Phalangeal microgeodic syndrome: a paediatric case series
Jasmine Zacharias1, Uday Mandalia1, Jason Palman1
1West Hertfordshire Teaching Hospitals NHS Trust, Hertfordshire, England.
Skeletal Radiology
|January 20, 2024
Summary
Phalangeal microgeodic syndrome (PMS) in children presents with digital swelling. MRI is more diagnostic than X-rays, revealing bone and soft tissue changes potentially linked to COVID-19 vasculopathy.
Area of Science:
- Pediatric Rheumatology
- Radiology
- Infectious Disease Epidemiology
Background:
- Phalangeal microgeodic syndrome (PMS) is a rare pediatric condition affecting the digits with unknown etiology.
- The study occurred during the second peak of the COVID-19 pandemic in the UK, observing a cluster of affected children.
Purpose of the Study:
- To describe the clinical and radiological characteristics of PMS in a pediatric cohort.
- To investigate potential associations between PMS and the COVID-19 pandemic.
Main Methods:
- Case series analysis of five children presenting with phalangeal swelling and erythema.
- Clinical evaluation, laboratory investigations, X-rays, and Magnetic Resonance Imaging (MRI) were performed.
- Rheumatological work-up was conducted for all participants.
Main Results:
- Four children had hand involvement, one had foot involvement; ages ranged from 10.4 to 16.6 years.
- X-rays showed microgeodes and bone resorption in some cases, but MRI revealed more extensive marrow edema, soft tissue swelling, and cortical erosions.
- MRI findings were more pathognomonic in the acute clinical context.
Conclusions:
- Phalangeal microgeodic syndrome diagnosis benefits from MRI due to its sensitivity to bone marrow edema and soft tissue abnormalities, surpassing plain X-rays.
- The temporal association with the COVID-19 pandemic suggests a potential role for COVID-related thrombophilia or immune-mediated vasculopathy as triggers for PMS.
- COVID-19 vasculopathy may be a previously unrecognized cause of PMS.
More Related Videos
Related Concept Videos
Genomic Imprinting and Inheritance
34.5K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
34.5K
Pleiotropy
40.5K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.5K


