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Epitranscriptomic regulation via m6A RNA methylation: a determinant of cancer immunotherapy response. 通过m6A RNA甲基化的表转录组调控:癌症免疫治疗反应的决定因素。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004700
Syeda Tayyaba Batool, Umair Ali, Raghabendra Kumar Mahato
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引用次数: 0
Short-chain fatty acids (SCFAs) and the "Regulatory" B-cell: why fiber diet may reduce relapse in IgA vasculitis. 短链脂肪酸(SCFAs)和“调节性”b细胞:为什么纤维饮食可以减少IgA血管炎的复发。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004765
Fatima Zohra Ali, Eashaal Imtiaz, Riyasat Hamza Ali, Muhammad Shahmeer Khan, Raghabendra Kumar Mahato
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引用次数: 0
Augmented reality (AR) rehabilitation for homonymous hemianopia: 'prism-free' field expansion via smart glasses. 增强现实(AR)治疗同义性偏视:通过智能眼镜实现“无棱镜”视野扩展。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004750
Fatima Zohra Ali, Eashaal Imtiaz, Raghabendra Kumar Mahato, Mustabshirah Jadoon, Sofia Intikhab
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引用次数: 0
Intensive versus standard blood pressure management after endovascular therapy in acute ischemic stroke: a systematic review and meta-analysis. 急性缺血性卒中血管内治疗后强化与标准血压管理:一项系统回顾和荟萃分析。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004740
Fatima Sajjad, Maria Qadri, Ayesha Arshad, Iqra Shahid, Asad Iqbal, Zoya Riaz, Umama Alam, Ammara Rehman, Gul Rukh Noreen, Muhammad Abdullah Ali, Zaryab Bacha, Fathimathul Henna, Malaika Usman, Umama Rehman, Kamil Ahmad Kamil

Endovascular thrombectomy (EVT) has improved the therapy of acute ischemic stroke, patients still have functional impairments after reperfusion. This updated meta-analysis assesses whether intense blood pressure (BP) management following successful EVT enhances results and reduces problems associated with reperfusion. PubMed, Embase, and Cochrane databases were systematically searched using relevant keywords from inception until July 2025. A total of five studies were included after final screening. Outcomes were reported as excellent clinical outcomes, functional independence, all-cause mortality at 90 days, any intracranial hemorrhage within 24 h, etc. Interstudy heterogeneity was assessed using I 2 and X 2 statistics (I 2 > 50% = significant heterogeneity). Statistical calculations used Review Manager 5.4.1, with a P-value of <0.05 indicating statistical significance. A moderate but substantial improvement in neurological outcomes (mean National Institutes of Health Stroke Scale difference = 1.07; P = 0.03) and functional independence (mRS modified Rankin Scale 0-2) was both markedly enhanced by intensive BP control (RR = 0.82; 95% CI: 0.74-0.91; P = 0.0002). It did not, however, have a significant effect on all-cause death at 90 days, symptomatic or any cerebral bleeding, stroke recurrence, or excellent clinical outcomes (mRS 0-1). A significant correlation was seen between a greater incidence of hypotensive episodes and severe BP lowering (RR = 1.77; P < 0.00001). It also raises the risk of hypotension without reducing the danger of hemorrhage or death. Following EVT, intense BP control may enhance early neurological results and functional independence, but it also raises the risk of hypotension without reducing death or hemorrhage.

