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Paraneoplastic Neurological Syndrome Presenting as New-Onset Refractory Status Epilepticus 副肿瘤神经综合征表现为新发难治性癫痫持续状态
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.02.00005
Amanda Nayberg, Linda Liu, Tanya Kappor-Maini, D. Ledoux
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引用次数: 0
Acholic Stools as a Primary Presenting Symptom of Incomplete Kawasaki Disease 不完全性川崎病的主要表现为胆汁性便
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.06.00008
Lexi M Crawford, Manju Korattiyil, Gabrina Dixon, Ashley L Siems
{"title":"Acholic Stools as a Primary Presenting Symptom of Incomplete Kawasaki Disease","authors":"Lexi M Crawford, Manju Korattiyil, Gabrina Dixon, Ashley L Siems","doi":"10.25270/con.2022.06.00008","DOIUrl":"https://doi.org/10.25270/con.2022.06.00008","url":null,"abstract":"","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69418123","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
Rapid, Spontaneous Resolution of Adolescent Idiopathic Scoliosis 快速,自发解决青少年特发性脊柱侧凸
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.07.00007
Jacob Moser, A. Bourland, Richard W. Byrd
{"title":"Rapid, Spontaneous Resolution of Adolescent Idiopathic Scoliosis","authors":"Jacob Moser, A. Bourland, Richard W. Byrd","doi":"10.25270/con.2022.07.00007","DOIUrl":"https://doi.org/10.25270/con.2022.07.00007","url":null,"abstract":"","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69418533","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
Pyoderma Gangrenosum on the Lower Extremity 下肢坏疽脓皮病
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.08.000002
R. Brubaker, Rudy Schmiedecke
{"title":"Pyoderma Gangrenosum on the Lower Extremity","authors":"R. Brubaker, Rudy Schmiedecke","doi":"10.25270/con.2022.08.000002","DOIUrl":"https://doi.org/10.25270/con.2022.08.000002","url":null,"abstract":"","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69418746","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
Lingual Osseous Choristoma in a 7-Year-Old 7岁儿童舌骨脉络瘤一例
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.10.000007
R. Sims, IV, Richard W. Byrd
{"title":"Lingual Osseous Choristoma in a 7-Year-Old","authors":"R. Sims, IV, Richard W. Byrd","doi":"10.25270/con.2022.10.000007","DOIUrl":"https://doi.org/10.25270/con.2022.10.000007","url":null,"abstract":"","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69420400","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 Potential Alternative Therapy for MPO-ANCA Vasculitis with IVIG in a Patient with COVID-19 COVID-19患者MPO-ANCA血管炎联合IVIG的潜在替代疗法
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.10.000001
Resham Khan, M. Zafar, Bianca Leuzzi
{"title":"A Potential Alternative Therapy for MPO-ANCA Vasculitis with IVIG in a Patient with COVID-19","authors":"Resham Khan, M. Zafar, Bianca Leuzzi","doi":"10.25270/con.2022.10.000001","DOIUrl":"https://doi.org/10.25270/con.2022.10.000001","url":null,"abstract":"","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69419617","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
Cerebral Venous Sinus Thrombosis in a Patient With a History of COVID-19 mRNA Vaccination COVID-19 mRNA疫苗接种史患者的脑静脉窦血栓形成
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2021.12.00012
Meet J Patel, Mahvish Qazi, Ryan T. Dougherty, Joshua J. Raymond
{"title":"Cerebral Venous Sinus Thrombosis in a Patient With a History of COVID-19 mRNA Vaccination","authors":"Meet J Patel, Mahvish Qazi, Ryan T. Dougherty, Joshua J. Raymond","doi":"10.25270/con.2021.12.00012","DOIUrl":"https://doi.org/10.25270/con.2021.12.00012","url":null,"abstract":"A 43-year-old woman with no significant medical history was admitted to our hospital's step down unit with a headache secondary to a cerebral venous sinus thrombosis (CVST), which had been discovered on computed tomography (CT) scan and confirmed with CT angiography. Copyright © 2022 Cliggott Publishing Co.. All rights reserved.","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69417065","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 Concerning Uvula Abnormality A关于小舌异常
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.01.00001
N. Lam, Patricia Campbell
