发布求助
文献互助 智能选刊 最新文献

Türkiye Klinikleri Journal of Case Reports最新文献

筛选
英文 中文
An Overview of Immunoglobulin G4-related Ophthalmic Diseases Accompanied by a Case Report 免疫球蛋白g4相关眼科疾病综述附1例报告
Türkiye Klinikleri Journal of Case Reports Pub Date : 2021-01-01 DOI: 10.5336/CASEREP.2020-78271
B. Şimşek, G. E. Cecikoğlu, E. Durmus, Umut Perçem Orhan Söylemez
{"title":"An Overview of Immunoglobulin G4-related Ophthalmic Diseases Accompanied by a Case Report","authors":"B. Şimşek, G. E. Cecikoğlu, E. Durmus, Umut Perçem Orhan Söylemez","doi":"10.5336/CASEREP.2020-78271","DOIUrl":"https://doi.org/10.5336/CASEREP.2020-78271","url":null,"abstract":"","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"25 1","pages":"33-37"},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85798964","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
Delayed Diagnosis of Spontaneous Intraperitoneal Rupture of Hydatid Cyst of the Liver 肝包虫囊自发性腹膜内破裂的延迟诊断
Türkiye Klinikleri Journal of Case Reports Pub Date : 2021-01-01 DOI: 10.5336/CASEREP.2020-78056
S. Eren, B. Taştan, Ömer Topuz, T. Ertan
{"title":"Delayed Diagnosis of Spontaneous Intraperitoneal Rupture of Hydatid Cyst of the Liver","authors":"S. Eren, B. Taştan, Ömer Topuz, T. Ertan","doi":"10.5336/CASEREP.2020-78056","DOIUrl":"https://doi.org/10.5336/CASEREP.2020-78056","url":null,"abstract":"","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"47 1","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75401734","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 Malignancy in an Adolescent: Desmoplastic Small Round Cell Tumor 一罕见的青少年恶性肿瘤:结缔组织增生小圆细胞瘤
Türkiye Klinikleri Journal of Case Reports Pub Date : 2021-01-01 DOI: 10.5336/CASEREP.2020-77722
G. Dogan, A. Sığırcı, A. Akyay, S. Uğuralp, Merve Nur Güvenç
{"title":"A Rare Malignancy in an Adolescent: Desmoplastic Small Round Cell Tumor","authors":"G. Dogan, A. Sığırcı, A. Akyay, S. Uğuralp, Merve Nur Güvenç","doi":"10.5336/CASEREP.2020-77722","DOIUrl":"https://doi.org/10.5336/CASEREP.2020-77722","url":null,"abstract":"","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"45 1","pages":"45-50"},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77585519","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 Problem of Diagnosis in Occupational Brucellosis 职业性布鲁氏菌病的诊断问题
Türkiye Klinikleri Journal of Case Reports Pub Date : 2020-01-01 DOI: 10.5336/caserep.2020-74317
D. Karagül, Elif Altundaş Hatman, S. Canbaz
{"title":"The Problem of Diagnosis in Occupational Brucellosis","authors":"D. Karagül, Elif Altundaş Hatman, S. Canbaz","doi":"10.5336/caserep.2020-74317","DOIUrl":"https://doi.org/10.5336/caserep.2020-74317","url":null,"abstract":"180 In the Social Insurance and General Health Insurance Law, occupational disease refer to the temporary or permanent disease, physical or mental handicapped status, caused by a reason reiterated due to the quality of the work made or worked by the insurance holder or by the working conditions.1 Although it is possible to protect employees from occupational diseases, they are still an important cause of morbidity and mortality today.2 In cases where protection from occupational diseases is unsuccessful, early detection of the disease is required. The aim of the determination of occupational diseases is to diagnose and treat the sick employee early, to minimize sequelae, to provide the necessary rehabilitation, to prevent other employees from affecting the disease and to ensure that employees benefit from legal rights.3","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"59 1","pages":"180-185"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75653221","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
Neonatal Ileal Perforation due to Type IV Ileocecal Valve Atresia IV型回盲瓣闭锁致新生儿回肠穿孔
Türkiye Klinikleri Journal of Case Reports Pub Date : 2020-01-01 DOI: 10.5336/caserep.2020-75177
Tuğba Acer Demir, E. Arslan