血管内取栓(EVT)改善了急性缺血性脑卒中的治疗,但患者在再灌注后仍存在功能障碍。这项最新的荟萃分析评估了EVT成功后的高血压(BP)管理是否能提高结果并减少与再灌注相关的问题。PubMed、Embase和Cochrane数据库使用相关关键词进行系统检索,检索时间从数据库建立到2025年7月。最终筛选后共纳入5项研究。结果报告为良好的临床结果,功能独立性,90天全因死亡率,24小时内无颅内出血等。使用i2和x2统计量评估研究间异质性(i2 bb0 50% =显著异质性)。使用Review Manager 5.4.1进行统计计算,P值为P = 0.03),强化血压控制显著提高了功能独立性(mRS修正Rankin量表0-2)(RR = 0.82; 95% CI: 0.74-0.91; P = 0.0002)。然而,它对90天全因死亡、症状性或任何脑出血、中风复发或优秀临床结果(mRS 0-1)没有显著影响。低血压发作发生率增高与严重降压之间存在显著相关性(RR = 1.77; P < 0.00001)。它还会增加低血压的风险,而不会降低出血或死亡的危险。在EVT后,强烈的血压控制可能会提高早期神经学结果和功能独立性,但也会增加低血压的风险,而不会减少死亡或出血。
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引用次数: 0
Heart failure and tobacco use disorder: mortality trends and disparities in the United States. 心力衰竭和烟草使用障碍:美国的死亡率趋势和差异。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004729
Affaf Mahmood, Farah Latif, Sana Latif, David N Smith, Biruk D Ayalew, Adarsh Raja, Sumet Kumar, Neeraj Kumar, Kuldeep D Rai, Aneesh K Sangtiani, Tanzeela Khan, Hafsa Hanif, Laksh Kumar, Abdullah Bs, Aayush Chaulagain

Introduction: Tobacco use disorder is associated with increased morbidity and mortality from heart failure (HF) in the United States. Despite this burden, long-term trends in HF mortality among tobacco users and the extent of demographic and geographic disparities remain poorly understood, limiting targeted prevention and intervention strategies. This study examines these trends and disparities using the CDC WONDER database.

Methods: Mortality data from 2003 to 2020 were analyzed for individuals aged ≥25 years with tobacco use disorder who died from HF. Age-adjusted mortality rates (AAMRs) per 100 000 general population were calculated. Joinpoint regression estimated annual percentage changes. Subgroup analyses were conducted by sex, race/ethnicity, region, and rural-urban classification.

Results: From 2003 to 2020, 576 781 HF deaths occurred among tobacco users aged ≥25 years. The overall AAMR nearly quadrupled during this period. Men consistently exhibited higher AAMRs than women. Among racial/ethnic groups, American Indians or Alaska Natives had the highest rates, followed by Whites, Blacks, and Asian or Pacific Islanders. Regionally, the Midwest recorded the highest mortality, followed by the South, Northeast, and West. Rural populations had higher AAMRs than urban populations. At the state level, Oregon showed the highest AAMR, while California had the lowest.

Conclusion: The sharp rise in HF mortality among tobacco users underscores critical public health gaps. Disparities were most pronounced among men, American Indians or Alaska Natives, Midwestern residents, and rural populations. By identifying high-risk populations and regions, this study provides actionable insights to guide targeted interventions, tobacco cessation programs, and equitable healthcare access, helping to address the growing burden of HF in tobacco users.

在美国,烟草使用障碍与心力衰竭(HF)的发病率和死亡率增加有关。尽管存在这种负担,但烟草使用者心力衰竭死亡率的长期趋势以及人口和地理差异的程度仍然知之甚少,这限制了有针对性的预防和干预战略。本研究使用CDC WONDER数据库检查了这些趋势和差异。方法:分析2003 - 2020年年龄≥25岁的烟草使用障碍患者死于心衰的死亡率数据。计算每10万普通人口的年龄调整死亡率(AAMRs)。接合点回归估计年百分比变化。亚组分析按性别、种族/民族、地区和城乡分类进行。结果:从2003年到2020年,年龄≥25岁的烟草使用者中发生了577681例HF死亡。在此期间,总体AAMR几乎翻了两番。男性的aamr始终高于女性。在种族/民族群体中,美国印第安人或阿拉斯加原住民的发病率最高,其次是白人、黑人、亚洲人或太平洋岛民。从地区来看,中西部地区的死亡率最高,其次是南部、东北部和西部。农村人口aamr高于城市人口。在州一级,俄勒冈州的AAMR最高,而加利福尼亚州最低。结论:烟草使用者心衰死亡率的急剧上升凸显了严重的公共卫生缺口。差异在男性、美洲印第安人或阿拉斯加原住民、中西部居民和农村人口中最为明显。通过确定高危人群和地区,本研究为指导有针对性的干预措施、戒烟计划和公平的医疗服务提供了可行的见解,有助于解决烟草使用者日益增加的心衰负担。
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引用次数: 0
Novel prone retroperitoneal robotic-assisted approach for bilateral partial nephrectomy: a case report. 新型俯卧后腹膜机器人辅助双侧肾部分切除术1例报告。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004716
Qingyu Ge, Guanqun Ju, Chuanmin Chu, Xinyu Zhai, Mingyue Tan, Dongliang Xu

Introduction and importance: Partial nephrectomy is the standard surgical technique for the management of early-stage renal neoplasms. Bilateral synchronous sporadic renal tumors are a rare subtype of renal tumors, for which no consensus has been reached on the optimal surgical strategy.

