APSP journal of case reports最新文献_第7页

Giant Lingual Teratoma with Cleft Palate in Male New-Born 新生儿巨大舌畸胎瘤伴腭裂

APSP journal of case reports Pub Date : 2016-11-01 DOI: 10.21699/AJCR.V7I5.474

J. Rawat, Piyush Kumar, Sudhir Singh, Hemlata

引用次数: 0

Foreign Body in Duodenum Mimicking a Duplication Cyst on Imaging 十二指肠异物影像学表现酷似重复囊肿

APSP journal of case reports Pub Date : 2016-11-01 DOI: 10.21699/ajcr.v7i5.468

A. Singh, Vinay Mathur, Ramesh Tanger, Arun Gupta, Ayush Kumar

引用次数: 6

Incidentally Diagnosed Multiple Vascular Lesions of the Spleen: Littoral Cell Angioma or Hemangioma? 偶然诊断的脾脏多发血管病变:滨海细胞血管瘤还是血管瘤?

APSP journal of case reports Pub Date : 2016-11-01 DOI: 10.21699/ajcr.v7i5.492

E. Aydın

引用次数: 3

Huge Gastric Teratoma in an 8-Year Old Boy. 8岁男童巨大胃畸胎瘤。

APSP journal of case reports Pub Date : 2016-11-01 DOI: 10.21699/ajcr.v7i5.495

Rajpal S Sisodiya, Simmi K Ratan, Parveen K Man

引用次数: 2

Severe Hematuria and Prevesical Hematoma after Open Ureterocystoneostomy: Sequel of Undiagnosed Hemophilia 开放输尿管膀胱造口术后严重血尿和膀胱前血肿:未确诊血友病的后遗症

APSP journal of case reports Pub Date : 2016-11-01 DOI: 10.21699/AJCR.V7I5.486

E. Hisamatsu, K. Yoshino

引用次数: 0

Postoperative Ileocolic Intussusception in a Neonate with Anorectal Malformation 新生儿肛肠畸形术后回结肠肠套叠1例

APSP journal of case reports Pub Date : 2016-11-01 DOI: 10.21699/AJCR.V7I5.473

Piyush Kumar, Sudhir Singh, J. Rawat, Sarita Singh

{"title":"Postoperative Ileocolic Intussusception in a Neonate with Anorectal Malformation","authors":"Piyush Kumar, Sudhir Singh, J. Rawat, Sarita Singh","doi":"10.21699/AJCR.V7I5.473","DOIUrl":"https://doi.org/10.21699/AJCR.V7I5.473","url":null,"abstract":"A 7-days-old male neonate with anorectal malformation (ARM) presented with abdominal distension and bleeding per rectum. He had an operation for ARM (Anoplasty) a day after birth and the patient had history of passing stool normally for two days. It was followed by blood mixed stool and abdominal distension. On examination, the patient had features of mild dehydration and sepsis. The abdomen was distended and a mass was palpable on left side of abdomen. Perineal examination showed attempt of a primary anoplasty performed at other hospital for absent anal opening to decompress the bowel. Haematological and biochemical investigations including coagulation profile were in the normal limits. X-ray abdomen in AP erect view revealed multiple air fluid levels. Patient was resuscitated with intravenous (IV) fluids. Antibiotics and analgesics were started. In view of abdominal distension, palpable abdominal mass, and history of bloody stool, we kept the possibility of intussusception in mind. Exploratory laparotomy was performed after about four hours of admission. Intraoperatively, ileocolic intussusception was found, which was advancing up to the sigmoid colon (Fig.1). It was not possible to manually reduce the intussusception owing to ischemic intussusceptum, thus resection of bowel with ileostomy and colonic mucous fistula (Transverse colon) were made. On opening the resected bowel, no pathological lead point was found. Patient was discharged in good general condition on fifth post-operative day of procedure. Sitz bath and care of perineal wound was advised. Patient was in regular follow up or two months with satisfactory condition. However, he did not turn up in third month. On telephonic inquiry, it was informed that the patient developed ileostomy diarrhoea and succumbed to dehydration.","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":"68185768","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

Giant Primary Epithelial Splenic Cyst in an Adolescent Girl 青春期女孩原发性巨大上皮性脾囊肿

APSP journal of case reports Pub Date : 2016-11-01 DOI: 10.21699/ajcr.v7i5.485

Pradeep Kajal, K. Rattan, Namita Bhutani, K. Bhalla

{"title":"Giant Primary Epithelial Splenic Cyst in an Adolescent Girl","authors":"Pradeep Kajal, K. Rattan, Namita Bhutani, K. Bhalla","doi":"10.21699/ajcr.v7i5.485","DOIUrl":"https://doi.org/10.21699/ajcr.v7i5.485","url":null,"abstract":"A 13-year old girl presented with abdominal pain and upper abdominal fullness for 4 months. On examination, there was a large, smooth, and firm lump palpable involving the left hypochondrium, epigastrium, left lumbar region, and reaching almost up to the umbilicus. It was moving with respiration and the upper limit was not reachable. Rest of the examination was normal. All routine hematological and biochemical investigations were within normal range. Hematological tests for human immunodeficiency virus (HIV), hepatitis C virus (HCV) and hepatitis B virus (HBV) viz. ELISA for HIV, anti-HCV and HBsAg were negative. X-ray chest revealed slight elevation of left diaphragm. Abdominal ultrasonography revealed a giant unilocular cystic lesion in the spleen. Casoni’s skin test and complement fixation test for Echinococcus granulosus were negative. Stool examination done over 3 consecutive days was found to be normal. Computed tomography confirmed the splenic large cyst with dimensions of 22x17x15cm with thin, compressed rim of normal parenchyma posterolaterally (Fig.1). At laparotomy, a huge splenic cyst of more than 20 cm of maximum diameter was found with almost total displacement and compression of remaining splenic parenchyma. However due to cyst size and location, preservation of spleen was considered impossible and total splenectomy was carried out after decompression of the cyst by aspiration of about 2000 ml of turbid serous fluid (Fig.2). The postoperative period was uneventful and patient was discharged in fair health on 5th postoperative day.","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":"68185650","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

Neurenteric Cyst Presenting with Bleeding Per Rectum 神经直肠囊肿表现为直肠出血

APSP journal of case reports Pub Date : 2016-09-01 DOI: 10.21699/ajcr.v7i4.454

T. Yadav, P. Parmar, K. Rattan

引用次数: 0

Inflammatory Myofibroblastic Tumor of Common Bile Duct in a Girl 1例女孩胆总管炎性肌成纤维细胞瘤

APSP journal of case reports Pub Date : 2016-09-01 DOI: 10.21699/ajcr.v7i4.445

Aureen D’cunha, Susan Jehangir, R. Thomas

引用次数: 7

Malrotation and Midgut Volvulus associated with Asymptomatic Duplication Cyst of Jejunum 空肠无症状重复囊肿伴旋转不良和中肠扭转

APSP journal of case reports Pub Date : 2016-09-01 DOI: 10.21699/ajcr.v7i4.447

Sandip K. Rahul, V. Upadhyaya, B. Kumar

引用次数: 8