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Stromme Syndrome: New Clinical Features. Stromme综合征:新的临床特征
APSP journal of case reports Pub Date : 2017-03-18 eCollection Date: 2017-03-01 DOI: 10.21699/ajcr.v8i2.564
Bayram Ali Dorum, Irmak Tanal Sambel, Hilal Ozkan, Irfan Kiristioglu, Nilgun Koksal
{"title":"Stromme Syndrome: New Clinical Features.","authors":"Bayram Ali Dorum,&nbsp;Irmak Tanal Sambel,&nbsp;Hilal Ozkan,&nbsp;Irfan Kiristioglu,&nbsp;Nilgun Koksal","doi":"10.21699/ajcr.v8i2.564","DOIUrl":"https://doi.org/10.21699/ajcr.v8i2.564","url":null,"abstract":"A baby girl was born, on the 35th week of gestation via cesarean section, to an 18-year old mother. Apgar score at the 1st and 5th minute was 8 and 9, respectively. Antenatal scan at 20th gestational week found microcephaly, edema in both lower extremities and the dilation of the proximal intestinal loops. No pathology was found on FISH examination in relation to chromosome 13, 18, 21, X and Y during amniocentesis. At birth baby had weight of 1890 gram (10-50 percentile), the height of 40cm (<10 percentile) and head circumference of 26cm (<10 percentile). Examination of the head revealed microcephaly, micrognathia and a high-bridged nose (Fig. 1). Edema was seen in both lower extremities (Fig. 1). CBC showed thrombocytopenia (86.000/mm3). Liver and kidney function tests, and albumin level were in normal range. Serologic tests for TORCH and Parvovirus were negative. Abdominal ultrasonography (USG) showed bilateral renal hypodysplasia. Ventricular septal defect was found on Echocardiography. Ophthalmologic examination showed microphthalmia, microcornea, and sclerocornea.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"8 2","pages":"14"},"PeriodicalIF":0.0,"publicationDate":"2017-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371687/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34906548","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
Giant Omphalocele Complicated by Postoperative Duodenal Obstruction. 巨大脐膨出并发术后十二指肠梗阻
APSP journal of case reports Pub Date : 2017-01-05 eCollection Date: 2017-01-01 DOI: 10.21699/ajcr.v8i1.518
Sunita Ojha, Shobha Parashar, Dharmil Doshi, Rajiv Kumar Bansal
{"title":"Giant Omphalocele Complicated by Postoperative Duodenal Obstruction.","authors":"Sunita Ojha, Shobha Parashar, Dharmil Doshi, Rajiv Kumar Bansal","doi":"10.21699/ajcr.v8i1.518","DOIUrl":"10.21699/ajcr.v8i1.518","url":null,"abstract":"<p><p>Omphalocele is a congenital defect in the abdominal wall, usually treated at birth or within 1-2 years of life depending on condition of patient and size and contents of the defect. We repaired a giant omphalocele without mesh in a 9-year-old girl. She developed duodenal obstruction in the postoperative period requiring another laparotomy and duodeno-jejunostomy to bypass obstruction.</p>","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":"5"},"PeriodicalIF":0.0,"publicationDate":"2017-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.21699/ajcr.v8i1.518","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43719840","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
Food Allergy: A Rare Cause of Recurrent Intussusception 食物过敏：复发性肠套叠的罕见原因
APSP journal of case reports Pub Date : 2017-01-04 DOI: 10.21699/ajcr.v8i1.513
E. Aydın, Ö. F. Beşer
{"title":"Food Allergy: A Rare Cause of Recurrent Intussusception","authors":"E. Aydın, Ö. F. Beşer","doi":"10.21699/ajcr.v8i1.513","DOIUrl":"https://doi.org/10.21699/ajcr.v8i1.513","url":null,"abstract":"Recurrent intussusception is a management dilemma and have many causes. We report a 22-month old boy who presented multiple times for recurrent intussusception. At diagnostic work-up he was found to be suffering from non-IgE food allergy. The child did not develop further episodes of intussusception after removal of allergenic diet.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"11 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41292833","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: 5
