Proteus syndrome revealing itself after the treatment of a bilateral subdural haematoma
Autor: | Bénédict Rilliet, Paolo Scolozzi, Armand Bottani, Benoit John Jenny, Yassine El Hassani, Brigitte Pittet-Cuénod, Hulya Ozsahin Ayse |
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Rok vydání: | 2013 |
Předmět: |
medicine.medical_specialty
Pathology Subdural haematoma Scoliosis Proteus Syndrome Muscle hypertrophy Hematoma medicine Humans ddc:576.5 Craniofacial Child ddc:617 business.industry General Medicine medicine.disease Proteus syndrome Hypoplasia ddc:616.8 Surgery Hematoma Subdural Pediatrics Perinatology and Child Health bacteria Female Neurology (clinical) Complication business |
Zdroj: | Child's Nervous System, Vol. 29, No 10 (2013) pp. 1927-31 |
ISSN: | 1433-0350 0256-7040 |
DOI: | 10.1007/s00381-013-2090-z |
Popis: | Introduction: Hypertrophy of the calvarium has different aetiologies, among them the rare Proteus syndrome. Case report: We report here the case of a young girl initially treated for relapsing right then left large chronic subdural haematoma, who progressively developed craniofacial hypertrophy consistent with the diagnosis of Proteus syndrome. Calvarium hypertrophy was shaved and remodelled combining midface advancement, essentially for cosmetic purposes. During the first calvarium remodelling, important bleeding of the bone required large volume of blood replacement. Haemostasis workup revealed platelets aggregation anomalies. Bleeding issues during subsequent surgeries were controlled with tranexamic acid and desmopressin acetate. Discussion: Other manifestations of Proteus syndrome, such as a right hypertrophy of the face with hypoplasia of its middle third, a pigmented epidermal nevus and asymmetric limbs and scoliosis, appeared progressively over time. Blood and fibroblast phosphatase and tensin homolog mutation was not found. Conclusion: Literature review of operated patients with Proteus syndrome did not reveal an association with platelets anomalies. A complete haemostasis workup following this unexpected haemorrhagic complication is recommended for this rare pathology |
Databáze: | OpenAIRE |
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