Oxford Medical Case Reports最新文献_第10页

When the farm turns fatal: a rare infection causing heart block. 当农场变得致命时：一种罕见的感染导致心脏传导阻滞。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omaf010

Shaun Abid, Anton Stolear, Maxim Dulgher, Samdish Sethi, Stuart Zarich

引用次数: 0

Pulmonary amyloidosis: a case report. 肺淀粉样变1例。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omaf007

Fenna Ahsino, Mouad Al Moudni, Jamal Eddine Bourkadi, Karima Marc

引用次数: 0

Impact of selegiline on ¹²³I-meta-iodobenzylguanidine myocardial scintigraphy. selegiline对123i -间碘苄基胍心肌显像的影响。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omae212

Katsuya Nishida

引用次数: 0

Long-term follow-up of vasculitis with metal allergy after cerebrovascular coil embolization. 脑血管圈栓塞后血管炎伴金属过敏的长期随访。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omaf004

Yukiko Takakuwa, Seido Ooka, Nobuyuki Endo, Hisao Nakamura, Tatsuro Okano, Tomomitsu Miyagaki, Takafumi Kadono, Kimito Kawahata

{"title":"Long-term follow-up of vasculitis with metal allergy after cerebrovascular coil embolization.","authors":"Yukiko Takakuwa, Seido Ooka, Nobuyuki Endo, Hisao Nakamura, Tatsuro Okano, Tomomitsu Miyagaki, Takafumi Kadono, Kimito Kawahata","doi":"10.1093/omcr/omaf004","DOIUrl":"10.1093/omcr/omaf004","url":null,"abstract":"Interventional treatment using catheters, particularly coil embolization, is a common therapy for cerebral aneurysms. While generally safe, complications such as allergic vasculitis due to metal allergies can occur. We report the case of a 57-year-old Japanese woman who developed vasculitis after undergoing coil embolization for a cerebral aneurysm. Two days post-procedure, she presented with left-sided facial paralysis, paresis, and hearing loss. MRI revealed multiple small lesions, and vasculitis due to metal allergy was suspected. Treatment with steroids led to improvement, and steroid therapy was tapered off within a year. Allergy tests performed post-treatment identified a positive reaction to the GDC coil and potassium dichromate but not to nickel or platinum. Unfortunately, recurrent vasculitis lesions were detected following the patch test. This case highlights the importance of considering metal allergies before coil embolization and the potential risks of allergy testing after the procedure.","PeriodicalId":45318,"journal":{"name":"Oxford Medical Case Reports","volume":"2025 4","pages":"omaf004"},"PeriodicalIF":0.5,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11952890/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143754718","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Oral contraceptive pill-induced esophagitis: a rare cause of pill esophagitis in a Rwandan woman. 口服避孕药引起的食管炎：一名卢旺达妇女的罕见原因。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omaf001

Gordon P Bensen, Matthew R Bryan, Esther Nishimwe, Bao Sean Nguyen, Kenechukwu Chudy-Onwugaje

引用次数: 0

Aase-Smith syndrome type 2 with new neurological findings. 有新的神经学发现的2型Aase-Smith综合征。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omaf006

Sarah Aljarad, Ahmad Alhamid, Hamdah Hanifa, Obada Zayegh, Jamal Ataya, Ziad Aljarad

引用次数: 0

Unmasking the uncommon: retroperitoneal Leiomyosarcoma case report. 揭露不寻常：腹膜后平滑肌肉瘤病例报告。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omaf002

Boujguenna Imane, Mohammed Essaid Ramraoui, Fatima Boukis, Faisal ElMouhafid

引用次数: 0

Diagnostic evaluation and management of pulmonary hypertension with concomitant incidental partial anomalous pulmonary venous return. 肺动脉高压伴发偶发部分肺静脉回流异常的诊断评价与治疗。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omae214

Isaac K S Ng, Christopher Thong, Gaurav Deep Singh, Peter Daniel, Kei Jun Poon, Ching Ching Ong, Adrian C L Kee