Ingested Metallic Spool: A Rare Cause of Acquired Tracheoesophageal Fistula 摄取金属线轴:获得性气管食管瘘的罕见原因
APSP journal of case reports Pub Date : 2017-01-04 DOI: 10.21699/ajcr.v8i1.531
Imran Hashim, N. Talat
{"title":"Ingested Metallic Spool: A Rare Cause of Acquired Tracheoesophageal Fistula","authors":"Imran Hashim, N. Talat","doi":"10.21699/ajcr.v8i1.531","DOIUrl":"https://doi.org/10.21699/ajcr.v8i1.531","url":null,"abstract":"Foreign body (FB) ingestion is a common problem in children. Prolonged impaction of FB in esophagus may result in tracheoesophageal fistula (TEF). A 6-year-old girl presented with progressive dysphagia and recurrent chest infections. No history of FB ingestion was given by parents. Further investigations revealed FB (spool) in cervical esophagus. Patient was successfully managed by surgery through trans-cervical approach.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43924670","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
Abdominal Mass Secondary to Human Toxocariasis 继发于人类弓形虫病的腹部肿块
APSP journal of case reports Pub Date : 2017-01-04 DOI: 10.21699/ajcr.v8i1.490
J. Ghoroobi, L. Mohajerzadeh, M. Khoddami, A. Mirshemirani, N. Sadeghian, A. Mahdavi, Sayeh Hatefi
{"title":"Abdominal Mass Secondary to Human Toxocariasis","authors":"J. Ghoroobi, L. Mohajerzadeh, M. Khoddami, A. Mirshemirani, N. Sadeghian, A. Mahdavi, Sayeh Hatefi","doi":"10.21699/ajcr.v8i1.490","DOIUrl":"https://doi.org/10.21699/ajcr.v8i1.490","url":null,"abstract":"Toxocariasis is an extensive helminthic infection that leads to visceral larva migrans in humans. A 2.5-year-old girl referred for abdominal mass. She had history of pharyngitis for two weeks. There were no other symptoms. Abdominal examination revealed an irregular solid mass in right lower quadrant (RLQ). Abdominal ultrasonography revealed an echohetrogenic large mass in RLQ, liver, and retroperitoneal area. Abdominal CT scan showed a huge mass. At laparotomy a large retroperitoneal mass that involved right liver lobe, bladder, ileocecal valve, small and large intestines was found. At histopathology diagnosis of toxocariasis was made.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43140246","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: 6
Spinal Dural Arteriovenous Fistula and Cecal Arteriovenous Malformation in a Boy 1例男孩硬脊膜动静脉瘘及盲肠动静脉畸形
APSP journal of case reports Pub Date : 2017-01-04 DOI: 10.21699/ajcr.v8i1.510
Vimlesh Soni, P. Vaidya, J. Sahu, M. Yadav, P. Singhi
{"title":"Spinal Dural Arteriovenous Fistula and Cecal Arteriovenous Malformation in a Boy","authors":"Vimlesh Soni, P. Vaidya, J. Sahu, M. Yadav, P. Singhi","doi":"10.21699/ajcr.v8i1.510","DOIUrl":"https://doi.org/10.21699/ajcr.v8i1.510","url":null,"abstract":"Concurrent spinal dural arteriovenous fistula (AVF) and cecal arteriovenous malformation (AVM) are very rare. A 6-year old boy presented with lower limb paresis after trauma. On imaging work-up spinal dural AVF was found. It was managed with endovascular glue embolization. After two years, the boy presented with severe anemia and occult gastrointestinal tract (GIT) bleed. Cecal AVM was diagnosed and managed with embolization.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45651586","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
Atypical Presentation of Multiple Foreign Body Ingestion 多异物摄入的非典型表现
APSP journal of case reports Pub Date : 2017-01-04 DOI: 10.21699/ajcr.v8i1.525
E. Aydın, S. Bent, Burak Ayan