Case presentation: A 73-year-old man was diagnosed with bilateral renal masses. Owing to a history of prior abdominal surgeries and underlying medical conditions, including ankylosing spondylitis, we herein report for the first time the performance of robotic-assisted one-stage bilateral partial nephrectomy in the prone position. No severe intraoperative or postoperative complications or renal failure were observed, and the patient achieved a satisfactory recovery at the 3-month postoperative follow-up.

Clinical discussion: Conventional partial nephrectomy via either transperitoneal or retroperitoneal approaches has been performed in the lateral decubitus position. For patients with bilateral renal tumors, this approach necessitates intraoperative repositioning, while prolonged lateral decubitus may compromise respiratory function and cause compression of peripheral nerves. In contrast, the prone position approach not only resolves these issues but also simplifies the surgical procedure and provides greater benefits to patients.

Conclusion: Prone retroperitoneal robotic assisted partial nephrectomy is a novel approach for the management of BSSRCC, and expanded samples and large-scale clinical studies are warranted to confirm the safety and feasibility of this surgical technique in future investigations.

简介及重要性:肾部分切除术是治疗早期肾肿瘤的标准手术技术。双侧同步散发性肾肿瘤是一种罕见的肾肿瘤亚型,对于其最佳手术策略尚未达成共识。病例介绍:一名73岁男性被诊断为双侧肾肿块。由于既往腹部手术史和潜在的医疗条件,包括强直性脊柱炎,我们在此首次报道机器人辅助俯卧位一期双侧部分肾切除术的表现。无严重术中、术后并发症及肾功能衰竭,术后随访3个月,患者恢复良好。临床讨论:经腹膜或腹膜后入路的常规肾部分切除术已在侧卧位进行。对于双侧肾肿瘤患者,这种入路需要术中重新定位,而长时间侧卧可能损害呼吸功能并导致周围神经受压。相比之下,俯卧位入路不仅解决了这些问题,而且简化了手术程序,为患者提供了更大的好处。结论:俯卧式腹膜后机器人辅助部分肾切除术是治疗BSSRCC的一种新方法,在未来的研究中,需要扩大样本和大规模的临床研究来证实该手术技术的安全性和可行性。
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引用次数: 0
Mortality trends for chronic kidney disease and dementia in the United States, 1999-2020: a 22-year retrospective analysis. 1999-2020年美国慢性肾脏疾病和痴呆死亡率趋势:22年回顾性分析
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004761
Muhammad S Ahmad, Sarmad Imran, Muhammad A Kamal, Archi Mehta, Iqra Nawaz, Iman O Abufatima, Abdulhadi M A Mahgoub, Mohammedsadeq A Shweliya

Background: Chronic kidney disease (CKD) and dementia are major causes of morbidity and mortality among older adults and frequently coexist due to shared vascular and metabolic risk factors. Despite their clinical importance, national mortality trends for these conditions remain underexplored. This study aimed to examine temporal and demographic patterns of mortality among individuals with coexisting CKD and dementia in the United States from 1999 to 2020.

Methods: In this retrospective, population-based study, mortality data for adults aged ≥25 years were extracted from the Centers for Disease Control and Prevention's Wide-ranging Online Data for Epidemiologic Research database. Deaths listing both CKD [International Statistical Classification of Diseases and Related Health Problems, 10th Revision (ICD-10 N18.x)] and dementia (ICD-10 F01.x, F03, G30.x) as causes were included. Age-adjusted mortality rates (AAMRs) per 100 000 were calculated using the 2000 U.S. standard population. Temporal trends were analyzed using Joinpoint regression to estimate annual percent change and average annual percent change (AAPC) with P < 0.05 considered significant. Subgroup analyses were stratified by gender, race/ethnicity, age, region, and urbanization.

