Zacharias Jasmine, Mandalia Uday, Palman Jason, Kagalwala Fatima, Colaco Cecil Bernard, Pillai Janani K
West Hertfordshire Teaching Hospitals NHS Trust, Hertfordshire, England.
East and North Hertfordshire NHS Trust, Hertfordshire, England.
Skeletal Radiol. 2024 Nov;53(11):2519-2528. doi: 10.1007/s00256-024-04581-y. Epub 2024 Jan 20.
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.
我们呈现了在英国新冠疫情第二波高峰期间一组五名儿童的指骨微地理综合征的临床和放射学特征。每个儿童均表现为指骨肿胀和红斑,促使多学科团队进行全面评估,以分析临床表现、血液检查结果和影像学检查。该队列的平均年龄为14.1岁,年龄范围在10.4至16.6岁之间,其中有两名女孩和三名男孩。四名儿童手部指骨受累,而一名儿童仅足部受累。对所有儿童均进行了风湿病学检查。对三名儿童进行的手部X线检查显示出独特的放射学特征,如微地理现象、骨膜下骨质吸收,其中两例还伴有骨质稀疏。然而,进一步的MRI检查显示广泛的改变,与皮肤血管病变性皮疹的临床体征密切相关。MRI异常显著,包括主要影响干骺端和骨骺的骨髓水肿,呈现出广泛的过渡区。还观察到软组织肿胀和皮质侵蚀。在急性临床情况下,这些MRI特征更具诊断意义。该研究得出结论,以手指肿胀和红斑为特征的指骨微地理综合征,普通X线检查可能无法对其进行充分评估。包括骨髓水肿和软组织异常在内的更全面的MRI特征,在诊断该疾病时似乎更具指示性。考虑到该综合征的罕见性及其与新冠疫情的时间关联,该研究推测,与新冠相关的血栓形成倾向和免疫介导的血管病变可能是该综合征中所见活跃骨表现的关键触发因素。要点:•指骨微地理综合征是一种罕见的、主要发生在儿童的疾病,病因不明,累及手指。•实验室检查通常为阴性;然而,在适当的临床背景下,X线检查发现的微地理现象以及MRI上所见的骨髓水肿模式具有诊断意义。•考虑到指骨微地理综合征的罕见性及其与新冠疫情的时间关联,新冠血管病变可能是指骨微地理综合征一种先前未被认识的病因。