{"title":"A Concerning Uvula Abnormality","authors":"N. Lam, Patricia Campbell","doi":"10.25270/con.2022.01.00001","DOIUrl":"https://doi.org/10.25270/con.2022.01.00001","url":null,"abstract":"A 21-year-old woman with no significant medical history presented to our clinic with “something hanging” from her uvula. She had noticed it a few months prior to presentation when she felt a tickling sensation at the back of her throat. At presentation, she said it now felt like it grew, because it was causing her to gag at times when swallowing. She denied any pain, difficulty swallowing, difficulty breathing, snoring, bleeding, or any changes in her voice. She is concerned because she believes her uvula is now connected to her tongue and is worried it may be cancerous. On physical examination, her vital signs were stable with 100% oxygen saturation on room air. Results of a head, eyes, ears, nose, and throat examination were normal except for the uvula abnormality. An oropharynx examination revealed a thin strand of tissue connecting the tip of her uvula to the base of her tongue (Figure). No cervical lymphadenopathy was noted, and the rest of her examination was unremarkable. Based on the patient’s history and physical examination, which one of the following is the most likely diagnosis?","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69417100","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
Intradermal Injection of Normal Saline for Treatment of Fat Atrophy Following Corticosteroid Injection 皮内注射生理盐水治疗皮质类固醇注射后脂肪萎缩
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.02.00008
Sierra Crowe, E. C. Schmidgal
{"title":"Intradermal Injection of Normal Saline for Treatment of Fat Atrophy Following Corticosteroid Injection","authors":"Sierra Crowe, E. C. Schmidgal","doi":"10.25270/con.2022.02.00008","DOIUrl":"https://doi.org/10.25270/con.2022.02.00008","url":null,"abstract":"A 20-year-old woman with a Fitzpatrick score of 2 presented via telehealth with “divots” on her forehead and scalp. She reported that 2 months prior to presentation she had received multiple steroid injections into her forehead and posterior skull by a neurologist for treatment of migraines. She had soon thereafter developed fat atrophy in 3 areas: 2 on her forehead and 1 on her occipital scalp. Although they were not painful or otherwise symptomatic, she was unhappy with the cosmetic appearance. She had no other skin or systemic symptoms. She visited the office the following day, and on examination, 2 atrophic plaques were noted on her bilateral forehead around the mid-pupillary lines, with a larger atrophic plaque on the occipital scalp (Figures 1 and 2). Given the location and timing of the lesions, they were consistent with skin atrophy induced by her prior steroid injections. Therefore, a biopsy was not performed.","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69417523","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
Unilateral Submandibular Lymphadenopathy in a 7-Year-Old Boy 1例7岁男童单侧下颌下淋巴结病变
Consultant Pub Date : 2022-01-01 DOI: 10.25270/con.2022.06.00004
Ebony Beaudoin, Malvi Mehta, Stephanie A Valek
{"title":"Unilateral Submandibular Lymphadenopathy in a 7-Year-Old Boy","authors":"Ebony Beaudoin, Malvi Mehta, Stephanie A Valek","doi":"10.25270/con.2022.06.00004","DOIUrl":"https://doi.org/10.25270/con.2022.06.00004","url":null,"abstract":"Background. A 7-year-old boy presented with a 3-week history of an ulcerated vesicle on his left cheek, left-sided facial swelling, and left submandibular lymphadenopathy after being scratched by a kitten. The swelling wors-ened despite a course of cephalexin for an assumed case of lymphangitis. Given his history of contact with a cat and clinical presentation, he was given a presumptive diagnosis of cat-scratch disease. He was prescribed a 5-day course of azithromycin and had full resolution of his symptoms approximately 2 weeks later. Cat-scratch disease, a bacterial infection caused by Bartonella henselae , is a common pediatric condition characterized by local lymphadenopathy and fever after being scratched by a cat. It can be diagnosed clinically based on history and physical exam findings and is usually a benign and self-limited condition in immunocompetent pediatric patients. afebrile, alert, active, and in no acute distress. Examination of the skin revealed a 1-cm raised, firm, nontender, erythematous circular nodule adjacent to the nose on the left cheek with an overlying 3-4 mm vesicle. The vesicle was open, circular, and appeared to be healing well without exudate. The submandibular area was swollen, painless to palpation, nonerythematous and nonfluctuant. The patient had mildly boggy nasal turbinates with no Physical examination was otherwise unremarkable.","PeriodicalId":35575,"journal":{"name":"Consultant","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69417915","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
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