Journal of clinical case reports最新文献

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Differential Diagnosis of Cognitive Impairment in Bipolar Disorder: A Case Report 双相情感障碍认知障碍的鉴别诊断:1例报告
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001203
Tavares Df
{"title":"Differential Diagnosis of Cognitive Impairment in Bipolar Disorder: A Case Report","authors":"Tavares Df","doi":"10.4172/2165-7920.10001203","DOIUrl":"https://doi.org/10.4172/2165-7920.10001203","url":null,"abstract":"In old age bipolar disorder (BD) patients, cognitive complaints difficults an accurate differential diagnosis between cognitive deficits secondary to a primary affective disorder and neurocognitive disorders, such as dementia in Alzheimer’s disease (AD). This case report refers to a female 56-year-old patient with severe and treatment resistant BD type I that presented cognitive decline with loss in recent episodic memory and executive functions in the past year. The diagnosis of mild stage dementia associated to BD was suggested, however neuroimaging tests such as magnetic resonance imaging (MRI) and positron emission tomography with fluordeoxiglicose (PET - FDG) were not enough to exclude the differential diagnosis of AD. The CSF biomarkers (reduced levels of amyloid peptide Aâ1-42 and the elevation of total tau protein and phosphorylated tau levels) resources were decisive for exclusion of an etiological diagnosis of AD.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001203","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70706776","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
Stroke in Early Postpartum Period in a Young Woman: A Case Study 一位年轻女性产后早期中风的个案研究
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001205
Ubaid Mf, A. Salim, Faiz Sa, Z. Azeem, R. Abid, M. Shakeel
{"title":"Stroke in Early Postpartum Period in a Young Woman: A Case Study","authors":"Ubaid Mf, A. Salim, Faiz Sa, Z. Azeem, R. Abid, M. Shakeel","doi":"10.4172/2165-7920.10001205","DOIUrl":"https://doi.org/10.4172/2165-7920.10001205","url":null,"abstract":"This is a case of 35-years-old woman who presented with visual disturbances, gait disturbances and headache ten days postpartum. Imaging studies identified an acute infarction in the right parietal region. This case report discusses her presentation, investigations and management and the Etiology of stroke in pregnancy and the post-partum period. *Corresponding author: Ubaid MF, Department of Obstetrics and Gynecology, Azad Jammu and Kashmir Medical College, Muzaffarabad, Pakistan, Tel: 00923318189509; E-mail: Muhammadfurqanubaid0@gmail.com Received January 07, 2019; Accepted January 27, 2019; Published January 31, 2019 Citation: Ubaid MF, Salim A, Faiz SA, Azeem Z, Abid R, et al. (2019) Stroke in Early Postpartum Period in a Young Woman: A Case Study. J Clin Case Rep 9: 1205. doi: 10.4172/2165-7920.10001205 Copyright: © 2019 Ubaid MF, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"47 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001205","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70706997","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
Ocular Metastasis from Breast Cancer: A Case Report and Review of Literatures 乳腺癌眼部转移1例报告及文献复习
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001223
E. Abdelaal, D. Hacking, W. Sąsiadek, M. O’Connor, I. Owens, K. Murphy, C. McGeeney, S. Matthew
{"title":"Ocular Metastasis from Breast Cancer: A Case Report and Review of Literatures","authors":"E. Abdelaal, D. Hacking, W. Sąsiadek, M. O’Connor, I. Owens, K. Murphy, C. McGeeney, S. Matthew","doi":"10.4172/2165-7920.10001223","DOIUrl":"https://doi.org/10.4172/2165-7920.10001223","url":null,"abstract":"Male breast cancer is relatively uncommon, representing less than 1% of all breast cancer with a peak incidence at 70 years. The principles of management are like that for female patients, including surgery (more mastectomy in men), radiotherapy and systemic treatment. The prognosis is stage dependent and it is generally worse than female breast cancer due to late presentation. The choroid is a relatively common site for metastasis due to rich blood supply and the most common primaries are the breast and the lung. We are presenting a case of a male patient with locally advanced breast cancer, who had mastectomy and radiotherapy in 2015 and who presented three years later with blurred vision in the left eye and was found to have choroidal metastasis. He had urgent palliative radiotherapy to the left eye. Further investigation followed showing widespread metastatic disease and he demised shortly thereafter.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001223","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70708077","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 Measurable and Unmeasurable Visual Benefits of 3D Saline Infusion Sonohysterography 三维生理盐水输注超声宫腔镜可测量和不可测量的视觉效果