{"title":"Neonatal Ileal Perforation due to Type IV Ileocecal Valve Atresia","authors":"Tuğba Acer Demir, E. Arslan","doi":"10.5336/caserep.2020-75177","DOIUrl":"https://doi.org/10.5336/caserep.2020-75177","url":null,"abstract":"ing in patients with congenital intestinal atresia. Colonic atresia accounts for only 1.8-5% of intestinal atresia with the reported incidence of 1 in 66 000 births.1,2 Mortality rate of colonic atresia, which increases with delayed treatment, is 25.7%.3 Colonic atresia is mostly located in the right colon.3 Like other intestinal atresia colonic atresia is classified as: Type I, membranous atresia with continuous intestinal wall; Type II, blind ending intestines separated by fibrous cord (no continuous intestinal wall but intact mesentery); Type III, blind ending intestines with mesenteric defect between two ends; Type IV, multiple atresias.4 Most of the colonic atresia is type III (60.4%). The rate of type I (membranous) atresia is 15% and type IV (multiple) atresia is 10% among all colonic atresia.3","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"306 2 1","pages":"215-219"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73194275","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: 2
A Case of Eosinophilic Granuloma Presenting as Post-traumatic Scalp Hematoma 以创伤后头皮血肿表现的嗜酸性肉芽肿1例
Türkiye Klinikleri Journal of Case Reports Pub Date : 2020-01-01 DOI: 10.5336/caserep.2020-74185
G. Dogan, A. Sığırcı
{"title":"A Case of Eosinophilic Granuloma Presenting as Post-traumatic Scalp Hematoma","authors":"G. Dogan, A. Sığırcı","doi":"10.5336/caserep.2020-74185","DOIUrl":"https://doi.org/10.5336/caserep.2020-74185","url":null,"abstract":"206 Eosinophilic granuloma is a benign bone disease which is local. It is a mild form of Langerhans cell histiocytosis (LCH). Children, adolescents, and young adults are predominantly affected. The most common site of involvement is the skull.1 Although eosinophilic granuloma (EG) can be asymptomatic and incidentally found, it can be seen as tender, growing scalp mass. A mild head trauma history before clinical symptoms is common.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"1 1","pages":"206-210"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81532280","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
Desmoid Fibromatosis Mimicking Breast Cancer After Nipple-Sparing Mastectomy 保留乳头乳房切除术后的硬纤维瘤病模拟乳腺癌
Türkiye Klinikleri Journal of Case Reports Pub Date : 2020-01-01 DOI: 10.5336/caserep.2019-72157
H. Vayvada, C. Demirdöver, E. Tuna, Alper Geyik
{"title":"Desmoid Fibromatosis Mimicking Breast Cancer After Nipple-Sparing Mastectomy","authors":"H. Vayvada, C. Demirdöver, E. Tuna, Alper Geyik","doi":"10.5336/caserep.2019-72157","DOIUrl":"https://doi.org/10.5336/caserep.2019-72157","url":null,"abstract":"women aged 40-55.1,2 The overall risk of breast cancer in the occidental female population is 9.6-13.1% and the risk of death is 3.4%.3 Surgery is the main approach for the treatment of breast cancer. There are several types of breast cancer surgeries and today conservative breast surgery (CBS) is taking the place of radical procedures.4 Mainly, CBS could be classified as wide local excision, quadranectomy, and nipple and skin sparing mastectomy (NSSM). Although there is still a lack of long term data up to date studies for the NSSM, locoregional recurrence is evaluated less than 1% per year which is acceptable when compared to radical and modified radical mastectomy.5","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"16 1","pages":"95-98"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72906187","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
Glycogen Storage Disease Type IIIa Presenting with Hyperglycemia: A Novel Mutation 以高血糖为表现的IIIa型糖原储存病:一种新的突变
Türkiye Klinikleri Journal of Case Reports Pub Date : 2020-01-01 DOI: 10.5336/caserep.2020-74932
M. Güven, Mehmet Şimşek, Müslüm Güneş, S. Tekeş
