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Thoracoschisis associated with Limb Body Wall Complex. 胸裂与肢体体壁复合体有关。
APSP journal of case reports Pub Date : 2017-05-01 DOI: 10.21699/ajcr.v8i3.568
Dragana Vujovic, Aleksandar Sretenovic, Maja Raicevic, MarijaLukac MarijaLukac, Tamara Krstajic, Vesna Ljubic, Sanja Sindjic Antunovic
{"title":"Thoracoschisis associated with Limb Body Wall Complex.","authors":"Dragana Vujovic,&nbsp;Aleksandar Sretenovic,&nbsp;Maja Raicevic,&nbsp;MarijaLukac MarijaLukac,&nbsp;Tamara Krstajic,&nbsp;Vesna Ljubic,&nbsp;Sanja Sindjic Antunovic","doi":"10.21699/ajcr.v8i3.568","DOIUrl":"https://doi.org/10.21699/ajcr.v8i3.568","url":null,"abstract":"<p><p>Thoracoschisis is a rare condition. A female newborn presented with right-sided thoracoschisis, associated with diaphragmatic hernia and protrusion of an accessory liver lobe through the chest wall defect along with deformity of the right forearm and hand duplication. Diagnosed as part of the limb-body wall complex (LBWC), management included resection of the exteriorized liver lobe followed by right hemidiaphragm and thoracic wall reconstruction.</p>","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 3","pages":"19"},"PeriodicalIF":0.0,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423888/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35024320","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
Bilateral Testicular Loss due to Dog Bite in a Child. 狗咬伤儿童双侧睾丸丢失。
APSP journal of case reports Pub Date : 2017-05-01 DOI: 10.21699/ajcr.v8i3.575
Taketoshi Nara, Eiji Hisamatsu, Akiko Haruna, Yoshifumi Sugita
{"title":"Bilateral Testicular Loss due to Dog Bite in a Child.","authors":"Taketoshi Nara,&nbsp;Eiji Hisamatsu,&nbsp;Akiko Haruna,&nbsp;Yoshifumi Sugita","doi":"10.21699/ajcr.v8i3.575","DOIUrl":"https://doi.org/10.21699/ajcr.v8i3.575","url":null,"abstract":"<p><p>Although animal bites are common, genital trauma caused by animal bites is rare. Here we report a case of bilateral testicular loss in an infant due to a dog bite. The patient was bitten by a friend's dog while his mother was intoxicated and, therefore, did not receive immediate medical attention. Although initial treatment with subsequent genital reconstruction and hormone replacement is important for children with genital trauma, it is too important to make home safe for them.</p>","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 3","pages":"20"},"PeriodicalIF":0.0,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423889/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35023752","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
Multiple Foreign bodies entrapped at Duodenal Web. 十二指肠网内有多处异物。
APSP journal of case reports Pub Date : 2017-05-01 DOI: 10.21699/ajcr.v8i3.578
Aditya Pratap Singh, Ramesh Tanger, Dinesh Kumar Barolia, Arun Kumar Gupta, Sunil Kumar Mehra
{"title":"Multiple Foreign bodies entrapped at Duodenal Web.","authors":"Aditya Pratap Singh,&nbsp;Ramesh Tanger,&nbsp;Dinesh Kumar Barolia,&nbsp;Arun Kumar Gupta,&nbsp;Sunil Kumar Mehra","doi":"10.21699/ajcr.v8i3.578","DOIUrl":"https://doi.org/10.21699/ajcr.v8i3.578","url":null,"abstract":"An 18-month-old male infant presented with intermittent non-bilious vomiting with pain abdomen for last six months. There was history of localized abdominal distension which gets relieved partially, with vomiting. Patient was born at full term and had no previous medical or surgical history. On examination, patient’s weight was 8.8 kg. Biochemical profile was normal. X-ray abdomen revealed gastric distension with paucity of gas in rest of abdomen. In upper GI study, stomach and duodenum were distended with narrowing of the 2rd part of the duodenum with passage of the contrast distally, suggestive of the perforated duodenal web (Fig.1). At laparotomy, duodenotomy revealed a web with a pin point hole in the center. Multiple FBs were present in the duodenum. The web was excised and the foreign bodies were retrieved (Fig.2). The foreign bodies were mostly buttons, seeds and diamonds. Postoperative period was uneventful.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 3","pages":"22"},"PeriodicalIF":0.0,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423891/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35023753","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
Intrauterine Intussusception Leading to Ileal Atresia in a Premature Baby. 宫内肠套叠导致早产儿回肠闭锁。
APSP journal of case reports Pub Date : 2017-03-18 eCollection Date: 2017-03-01 DOI: 10.21699/ajcr.v8i2.567
Sirajuddin Soomro, Sikandar Ali Mughal, Fida Hussain Depar
