name":"Cocuk Cerrahisi Dergisi","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70851756","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
期刊
Cocuk Cerrahisi Dergisi
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1