Phalangeal microgeodic syndrome: a paediatric case series.

IF 1.9 3区 医学 Q2 ORTHOPEDICS
Skeletal Radiology Pub Date : 2024-11-01 Epub Date: 2024-01-20 DOI:10.1007/s00256-024-04581-y
Jasmine Zacharias, Uday Mandalia, Jason Palman, Fatima Kagalwala, Cecil Bernard Colaco, Janani K Pillai
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引用次数: 0

Abstract

We present the clinical and radiological characteristics of phalangeal microgeodic syndrome in a cluster of five children during the second peak of COVID-19 pandemic in the UK. Each child presented with phalangeal swelling and erythema, prompting a comprehensive multi-disciplinary team review to analyse the clinical presentation, blood test results and imaging. The cohort's average age was 14.1 years, ranging from 10.4 to 16.6 years, with two girls and three boys. Four children experienced phalangeal involvement in the hands, whilst one was affected solely in the feet. A rheumatological work-up was performed for all. Hand X-rays performed on three children revealed distinct radiographic features like microgeodes, subperiosteal bone resorption and rarefaction in two cases. However, further MRI showed extensive changes closely correlated with the clinical signs of cutaneous vasculopathic rashes. The MRI abnormalities were notable, encompassing marrow oedema primarily affecting metaphyses and epiphyses, displaying broad transition zones. Soft tissue swelling and cortical erosions were also observed. These MRI features proved more pathognomonic in the acute clinical context. The study concluded that phalangeal microgeodic syndrome, characterised by digital swelling and erythema, might not be adequately assessed by plain X-rays. The more comprehensive MRI features, including marrow oedema and soft tissue abnormalities, appeared to be more indicative in diagnosing the condition. Considering the rarity of this syndrome and its temporal association with the COVID-19 pandemic, the study hypothesised that COVID-related thrombophilia and immune-mediated vasculopathy might act as crucial triggers for the active bony manifestations seen in this syndrome. KEY POINTS: • PMS is a rare, predominantly paediatric condition, of unknown aetiology which affects the digits. • Laboratory investigations are generally negative; however, in the appropriate clinical context, the X-ray findings of microgeodes and pattern of bone marrow oedema seen on MRI are pathognomonic. • Considering the rarity of PMS and temporal association with the COVID-19 pandemic, COVID vasculopathy may represent a previously unrecognised aetiology for PMS.

趾骨小关节综合征:儿科病例系列。
我们介绍了在英国 COVID-19 大流行的第二个高峰期,一组五名儿童趾骨小关节综合征的临床和放射学特征。每名儿童均出现趾骨肿胀和红斑,促使多学科团队对其进行全面复查,分析临床表现、血液化验结果和影像学检查。患儿的平均年龄为 14.1 岁,从 10.4 岁到 16.6 岁不等,其中有两名女孩和三名男孩。四名儿童的手部趾骨受累,一名儿童仅足部受累。所有患儿都接受了风湿病检查。三名患儿的手部 X 光片显示出明显的放射学特征,如微结节、骨膜下骨吸收和两个病例的骨质稀疏。然而,进一步的核磁共振成像却显示出与皮肤血管病性皮疹的临床症状密切相关的广泛变化。核磁共振成像异常非常明显,包括骨髓水肿,主要影响骨骺和骨骺,显示出广泛的过渡区。此外,还观察到软组织肿胀和皮质侵蚀。这些核磁共振成像特征在急性临床情况下被证明更具诊断意义。研究认为,以数字肿胀和红斑为特征的趾骨小关节综合征可能无法通过普通X光片进行充分评估。更全面的核磁共振成像特征,包括骨髓水肿和软组织异常,似乎更能说明病情。考虑到该综合征的罕见性及其与 COVID-19 大流行的时间关联性,研究假设 COVID 相关的血栓性疾病和免疫介导的血管病变可能是该综合征中出现的活动性骨骼表现的关键诱因。要点:- PMS是一种罕见的、主要是儿科疾病,病因不明,主要影响手指。- 实验室检查通常呈阴性,但在适当的临床情况下,X 射线检查发现的微小结节和核磁共振成像上看到的骨髓水肿模式具有病理诊断意义。- 考虑到PMS的罕见性以及与COVID-19大流行的时间关联性,COVID血管病变可能是PMS的一种以前未被发现的病因。
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来源期刊
Skeletal Radiology
Skeletal Radiology 医学-核医学
CiteScore
4.40
自引率
9.50%
发文量
253
审稿时长
3-8 weeks
期刊介绍: Skeletal Radiology provides a forum for the dissemination of current knowledge and information dealing with disorders of the musculoskeletal system including the spine. While emphasizing the radiological aspects of the many varied skeletal abnormalities, the journal also adopts an interdisciplinary approach, reflecting the membership of the International Skeletal Society. Thus, the anatomical, pathological, physiological, clinical, metabolic and epidemiological aspects of the many entities affecting the skeleton receive appropriate consideration. This is the Journal of the International Skeletal Society and the Official Journal of the Society of Skeletal Radiology and the Australasian Musculoskelelal Imaging Group.
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