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Annals of internal medicine. Clinical cases最新文献

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Alternating Transient Monocular Vision Loss Due to Giant Cell Arteritis 巨细胞动脉炎引起的交替性短暂性单眼视力丧失
Annals of internal medicine. Clinical cases Pub Date : 2023-10-01 DOI: 10.7326/aimcc.2023.0639
Benjamin J. McCormick, Rex K. Siu, Eric Eggenberger, Ronald R. Butendieck, Michael J. Maniaci
{"title":"Alternating Transient Monocular Vision Loss Due to Giant Cell Arteritis","authors":"Benjamin J. McCormick, Rex K. Siu, Eric Eggenberger, Ronald R. Butendieck, Michael J. Maniaci","doi":"10.7326/aimcc.2023.0639","DOIUrl":"https://doi.org/10.7326/aimcc.2023.0639","url":null,"abstract":"Giant cell arteritis is a systemic granulomatous vasculitis commonly involving the temporal artery and associated with visual deficits. The most common ocular presentation of giant cell arteritis involves anterior ischemic ocular neuropathy with sudden unilateral vision loss. We present a rare case of alternating painless monocular vision loss in an older man who responded clinically to prolonged glucocorticoid therapy, tocilizumab, and intraocular pressure–lowering ophthalmic medications.","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"116 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134935071","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
Vasculitis After a Vaccine: Rare Adverse Reaction Following a COVID-19 Vaccine 疫苗后血管炎:COVID-19疫苗后罕见的不良反应
Annals of internal medicine. Clinical cases Pub Date : 2023-10-01 DOI: 10.7326/aimcc.2022.1043
Prutha Pathak, Siddharth Patel, Brendan Gaylord, Punuru J. Reddy
{"title":"Vasculitis After a Vaccine: Rare Adverse Reaction Following a COVID-19 Vaccine","authors":"Prutha Pathak, Siddharth Patel, Brendan Gaylord, Punuru J. Reddy","doi":"10.7326/aimcc.2022.1043","DOIUrl":"https://doi.org/10.7326/aimcc.2022.1043","url":null,"abstract":"Fatigue, fever, localized soreness, urticaria, and rash are common adverse reactions of COVID-19 vaccines. However, the occurrence of serious autoimmune reactions is quite rare. Cutaneous small-vessel vasculitis is an autoimmune disorder that manifests with palpable purpura and petechiae involving extremities. It results from neutrophilic inflammation within and around dermal vessels and is usually self-limited. We report a 55-year-old woman presenting with a rash 48 hours after receiving the third (Moderna) COVID-19 vaccine dose. Blood investigations and a skin punch biopsy confirmed the diagnosis of COVID-19 vaccine–induced cutaneous small-vessel vasculitis. The patient ultimately improved after inpatient treatment with systemic steroids.","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"21 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135809932","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 Case of Relugolix-Associated Rhabdomyolysis relugolix相关横纹肌溶解1例
Annals of internal medicine. Clinical cases Pub Date : 2023-10-01 DOI: 10.7326/aimcc.2023.0095
Benjamin Tanenbaum, Julie Kolnik, Taruna Arora, Kriti Mittal
{"title":"A Case of Relugolix-Associated Rhabdomyolysis","authors":"Benjamin Tanenbaum, Julie Kolnik, Taruna Arora, Kriti Mittal","doi":"10.7326/aimcc.2023.0095","DOIUrl":"https://doi.org/10.7326/aimcc.2023.0095","url":null,"abstract":"","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"27 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135811033","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 Case Report of Systemic Lupus Erythematosus With IgA Nephropathy and Crescentic Nephritis 系统性红斑狼疮合并IgA肾病合并月牙状肾炎1例
Annals of internal medicine. Clinical cases Pub Date : 2023-10-01 DOI: 10.7326/aimcc.2023.0157
Zhifeng Jiang, Aiqiao Feng
