Journal of clinical case reports最新文献_第8页

Microsurgical Treatment of Intracranial Aneurysms: Report of a Series of Cases in a Single Cuban Hospital 显微外科治疗颅内动脉瘤:古巴一家医院的一系列病例报告

Journal of clinical case reports Pub Date : 2018-06-21 DOI: 10.26420/AUSTINJCLINCASEREP.2019.1132

Dr. C. Angel Jesus Lacerda Gallardo

引用次数: 0

Pleomorphic Adenoma of Buccal Minor Salivary Gland: A Case Report 颊小涎腺多形性腺瘤1例报告

Journal of clinical case reports Pub Date : 2018-06-18 DOI: 10.4172/2165-7920.10001132

H. Khoja, D. Jain

引用次数: 0

A Patient Diagnosed with POEMS Syndrome with Atypical Presentation: A Case Report 一位被诊断为POEMS综合征的非典型患者:一例报告

Journal of clinical case reports Pub Date : 2018-06-15 DOI: 10.4172/2165-7920.10001130

H. Semiz, Roxana Carmen Geana, D. Sorostinean, Iliescu Va, A. Drăgan

引用次数: 0

Bilateral Ruptured Ectopic Pregnancies with Massive Hemo-Peritonium: A Case Report in a Resource-Low Setting in Sub-Saharan Africa 撒哈拉以南非洲资源匮乏地区双侧破裂型异位妊娠伴大量出血性腹膜炎一例报告

Journal of clinical case reports Pub Date : 2018-06-08 DOI: 10.4172/2165-7920.10001127

Dongmo Gael, Binwe Hapmo Bienvenu, D. Francois, Silatsa Dongmo Fabrice, Kengne Mbobda Willy Stephane, P. Tolefac, Biyoma Marcella Derboise Christelle, Tocki Toutou Grâce, Tameyi Tatsa Joel, Danwang Celestin, N. Marcelin

{"title":"Bilateral Ruptured Ectopic Pregnancies with Massive Hemo-Peritonium: A Case Report in a Resource-Low Setting in Sub-Saharan Africa","authors":"Dongmo Gael, Binwe Hapmo Bienvenu, D. Francois, Silatsa Dongmo Fabrice, Kengne Mbobda Willy Stephane, P. Tolefac, Biyoma Marcella Derboise Christelle, Tocki Toutou Grâce, Tameyi Tatsa Joel, Danwang Celestin, N. Marcelin","doi":"10.4172/2165-7920.10001127","DOIUrl":"https://doi.org/10.4172/2165-7920.10001127","url":null,"abstract":"Background: Bilateral ruptured ectopic pregnancy is the rupture of two implanted product of conception outside of the uterine cavity. Bilateral ruptured ectopic pregnancy without an initial induction of ovulation is extremely rare. It’s occurrence with a major life threatening complication such as massive hemo-peritonium worsens the prognosis. Immediate diagnosis and surgical intervention is required. Few cases have been identified. Case report: We report the case of bilateral ruptured ectopic pregnancy with massive hemo-peritonium diagnosed in a 28-year- old female and managed at African Genesis Health Clinic Yaounde. Discussion and Conclusion: prompt diagnosis and surgical intervention is needed to improve the prognosis related to bilateral ruptured ectopic pregnancies with massive hemo-peritonium. Counseling for assisted means of procreation is important.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":" ","pages":"1-2"},"PeriodicalIF":0.0,"publicationDate":"2018-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001127","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44871432","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

Recurrent Infective Endocarditis in a Drug Addict: A Case Report 吸毒成瘾者复发性感染性心内膜炎1例报告

Journal of clinical case reports Pub Date : 2018-05-30 DOI: 10.4172/2165-7920.10001123

G. Menafra, A. Pingitore, A. Gurgo, D. Magrí, E. Pagannone, M. Testa, M. Volpe

{"title":"Recurrent Infective Endocarditis in a Drug Addict: A Case Report","authors":"G. Menafra, A. Pingitore, A. Gurgo, D. Magrí, E. Pagannone, M. Testa, M. Volpe","doi":"10.4172/2165-7920.10001123","DOIUrl":"https://doi.org/10.4172/2165-7920.10001123","url":null,"abstract":"Infective endocarditis is a disease with a high mortality rate; mortality increases with the number of new episodes. Patients with relapsing endocarditis have a higher mortality rate per year (20%) than patients with a single episode (9%); moreover, the episodes of infective endocarditis on the prosthetic valve have a worse prognosis, with a mortality rate of 45% for each episode. In relapsing endocarditis, the following are distinguished: the relapses, characterized by the same germ, less than six months after the previous episode, and the reinfections, which may be caused by a different germ, or by the same germ, more than six months after previous episode. A recent analysis of the risk factors of recurrent bacterial endocarditis showed that the use of intravenous drugs, hemodialysis, immunosuppression and previous episodes of infective endocarditis played a major role, especially if they occurred on the prosthetic valve and if caused by S. aureus. Recurrent infectious endocarditis occurs more frequently in young male patients with HIV seropositivity, who routinely use intravenous drugs. We have analyzed the clinical case of a 36-year-old immunocompetent man with a long history of parenteral drug abuse, who has presented 6 new episodes of relapsing infective endocarditis on mitral valve and 2 reinfections since 2013. Between 2013 and 2016, the patient underwent two mitral valve replacements with a biological prosthesis implant and a mitral valve replacement with a mechanical prosthesis implant and a tricuspid annuloplasty. The remaining episodes were treated with medical therapy only. Currently in the literature 6 episodes of relapsing infective endocarditis and 1 reinfection in a single patient is the highest number of reported events.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":" ","pages":"1-3"},"PeriodicalIF":0.0,"publicationDate":"2018-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001123","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47507050","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

