Langerhans cell histiocytosis in the glenoid neck with rare mutation: A case report

Langerhans cell histiocytosis (LCH) is a rare disease that occurs mainly in children. It has several forms of clinical presentation. Early diagnosis is important for better results. A 17-year-old male patient presented with right sharp shoulder pain for 2 months. Magnetic resonance image (MRI) of th...

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Detalles Bibliográficos
Autores principales: Ortegón, José David Cardona, Valencia, Valentina Ferrer, Yepes, María Mónica, Maldonado, Sandra Patricia, Rueda, Hernan Dario Paez, Palau-Lazaro, Mauricio, Quiroga, Luisa Maria Muñoz, Paternina, Salim Nayib Cueter, Quintana, Jose Valderrama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829550/
https://www.ncbi.nlm.nih.gov/pubmed/36636479
http://dx.doi.org/10.1016/j.radcr.2022.12.016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829550/
https://www.ncbi.nlm.nih.gov/pubmed/36636479
http://dx.doi.org/10.1016/j.radcr.2022.12.016

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