{"title":"A Case Report of Systemic Lupus Erythematosus With IgA Nephropathy and Crescentic Nephritis","authors":"Zhifeng Jiang, Aiqiao Feng","doi":"10.7326/aimcc.2023.0157","DOIUrl":"https://doi.org/10.7326/aimcc.2023.0157","url":null,"abstract":"We report a case of systemic lupus erythematosus with IgA nephropathy and acute progressive glomerulonephritis. Renal function failed to recover after the administration of glucocorticoid and cyclophosphamide pulse therapy, which shows that systemic lupus erythematosus and IgA nephropathy may coexist at the same time.","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"45 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135811800","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 Complication of Silicone Breast Implant Rupture 硅胶乳房植入物破裂的罕见并发症
Annals of internal medicine. Clinical cases Pub Date : 2023-10-01 DOI: 10.7326/aimcc.2023.0290
Sateesh Sakhamuri, Kabeer Ali, Vijay Naraynsingh, Ian Ramnarine, Surujpal Teelucksingh
{"title":"A Rare Complication of Silicone Breast Implant Rupture","authors":"Sateesh Sakhamuri, Kabeer Ali, Vijay Naraynsingh, Ian Ramnarine, Surujpal Teelucksingh","doi":"10.7326/aimcc.2023.0290","DOIUrl":"https://doi.org/10.7326/aimcc.2023.0290","url":null,"abstract":"","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"31 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135809948","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
Euglycemic Diabetic Ketoacidosis in a Patient Post Cardiac Surgery Receiving Continuous Renal-Replacement Therapy 心脏手术后接受持续肾脏替代治疗的糖尿病酮症酸中毒患者
Annals of internal medicine. Clinical cases Pub Date : 2023-10-01 DOI: 10.7326/aimcc.2023.0663
Walter Yaw Agyeman, Inemesit Akpan, Kwasi Opare-Addo, Saheed Soleye, Alfred Solomon
{"title":"Euglycemic Diabetic Ketoacidosis in a Patient Post Cardiac Surgery Receiving Continuous Renal-Replacement Therapy","authors":"Walter Yaw Agyeman, Inemesit Akpan, Kwasi Opare-Addo, Saheed Soleye, Alfred Solomon","doi":"10.7326/aimcc.2023.0663","DOIUrl":"https://doi.org/10.7326/aimcc.2023.0663","url":null,"abstract":"","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"6 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134931115","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
Neurologic Manifestations of Germline GATA2 Deficiency: A Report of Two Cases 种系GATA2缺乏的神经学表现:附2例报告
Annals of internal medicine. Clinical cases Pub Date : 2023-10-01 DOI: 10.7326/aimcc.2022.1087
Alastair K. Williams, Ryan J. Stubbins, Eric McGinnis, John A. Maguire, Persia Pourshahnazari, Claudie Roy, Luke Y.C. Chen, Thomas J. Nevill
{"title":"Neurologic Manifestations of Germline <i>GATA2</i> Deficiency: A Report of Two Cases","authors":"Alastair K. Williams, Ryan J. Stubbins, Eric McGinnis, John A. Maguire, Persia Pourshahnazari, Claudie Roy, Luke Y.C. Chen, Thomas J. Nevill","doi":"10.7326/aimcc.2022.1087","DOIUrl":"https://doi.org/10.7326/aimcc.2022.1087","url":null,"abstract":"Germline pathogenic mutations in the GATA2 gene, a critical transcription factor in hematopoietic and neurologic development, are known to cause various syndromes characterized by both hematopoietic (for example, monocytopenia, myelodysplastic syndrome) and extra-hematopoietic (for example, lymphedema, atypical and mycobacterial infections) manifestations. Neurologic features of this disease need to be better understood. We describe 2 patients with germline GATA2 deficiency who developed a progressive neurologic illness characterized by upper motor neuron weakness, bulbar and cerebellar dysfunction, pronounced white matter magnetic resonance imaging abnormalities, and noninfectious leukoencephalopathy with cerebellar degeneration. These neurologic findings may be a novel extra-hematopoietic manifestation of germline GATA2 deficiency.","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"7 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135811027","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