Results: Between 1999 and 2020, 170 375 deaths were attributed to CKD and dementia. The overall AAMR increased from 1.03 to 5.92 per 100 000 (AAPC 7.41%). Mortality increased significantly across both genders, older adults, and all census regions, peaking in 2012, briefly declining between 2012 and 2015, then rising during 2015 to 2020. Males had higher mortality (AAMR 4.24) than females (3.16). Non-Hispanic Black individuals exhibited the highest rate (6.20), followed by non-Hispanic White (3.35) and Hispanic (3.09) populations. The Midwest showed the highest regional burden (AAMR 3.90), while rural counties recorded greater mortality (3.89) than urban areas (3.49).

Conclusion: The increasing mortality trends show a close relationship between CKD and dementia. Thus, improving early diagnosis, ensuring equal access to care, and providing a holistic treatment approach targeting both the organs is key to enhancing optimal patient care and consequently reducing mortality.

背景:慢性肾脏疾病(CKD)和痴呆是老年人发病和死亡的主要原因,由于共同的血管和代谢危险因素,它们经常共存。尽管具有临床重要性,但这些疾病的全国死亡率趋势仍未得到充分探讨。本研究旨在研究1999年至2020年美国慢性肾病和痴呆患者死亡率的时间和人口统计学模式。方法:在这项基于人群的回顾性研究中,年龄≥25岁的成年人的死亡率数据从疾病控制和预防中心的广泛在线流行病学研究数据数据库中提取。CKD[国际疾病和相关健康问题统计分类,第十次修订版(ICD-10 N18)]。x)]和痴呆(ICD-10 F01)。x, F03, G30X),因为原因包括在内。使用2000年美国标准人口计算每10万人的年龄调整死亡率(AAMRs)。使用Joinpoint回归分析时间趋势,估计年百分比变化和平均年百分比变化(AAPC)与P。结果:1999年至2020年,17375例死亡归因于CKD和痴呆。总体AAMR从1.03 / 10万增加到5.92 / 10万(AAPC为7.41%)。男女、老年人和所有人口普查地区的死亡率都显著上升,在2012年达到顶峰,在2012年至2015年期间短暂下降,然后在2015年至2020年期间上升。男性死亡率(AAMR 4.24)高于女性(3.16)。非西班牙裔黑人的发病率最高(6.20),其次是非西班牙裔白人(3.35)和西班牙裔人群(3.09)。中西部地区的地区负担最高(AAMR为3.90),农村地区的死亡率(3.89)高于城市地区(3.49)。结论:CKD死亡率上升趋势与痴呆密切相关。因此,改善早期诊断,确保平等获得护理,并提供针对这两个器官的整体治疗方法,是加强最佳患者护理并从而降低死亡率的关键。
{"title":"Mortality trends for chronic kidney disease and dementia in the United States, 1999-2020: a 22-year retrospective analysis.","authors":"Muhammad S Ahmad, Sarmad Imran, Muhammad A Kamal, Archi Mehta, Iqra Nawaz, Iman O Abufatima, Abdulhadi M A Mahgoub, Mohammedsadeq A Shweliya","doi":"10.1097/MS9.0000000000004761","DOIUrl":"https://doi.org/10.1097/MS9.0000000000004761","url":null,"abstract":"<p><strong>Background: </strong>Chronic kidney disease (CKD) and dementia are major causes of morbidity and mortality among older adults and frequently coexist due to shared vascular and metabolic risk factors. Despite their clinical importance, national mortality trends for these conditions remain underexplored. This study aimed to examine temporal and demographic patterns of mortality among individuals with coexisting CKD and dementia in the United States from 1999 to 2020.</p><p><strong>Methods: </strong>In this retrospective, population-based study, mortality data for adults aged ≥25 years were extracted from the Centers for Disease Control and Prevention's Wide-ranging Online Data for Epidemiologic Research database. Deaths listing both CKD [International Statistical Classification of Diseases and Related Health Problems, 10th Revision (ICD-10 N18.x)] and dementia (ICD-10 F01.x, F03, G30.x) as causes were included. Age-adjusted mortality rates (AAMRs) per 100 000 were calculated using the 2000 U.S. standard population. Temporal trends were analyzed using Joinpoint regression to estimate annual percent change and average annual percent change (AAPC) with <i>P</i> < 0.05 considered significant. Subgroup analyses were stratified by gender, race/ethnicity, age, region, and urbanization.</p><p><strong>Results: </strong>Between 1999 and 2020, 170 375 deaths were attributed to CKD and dementia. The overall AAMR increased from 1.03 to 5.92 per 100 000 (AAPC 7.41%). Mortality increased significantly across both genders, older adults, and all census regions, peaking in 2012, briefly declining between 2012 and 2015, then rising during 2015 to 2020. Males had higher mortality (AAMR 4.24) than females (3.16). Non-Hispanic Black individuals exhibited the highest rate (6.20), followed by non-Hispanic White (3.35) and Hispanic (3.09) populations. The Midwest showed the highest regional burden (AAMR 3.90), while rural counties recorded greater mortality (3.89) than urban areas (3.49).</p><p><strong>Conclusion: </strong>The increasing mortality trends show a close relationship between CKD and dementia. Thus, improving early diagnosis, ensuring equal access to care, and providing a holistic treatment approach targeting both the organs is key to enhancing optimal patient care and consequently reducing mortality.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"88 2","pages":"1264-1274"},"PeriodicalIF":1.6,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12889323/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146163818","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
A 65-year-old male with phosphaturic mesenchymal tumor presenting as tumor-induced osteomalacia: a case report. 65岁男性磷化间充质肿瘤表现为肿瘤诱导的骨软化症1例。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004727
Hamza Khaiata, Feras Abo Dala, Rawan Alahmad, Abdulrahman Kmaleh, Nour Alhamod, Bilal Sleiay

