发布求助
文献互助 智能选刊 最新文献

Journal of Case Reports and Medical History最新文献

筛选
英文 中文
Papillary Urothelial Neoplasm With Low Malignancy Potential in Adolescence 青少年低恶性潜能乳头状尿路上皮肿瘤
Journal of Case Reports and Medical History Pub Date : 2023-10-19 DOI: 10.54289/jcrmh2300132
{"title":"Papillary Urothelial Neoplasm With Low Malignancy Potential in Adolescence","authors":"","doi":"10.54289/jcrmh2300132","DOIUrl":"https://doi.org/10.54289/jcrmh2300132","url":null,"abstract":"Bladder urothelial neoplasms are very rare in people in the first two decades of life. We presented our experience in the diagnosis and treatment of a fourteen-year-old adolescent girl with a tumor process on the urinary bladder.","PeriodicalId":484263,"journal":{"name":"Journal of Case Reports and Medical History","volume":"68 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135666708","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
The History of Chronic Diseases and Industrial Revolution 慢性疾病和工业革命的历史
Journal of Case Reports and Medical History Pub Date : 2023-10-16 DOI: 10.54289/jcrmh2300131
{"title":"The History of Chronic Diseases and Industrial Revolution","authors":"","doi":"10.54289/jcrmh2300131","DOIUrl":"https://doi.org/10.54289/jcrmh2300131","url":null,"abstract":"The current research investigates the historical association between the industrial revolution and an increase in the prevalence of chronic diseases. Less time spent being physically active and more calories consumed have been linked to an increased risk of developing chronic diseases such as diabetes. This resulted in obesity, which then contributed to the development of cardiovascular disease and other illnesses. According to the findings of this research, the main characteristics of chronic diseases are linked to the transition to modernity. These shifts in the composition of the community have been observed in more recent times in history. When viewed as a whole, changes in lifestyle are a contributing factor in the problem of rising disease rates and have the potential to be both part of the problem and part of the solution.","PeriodicalId":484263,"journal":{"name":"Journal of Case Reports and Medical History","volume":"6 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136113547","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
Embracing the Legacy of Medical History 拥抱医学史的遗产
Journal of Case Reports and Medical History Pub Date : 2023-10-11 DOI: 10.54289/jcrmh2300129
{"title":"Embracing the Legacy of Medical History","authors":"","doi":"10.54289/jcrmh2300129","DOIUrl":"https://doi.org/10.54289/jcrmh2300129","url":null,"abstract":"","PeriodicalId":484263,"journal":{"name":"Journal of Case Reports and Medical History","volume":"102 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136097718","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
Tuberculous Pericarditis: Clinical, Diagnostic, and Therapeutic Features 结核性心包炎:临床、诊断和治疗特点
Journal of Case Reports and Medical History Pub Date : 2023-10-11 DOI: 10.54289/jcrmh2300130
{"title":"Tuberculous Pericarditis: Clinical, Diagnostic, and Therapeutic Features","authors":"","doi":"10.54289/jcrmh2300130","DOIUrl":"https://doi.org/10.54289/jcrmh2300130","url":null,"abstract":"Introduction: Tuberculous pericarditis is a rare manifestation of extrapulmonary tuberculosis. Due to the infrequency of this condition, the most effective management approach has not been clearly established. Our study analyzed 14 cases with tuberculous pericarditis treated at Ibn Rochd Hospital in Casablanca over two years from 2020 to 2022. Methods: Medical records of tuberculous pericarditis patients were reviewed. Data on demographics, clinical presentation, diagnostic methods, and treatments were collected. Results were expressed in terms of frequencies, averages, and percentages. Results: The mean patient age was 37.7 years, with 64% males. Common symptoms included fever (50%), chest pain (57%), and dyspnea (92.8%). Clinical signs included right heart failure (35%) and muffled heart sounds (57%). ECG findings showed sinus tachycardia (71.4%) and low voltage (57%). Echocardiography revealed pericardial effusion (78%) and other abnormalities. Pericardial fluid was mostly citrine yellow (64%) and serohemorrhagic (36%). Adenosine deaminase was positive in 57% of cases. GeneXpert confirmed 71% of cases, while pericardial biopsy confirmed 29%. All received antitubercular treatment, with corticosteroids in three cases. In-hospital, 92% showed pericardial effusion regression, but one death due to tamponade occurred. Long term, 21% had effusion recurrence, and 35% transitioned to constrictive pericarditis. Conclusion: Tuberculous pericarditis presents diagnostic challenges. Clinical, radiological, and biological evidence is crucial for diagnosis. Antitubercular treatment is effective, but the risk of constrictive pericarditis remains high, necessitating further research into corticosteroid therapy's role in prevention.","PeriodicalId":484263,"journal":{"name":"Journal of Case Reports and Medical History","volume":"5 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136211638","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 Non-Ischemic Dilated Cardiomyopathy Revealing Inclusion Body Myositis 一例罕见的非缺血性扩张型心肌病表现为包涵体肌炎