Familial Glucocorticoid Deficiency Presenting as Progressive Hyperpigmentation: A Case Report 家族性糖皮质激素缺乏表现为进行性色素沉着:1例报告

Journal of clinical case reports Pub Date : 2018-05-28 DOI: 10.4172/2165-7920.10001120

A. Refaei, A. Alali, M. Soeid, N. A. Jurayyan, B. Alenazi, Taleb Ra

{"title":"Familial Glucocorticoid Deficiency Presenting as Progressive Hyperpigmentation: A Case Report","authors":"A. Refaei, A. Alali, M. Soeid, N. A. Jurayyan, B. Alenazi, Taleb Ra","doi":"10.4172/2165-7920.10001120","DOIUrl":"https://doi.org/10.4172/2165-7920.10001120","url":null,"abstract":"Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disease caused by resistant of ACTH receptor at adrenal cortex leading to (usually) isolated glucocorticoid deficiency with normal mineralocorticoid secrete. Patients with FGD usually presented in neonatal–childhood period with signs/symptoms of glucocorticoid deficiency such as hypoglycemia, hyperpigmentation, Failure to thrive, shock and death if treatment was delayed. Labs usually revealed high ACTH, low cortisol but normal 17 OHP, electrolyte, androgen. Here we describe a 3-yearsold Saudi girl, with history of progressive hyperpigmentation for first year of life, but no history of hypoglycaemia or neonatal jaundice, no history of a lacrimation or dysphagia and positive similar family history. She had generalized Hyperpigmentation with normal female genitalia. Her cortisol was low with high ACTH level, but normal electrolyte 17, Hydroxyprogesterone, aldosterone, renin, androgen. Familial Glucocorticoid Deficiency was diagnosed, and maintenance dose of hydro cortisol was started, and patient pigmentation was improved few week latter.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":" ","pages":"1-2"},"PeriodicalIF":0.0,"publicationDate":"2018-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47553355","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

Report Case of Van Der Knaap Syndrome in Two Ecuadorian Siblings 厄瓜多尔两名兄弟姐妹罹患Van Der Knaap综合征

Journal of clinical case reports Pub Date : 2018-05-28 DOI: 10.4172/2165-7920.10001122

M. Ja

引用次数: 0

Treatment for Severe Pregnancy Induced Hypertension and Preterm Labor with Concomitant Administration of Estradiol and Progesterone under Monitoring Aminopeptidases: A Case Report 氨基肽酶监测下雌孕激素联合应用治疗严重妊娠高血压和早产1例

Journal of clinical case reports Pub Date : 2018-05-25 DOI: 10.4172/2165-7920.10001115

S. Mizutani, E. Mizutani, A. Iwase, K. Shibata

引用次数: 3

Psychogenic Nonepileptic Seizures in a Mother and Her Son–Fate or Chance? 母亲和儿子的心因性非癫痫性癫痫发作是命运还是偶然?

Journal of clinical case reports Pub Date : 2018-05-21 DOI: 10.4172/2165-7920.10001114

Shah V, Hamouda D, Masel T

{"title":"Psychogenic Nonepileptic Seizures in a Mother and Her Son–Fate or Chance?","authors":"Shah V, Hamouda D, Masel T","doi":"10.4172/2165-7920.10001114","DOIUrl":"https://doi.org/10.4172/2165-7920.10001114","url":null,"abstract":"Psychogenic Nonepileptic Seizures (PNES) are defined as typical seizure-like activities or behaviors without cortical epileptiform discharges. The diagnosis of PNES remains a challenge and continuous video electroencephalography (cEEG) remains the gold standard to differentiate between epileptic seizures and PNES. Despite advances made in our understanding of PNES, diagnosing and treating this well-known entity remains a challenge. 25% of patients with seizures will be misdiagnosed as having PNES or epileptic seizures even by certified Neurologists. Do patient characteristics and demographics increase our accuracy to diagnose PNES? We present a case of a mother and her son, both diagnosed with PNES by cEEG monitoring in our epilepsy monitoring unit. While familial prevalence of conversion disorders is reported in the literature, this will be the first case report describing the incidence of PNES in two members of the same family. Do psychogenic epilepsies run in families? Will the diagnosis of PNES in one family member increase the probability of PNES in their relatives with seizures? Larger patient pools need to be studied to draw a definite conclusion regarding our observation.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"2018 1","pages":"1-3"},"PeriodicalIF":0.0,"publicationDate":"2018-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001114","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44961753","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

Torpedo Maculopathy: A Case Report of a 9-Year-Old Girl in Albania 鱼雷黄斑病变:阿尔巴尼亚1例9岁女童报告

Journal of clinical case reports Pub Date : 2018-05-18 DOI: 10.4172/2165-7920.10001112

M. Krasniqi

引用次数: 0