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Fat embolism syndrome in Duchenne muscular dystrophy: Report on a novel case and systematic literature review.
Specht, Sabine; Zhukova, Irina; Westhoff, Jens H; Erb, Larissa; Ziegler, Andreas; Kölker, Stefan; Hoffmann, Georg F; Hagmann, Sébastien; Syrbe, Steffen.
Afiliación
  • Specht S; Division of Paediatric Neurology and Metabolic Medicine, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Zhukova I; Division of Paediatric Epileptology, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Westhoff JH; Department of Paediatrics I, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Erb L; Department of Paediatrics I, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Ziegler A; Division of Paediatric Neurology and Metabolic Medicine, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Kölker S; Division of Paediatric Neurology and Metabolic Medicine, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Hoffmann GF; Department of Paediatrics I, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Hagmann S; Department of Orthopaedics and Trauma Surgery, Centre for Orthopaedics, Trauma Surgery and Spinal Cord Injury, Heidelberg University Hospital, Heidelberg, Germany.
  • Syrbe S; Division of Paediatric Epileptology, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany. Electronic address: Steffen.Syrbe@med.uni-heidelberg.de.
Eur J Paediatr Neurol ; 48: 91-100, 2024 Jan.
Article en En | MEDLINE | ID: mdl-38096597
ABSTRACT
We report a non-ambulatory 13-year-old boy with Duchenne muscular dystrophy who experienced severe acute respiratory distress syndrome and cerebral fat embolism following elective soft tissue surgery. Post-surgery radiological examination revealed bilateral femoral fractures and marked osteopenia that were believed to have caused disseminated pulmonary and cerebral fat embolism. The patient had never been on glucocorticoid treatment. Five months post-surgery, he remained in a state of minimal consciousness. A literature review was performed and eleven publications included, providing case reports of a total number of 23 patients with Duchenne muscular dystrophy with fat embolism syndrome. The most common causes were falls from the wheelchair that predominantly resulted in femoral fractures. Median age at the event was around 14 years. Seven patients succumbed to complications of fat embolism. No event was described in the context of surgery. We want to raise awareness that spontaneous unnoticed fractures may occur especially in adolescents with DMD from traumatic injury of large bones and also during elective surgery with a high risk of causing fat embolism with severe sequelae.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Distrofia Muscular de Duchenne / Embolia Grasa / Fracturas del Fémur Tipo de estudio: Systematic_reviews Idioma: En Revista: Eur J Paediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Distrofia Muscular de Duchenne / Embolia Grasa / Fracturas del Fémur Tipo de estudio: Systematic_reviews Idioma: En Revista: Eur J Paediatr Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article