Invasive Squamous Cell Carcinoma of Anterior Mediastinum of Unknown Primary Site 原发部位未知的前纵隔浸润性鳞状细胞癌
Annals of internal medicine. Clinical cases Pub Date : 2023-09-01 DOI: 10.7326/aimcc.2023.0111
Bibek Koirala, Min Zhang, Ali Akalin
{"title":"Invasive Squamous Cell Carcinoma of Anterior Mediastinum of Unknown Primary Site","authors":"Bibek Koirala, Min Zhang, Ali Akalin","doi":"10.7326/aimcc.2023.0111","DOIUrl":"https://doi.org/10.7326/aimcc.2023.0111","url":null,"abstract":"The most common lesions in the anterior mediastinum are thymomas, lymphomas, teratomas, and thyroid masses. Squamous cell carcinoma of anterior mediastinum is most commonly due to thymic carcinoma. We present an unusual case of a patient presenting with anterior mediastinal mass that was later found to be biopsy-proven invasive squamous cell carcinoma of unknown primary site based on the available imaging studies. We also review the broad differential diagnoses, clinical presentation, and diagnostic work-up of anterior mediastinal mass, especially the one with no clear primary site.","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"21 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135387570","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
EBV Acalculous Cholecystitis Secondary to Cystic Duct Node Lymphadenitis With Positive EBER in Situ Hybridization EBV继发于囊管结淋巴结炎的无结石性胆囊炎伴原位杂交阳性
Annals of internal medicine. Clinical cases Pub Date : 2023-09-01 DOI: 10.7326/aimcc.2023.0589
Madeline Vithya Barnaba Durairaj, Samuel Addo, Rahul Sampath, Kyle David Burnette, Suneel Mohammed
{"title":"EBV Acalculous Cholecystitis Secondary to Cystic Duct Node Lymphadenitis With Positive EBER in Situ Hybridization","authors":"Madeline Vithya Barnaba Durairaj, Samuel Addo, Rahul Sampath, Kyle David Burnette, Suneel Mohammed","doi":"10.7326/aimcc.2023.0589","DOIUrl":"https://doi.org/10.7326/aimcc.2023.0589","url":null,"abstract":"Primary Epstein-Barr virus (EBV) infections are commonly subclinical and seen in adolescents. Although infectious mononucleosis is the most common manifestation, EBV has diverse manifestations within the gastrointestinal system. We describe a rare case of a 27-year-old woman with acute EBV acalculous cholecystitis and hepatitis secondary to cystic duct node lymphadenitis causing compression. EBV-encoded RNA in situ hybridization stained positive within sinusoids of liver and cystic duct lymphoid tissue but negative in gallbladder tissue. Work-up for a cause of hepatitis was negative except for serology confirming primary EBV infection. She underwent laparoscopic cholecystectomy, with a resolution of symptoms.","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":"13 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135387578","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
Hyperlipasemia Due to Duodenal Obstruction Secondary to Gastrostomy Tube Migration 胃造口管迁移继发于十二指肠阻塞引起的高脂血症
Annals of internal medicine. Clinical cases Pub Date : 2023-09-01 DOI: 10.7326/aimcc.2023.0482
S. Amin, Parth M. Desai, J. Altomare
{"title":"Hyperlipasemia Due to Duodenal Obstruction Secondary to Gastrostomy Tube Migration","authors":"S. Amin, Parth M. Desai, J. Altomare","doi":"10.7326/aimcc.2023.0482","DOIUrl":"https://doi.org/10.7326/aimcc.2023.0482","url":null,"abstract":"","PeriodicalId":72222,"journal":{"name":"Annals of internal medicine. Clinical cases","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42828901","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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