Introduction and importance: Tumor-induced osteomalacia (TIO) is a rare paraneoplastic disorder caused by phosphaturic mesenchymal tumors (PMTs), characterized by chronic hypophosphatemia and impaired bone mineralization.

Case presentation: A 65-year-old man presented with progressive bone pain lasting 3 years. Laboratory results showed persistent hypophosphatemia and elevated fibroblast growth factor 23. Imaging revealed a hypermetabolic lesion in the left acetabulum. The tumor was surgically resected, and histology confirmed a spindle cell neoplasm without vascular invasion. Serum phosphorus normalized postoperatively, and the patient showed sustained clinical improvement over 1 year.

Clinical discussion: This case underscores the diagnostic challenges of TIO, often mimicking other metabolic bone diseases and leading to significant delays. Compared with similar reports, our case highlights the utility of combined positron emission tomography and magnetic resonance imaging in localizing PMTs and the dramatic clinical improvement following resection.

Conclusion: This case underscores the importance of recognizing TIO early to enable effective treatment and avoid prolonged morbidity.

肿瘤诱导骨软化症(TIO)是一种罕见的由磷质间充质肿瘤(pmt)引起的副肿瘤疾病,以慢性低磷血症和骨矿化受损为特征。病例介绍:一名65岁男性,表现为持续3年的进行性骨痛。实验室结果显示持续性低磷血症和成纤维细胞生长因子23升高。影像学显示左髋臼有高代谢性病变。手术切除肿瘤,组织学证实为梭形细胞肿瘤,无血管浸润。术后血清磷恢复正常,患者临床持续改善1年以上。临床讨论:该病例强调了TIO的诊断挑战,通常模仿其他代谢性骨病并导致显著延迟。与类似的报道相比,本病例强调了正电子发射断层扫描和磁共振成像在定位pmt方面的应用,以及切除后显著的临床改善。结论:本病例强调了早期发现TIO的重要性,以便有效治疗,避免长期发病。
{"title":"A 65-year-old male with phosphaturic mesenchymal tumor presenting as tumor-induced osteomalacia: a case report.","authors":"Hamza Khaiata, Feras Abo Dala, Rawan Alahmad, Abdulrahman Kmaleh, Nour Alhamod, Bilal Sleiay","doi":"10.1097/MS9.0000000000004727","DOIUrl":"https://doi.org/10.1097/MS9.0000000000004727","url":null,"abstract":"<p><strong>Introduction and importance: </strong>Tumor-induced osteomalacia (TIO) is a rare paraneoplastic disorder caused by phosphaturic mesenchymal tumors (PMTs), characterized by chronic hypophosphatemia and impaired bone mineralization.</p><p><strong>Case presentation: </strong>A 65-year-old man presented with progressive bone pain lasting 3 years. Laboratory results showed persistent hypophosphatemia and elevated fibroblast growth factor 23. Imaging revealed a hypermetabolic lesion in the left acetabulum. The tumor was surgically resected, and histology confirmed a spindle cell neoplasm without vascular invasion. Serum phosphorus normalized postoperatively, and the patient showed sustained clinical improvement over 1 year.</p><p><strong>Clinical discussion: </strong>This case underscores the diagnostic challenges of TIO, often mimicking other metabolic bone diseases and leading to significant delays. Compared with similar reports, our case highlights the utility of combined positron emission tomography and magnetic resonance imaging in localizing PMTs and the dramatic clinical improvement following resection.</p><p><strong>Conclusion: </strong>This case underscores the importance of recognizing TIO early to enable effective treatment and avoid prolonged morbidity.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"88 2","pages":"2057-2060"},"PeriodicalIF":1.6,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12889496/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146163485","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
First case of IgA vasculitis atypically presenting as recurrent gastroenteritis from Nepal: a case report and review of the literature. 第一例IgA血管炎的非典型表现为复发性肠胃炎从尼泊尔:一个病例报告和文献回顾。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004758
Sanjay Dhungana, Bipin Bashyal, Jenish Adhikari, Mukunda Thakur, Rahul Shakya, Sujan Sharma, Anish Paudyal, Sachin Bhatta, Sphurna Karki, Santosh Pandey, Rabin Baniya, Sandesh Shah

Introduction and importance: Immunoglobulin A vasculitis (IgAV), though primarily a childhood disease, is uncommon in adults and often presents atypically, leading to diagnostic delays. We report the first known case of adult-onset IgAV from Nepal, presenting as recurrent episodes of acute gastroenteritis. The delayed appearance of purpuric rash - nearly a year after symptom onset - and the rapid response to oral corticosteroids make this case unique and thus add to the existing literature on adult IgAV.

Case presentation: A 57-year-old male presented with 4 days of purpuric rash, abdominal pain, and loose stools. He reported five similar gastroenteritis-like episodes over the prior year, resolving temporarily with antibiotics. Examination revealed palpable purpuric lesions on limbs and trunk. IgAV was diagnosed clinically per EULAR/PRINTO/PRES criteria. Oral prednisolone (60 mg/day) with gastric protection led to complete symptom resolution within 1 week. Antibiotics were discontinued after negative stool cultures. Steroids were tapered over 2 months without relapse.

Clinical discussion: IgAV presents with purpura, abdominal pain, arthralgia, and renal involvement. Diagnosis is often delayed in adults due to atypical symptoms and the absence of rash. Early corticosteroid therapy is effective even without biopsy confirmation in resource-constrained settings. This case underscores the importance of considering IgAV in recurrent gastrointestinal complaints and highlights the effectiveness of corticosteroids, emphasizing the need for clinical vigilance.

Conclusion: IgAV should be considered in adults with unexplained recurrent abdominal pain. Early recognition of the condition, even before the skin manifestations, can significantly improve the prognosis and patient outcome.