{"title":"Intrauterine Intussusception Leading to Ileal Atresia in a Premature Baby.","authors":"Sirajuddin Soomro,&nbsp;Sikandar Ali Mughal,&nbsp;Fida Hussain Depar","doi":"10.21699/ajcr.v8i2.567","DOIUrl":"https://doi.org/10.21699/ajcr.v8i2.567","url":null,"abstract":"Intussusception is relatively common in infants but occurs only 0.3% of cases during the first month of life.[1] Majority of neonatal intussusceptions occur in full term babies and it is rare in the premature newborns. Poynter suggested intrauterine intussusception as a cause of intestinal atresia in 1922. Less than 100 cases of intrauterine intussusception in association with ileal atresia have been reported in the literature.[2,3] We are adding another case with similar anomaly.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 2","pages":"15"},"PeriodicalIF":0.0,"publicationDate":"2017-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371688/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34905966","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
Lumbo-Costo-Vertebral Syndrome: An Iceberg with Tip of Hernia and Body of Spinal and Neurological Malformations. 腰肋椎综合征:以疝为尖，脊柱和神经系统畸形为体的冰山。
APSP journal of case reports Pub Date : 2017-03-18 eCollection Date: 2017-03-01 DOI: 10.21699/ajcr.v8i2.573
Xenophon Sinopidis, Georgia Antoniou, Vasileios Alexopoulos, Antonios Panagidis, George Georgiou
{"title":"Lumbo-Costo-Vertebral Syndrome: An Iceberg with Tip of Hernia and Body of Spinal and Neurological Malformations.","authors":"Xenophon Sinopidis,&nbsp;Georgia Antoniou,&nbsp;Vasileios Alexopoulos,&nbsp;Antonios Panagidis,&nbsp;George Georgiou","doi":"10.21699/ajcr.v8i2.573","DOIUrl":"https://doi.org/10.21699/ajcr.v8i2.573","url":null,"abstract":"We read with great interest the contribution of Gupta et al on the lumbo-costo-vertebral syndrome (LCVS).[1] We encountered this rare anomaly in a 39 week-of-gestation female patient, who after an uncomplicated birth underwent investigation because of a left lumbar hernia, and vertebral anomalies. Imaging assay with plain radiography, revealed the presence of tenth and eleventh thoracic hemivertebrae, and intervertebral cleft of the twelfth thoracic vertebra. These anomalies resulted in clockwise thoracic and counterclockwise lumbar scoliosis. Magnetic resonance imaging revealed syringomyelia at the level of the three lower thoracic dysplastic vertebrae, and low termination of the spinal cord at the level of the fourth lumbar vertebra.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 2","pages":"16"},"PeriodicalIF":0.0,"publicationDate":"2017-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371689/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34905967","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
Anomalous Origin of the Left Pulmonary Artery: Hemi-Truncus Arteriosus. 左肺动脉异常起源:半动脉干。
APSP journal of case reports Pub Date : 2017-03-18 eCollection Date: 2017-03-01 DOI: 10.21699/ajcr.v8i2.556
Ali Shabbir Hussain, Mariam Shakir, Shabina Ariff, Rehan Ali, Babar Hassan
{"title":"Anomalous Origin of the Left Pulmonary Artery: Hemi-Truncus Arteriosus.","authors":"Ali Shabbir Hussain,&nbsp;Mariam Shakir,&nbsp;Shabina Ariff,&nbsp;Rehan Ali,&nbsp;Babar Hassan","doi":"10.21699/ajcr.v8i2.556","DOIUrl":"https://doi.org/10.21699/ajcr.v8i2.556","url":null,"abstract":"<p><p>Hemi-truncus arteriosus is a rare congenital cardiovascular malformation. It usually presents in infancy and leads to development of progressive pulmonary vascular disease, heart failure, and death. We report a case of hemi truncus arteriosus in a 12-day-old neonate who was successfully managed at our institute.</p>","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 2","pages":"9"},"PeriodicalIF":0.0,"publicationDate":"2017-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371690/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34906542","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
Ileal Trichobezoar Presenting as Intestinal Obstruction and Peritonitis. 表现为肠梗阻和腹膜炎。
APSP journal of case reports Pub Date : 2017-03-18 eCollection Date: 2017-03-01 DOI: 10.21699/ajcr.v8i2.549
Kamal Nain Rattan, Vikas Yadav, Varun Yadav, Jasbir Singh
