Case Reports in Clinical Practice最新文献_第9页

Starry Sky on MRI Brain: Unusually Observed in a Pediatric Case of Japanese Encephalitis MRI脑上的星空：一例日本脑炎患儿的异常观察

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11128

Durgesh Kumar, D. Kumar, Rajesh Kumar Yadav

引用次数: 1

Endoscopic Endonasal Approach to Cavernous Sinus Hemangioma: A Report of Two Cases and Review of the Literature 内窥镜入路治疗海绵窦血管瘤2例报告并文献复习

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11121

A. Fathi, M. Rashidbeygi, Maryamalsadat Mousavi, Zahra Azizan, S. Sadrehosseini, Azin Tabari, Mehdi Zeinalizadeh

{"title":"Endoscopic Endonasal Approach to Cavernous Sinus Hemangioma: A Report of Two Cases and Review of the Literature","authors":"A. Fathi, M. Rashidbeygi, Maryamalsadat Mousavi, Zahra Azizan, S. Sadrehosseini, Azin Tabari, Mehdi Zeinalizadeh","doi":"10.18502/crcp.v7i3.11121","DOIUrl":"https://doi.org/10.18502/crcp.v7i3.11121","url":null,"abstract":"Cavernous sinus hemangiomas (CSHs) are rare, benign, slow-growing neoplasms within the cavernous sinus. Laterally located to these lesions, the cranial nerves and carotid artery are subject to injury during removal of hemangiomas through a transcranial route. Therefore, forsurgi- cal management of cavernous sinus hemangiomas a medial corridor granted through an endoscop- ic endonasal approach may be less traumatic to the neurovascular bundle. \u0000Case-1 describes a 23-year old male who presented with intermittent blurred vision and very mild ptosis on the right side for two yearsbefore admission. Fundoscopic exam, visual acuity and perimetry tests were normal. With intense enhancement after contrastadministration, both brain MRI and CT scan demonstrated an extra-axial mass in the right cavernous sinus. \u0000Case-2 presents a 59-year-old male, a known case of renal oncocytoma who underwent nephrec- tomy a year before, with chief complain ofmoderate intermittent headaches. Imaging study of the brain by MRI revealed a sellar mass. \u0000Near-total resection for case-1 and gross total resection for case-2 were performed through the an extended endoscopic endonasal approach. \u0000We report two cases of near-total and gross total resection of CSHs via an extend- ed endoscopic endonasal approach substantiatingadvances in minimal access neurosurgery to the treatment of such grim lesions of an intricate vicinity of the skull base. At the same time, we focus to review extensively the growing yet heterogenous literature of the past twenty \u0000years on the broached topic. The evolution of extended endoscopic endonasal approach over the past two decades changes the dynamism of the surgical practices steeped in tradition and provides a safer alternate route for preserving cranial nerves of this anatomic region.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46112912","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

Prenatal Diagnosis of Congenitally Corrected Transposition of the Great Arteries (CCTGA): A Case Report 先天性大动脉转位(CCTGA)的产前诊断:1例报告

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11119

Nasir Hematian, S. Torabi, S. Hantoushzadeh, Maasoumeh Saleh, Mahboubeh Saleh

{"title":"Prenatal Diagnosis of Congenitally Corrected Transposition of the Great Arteries (CCTGA): A Case Report","authors":"Nasir Hematian, S. Torabi, S. Hantoushzadeh, Maasoumeh Saleh, Mahboubeh Saleh","doi":"10.18502/crcp.v7i3.11119","DOIUrl":"https://doi.org/10.18502/crcp.v7i3.11119","url":null,"abstract":"CCTGA, also known as levo- or L-loop transposition (L-TGA), double discordance, or ventricular inversion, is a rare cardiovascular anomaly with inversion of the ventricles and great arteries. In this anomaly, the right atrium communicates with the morpho- logic left ventricle, which gives rise to the pulmonary artery, while the left atrium communicates with the morphologic right ventricle, which gives rise to the aorta. Thus, atrioventricular and ventriculoarterial discordance (double discordance) exist, and although the blood flows in the normal direction, it passes through the wrong ventricular chambers. It is a unique conotruncal anomaly, inwhich the four-chamber view is abnormal. It may be associated with other heart disorders. In most fetuses, TGA remains undiagnosed before birth. The diagnosis of TGA can be made by care- fully and appropriately evaluating the anatomic locationsof cardiac chambers and the connections between the atria, ventricles, and great arteries with high-resolution ultrasound. Patients with isolated CTGA generally present later in life with signs and symptoms related to either arrhythmias or heart failure. TGA is rarely associated with chromosomal abnormality and amniocentesis is usually not undertaken. We report a case of CTGA detected at 18 week’s gestation on screening ultrasound.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45056949","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

Sarcoidosis in Close Family Members and Susceptibility to High Grade B-Cell Lymphoma: A Case Report Study 近亲属结节病与高级别b细胞淋巴瘤易感性:一个病例报告研究

