发布求助
文献互助 智能选刊 最新文献

Case Reports in Clinical Radiology最新文献

筛选
英文 中文
The “expanded Goldenhar syndrome” – A rare entity 扩大的戈登哈尔综合征"--一种罕见的病症
Case Reports in Clinical Radiology Pub Date : 2024-03-06 DOI: 10.25259/crcr_6_2024
Srijan Utkarsh, Pratibha Sharma, Harshit Tyagi, N. Nischal
{"title":"The “expanded Goldenhar syndrome” – A rare entity","authors":"Srijan Utkarsh, Pratibha Sharma, Harshit Tyagi, N. Nischal","doi":"10.25259/crcr_6_2024","DOIUrl":"https://doi.org/10.25259/crcr_6_2024","url":null,"abstract":"Goldenhar syndrome is a rare congenital condition occurring due to defects in the first and second branchial arches and encompasses a wide range of anomalies involving craniofacial structures, vertebrae, and internal organs, typically manifesting unilaterally. The causes for the defects are heterogenous with most cases being sporadic; however, the exact etiology of the disorder is still unknown. In this case report, we present a case of an adult male presenting with features of Goldenhar syndrome with ipsilateral pulmonary aplasia, which is a rare association.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"9 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140261182","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
A rare case of persistent mullerian duct syndrome with adenocarcinoma of ascending colon 一例罕见的持续性穆勒氏管综合征合并升结肠腺癌病例
Case Reports in Clinical Radiology Pub Date : 2024-02-19 DOI: 10.25259/crcr_190_2023
Nalin G. Patel, Shaiv Patel, Vaibhavkumar Maganbhai Vekaria, Himani Sharma, Chintan P. Banugariya
{"title":"A rare case of persistent mullerian duct syndrome with adenocarcinoma of ascending colon","authors":"Nalin G. Patel, Shaiv Patel, Vaibhavkumar Maganbhai Vekaria, Himani Sharma, Chintan P. Banugariya","doi":"10.25259/crcr_190_2023","DOIUrl":"https://doi.org/10.25259/crcr_190_2023","url":null,"abstract":"Persistent mullerian duct syndrome (PMDS) is a rare congenital disorder. This condition results from a failure of Mullerian duct regression during fetal development, leading to the presence of uterus, fallopian tubes, and upper vagina in otherwise phenotypically male individuals. Radiological evaluation plays a crucial role in the diagnosis and management of PMDS. Various imaging modalities including ultrasound, magnetic resonance imaging, and computed tomography are employed to visualize and confirm the presence of Mullerian structures in affected individuals.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"3 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139958732","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
In a fetus’ “CHAOS” there is no cosmos, in this disorder exists only one order 在胎儿的 "混乱 "中没有宇宙，在这种混乱中只存在一种秩序
Case Reports in Clinical Radiology Pub Date : 2024-02-03 DOI: 10.25259/crcr_167_2023
Vivek Gupta, Kimal Bhandari, Shishira Ramesh Shetty
{"title":"In a fetus’ “CHAOS” there is no cosmos, in this disorder exists only one order","authors":"Vivek Gupta, Kimal Bhandari, Shishira Ramesh Shetty","doi":"10.25259/crcr_167_2023","DOIUrl":"https://doi.org/10.25259/crcr_167_2023","url":null,"abstract":"Congenital high airway obstruction syndrome (CHAOS) is a partial or complete obstruction of the fetal upper airways and is an extremely rare entity. The most common cause of CHAOS is tracheal or laryngeal atresia. Laryngeal agenesis, laryngeal webs or cysts, and even subglottic stenosis can be rare causes. We present the rare case of a large cervical teratoma impinging on the upper airways of a fetus and causing CHAOS.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"15 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139808523","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
In a fetus’ “CHAOS” there is no cosmos, in this disorder exists only one order 在胎儿的 "混乱 "中没有宇宙，在这种混乱中只存在一种秩序
Case Reports in Clinical Radiology Pub Date : 2024-02-03 DOI: 10.25259/crcr_167_2023
Vivek Gupta, Kimal Bhandari, Shishira Ramesh Shetty
{"title":"In a fetus’ “CHAOS” there is no cosmos, in this disorder exists only one order","authors":"Vivek Gupta, Kimal Bhandari, Shishira Ramesh Shetty","doi":"10.25259/crcr_167_2023","DOIUrl":"https://doi.org/10.25259/crcr_167_2023","url":null,"abstract":"Congenital high airway obstruction syndrome (CHAOS) is a partial or complete obstruction of the fetal upper airways and is an extremely rare entity. The most common cause of CHAOS is tracheal or laryngeal atresia. Laryngeal agenesis, laryngeal webs or cysts, and even subglottic stenosis can be rare causes. We present the rare case of a large cervical teratoma impinging on the upper airways of a fetus and causing CHAOS.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"48 13","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139868119","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
