• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Singleton-Merten 综合征:一种罕见的股骨头坏死病因。

Singleton-Merten syndrome: A rare cause of femoral head necrosis.

机构信息

Department of Orthopedics and Trauma Surgery, University Medical Centre, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.

Institute of Pathology, University Medical Centre, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.

出版信息

Am J Med Genet A. 2021 Oct;185(10):3170-3175. doi: 10.1002/ajmg.a.62395. Epub 2021 Jun 30.

DOI:10.1002/ajmg.a.62395
PMID:34189824
Abstract

Singleton-Merten syndrome (SMS) is a type I interferonopathy. In this report, we disclose the first-to the best of our knowledge-direct association of SMS with femoral head necrosis (FHN). The following case report presents the condition of a 38-year-old male suffering from SMS with FHN, characterized by acute symptoms and rapid disease progression. As per the recommendations of the Association Research Circulation Osseous (ARCO) and the S3-guidelines, we successfully treated the FHN with core decompression. Our histological results correlate with the changes described in medical literature in patients with SMS and MDA5-knockout in vivo experiments such as osteopenia, widened medullary cavity, and thin cortical bone. Moreover, the conducted immunohistochemistry shows strong CD56 positivity of the osteoblasts and osteocytes, as well as significant CD68 and CD163 positivity of the middle-sized osteoclasts. Collectively, these findings suggest an underlying syndrome in the FHN. A six-month post-operative follow-up revealed complete recovery with the absence of the initial symptoms and ability to resume normal daily activities. Taken together, our findings suggest that SMS is an additional cause of FHN in young adults. Early detection and adequate treatment using well-established joint-preserving techniques demonstrate a favorable improvement of the patient's clinical condition.

摘要

Singleton-Merten 综合征 (SMS) 是一种 I 型干扰素病。在本报告中,我们首次披露了 SMS 与股骨头坏死 (FHN) 之间的直接关联。该病例报告介绍了一名 38 岁男性患有 SMS 和 FHN 的情况,其特点是症状急性发作且疾病快速进展。根据 Association Research Circulation Osseous (ARCO) 和 S3 指南的建议,我们成功地对 FHN 进行了核心减压治疗。我们的组织学结果与在 SMS 患者和 MDA5 敲除体内实验中描述的变化相吻合,例如骨质疏松症、骨髓腔增宽和皮质骨变薄。此外,进行的免疫组织化学显示成骨细胞和骨细胞的 CD56 阳性表达强烈,以及中型破骨细胞的 CD68 和 CD163 阳性表达显著。综上所述,这些发现提示 FHN 存在潜在的综合征。术后 6 个月的随访显示,患者完全康复,初始症状消失,能够恢复正常日常活动。综上所述,我们的发现提示 SMS 是年轻人 FHN 的另一个病因。早期发现和使用成熟的保关节技术进行充分治疗可显著改善患者的临床状况。

相似文献

1
Singleton-Merten syndrome: A rare cause of femoral head necrosis.Singleton-Merten 综合征:一种罕见的股骨头坏死病因。
Am J Med Genet A. 2021 Oct;185(10):3170-3175. doi: 10.1002/ajmg.a.62395. Epub 2021 Jun 30.
2
A case of Singleton-Merten syndrome without cardiac involvement harboring a novel IFIH1 variant.一例无心脏受累的Singleton-Merten综合征病例,携带一种新的IFIH1变异体。
Am J Med Genet A. 2020 Jun;182(6):1535-1536. doi: 10.1002/ajmg.a.61556. Epub 2020 Mar 23.
3
A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patient.一名患者中,钳子结构域的一种新型IFIH1突变是Aicardi-Goutières综合征和Singleton-Merten综合征临床特征的基础。
Br J Dermatol. 2018 Feb;178(2):e111-e113. doi: 10.1111/bjd.15869. Epub 2017 Dec 22.
4
Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome.编码视黄酸诱导基因I(RIG-I)的DDX58基因突变会导致非典型Singleton-Merten综合征。
Am J Hum Genet. 2015 Feb 5;96(2):266-74. doi: 10.1016/j.ajhg.2014.11.019. Epub 2015 Jan 22.
5
Unified mechanisms for self-RNA recognition by RIG-I Singleton-Merten syndrome variants.RIG-I 单体酶突变体识别自身 RNA 的统一机制。
Elife. 2018 Jul 26;7:e38958. doi: 10.7554/eLife.38958.
6
Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromes.与IFIH1杂合功能获得性突变相关的不寻常皮肤特征:Aicardi-Goutières综合征与Singleton-Merten综合征的重叠
Br J Dermatol. 2015 Dec;173(6):1505-13. doi: 10.1111/bjd.14073. Epub 2015 Oct 29.
7
R516Q mutation in Melanoma differentiation-associated protein 5 (MDA5) and its pathogenic role towards rare Singleton-Merten syndrome; a signature associated molecular dynamics study.黑色素瘤分化相关蛋白 5(MDA5)中的 R516Q 突变及其对罕见Singleton-Merten 综合征的致病作用:一个相关的特征分子动力学研究。
J Biomol Struct Dyn. 2019 Feb;37(3):750-765. doi: 10.1080/07391102.2018.1439770. Epub 2018 Feb 20.
8
Singleton-Merten Syndrome-like Skeletal Abnormalities in Mice with Constitutively Activated MDA5.MDA5 持续激活的小鼠中类似Singleton-Merten 综合征的骨骼异常
J Immunol. 2019 Sep 1;203(5):1356-1368. doi: 10.4049/jimmunol.1900354. Epub 2019 Jul 31.
9
MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum.MDA5相关神经炎症与辛格尔顿-默滕综合征:同一I型干扰素病谱系的两面
J Interferon Cytokine Res. 2017 May;37(5):214-219. doi: 10.1089/jir.2017.0004.
10
A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome.一种特定的IFIH1功能获得性突变导致辛格尔顿-默滕综合征。
Am J Hum Genet. 2015 Feb 5;96(2):275-82. doi: 10.1016/j.ajhg.2014.12.014. Epub 2015 Jan 22.

引用本文的文献

1
Case Report: Transcatheter valve implantation in a 13-year-old teenager with critical aortic stenosis and Singleton-Merten syndrome.病例报告:对一名患有严重主动脉瓣狭窄和辛格尔顿 - 默滕综合征的13岁青少年进行经导管瓣膜植入术。
Front Cardiovasc Med. 2025 May 8;12:1506887. doi: 10.3389/fcvm.2025.1506887. eCollection 2025.
2
Early-Age Manifestation of Singleton Merten Syndrome With Systemic Lupus Erythematosus Features: A Case Report.具有系统性红斑狼疮特征的单例默滕斯综合征的早期表现:病例报告
Cureus. 2022 May 23;14(5):e25244. doi: 10.7759/cureus.25244. eCollection 2022 May.