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11120

Hana Magrooni, N. Javadian, Ghasem Farahmand, Sakineh Ranji-Burachaloo

{"title":"Sarcoidosis in Close Family Members and Susceptibility to High Grade B-Cell Lymphoma: A Case Report Study","authors":"Hana Magrooni, N. Javadian, Ghasem Farahmand, Sakineh Ranji-Burachaloo","doi":"10.18502/crcp.v7i3.11120","DOIUrl":"https://doi.org/10.18502/crcp.v7i3.11120","url":null,"abstract":"The presented case is an 81- year-old woman who had experienced episodes of facial twitching without loss of consciousness and flu like symptoms for a few weeks prior to her admission. examinations were unremarkable except for left 3rd nerve and right 6th nerve palsy, right peripheral facial palsy and right -side hemiparesis. FH was positive for sarcoidosis. neuroimaging were in favor of PCNSL. \u0000Sarcoidosis and malignancy maybe etiologically related in at least 25% of cases. Coexis- tence of sarcoidosis and lymphoma have been reported previously. Our patient had two daughters with sarcoidosis and her chest CT scan showed multiple lymph nodes inmedias- tinum. Unfortunately, due to the location and the technical restriction, biopsy of mediasti- nal lymph nodes was not performedfor our patient and we could not differentiate whether it was reactive, paraneoplastic or granulomatous. We present this case as concurrence of lymphoma and sarcoidosis in a family, which could guide a new concern for the patient with granulomatous infiltrative disease for early diagnosis and familial screening.","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49013572","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

Appendicovesical Fistula, as the First Presentation of Mucinous Adenocarcinoma of Appendix: A Case Report 阑尾粘液腺癌首次表现为阑尾膀胱瘘1例报告

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11118

Narjes Mohammadzadeh, S. Hashemi

引用次数: 0

Hereditary Hemochromatosis and Alpha-Thalassemia Presenting with Diabetes Mellitus: A Rare Case Report 糖尿病并发遗传性血色素沉着症和α地中海贫血：一例罕见病例报告

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11125

Pourya Farhangi, M. Hajmiri, N. Shirzad, M. Hemmatabadi

引用次数: 1

Pancreatic Tuberculosis Mimicking a Mass: A Case Report 模拟肿块的胰腺结核一例报告

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11127

S. Deme, Bhaskar Kakarla, R. Thakur, Purushotham Ramireddygari, Nageswara Rao Modugu

{"title":"Pancreatic Tuberculosis Mimicking a Mass: A Case Report","authors":"S. Deme, Bhaskar Kakarla, R. Thakur, Purushotham Ramireddygari, Nageswara Rao Modugu","doi":"10.18502/crcp.v7i3.11127","DOIUrl":"https://doi.org/10.18502/crcp.v7i3.11127","url":null,"abstract":"Tuberculosis, a preventable and curable disease caused by Mycobacterium tuberculosis, is the leading infectious cause of mortality worldwide. Organs commonly affected are lungs and extrapulmonary organs like lymph nodes, meninges, bones, genitourinary and gastrointestinal tract. Ileocaecal tuberculosis is the commonest form of the gastrointestinal tract. Disseminated infection can involve almost all organs in the body but isolated pancreatic tuberculosis is rarely reported in the literature. Hereby,we report a case of a young female presenting with abdominal pain and further evaluation with imaging revealed pancreatic mass raising suspicion of malignancy. Endoscopic ultrasound (EUS) guided FNAC of pancreatic mass surprisingly revealed necrotizing granulomatous lesions favoring tuberculosis. This was further supported by the complete resolution of the mass with Antituberculous Therapy (ATT). What is important: All pancreatic masses are not malignant. Infectious causes like tuberculosis should be considered in the differential diagnosis which is curable by medication. With a high index of suspicion and adequate workup, unnecessary invasive procedures can be avoided. \u0000 \u0000 ","PeriodicalId":34254,"journal":{"name":"Case Reports in Clinical Practice","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47143376","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

Case Series of Pneumomediastinum and Subcutaneous Emphysema in COVID-19 Patients COVID-19患者纵隔气肿与皮下肺气肿病例系列分析

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11126

Y. Tan, Vivek Vijayan, K. K. Sia

引用次数: 0

Abdominal Wall Synovial Sarcoma, a Rare Presentation 罕见的腹壁滑膜肉瘤

Case Reports in Clinical Practice Pub Date : 2022-11-13 DOI: 10.18502/crcp.v7i3.11117

E. Nazar, Zohre Shabanzade, Amir Ahmadi

引用次数: 0

Massive Enlargement of The Tongue: A Report of Unusual Case 舌肿大:一罕见病例报告

Case Reports in Clinical Practice Pub Date : 2022-10-11 DOI: 10.18502/crcp.v7i2.10823

R. Erfanian, F. Heidari, Saeed Sohrabpour, S. Shakiba

引用次数: 0