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APSP journal of case reports最新文献

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What I Would Like to be Remembered for! 我想被人记住的是什么！
APSP journal of case reports Pub Date : 2018-10-14 DOI: 10.21699/AJCR.V9I3.55
C. A. Safdar
{"title":"What I Would Like to be Remembered for!","authors":"C. A. Safdar","doi":"10.21699/AJCR.V9I3.55","DOIUrl":"https://doi.org/10.21699/AJCR.V9I3.55","url":null,"abstract":"Please see fulltext","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42646993","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
Multiple Jejunoileal Atresia and Stenosis with Duplication Cyst in a Newborn 新生儿多发空肠回肠闭锁狭窄伴重复囊肿1例
APSP journal of case reports Pub Date : 2018-09-26 DOI: 10.21699/ajcr.v9i3.13
A. Singh, Rajlaxmi Pardeshi, Ramesh Tanger, Maryem Ansari, Arun Gupta
{"title":"Multiple Jejunoileal Atresia and Stenosis with Duplication Cyst in a Newborn","authors":"A. Singh, Rajlaxmi Pardeshi, Ramesh Tanger, Maryem Ansari, Arun Gupta","doi":"10.21699/ajcr.v9i3.13","DOIUrl":"https://doi.org/10.21699/ajcr.v9i3.13","url":null,"abstract":"Jejunoileal atresia is a congenital anomaly that is characterized clinically by bilious vomiting and abdominal dis-tension. It has been associated with various other anomalies but its association with mesenteric cyst is rare. We are presenting a patient with antenatally diagnosed duplication cyst with multiple jejunoileal atresia and stenosis with possible etiology behind such an association.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47277847","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
Anorectal Laceration due to Crush Injury: A Case of Rarity 因挤压伤致肛门直肠撕裂:一例罕见病例
APSP journal of case reports Pub Date : 2018-09-26 DOI: 10.21699/ajcr.v9i3.25
S. Sancar, E. Ozcakir, M. Kaya
{"title":"Anorectal Laceration due to Crush Injury: A Case of Rarity","authors":"S. Sancar, E. Ozcakir, M. Kaya","doi":"10.21699/ajcr.v9i3.25","DOIUrl":"https://doi.org/10.21699/ajcr.v9i3.25","url":null,"abstract":"Please see fulltext","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44297429","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 Umbilical Appendix Misdiagnosed as Umbilical Granuloma: Report of 2 Cases 先天性脐尾误诊为脐肉芽肿2例报告
APSP journal of case reports Pub Date : 2018-09-25 DOI: 10.21699/AJCR.V9I3.45
J. Ghoroubi, L. Mohajerzadeh, Saran Lotfollahzadeh, Khashayar Atqiaee
{"title":"Congenital Umbilical Appendix Misdiagnosed as Umbilical Granuloma: Report of 2 Cases","authors":"J. Ghoroubi, L. Mohajerzadeh, Saran Lotfollahzadeh, Khashayar Atqiaee","doi":"10.21699/AJCR.V9I3.45","DOIUrl":"https://doi.org/10.21699/AJCR.V9I3.45","url":null,"abstract":"Background: Umbilical cord hernia is an uncommon umbilical anomaly which develops during 10th to 12th weeks of gestational age owing to failure of complete bowel return into coelomic cavity. In extremely rare cases appendix is the only trapped organ in hernia sac which may erode the overlying membrane and simulate umbili-cal granuloma. \u0000Case Report: Two infants presented with delayed umbilical cord separation with a reddish mass at umbilicus which was initially diagnosed as umbilical granuloma. Surgical exploration on failure of conservative measures revealed it as vermiform appendix. Appendectomy was done in both cases. \u0000Conclusion: Vermiform appendix at umbilicus is a rare congenital anomaly and may simulate other pathologies at umbilicus.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42245954","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
Intramural Duodenal Hematoma In 2-year Old Child 2岁儿童十二指肠壁内血肿
APSP journal of case reports Pub Date : 2018-09-23 DOI: 10.21699/AJCR.V9I3.42
D. Hota, K. Rattan, A. Khursheed, M. Swami, H. Bhardwaj
{"title":"Intramural Duodenal Hematoma In 2-year Old Child","authors":"D. Hota, K. Rattan, A. Khursheed, M. Swami, H. Bhardwaj","doi":"10.21699/AJCR.V9I3.42","DOIUrl":"https://doi.org/10.21699/AJCR.V9I3.42","url":null,"abstract":"Background: Intramural hematoma of the duodenum is a rare cause of acquired duodenal obstruction. It is often a diagnostic dilemma and a high degree of suspicion is required to make an early and accurate diagnosis in children. \u0000Case Report: A 2-year-old child presented with bilious vomiting and abdominal distension. X-ray abdomen showed high intestinal obstruction. Ultrasound and CT scan abdomen gave suspicion of pancreatic pseudo-cyst near head of pancreas. At surgery, an intramural hematoma of the duodenum was found and drained. \u0000Conclusion: Intramural duodenal hematoma is a rare entity especially in children and should be considered in differential diagnosis of acquired duodenal obstruction.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42326308","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
Antenatally Diagnosed Suprarenal Mature Cystic Teratoma with Down Syndrome 产前诊断为唐氏综合征的鞍上成熟囊性畸胎瘤
APSP journal of case reports Pub Date : 2018-09-23 DOI: 10.21699/AJCR.V9I3.44
A. Singh, Ramesh Tanger, Maryem Ansari, Arun Gupta, D. Barolia