{"title":"Atypical Presentation of Multiple Foreign Body Ingestion","authors":"E. Aydın, S. Bent, Burak Ayan","doi":"10.21699/ajcr.v8i1.525","DOIUrl":"https://doi.org/10.21699/ajcr.v8i1.525","url":null,"abstract":"Foreign body ingestion is very common in childhood especially under 3 year of age. Pica syndrome is characterized by an appetite for substances that are largely non-nutritive. We present a 3-year old girl who presented to ER with symptoms and signs of intestinal obstruction.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46210618","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
Bilateral Cystic Adrenal Neuroblastoma with Cystic Liver metastasis 双侧囊性肾上腺神经母细胞瘤伴囊性肝转移
APSP journal of case reports Pub Date : 2017-01-04 DOI: 10.21699/ajcr.v8i1.517
M. Aslan, D. Alis, A. U. Kalyoncu, H. Habibi, G. Ozdemir, B. Koç, I. Adaletli
{"title":"Bilateral Cystic Adrenal Neuroblastoma with Cystic Liver metastasis","authors":"M. Aslan, D. Alis, A. U. Kalyoncu, H. Habibi, G. Ozdemir, B. Koç, I. Adaletli","doi":"10.21699/ajcr.v8i1.517","DOIUrl":"https://doi.org/10.21699/ajcr.v8i1.517","url":null,"abstract":"Bilateral congenital cystic adrenal neuroblastoma (NB) with cystic liver metastasis is a very rare condition and only few cases have been reported in the literature. Herein we report a case of a congenital bilateral cystic adrenal NB with cystic liver metastasis and briefly discuss characteristic imaging features of cystic NB.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43712089","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: 6
Urachal Cyst, Meckel’s Diverticulum and Band, and Urachus 尿管囊肿，梅克尔憩室和束，以及尿管
APSP journal of case reports Pub Date : 2017-01-04 DOI: 10.21699/ajcr.v8i1.477
Dileep Garg, A. Singh, S. Kothari, Ayush Kumar
{"title":"Urachal Cyst, Meckel’s Diverticulum and Band, and Urachus","authors":"Dileep Garg, A. Singh, S. Kothari, Ayush Kumar","doi":"10.21699/ajcr.v8i1.477","DOIUrl":"https://doi.org/10.21699/ajcr.v8i1.477","url":null,"abstract":"A 4-year old boy presented with pain abdomen, bilious vomiting and constipation for three days. On examination, abdomen was distended and tender. X-ray abdomen revealed multiple air-fluid levels suggestive of intestinal obstruction. Ultrasonography abdomen revealed dilated bowel loops with minimal free fluid in peritoneal cavity. On exploration, there was a band causing obstruction of terminal ileum which was released. Band was arising from Meckel’s diverticulum which was connected to a cyst at umbilicus. On further exploration, the cyst was connected to urachus which was patent (Fig.1). There was no communication between bladder and urachus, cyst and urachus, Meckel's diverticulum and the cyst. Resection of Meckel’s diverticulum with ileum and end to end ileo-ileal anastomosis was done. Urachus and cyst were also excised. Patient recovered well postoperatively. Histopathology confirmed urachal cyst, urachus, and Meckel’s diverticulum.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46213671","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
Metanephric Adenofibroma Masquerading as Wilms’ Tumor 后肾腺纤维瘤伪装成威尔姆斯瘤
APSP journal of case reports Pub Date : 2016-11-01 DOI: 10.21699/ajcr.v7i5.463
Prince Raj, A. Khanolkar, Y. Sarin
{"title":"Metanephric Adenofibroma Masquerading as Wilms’ Tumor","authors":"Prince Raj, A. Khanolkar, Y. Sarin","doi":"10.21699/ajcr.v7i5.463","DOIUrl":"https://doi.org/10.21699/ajcr.v7i5.463","url":null,"abstract":"Metanephric adenofibroma is a rare, biphasic, benign tumor containing both stromal and epithelial components and could be potentially mistaken as Wilms’ tumor (WT). We present a 5-year-old girl who was suspected to have metastatic Wilms’ tumor on radiological investigations/tru-cut biopsy and had received neoadjuvant chemotherapy, but postoperatively final histopathology revealed it as metanephric adenofibroma. No postoperative chemotherapy was given","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"7 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68185059","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: 5
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