Role of imaging in atypical infantile lipofibromatosis 成像在非典型婴儿脂肪纤维瘤病中的作用
Case Reports in Clinical Radiology Pub Date : 2023-12-23 DOI: 10.25259/crcr_162_2023
Mrinal Matish, Prem Kumar, Rahul Bhartiya, Sourav Jana
{"title":"Role of imaging in atypical infantile lipofibromatosis","authors":"Mrinal Matish, Prem Kumar, Rahul Bhartiya, Sourav Jana","doi":"10.25259/crcr_162_2023","DOIUrl":"https://doi.org/10.25259/crcr_162_2023","url":null,"abstract":"Lipofibromatosis is an extremely rare, hamartomatous soft-tissue tumor seen almost exclusively in the pediatric age group. They are typically found in the extremities. Varied clinical presentations and lack of specificity in imaging findings often create a diagnostic dilemma. A systematic approach with emphasis on tumor composition is needed to arrive at a correct diagnosis. We report an unusual case of a giant lipofibromatosis that presented as a painless progressive back swelling in a 10-month-old male infant.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"3 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139163112","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
Retrograde jejunogastric intussusception 逆行性空肠胃肠吻合术
Case Reports in Clinical Radiology Pub Date : 2023-11-22 DOI: 10.25259/crcr_146_2023
V. Senthilvelmurugan, N. R. Prasanth, K. Arivarasan, S. A. Raj
{"title":"Retrograde jejunogastric intussusception","authors":"V. Senthilvelmurugan, N. R. Prasanth, K. Arivarasan, S. A. Raj","doi":"10.25259/crcr_146_2023","DOIUrl":"https://doi.org/10.25259/crcr_146_2023","url":null,"abstract":"Retrograde intussusception pertains to the invagination of the intussusceptum in a direction opposite to normal peristalsis. Jejunogastric intussusception (JGI) is an infrequent complication linked to procedures such as gastrojejunostomy, Billroth II gastrectomy, and Roux-en-Y anastomosis. There are four types of JGI based on the type of intussuscepted bowel loop and two types based on clinical presentation. In its acute form, JGI presents as severe intestinal blockage, a mass in the left hypochondriac region, and the occurrence of hematemesis. In a chronic situation, it leads to the recurrent episodes of feeling full in the upper abdomen and experiencing vomiting because of intermittent and reversible intussusception. The gold standard investigation for diagnosis is a contrast-enhanced computed tomography (CECT) scan. Here, we describe a case of retrograde JGI in a patient who presented with the complaints of hematemesis. The CECT scan revealed the invagination of jejunal bowel loops into the stomach. This condition was treated surgically.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"163 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139250387","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
Unusual case of biliary neuroendocrine tumor 胆道神经内分泌肿瘤罕见病例
Case Reports in Clinical Radiology Pub Date : 2023-08-18 DOI: 10.25259/crcr_104_2023
Haleema Sherene, V. Kasi, G. S. Mahadevan, S. Rajasekaran, S. Mehta
{"title":"Unusual case of biliary neuroendocrine tumor","authors":"Haleema Sherene, V. Kasi, G. S. Mahadevan, S. Rajasekaran, S. Mehta","doi":"10.25259/crcr_104_2023","DOIUrl":"https://doi.org/10.25259/crcr_104_2023","url":null,"abstract":"This case report showcases the imaging findings in a patient with a biliary neuroendocrine tumor (NET). NETs encompass a wide variety of diseases and comprise neoplasms arising from neural crest tissues during embryonic development. NETs can be found in different organs, including the gastrointestinal tract, adrenal medulla, pituitary gland, hypothalamus, and thyroid gland. Biliary NETs are uncommon and makeup <1% of all NETs.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"100 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115743507","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
Parotid duct sialocele following dental procedure: An uncommon cause of right oro-buccal swelling; with review of literature 牙科手术后腮腺导管涎腺囊肿:一种罕见的右口腔-颊肿胀的原因;通过文献回顾
Case Reports in Clinical Radiology Pub Date : 2023-08-18 DOI: 10.25259/crcr_106_2023
Shreyas Masrani, Debraj Saha., A. Singhai, Saumya Sanghavi