免疫球蛋白A血管炎(IgAV),虽然主要是一种儿童疾病,但在成人中并不常见,通常表现为非典型,导致诊断延迟。我们报告第一例已知的尼泊尔成人发病IgAV病例,表现为急性肠胃炎的反复发作。紫癜性皮疹的延迟出现-在症状出现近一年之后-以及口服皮质类固醇的快速反应使该病例独特,从而增加了关于成人IgAV的现有文献。病例介绍:一名57岁男性,表现为4天的紫癜疹、腹痛和稀便。在过去的一年里,他报告了五次类似的肠胃炎样发作,用抗生素暂时缓解。检查发现四肢和躯干有可触及的紫癜性病变。IgAV临床诊断符合EULAR/PRINTO/PRES标准。口服强的松龙(60mg /天)加胃保护可在1周内完全缓解症状。粪便培养阴性后停用抗生素。类固醇逐渐减少超过2个月没有复发。临床讨论:IgAV表现为紫癜、腹痛、关节痛和肾脏受累。由于非典型症状和无皮疹,成人的诊断常常延迟。在资源有限的情况下,即使没有活检证实,早期皮质类固醇治疗也是有效的。本病例强调了在胃肠道复发性疾病中考虑IgAV的重要性,并强调了皮质类固醇的有效性,强调了临床警惕的必要性。结论:成人不明原因复发性腹痛应考虑IgAV。早期识别病情,甚至在皮肤表现之前,可以显著改善预后和患者预后。
{"title":"First case of IgA vasculitis atypically presenting as recurrent gastroenteritis from Nepal: a case report and review of the literature.","authors":"Sanjay Dhungana, Bipin Bashyal, Jenish Adhikari, Mukunda Thakur, Rahul Shakya, Sujan Sharma, Anish Paudyal, Sachin Bhatta, Sphurna Karki, Santosh Pandey, Rabin Baniya, Sandesh Shah","doi":"10.1097/MS9.0000000000004758","DOIUrl":"https://doi.org/10.1097/MS9.0000000000004758","url":null,"abstract":"<p><strong>Introduction and importance: </strong>Immunoglobulin A vasculitis (IgAV), though primarily a childhood disease, is uncommon in adults and often presents atypically, leading to diagnostic delays. We report the first known case of adult-onset IgAV from Nepal, presenting as recurrent episodes of acute gastroenteritis. The delayed appearance of purpuric rash - nearly a year after symptom onset - and the rapid response to oral corticosteroids make this case unique and thus add to the existing literature on adult IgAV.</p><p><strong>Case presentation: </strong>A 57-year-old male presented with 4 days of purpuric rash, abdominal pain, and loose stools. He reported five similar gastroenteritis-like episodes over the prior year, resolving temporarily with antibiotics. Examination revealed palpable purpuric lesions on limbs and trunk. IgAV was diagnosed clinically per EULAR/PRINTO/PRES criteria. Oral prednisolone (60 mg/day) with gastric protection led to complete symptom resolution within 1 week. Antibiotics were discontinued after negative stool cultures. Steroids were tapered over 2 months without relapse.</p><p><strong>Clinical discussion: </strong>IgAV presents with purpura, abdominal pain, arthralgia, and renal involvement. Diagnosis is often delayed in adults due to atypical symptoms and the absence of rash. Early corticosteroid therapy is effective even without biopsy confirmation in resource-constrained settings. This case underscores the importance of considering IgAV in recurrent gastrointestinal complaints and highlights the effectiveness of corticosteroids, emphasizing the need for clinical vigilance.