{"title":"Ileal Trichobezoar Presenting as Intestinal Obstruction and Peritonitis.","authors":"Kamal Nain Rattan,&nbsp;Vikas Yadav,&nbsp;Varun Yadav,&nbsp;Jasbir Singh","doi":"10.21699/ajcr.v8i2.549","DOIUrl":"https://doi.org/10.21699/ajcr.v8i2.549","url":null,"abstract":"<p><p>Trichobezoar is less common in boys. We are reporting a case of isolated ileal trichobezoars in a 4-year old boy causing intestinal obstruction and gut ischemia with perforation and peritonitis. The case was managed surgically with ileal resection and anastomosis. Postoperative period was uneventful.</p>","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 2","pages":"11"},"PeriodicalIF":0.0,"publicationDate":"2017-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371684/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34906543","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
Two Cases of Massively Prolapsed Patent Vitellointestinal Duct. 卵黄肠管未闭大量脱垂2例。
APSP journal of case reports Pub Date : 2017-03-18 eCollection Date: 2017-03-01 DOI: 10.21699/ajcr.v8i2.534
Sudhir Singh, Digamber Chaubey, J D Rawat, Gurmeet Singh
{"title":"Two Cases of Massively Prolapsed Patent Vitellointestinal Duct.","authors":"Sudhir Singh,&nbsp;Digamber Chaubey,&nbsp;J D Rawat,&nbsp;Gurmeet Singh","doi":"10.21699/ajcr.v8i2.534","DOIUrl":"https://doi.org/10.21699/ajcr.v8i2.534","url":null,"abstract":"<p><p>Patent vitellointestinal duct (PVID) is a benign congrnital anomaly ususally presenting with fecal discharge from the umbilicus. In this report, we describe two cases of PVID presented with massive bowel prolapse through the PVID and signs of intestinal obstruction. Surgery revealed prolapse of the ileal intussusceptum through the PVID. Both of the babies were sucssesfully managed with surgery.</p>","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 2","pages":"12"},"PeriodicalIF":0.0,"publicationDate":"2017-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371685/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34906544","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
Female Epispadias Presenting as Urinary Incontinence. 女性上尿失禁。
APSP journal of case reports Pub Date : 2017-03-18 eCollection Date: 2017-03-01 DOI: 10.21699/ajcr.v8i2.548
Asmir Jonuzi, Nusret Popovic, Zlatan Zvizdic, Emir Milišic, Kenan Karavdic, Dewan Paddy
{"title":"Female Epispadias Presenting as Urinary Incontinence.","authors":"Asmir Jonuzi,&nbsp;Nusret Popovic,&nbsp;Zlatan Zvizdic,&nbsp;Emir Milišic,&nbsp;Kenan Karavdic,&nbsp;Dewan Paddy","doi":"10.21699/ajcr.v8i2.548","DOIUrl":"https://doi.org/10.21699/ajcr.v8i2.548","url":null,"abstract":"<p><p>Isolated female epispadias without bladder exstrophy is a rare congenital anomaly affecting 1 in 484,000 females. The presenting features of female epispadias are urinary incontinence and abnormal anatomical features. A 6-year-old girl presented with primary urinary incontinence who on physical examination had a bifid clitoris and labia minora. The vagina and hymen were normal. Voiding cystourethrogram showed no reflux and a funnel shaped proximal urethra. With the diagnosis of isolated female epispadias, one-stage reconstruction of the urethra, bladder neck, labia minora and clitoris was performed.</p>","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 2","pages":"10"},"PeriodicalIF":0.0,"publicationDate":"2017-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.21699/ajcr.v8i2.548","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34906547","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
Sewing Needle Penetration into Thorax: What Might be the Cause? 缝衣针穿胸:可能是什么原因?
APSP journal of case reports Pub Date : 2017-03-18 eCollection Date: 2017-03-01 DOI: 10.21699/ajcr.v8i2.560
J D Rawat, Sudhir Singh, Digamber Chaubey, Gurmeet Singh
{"title":"Sewing Needle Penetration into Thorax: What Might be the Cause?","authors":"J D Rawat,&nbsp;Sudhir Singh,&nbsp;Digamber Chaubey,&nbsp;Gurmeet Singh","doi":"10.21699/ajcr.v8i2.560","DOIUrl":"https://doi.org/10.21699/ajcr.v8i2.560","url":null,"abstract":"A 10-month-old male baby presented with irritability and inconsolable cry for last two weeks which increased on touching the chest. There was no history of fever, respiratory symptoms, or any accident. On examination, an indurated tender nodule over right lower chest was present. Chest x-rays showed a metallic foreign body at right lower chest extending from skin to pleural cavity (Fig.1A,1B). Foreign body was removed under anesthesia. It was a two inches long sewing needle. Child was discharged on day three of hospitalization after information to authority for further action.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 2","pages":"13"},"PeriodicalIF":0.0,"publicationDate":"2017-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371686/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34906545","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
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