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001220
A. A
{"title":"The Measurable and Unmeasurable Visual Benefits of 3D Saline Infusion Sonohysterography","authors":"A. A","doi":"10.4172/2165-7920.10001220","DOIUrl":"https://doi.org/10.4172/2165-7920.10001220","url":null,"abstract":"","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"248 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001220","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70708336","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
Metastatic Ameloblastoma to the Liver: Rare Presentation of a Rare Disease 肝转移成釉细胞瘤:一种罕见疾病的罕见表现
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001207
S. Lacin, A. Dogrul, E. Dikmen, N. Kertmen, A. Turker, A. Kars
{"title":"Metastatic Ameloblastoma to the Liver: Rare Presentation of a Rare Disease","authors":"S. Lacin, A. Dogrul, E. Dikmen, N. Kertmen, A. Turker, A. Kars","doi":"10.4172/2165-7920.10001207","DOIUrl":"https://doi.org/10.4172/2165-7920.10001207","url":null,"abstract":"Ameloblastoma is a slow growing odontogenic epithelial neoplasm which originates from remnants of the dental lamina with a high recurrence rate, but a low tendency to metastasize. Locally invasive ameloblastoma is often aggressive and destructive, which erodes bone and invades adjacent structures. Despite a benign histology metastatic disease may occur and samples taken from metastatic tumor usually maintains the features of the original tumor. Ameloblastic carcinoma differs from ameloblastoma with malignant cytological features. Here we report an unusual case of ameloblastoma metastatic to lung and liver, unresponsive to systemic treatment with cisplatin and adriamycin, and well controlled with local surgical treatment. *Corresponding author: Lacin S, Department of Medical Oncology, Hacettepe Cancer Institute, Hacettepe University Sıhhiye Campus, Oncology Hospital 2nd Floor, Altındag, Turkey, Tel: +905321591069; E-mail: sahin81lacin@yahoo.com Received January 20, 2019; Accepted January 29, 2019; Published January 31, 2019 Citation: Lacin S, Dogrul A, Dikmen E, Kertmen N, Turker A, et al. (2019) Metastatic Ameloblastoma to the Liver: Rare Presentation of a Rare Disease. J Clin Case Rep 9: 1207. doi: 10.4172/2165-7920.10001207 Copyright: © 2019 Lacin S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001207","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70707204","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: 4
Hepatic Hydatid Cyst in a Young Rural Female: A Case Report 农村年轻女性肝包虫病1例报告
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001218
Hoshy Ms, Hassan Fa
{"title":"Hepatic Hydatid Cyst in a Young Rural Female: A Case Report","authors":"Hoshy Ms, Hassan Fa","doi":"10.4172/2165-7920.10001218","DOIUrl":"https://doi.org/10.4172/2165-7920.10001218","url":null,"abstract":"Introduction: Hydatid disease in humans occurs as result of infection by the larval stages (hydatid cysts) of taeniid cestodes of the genus Echinococcus. The growth of the hydatid cysts in the internal organs (mainly liver and lungs) of humans may affect the health and lead to appearance of the disease manifestations. Case report: We report a case of hydatid cyst of the liver in a 29-years-old woman who originally lived in Jizan in Saudi Arabia and presented to Jeddah King Fahad hospital emergency unit with abdominal pain radiated to the right shoulder. Physical examination and imaging investigation in the form of chest X-ray, abdominal sonography and computed tomography were done to her. Results: Imaging investigations demonstrated a cystic lesion within right lobe of the liver extending to adjacent part of the left lobe. A hydatid cyst was diagnosed. The patient underwent radical excision of the cyst with total removal. She also received pre and postoperative oral albendazole. Conclusion: Hydatid disease cases of the liver may remain silent and become symptomatic and are usually diagnosed in adult patients because of the slowly growing nature of the cyst. The diagnosis needs careful history taking, examination and imaging investigations.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001218","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70707783","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
Remission in the Patient with Malignant Pleural Mesothelioma: A Case Report 恶性胸膜间皮瘤患者缓解1例报告
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001214
Firsov Is, Sivov Ig, Ingenik Llc