</p><p><strong>Conclusion: </strong>IgAV should be considered in adults with unexplained recurrent abdominal pain. Early recognition of the condition, even before the skin manifestations, can significantly improve the prognosis and patient outcome.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"88 2","pages":"2067-2072"},"PeriodicalIF":1.6,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12889422/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146163740","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
Advancing hypoparathyroidism treatment: FDA approval of Palopegteriparatide as a promising orphan drug. 推进甲状旁腺功能减退症的治疗:FDA批准Palopegteriparatide作为有前途的孤儿药。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 eCollection Date: 2026-02-01 DOI: 10.1097/MS9.0000000000004734
Syeda Rabiah Shahid, Kamran Shahid, Sikandar Ehsan, Maliha Khalid, Aminath Waafira

Hypoparathyroidism (HypoPT) is a rare endocrine disorder characterized by insufficient parathyroid hormone (PTH) levels, leading to hypocalcemia and hyperphosphatemia. Affecting approximately 70 000-90 000 individuals in the United States, HypoPT can arise from genetic mutations or, most commonly, as a result of surgical removal of the parathyroid glands. Traditional treatments involve calcium and vitamin D supplementation, which can pose long-term risks such as renal complications. On 9 August 2024, the U.S. Food and Drug Administration (FDA) approved Palopegteriparatide (Yorvipath, Ascendis, Denmark), a synthetic long-acting PTH analog, for subcutaneous use in adult patients with chronic HypoPT. Palopegteriparatide is designed as a pro-drug that undergoes auto-cleavage, offering sustained release and prolonged systemic exposure to recombinant PTH (1-34). Clinical trials have demonstrated its ability to maintain normocalcemia with minimal need for supplemental calcium or vitamin D. The treatment also showed a favorable safety profile, with mild transient side effects and no significant toxicity. Unlike standard-of-care therapies, Palopegteriparatide maintains balanced calcium-phosphate levels with less renal strain, making it a particularly promising option for patients with compromised kidney function. Although concerns remain regarding long-term safety, its FDA approval and orphan drug designation underscore its importance in addressing the unmet therapeutic needs of HypoPT. Continued investigation is warranted to optimize patient outcomes and further define its risk-benefit profile. This approval marks a critical milestone in endocrine therapeutics and offers renewed hope for patients struggling with the burdens of chronic HypoPT.