Journal of Case Reports and Medical History Pub Date : 2023-09-22 DOI: 10.54289/jcrmh2300128
{"title":"A Rare Case of Non-Ischemic Dilated Cardiomyopathy Revealing Inclusion Body Myositis","authors":"","doi":"10.54289/jcrmh2300128","DOIUrl":"https://doi.org/10.54289/jcrmh2300128","url":null,"abstract":"Inclusion body myositis is the most common inflammatory myopathy after age 50. Unlike polymyositis and dermatomyositis, in which cardiac involvement is relatively common, current evidence indicates that inclusion body myositis is not associated with cardiac disease such as dilated cardiomyopathy. We report the observation of a 57-year-old patient known to be type 2 diabetic under treatment, admitted with acute congestive heart failure. the paraclinical examinations carried out were in favor of inclusion body myositis complicated by heart failure and dilated cardiomyopathy, the patient was treated with boluses of corticosteroids and immunosuppressants as well as treatment of heart failure, this attitude has improved his symptoms as well as his quality of life. The interest of this work is to underline the importance of diagnosis and early treatment in the management of myositis complicated by cardiovascular manifestations, particularly dilated cardiomyopathy.","PeriodicalId":484263,"journal":{"name":"Journal of Case Reports and Medical History","volume":"79 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136061092","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
Naphthalene Ingestion Induced Acute Hemolytic Crisis in Young Adult with Undiagnosed G6PD Deficiency 摄入萘导致未确诊G6PD缺乏症的年轻成人急性溶血性危重
Journal of Case Reports and Medical History Pub Date : 2023-09-21 DOI: 10.54289/jcrmh2300126
{"title":"Naphthalene Ingestion Induced Acute Hemolytic Crisis in Young Adult with Undiagnosed G6PD Deficiency","authors":"","doi":"10.54289/jcrmh2300126","DOIUrl":"https://doi.org/10.54289/jcrmh2300126","url":null,"abstract":"Naphthalene ball ingestion is a common toxicological emergency with most cases seen in children. It is mostly a non-life-threatening condition, but some cases can be complicated by methemoglobinemia and hemolysis. The incidence of hemolysis is greater in predisposing conditions like G6PD. We are hereby presenting a case of a young male who presented after naphthalene ball ingestion with methemoglobinemia and later developed acute hemolytic crisis during course of treatment and was later found out to be an undiagnosed case of G6PD.","PeriodicalId":484263,"journal":{"name":"Journal of Case Reports and Medical History","volume":"20 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136235937","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 Preoperative Evaluation Revealing a Rare Coagulation Factor Deficiency 术前评估显示罕见凝血因子缺乏
Journal of Case Reports and Medical History Pub Date : 2023-09-20 DOI: 10.54289/jcrmh2300127
Tabat Meryem
{"title":"A Preoperative Evaluation Revealing a Rare Coagulation Factor Deficiency","authors":"Tabat Meryem","doi":"10.54289/jcrmh2300127","DOIUrl":"https://doi.org/10.54289/jcrmh2300127","url":null,"abstract":"Constitutional factor II deficiency is a rare coagulation disorder. The autosomal recessive form has an estimated prevalence of 1-2 million. Clinical symptoms depend on the rate of factor II deficiency. We report a fortuitous discovery of an isolated factor II deficiency in a 9-year-old girl of 1st degree consanguineous parents, following a preoperative assessment of drainage of her abundant pericardial effusion, the biological assessment showed a factor II rate < 1%, a prothrombin rate at 3% and a TCA > 120 sec, the dosage of the other coagulation factors are without anomalies. Through this observation we recall the rarity of this deficit and thought about it in the face of unusual bleeding in newborns of consanguineous parents, as well as the necessity of collaboration with international registries to establish codified diagnostic and therapeutic guidelines. Keywords: Factor II; Congenital Hemorrhagic Diseases; Rare Coagulation Factor Deficiency Abbreviations: FFP: Fresh Frozen Plasma","PeriodicalId":484263,"journal":{"name":"Journal of Case Reports and Medical History","volume":"84 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136308289","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
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