{"title":"Antenatally Diagnosed Suprarenal Mature Cystic Teratoma with Down Syndrome","authors":"A. Singh, Ramesh Tanger, Maryem Ansari, Arun Gupta, D. Barolia","doi":"10.21699/AJCR.V9I3.44","DOIUrl":"https://doi.org/10.21699/AJCR.V9I3.44","url":null,"abstract":"Background: Teratoma is a germ cell tumor (GCT) arising from totipotent stem cells that differentiate into the tissues that are foreign to the anatomic site. Teratoma at the suprarenal location is extremely rare. The associa-tion with the Down syndrome also makes it unusual. \u0000Case Report: We are presenting here a case of one-year-old female infant with Down syndrome who had an antenatal diagnosis of right suprarenal mass. Laparotomy revealed a large cystic mass in the right suprarenal location which was completely excised. Right adrenal gland could not be seen separately from the mass. The histological diagnosis was a mature cystic teratoma. \u0000Conclusion: Adrenal teratoma is rare and may be considered in the differential diagnosis of antenatally diag-nosed suprarenal lesion. Its association with Down syndrome is rare finding.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43429043","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
Post Necrotizing Enterocolitis Colonic Strictures: Report of 5 Cases 坏死性小肠结肠炎结肠狭窄5例报告
APSP journal of case reports Pub Date : 2018-09-20 DOI: 10.21699/AJCR.V9I3.17
Sandip K. Rahul, Vijayendra Kumar, V. Thakur, Ramdhani Yadav, Zaheer Hasan, Pankaj Kumar, Digamber Chaubey
{"title":"Post Necrotizing Enterocolitis Colonic Strictures: Report of 5 Cases","authors":"Sandip K. Rahul, Vijayendra Kumar, V. Thakur, Ramdhani Yadav, Zaheer Hasan, Pankaj Kumar, Digamber Chaubey","doi":"10.21699/AJCR.V9I3.17","DOIUrl":"https://doi.org/10.21699/AJCR.V9I3.17","url":null,"abstract":"Background: With increasing survival of patients suffering from necrotizing enterocolitis (NEC) colonic strictures, as its late sequelae, is increasingly being seen and most of these patients present with chronic constipation. \u0000Case Series: Five patients of acquired colonic stricture presenting with abdominal distension and constipation are being reported here. All five patients varied in clinical features, age at presentation and surgical manage-ment. Three of them had abdominal distension and constipation with poor nutritional status. Primary resection with anastomosis could be done in only one while stoma was made initially in other patients. One patient pre-sented with sealed perforation and fistula between jejunum and colon. All, except one patient, had stricture at splenic flexure. Histopathology of colon reported normal ganglion cells in all patients. \u0000Conclusion: All survivors of necrotizing enterocolitis, should be followed for the development of colonic stricture; It should be kept as important differential diagnoses of chronic constipation in children.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44988854","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
Acute Presentation of Eventration of Diaphragm with Gastrothorax in an Infant 婴儿膈肌膨出伴胃胸的急性表现
APSP journal of case reports Pub Date : 2018-09-20 DOI: 10.21699/AJCR.V9I3.18
F. Basheer, Q. Khan, J. Jalil, C. A. Safdar
{"title":"Acute Presentation of Eventration of Diaphragm with Gastrothorax in an Infant","authors":"F. Basheer, Q. Khan, J. Jalil, C. A. Safdar","doi":"10.21699/AJCR.V9I3.18","DOIUrl":"https://doi.org/10.21699/AJCR.V9I3.18","url":null,"abstract":"Please see fulltext","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43879823","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
Single System Ectopic Congenital Giant Megaureter Associated with Ipsilateral Multicystic Dysplastic Kidney 单系统异位先天性巨肾伴同侧多囊性发育不良肾
APSP journal of case reports Pub Date : 2018-06-19 DOI: 10.21699/AJCR.V9I2.699
S. Mahalik, B. Tripathy, A. Pati, M. Mohanty
{"title":"Single System Ectopic Congenital Giant Megaureter Associated with Ipsilateral Multicystic Dysplastic Kidney","authors":"S. Mahalik, B. Tripathy, A. Pati, M. Mohanty","doi":"10.21699/AJCR.V9I2.699","DOIUrl":"https://doi.org/10.21699/AJCR.V9I2.699","url":null,"abstract":"Congenital anomalies of the kidney and urinary tract (CAKUT) is a disease spectrum of a wide range of structural and functional anomalies. In this report, we have presented a rare case of CAKUT displaying the wide spectrum of renal and urinary tract anomalies with an unusual association like single system ectopic giant megaureter with the ipsilateral multicystic dysplastic kidney.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45037464","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
Multiple Congenital Granular Cell Tumor in a Neonate - A Rare Case 新生儿多发先天性颗粒细胞瘤1例
APSP journal of case reports Pub Date : 2018-06-18 DOI: 10.21699/ajcr.v9i2.719
A. Singh, Arun Gupta, Maryem Ansari, Ramesh Tanger, D. Barolia
{"title":"Multiple Congenital Granular Cell Tumor in a Neonate - A Rare Case","authors":"A. Singh, Arun Gupta, Maryem Ansari, Ramesh Tanger, D. Barolia","doi":"10.21699/ajcr.v9i2.719","DOIUrl":"https://doi.org/10.21699/ajcr.v9i2.719","url":null,"abstract":"Congenital granular cell tumor (CGCT) is an uncommon congenital benign epulis in neonates. A preliminary diagnosis is usually put forth clinically but may be confused with other anomalies. Herein, we report an unusual case of intra oral congenital granular cell tumor in a 4-day-old female newborn. The tumor was excised completely. At 3-month follow-up, the baby is doing fine without any recurrence.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42147808","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
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