{"title":"Glycogen Storage Disease Type IIIa Presenting with Hyperglycemia: A Novel Mutation","authors":"M. Güven, Mehmet Şimşek, Müslüm Güneş, S. Tekeş","doi":"10.5336/caserep.2020-74932","DOIUrl":"https://doi.org/10.5336/caserep.2020-74932","url":null,"abstract":"The disorder usually involves both liver and muscle and is termed glycogen storage diseases type IIIa. However, in about 15% of patients, the disease appears to involve only the liver and is classified as type IIIb. Hypoglycemia, hepatomegaly and progressive myopathy are prominent clinical findings. The presence of a wide variety of mutations in the AGL gene causing disease has been described in the literature.2-4 This new mutation we found in the AGL gene has not been yet published. In this case, we aimed to present our case of a 44-year-old Turkish male diagnosed as glycogen storage disease type IIIa, accompanied by this new mutation with hyperglycemia associated with type 2 diabetes mellitus without hypoglycemia. CASE REPORT A 44-year-old male patient was admitted to our clinic with complaints of inability to walk, dry mouth, polydipsia and polyuria. There is no known family history of diabetes mellitus and glycogen storage disease. Physical exam showed hepatomegaly, muscle weakness and atrophy of the distal extremities. The patient’s height was 165 cm and weight 50 kg.When he was 20 years old, he was diagnosed with glycogen storage disease (GSD) by muscle biopsy due to myopathy but at that time the type of the disease was not determined.The patient first noticed muscle weakness of the distal extremities at the age of 20. The symptoms gradually increased, and he could no longer walk without walking stick. In blood tests, glucose: 262 mg/dl, ALT: 74 U/L, AST: 50 U/L creatinine kinase (CK): 898 U/L HBA1c: 10.3% was detected. The laboratory results of the patient are shown in Table 1. Turkiye Klinikleri J Case Rep. 2020;28(3):173-6","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"10 1","pages":"173-176"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82466516","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 Mimicking Abdominal Wall Neoplasms: Meshoma 一例罕见的模拟腹壁肿瘤:Meshoma
Türkiye Klinikleri Journal of Case Reports Pub Date : 2020-01-01 DOI: 10.5336/caserep.2020-75013
T. Kalaycı, Ü. Iliklerden
{"title":"A Rare Case Mimicking Abdominal Wall Neoplasms: Meshoma","authors":"T. Kalaycı, Ü. Iliklerden","doi":"10.5336/caserep.2020-75013","DOIUrl":"https://doi.org/10.5336/caserep.2020-75013","url":null,"abstract":"","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"1966 1","pages":"220-223"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82729191","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
Spontaneous Massive Bladder Hematoma in the Late Period After Kidney Transplantation in Patients with AA Amyloidosis: Two Cases AA型淀粉样变性肾移植术后晚期自发性膀胱血肿2例
Türkiye Klinikleri Journal of Case Reports Pub Date : 2020-01-01 DOI: 10.5336/caserep.2019-70028
R. Sadioğlu, G. Kumru, Damla Örs Şendoğan, Şahin Eyüpoğlu, K. Keven
{"title":"Spontaneous Massive Bladder Hematoma in the Late Period After Kidney Transplantation in Patients with AA Amyloidosis: Two Cases","authors":"R. Sadioğlu, G. Kumru, Damla Örs Şendoğan, Şahin Eyüpoğlu, K. Keven","doi":"10.5336/caserep.2019-70028","DOIUrl":"https://doi.org/10.5336/caserep.2019-70028","url":null,"abstract":"ABS TRACT Massive bladder hematoma can occur following a trauma, neoplastic states, or as a longterm side effect of a pelvic irradiation therapy. It is reported, albeit rarely, in the patients with amyloidosis which can affect bladder and can manifest itself as hematoma. However, it hasn’t been yet reported in kidney transplant recipients. A 31 year-old male with chronic glomerulonephritis received kidney transplantation. He developed proteinuria and frequent episodes of lung infection because of bronchiectasis after seven years from transplantation. Duodenal biopsies showed AA-amyloidosis. Macroscopic hematuria appeared, and cystoscopy revealed hematoma and perforation of bladder wall. A 56 year-old male with secondary amyloidosis due to familial Mediterranean fever had kidney transplantation. After two years, cystoscopy was performed because of macroscopic hematuria and revealed large hematoma that completely filled the bladder. To our knowledge, these are the very first cases with AA amyloidosis who developed spontaneous bladder hematoma in kidney transplant recipients.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"33 1","pages":"60-62"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89380552","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：604180095
Book学术官方微信