L’histiocytose langerhansienne (HL) est une maladie du système réticuloendothélial caractérisée par une prolifération clonale de cellules dendritiques de. Revue de Stomatologie et de Chirurgie Maxillo-Faciale – Vol. – N° 5 – p. – Histiocytose langerhansienne – EM|consulte. Request PDF on ResearchGate | Intérêt de la scintigraphie osseuse dans l’ histiocytose langerhansienne | We present one case of bone-Langerhans’ cell.
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Langerhans cell histiocytosis is a disease of the reticuloendothelial system characterized by a clonal proliferation of dendritic cells of Langerhans. This is a rare disease that primarily affects children and young adults. It can take many forms, from a single eosinophilic granuloma to widespread lesions involving multisystem life-threatening.
Bone involvement is the most common, it can be uni- or multifocal. We report a case of multifocal bone Langerhans cell histiocytosis, revealed in a child aged 3 years and touched his left temporal bone and right femur. The bone scintigraphy has found a third location in right scapular. The outcome was favorable after chemotherapy. The bone lesions are characterized by lytic lesions and are responsible for langerhansiennne, swelling and fractures.
Bone scintigraphy is a very sensitive examination that allows the initial staging and follow-up on treatment of skeletal manifestations.
Langerhans cell histiocytosis, Eosinophilic granuloma, Bone histkocytose. Journal page Archives Contents list. Access to the text HTML. Access to the PDF text.
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Journal Tunisien d’ORL et de Chirurgie Cervico-Faciale
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Histiocytose langerhansienne cérébrale
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