{"title":"Parotid duct sialocele following dental procedure: An uncommon cause of right oro-buccal swelling; with review of literature","authors":"Shreyas Masrani, Debraj Saha., A. Singhai, Saumya Sanghavi","doi":"10.25259/crcr_106_2023","DOIUrl":"https://doi.org/10.25259/crcr_106_2023","url":null,"abstract":"There are various types of masses seen in the parotid region; however, parotid duct sialocele is a cystic mass seen arising at the expense of the parotid duct following a facial trauma or post-surgery. It may occur secondary to a stricture formed at the end of the duct or due to a complete laceration of the salivary gland. In our case, a 36-year-old female patient came to the outpatient department with a fullness of mouth in the right cheek, was evaluated clinically by the surgeon, and was sent to the radiology department for ultrasonography. Ultrasonography and a computed tomography (CT) scan were performed, and a diagnosis of parotid duct sialocele secondary to stenosis in the parotid duct was made. The patient underwent surgery, and the mass was removed. Parotid duct sialocele is a salivary cavity arising at the expense of the parotid duct. Facial trauma is the most common cause of this rare condition. If left untreated, a sialocele may develop into a significantly large facial swelling. Fistula formation may occur, often draining extraorally. We report a case of parotid duct sialocele that was assessed by sialography and ultrasonography and managed by the placement of an intraductal cannula for 15 days until the duct was found patent. We also discuss various treatment options for this condition in this case report.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"8 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128660709","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 pulmonary artery aneurysms in miliary tuberculosis 军人结核多发肺动脉动脉瘤
Case Reports in Clinical Radiology Pub Date : 2023-08-18 DOI: 10.25259/crcr_127_2023
A. Prakash, Srishti Sharma, S. Prasad
{"title":"Multiple pulmonary artery aneurysms in miliary tuberculosis","authors":"A. Prakash, Srishti Sharma, S. Prasad","doi":"10.25259/crcr_127_2023","DOIUrl":"https://doi.org/10.25259/crcr_127_2023","url":null,"abstract":"Pulmonary artery aneurysms are rare life threatening complications of tuberculosis (TB). Clinical symptoms range from being silent to fatal hemoptysis. Computed tomography angiography is diagnostic and shows the vascular nature of the lesions and their origin from the pulmonary arteries. The typically described Rasmussen’s aneurysm arises in cavitary TB due to inflammation induced damage to the tunica of the pulmonary artery. However, aneurysms may also rarely occur in non-cavitary TB. In this report, we describe a case of multiple aneurysms of the pulmonary artery in a case of non-cavitary miliary TB.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"65 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115113996","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
An often-forgotten cause of perihepatic abscess following cholecystectomy 胆囊切除术后肝周脓肿的一个常被遗忘的原因
Case Reports in Clinical Radiology Pub Date : 2023-08-11 DOI: 10.25259/crcr_126_2023
Vishaal Kondoor, D. Le, A. Kuo
{"title":"An often-forgotten cause of perihepatic abscess following cholecystectomy","authors":"Vishaal Kondoor, D. Le, A. Kuo","doi":"10.25259/crcr_126_2023","DOIUrl":"https://doi.org/10.25259/crcr_126_2023","url":null,"abstract":"Gallbladder perforation during laparoscopic cholecystectomy with gallstone spillage is common and typically without serious sequela. Rarely, retained gallstones may cause important complications such as focal infection, fistula formation, and adhesions. Here, a case of dropped gallstone related perihepatic abscess and sepsis is presented. Because the retained stone location and timeline of presentation are both highly variable, accurate diagnosis can be difficult. Knowledge of this condition is thus paramount to prompt consideration of this possibility.","PeriodicalId":419021,"journal":{"name":"Case Reports in Clinical Radiology","volume":"7 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121765006","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
首页 上一页 下一页 尾页
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
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
请完成安全验证×
相关产品
×
本文献相关产品
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号：481959085
Book学术官方微信