甲状旁腺功能减退症(HypoPT)是一种罕见的内分泌疾病,其特征是甲状旁腺激素(PTH)水平不足,导致低钙血症和高磷血症。在美国,大约有7万到9万人患有HypoPT,可能是由基因突变引起的,或者最常见的是由于手术切除甲状旁腺所致。传统的治疗方法包括补充钙和维生素D,这可能会带来肾脏并发症等长期风险。2024年8月9日,美国食品和药物管理局(FDA)批准Palopegteriparatide (Yorvipath, Ascendis, Denmark),一种合成长效甲状旁腺激素类似物,用于成人慢性HypoPT患者的皮下治疗。Palopegteriparatide被设计为一种经过自动切割的前药,提供持续释放和长时间的系统暴露于重组PTH(1-34)。临床试验已经证明它能够维持正常的钙血症,而不需要补充钙或维生素d。这种治疗也显示出良好的安全性,有轻微的短暂副作用,没有明显的毒性。与标准治疗方法不同,Palopegteriparatide维持平衡的磷酸钙水平,肾脏负荷较小,使其成为肾功能受损患者特别有希望的选择。尽管对长期安全性的担忧仍然存在,但其FDA批准和孤儿药指定强调了其在解决HypoPT未满足的治疗需求方面的重要性。有必要继续研究以优化患者预后并进一步确定其风险-收益概况。这一批准标志着内分泌治疗的一个重要里程碑,为与慢性HypoPT负担作斗争的患者带来了新的希望。
{"title":"Advancing hypoparathyroidism treatment: FDA approval of Palopegteriparatide as a promising orphan drug.","authors":"Syeda Rabiah Shahid, Kamran Shahid, Sikandar Ehsan, Maliha Khalid, Aminath Waafira","doi":"10.1097/MS9.0000000000004734","DOIUrl":"https://doi.org/10.1097/MS9.0000000000004734","url":null,"abstract":"<p><p>Hypoparathyroidism (HypoPT) is a rare endocrine disorder characterized by insufficient parathyroid hormone (PTH) levels, leading to hypocalcemia and hyperphosphatemia. Affecting approximately 70 000-90 000 individuals in the United States, HypoPT can arise from genetic mutations or, most commonly, as a result of surgical removal of the parathyroid glands. Traditional treatments involve calcium and vitamin D supplementation, which can pose long-term risks such as renal complications. On 9 August 2024, the U.S. Food and Drug Administration (FDA) approved Palopegteriparatide (Yorvipath, Ascendis, Denmark), a synthetic long-acting PTH analog, for subcutaneous use in adult patients with chronic HypoPT. Palopegteriparatide is designed as a pro-drug that undergoes auto-cleavage, offering sustained release and prolonged systemic exposure to recombinant PTH (1-34). Clinical trials have demonstrated its ability to maintain normocalcemia with minimal need for supplemental calcium or vitamin D. The treatment also showed a favorable safety profile, with mild transient side effects and no significant toxicity. Unlike standard-of-care therapies, Palopegteriparatide maintains balanced calcium-phosphate levels with less renal strain, making it a particularly promising option for patients with compromised kidney function. Although concerns remain regarding long-term safety, its FDA approval and orphan drug designation underscore its importance in addressing the unmet therapeutic needs of HypoPT. Continued investigation is warranted to optimize patient outcomes and further define its risk-benefit profile. This approval marks a critical milestone in endocrine therapeutics and offers renewed hope for patients struggling with the burdens of chronic HypoPT.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"88 2","pages":"1209-1212"},"PeriodicalIF":1.6,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12889382/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146163459","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
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