因鼻衄入院，服用免疫抑制剂后出院！- 混合性结缔组织病的不寻常表现。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL

Journal of Community Hospital Internal Medicine Perspectives Pub Date : 2024-09-09 eCollection Date: 2024-01-01 DOI:10.55729/2000-9666.1383

Anne C Laird, Basem Al Achras

{"title":"因鼻衄入院，服用免疫抑制剂后出院！- 混合性结缔组织病的不寻常表现。","authors":"Anne C Laird, Basem Al Achras","doi":"10.55729/2000-9666.1383","DOIUrl":null,"url":null,"abstract":"Mixed Connective Tissue Disease (MCTD) is a complex disease that is a combination of several other clinical conditions, including systemic lupus erythematosus (SLE), systemic sclerosis (SSc), and polymyositis/dermatomyositis (PM/DM). What makes MCTD challenging is the fact that there are no current management guidelines. Instead, treatment is usually chosen based on organ involvement using SLE, SSc, and PM/DM guidelines. In this paper, we will discuss an unusual presentation of MCTD, the workup that led to the diagnosis, the immunological profile, and the management plan for this rare disease.","PeriodicalId":15460,"journal":{"name":"Journal of Community Hospital Internal Medicine Perspectives","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11466346/pdf/","citationCount":"0","resultStr":"{\"title\":\"Admitted With Epistaxis, Discharged on Immunosuppressants! - An Unusual Presentation of Mixed Connective Tissue Disease.\",\"authors\":\"Anne C Laird, Basem Al Achras\",\"doi\":\"10.55729/2000-9666.1383\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Mixed Connective Tissue Disease (MCTD) is a complex disease that is a combination of several other clinical conditions, including systemic lupus erythematosus (SLE), systemic sclerosis (SSc), and polymyositis/dermatomyositis (PM/DM). What makes MCTD challenging is the fact that there are no current management guidelines. Instead, treatment is usually chosen based on organ involvement using SLE, SSc, and PM/DM guidelines. In this paper, we will discuss an unusual presentation of MCTD, the workup that led to the diagnosis, the immunological profile, and the management plan for this rare disease.\",\"PeriodicalId\":15460,\"journal\":{\"name\":\"Journal of Community Hospital Internal Medicine Perspectives\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2024-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11466346/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Community Hospital Internal Medicine Perspectives\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.55729/2000-9666.1383\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Community Hospital Internal Medicine Perspectives","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55729/2000-9666.1383","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}

引用次数: 0

摘要

混合性结缔组织病（MCTD）是一种复杂的疾病，它是系统性红斑狼疮（SLE）、系统性硬化症（SSc）和多发性肌炎/皮肌炎（PM/DM）等其他几种临床疾病的综合体。MCTD之所以具有挑战性，是因为目前还没有管理指南。相反，通常是根据系统性红斑狼疮、系统性硬化症和多发性肌炎/皮肌炎的指南，根据受累器官选择治疗方法。在本文中，我们将讨论 MCTD 的异常表现、诊断过程、免疫学特征以及这种罕见疾病的治疗方案。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Admitted With Epistaxis, Discharged on Immunosuppressants! - An Unusual Presentation of Mixed Connective Tissue Disease.

Mixed Connective Tissue Disease (MCTD) is a complex disease that is a combination of several other clinical conditions, including systemic lupus erythematosus (SLE), systemic sclerosis (SSc), and polymyositis/dermatomyositis (PM/DM). What makes MCTD challenging is the fact that there are no current management guidelines. Instead, treatment is usually chosen based on organ involvement using SLE, SSc, and PM/DM guidelines. In this paper, we will discuss an unusual presentation of MCTD, the workup that led to the diagnosis, the immunological profile, and the management plan for this rare disease.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Journal of Community Hospital Internal Medicine Perspectives MEDICINE, GENERAL & INTERNAL-

自引率

0.00%

发文量

106

审稿时长

17 weeks

期刊介绍： JCHIMP provides: up-to-date information in the field of Internal Medicine to community hospital medical professionals a platform for clinical faculty, residents, and medical students to publish research relevant to community hospital programs. Manuscripts that explore aspects of medicine at community hospitals welcome, including but not limited to: the best practices of community academic programs community hospital-based research opinion and insight from community hospital leadership and faculty the scholarly work of residents and medical students affiliated with community hospitals.