{"title":"Diagnostic evaluation and management of pulmonary hypertension with concomitant incidental partial anomalous pulmonary venous return.","authors":"Isaac K S Ng, Christopher Thong, Gaurav Deep Singh, Peter Daniel, Kei Jun Poon, Ching Ching Ong, Adrian C L Kee","doi":"10.1093/omcr/omae214","DOIUrl":"10.1093/omcr/omae214","url":null,"abstract":"Partial anomalous pulmonary venous return (PAPVR) is a rare congenital heart condition which is often asymptomatic and hence remains undiagnosed, but could occasionally be detected on thoracic imaging as an incidental finding. For rare cases of newly diagnosed pulmonary hypertension with concurrent PAPVRs, the diagnostic workup and subsequent management are more complicated, requiring a thorough evaluation of secondary causes of pulmonary hypertension, and assessing relative PAPVR shunt contribution to the pulmonary hypertension. We herein report a case of a 74-year-old Chinese male patient, a chronic smoker of 50 pack-years, and past medical history of hypertension and diabetes mellitus, who was admitted to our intensive care unit with acute decompensated type 2 respiratory failure, and subsequently found to have newly diagnosed pulmonary hypertension with right heart failure and an incidental PAPVR identified on inadvertent central venous cannulation (CVC) of the anomalous pulmonary vein draining into the left internal jugular vein. There are a few key learning points from this case study: firstly, we profile the characteristics and clinical outcomes of cases of incidental CVC cannulation of undiagnosed PAPVR from a literature review; and secondly, we discuss the diagnostic and management approach to newly diagnosed pulmonary hypertension with concomitant, incidental PAPVR that may be useful for internists and critical care physicians.","PeriodicalId":45318,"journal":{"name":"Oxford Medical Case Reports","volume":"2025 4","pages":"omae214"},"PeriodicalIF":0.5,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11952895/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143754697","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Case report of atypical presentation of Bartter's syndrome: hypertension and Hypokalemic nephropathy in a female patient. 巴特氏综合征的不典型表现的病例报告：高血压和低钾血症肾病的女性患者。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omae215

Emad A Odeh, Jaber H Jaradat, Raghad Amro, Seif Jankhout, Abdulqadir J Nashwan

{"title":"Case report of atypical presentation of Bartter's syndrome: hypertension and Hypokalemic nephropathy in a female patient.","authors":"Emad A Odeh, Jaber H Jaradat, Raghad Amro, Seif Jankhout, Abdulqadir J Nashwan","doi":"10.1093/omcr/omae215","DOIUrl":"10.1093/omcr/omae215","url":null,"abstract":"Bartter's syndrome (BS) is a rare hereditary disorder characterized by tubulopathies that affect salt reabsorption in the thick ascending limb of the Henle's loop. While BS typically presents with electrolyte imbalances and normal blood pressure, atypical presentations can complicate its diagnosis and management. We report the case of a 21-year-old female with BS diagnosed clinically at birth who presented with cough, vomiting, and elevated blood pressure. Despite a positive family history of BS, her presentation was unique with hypertension and hypokalemic nephropathy. Diagnostic evaluations during hospital admission revealed electrolyte imbalances, kidney dysfunction, and renal histopathological findings that were consistent with hypokalemic nephropathy. This case highlights the diverse clinical manifestations and potential complications of BS and emphasizes the importance of thorough evaluation and multidisciplinary management. Further research is needed to elucidate the underlying mechanisms linking BS with hypertension and hypokalemic nephropathy, and to guide targeted therapeutic strategies for complex presentations.","PeriodicalId":45318,"journal":{"name":"Oxford Medical Case Reports","volume":"2025 4","pages":"omae215"},"PeriodicalIF":0.5,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11952896/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143754696","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Neuroendocrine carcinoma causing common bile duct obstruction: a case report. 神经内分泌癌致胆总管梗阻1例。

IF 0.5

Oxford Medical Case Reports Pub Date : 2025-03-28 eCollection Date: 2025-04-01 DOI: 10.1093/omcr/omaf011

Richard Shamoon, Osman Elhassan, Lujain Al-Emadi, Abdulwahab Zabara, Mahir A Petkar, Sarah Sayed, Osama H Mohammad

引用次数: 0