Ashton L. Rogers, Alexander Burnett, Peter Eckard, Soroush Farsi, James R. Gardner, John L. Dornhoffer, Robert A. Saadi
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Study validity was assessed using the Joanna Briggs institute's critical appraisal tools and AMSTAR 2 criteria.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Seventeen cases (eight males and nine females) met inclusion criteria for analysis. On average, they presented at 59.7 (± 21.4) years old with sudden dysphagia (76.5%), anterior neck swelling (64.7%), neck pain (58.8%), and dysphonia (41.2%). Notably, 4 (23.5%) patients were taking an antithrombotic medication. Diagnosis was made using CT neck in 82.4% of cases. While 12 (70.6%) cases were managed medically, 5 (29.4%) received surgical intervention, and 6 (35.3%) required intubation. 16 (94.1%) cases had complete resolution within an average of 27.9 (± 24.8) days, and one patient (5.9%) died from airway compromise.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>SRH is a rare condition that presents with nonspecific dysphagia or neck discomfort. Antithrombotic medications may serve as a risk factor. Most patients will not require operative management, but close observation is needed as progression to fatal airway compromise has been documented.</p>\n </section>\n </div>","PeriodicalId":48529,"journal":{"name":"Laryngoscope Investigative Otolaryngology","volume":"10 3","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lio2.70162","citationCount":"0","resultStr":"{\"title\":\"A Systematic Review of Case Reports of Spontaneous Retropharyngeal Hematoma\",\"authors\":\"Ashton L. Rogers, Alexander Burnett, Peter Eckard, Soroush Farsi, James R. Gardner, John L. Dornhoffer, Robert A. Saadi\",\"doi\":\"10.1002/lio2.70162\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>Spontaneous retropharyngeal hematoma (SRH) is a rare and potentially life-threatening condition with the potential to cause acute airway obstruction. This review aims to describe the presentation, predisposing factors, and management of SRH cases to better understand the clinical course and guide strategies for identifying and managing this condition.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Data Sources</h3>\\n \\n <p>PubMed, Embase, and Web of Science.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Review Methods</h3>\\n \\n <p>Databases were queried for articles from inception to February 2025. Study protocols adhered to the PRISMA guidelines. Case reports and series describing SRH were included. Study validity was assessed using the Joanna Briggs institute's critical appraisal tools and AMSTAR 2 criteria.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Seventeen cases (eight males and nine females) met inclusion criteria for analysis. On average, they presented at 59.7 (± 21.4) years old with sudden dysphagia (76.5%), anterior neck swelling (64.7%), neck pain (58.8%), and dysphonia (41.2%). Notably, 4 (23.5%) patients were taking an antithrombotic medication. Diagnosis was made using CT neck in 82.4% of cases. While 12 (70.6%) cases were managed medically, 5 (29.4%) received surgical intervention, and 6 (35.3%) required intubation. 16 (94.1%) cases had complete resolution within an average of 27.9 (± 24.8) days, and one patient (5.9%) died from airway compromise.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>SRH is a rare condition that presents with nonspecific dysphagia or neck discomfort. 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Most patients will not require operative management, but close observation is needed as progression to fatal airway compromise has been documented.</p>\\n </section>\\n </div>\",\"PeriodicalId\":48529,\"journal\":{\"name\":\"Laryngoscope Investigative Otolaryngology\",\"volume\":\"10 3\",\"pages\":\"\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-05-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lio2.70162\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laryngoscope Investigative Otolaryngology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/lio2.70162\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OTORHINOLARYNGOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laryngoscope Investigative Otolaryngology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/lio2.70162","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的自发性咽后血肿(SRH)是一种罕见且可能危及生命的疾病,有可能引起急性气道阻塞。这篇综述旨在描述SRH病例的表现、易感因素和治疗,以更好地了解临床过程和指导识别和治疗这种疾病的策略。数据来源PubMed, Embase和Web of Science。检索数据库中自成立至2025年2月的文章。研究方案遵循PRISMA指南。包括病例报告和描述SRH的系列。使用乔安娜布里格斯研究所的关键评估工具和AMSTAR 2标准评估研究的有效性。结果17例(男8例,女9例)符合纳入标准。患者平均年龄为59.7(±21.4)岁,伴有突发性吞咽困难(76.5%)、颈部前肿胀(64.7%)、颈部疼痛(58.8%)和发音困难(41.2%)。值得注意的是,4例(23.5%)患者正在服用抗血栓药物。82.4%的病例通过颈部CT诊断。内科治疗12例(70.6%),手术治疗5例(29.4%),插管治疗6例(35.3%)。16例(94.1%)患者在平均27.9(±24.8)天内完全缓解,1例(5.9%)患者死于气道妥协。结论SRH是一种罕见的以非特异性吞咽困难或颈部不适为表现的疾病。抗血栓药物可能是一个危险因素。大多数患者不需要手术治疗,但需要密切观察,因为进展到致命的气道损害已被记录。
A Systematic Review of Case Reports of Spontaneous Retropharyngeal Hematoma
Objective
Spontaneous retropharyngeal hematoma (SRH) is a rare and potentially life-threatening condition with the potential to cause acute airway obstruction. This review aims to describe the presentation, predisposing factors, and management of SRH cases to better understand the clinical course and guide strategies for identifying and managing this condition.
Data Sources
PubMed, Embase, and Web of Science.
Review Methods
Databases were queried for articles from inception to February 2025. Study protocols adhered to the PRISMA guidelines. Case reports and series describing SRH were included. Study validity was assessed using the Joanna Briggs institute's critical appraisal tools and AMSTAR 2 criteria.
Results
Seventeen cases (eight males and nine females) met inclusion criteria for analysis. On average, they presented at 59.7 (± 21.4) years old with sudden dysphagia (76.5%), anterior neck swelling (64.7%), neck pain (58.8%), and dysphonia (41.2%). Notably, 4 (23.5%) patients were taking an antithrombotic medication. Diagnosis was made using CT neck in 82.4% of cases. While 12 (70.6%) cases were managed medically, 5 (29.4%) received surgical intervention, and 6 (35.3%) required intubation. 16 (94.1%) cases had complete resolution within an average of 27.9 (± 24.8) days, and one patient (5.9%) died from airway compromise.
Conclusions
SRH is a rare condition that presents with nonspecific dysphagia or neck discomfort. Antithrombotic medications may serve as a risk factor. Most patients will not require operative management, but close observation is needed as progression to fatal airway compromise has been documented.