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Orthopaedic manifestations of Proteus syndrome in a child with literature update
Tamer Ahmed El-Sobky1, Solaf M Elsayed2, Dalia M E El Mikkawy3
1Division of Paediatric Orthopaedics, Department of Orthopaedic Surgery, Faculty of Medicine, Ain-Shams University, 38 Abbasia, Cairo, Egypt.
Insights
Proteus syndrome, a rare overgrowth disorder, presents with characteristic skeletal abnormalities. Accurate diagnosis relies on consistent application of criteria and advanced imaging for this challenging condition.
Area of Science:
- Genetics and Developmental Biology
- Orthopedics and Radiology
Background:
- Proteus syndrome is a rare, complex developmental disorder with unknown causes.
- Characterized by postnatal overgrowth affecting multiple tissues, it frequently manifests as skeletal changes.
- Variable presentations and diagnostic inconsistencies lead to frequent misdiagnoses in medical literature.
Background:
Proteus syndrome is a rare developmental disorder of unknown aetiology. It is a disorder characterized by postnatal overgrowth affecting multiple tissues. Proteus syndrome is most frequently manifested in skeletal changes. As manifestations of Proteus syndrome are highly variable, and many are found in other overgrowth syndromes, and due to inconsistent application of diagnostic criteria, the literature has more reports of patients misdiagnosed than correctly diagnosed. The purpose of this study is to report the clinical and radiographic patterns of affection of the musculoskeletal system in Proteus syndrome in the light of the proposed diagnostic criteria and cases reported in the literature.
Methods:
The clinical and radiographic musculoskeletal characteristics of a child with Proteus syndrome are illustrated along with a literature update. The orthopaedic manifestations in our patient are correlated to cases and proposed diagnostic criteria reported in the literature.
Results:
The study of the presented case and review of available literature show that there tends to be a highly characteristic pattern of skeletal abnormalities in Proteus syndrome.
Conclusion:
The rarity of Proteus syndrome and the variability of signs make the diagnosis challenging. Clinical and radiographic examinations are important contributors to the diagnosis. The clinical utility of the reported cases is significantly dependent on consistent application of diagnostic criteria that augment diagnostic accuracy. The present case reinforces the need for supplementary musculoskeletal imaging modalities to be implemented in the diagnosis of Proteus syndrome.
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