{"title":"Remission in the Patient with Malignant Pleural Mesothelioma: A Case Report","authors":"Firsov Is, Sivov Ig, Ingenik Llc","doi":"10.4172/2165-7920.10001214","DOIUrl":"https://doi.org/10.4172/2165-7920.10001214","url":null,"abstract":"","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001214","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70707996","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
Microbiological Examination of Intrauterine Catheters Tips After Operative Hysteroscopy 宫腔镜术后宫内导管Tips的微生物学检查
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001211
A. A
{"title":"Microbiological Examination of Intrauterine Catheters Tips After Operative Hysteroscopy","authors":"A. A","doi":"10.4172/2165-7920.10001211","DOIUrl":"https://doi.org/10.4172/2165-7920.10001211","url":null,"abstract":"","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001211","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70707107","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 Cranial Nerve Palsies in Mantle Cell Lymphoma: A Case Report and Literature Review 套细胞淋巴瘤并发多发性脑神经麻痹1例并文献复习
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001215
M. Ababou, S. Jennane, Mehtat Em, H. Elmaaroufi, K. Doghmi
{"title":"Multiple Cranial Nerve Palsies in Mantle Cell Lymphoma: A Case Report and Literature Review","authors":"M. Ababou, S. Jennane, Mehtat Em, H. Elmaaroufi, K. Doghmi","doi":"10.4172/2165-7920.10001215","DOIUrl":"https://doi.org/10.4172/2165-7920.10001215","url":null,"abstract":"Involvement of cranial nerves is unspecific and can occur in inflammation, different types of nerve tumours and in malignancies. Central Nervous System (CNS) dissemination during the Mantle Cell Lymphoma (MCL) is unusual. We report a rare case of a patient followed for mantle cell lymphoma, which brutally instituted multiple cranial nerve palsies, brain imaging showed a bilateral sphenoid sinusitis. Cytology later showed the presence of mantle cells in cerebrospinal fluid analysis. We review literature for the Central Nervous System involvement in Mantle cell lymphoma and we discuss possible change of therapeutic strategies. Although the cranial nerves involvement is extremely rare in Mantle cell Lymphoma, physicians should be aware of such patterns of Central Nervous System (CNS) involvement for the early diagnosis and adequate selection of treatment modality.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"7 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001215","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70707675","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
Isolation of Streptococcus thoraltensis from an Abdominal Wall Abscess in a Young Female: A Case Report 从年轻女性腹壁脓肿中分离胸廓张力链球菌1例
Journal of clinical case reports Pub Date : 2019-01-01 DOI: 10.4172/2165-7920.10001212
Bustami N, Mismar A, Obeidat F
{"title":"Isolation of Streptococcus thoraltensis from an Abdominal Wall Abscess in a Young Female: A Case Report","authors":"Bustami N, Mismar A, Obeidat F","doi":"10.4172/2165-7920.10001212","DOIUrl":"https://doi.org/10.4172/2165-7920.10001212","url":null,"abstract":"Objective: Streptococcus thoraltensis is a recently described species, isolated from the intestinal and genital tracts of swine and from rabbit feces. We describe here a case of enterocutaneous fistula complicated by abdominal wall abscess formation attributable to S. thoraltensis. To our knowledge, this is the second reported human infection by this organism. Clinical features: Our patient is a 44-years-old diabetic female, with a previous history of ovarian mixed germ cell tumor treated with surgery and adjuvant chemoradiotherapy, presenting 18 years later with an enterocutaneous fistula complicated by abdominal wall abscess formation at the site of previous surgery. Culture from the drained pus and fistulous tract revealed Streptococcus thoraltensis. Outcome: The patient was treated conservatively with broad spectrum antibiotics and total parenteral nutrition. She suffered from disseminated intravascular coagulation and acute liver failure and passed away 4 weeks later. Conclusion: We report for the second time the isolation of streptococcus thoraltensis associated with a pathological process in humans. The infectious role of this newly identified organism pattern in human diseases is yet to be identified.","PeriodicalId":73664,"journal":{"name":"Journal of clinical case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2165-7920.10001212","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70707866","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
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