Langerhans Cell Histiocytosis: an orphan disease

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Langerhans cell histiocytosis

Introduction: Langerhans cell histiocytosis (LCH), which was previously known as histiocytosis X, refers to a group of lesions that stimulate uncontrolled proliferation of cells. The purpose of this case was to report and describe a LCH case with mandibular bone involvement in a 2.5-year-old boy. Case reports: A 2.5 years old boy with LCH of mandibular jaw who has been treated by surgical inter...

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Elements: in this month’s issue Langerhans Cell Histiocytosis: an orphan disease

There is no single agreed definition of a rare disease. The European Commission on Public Health defines rare diseases as those which are ‘life-threatening or chronically debilitating and which are of such low prevalence that special combined efforts are needed to address them’. The term ‘orphan’ has been used in association with rare diseases in order to emphasise their relative neglect in ter...

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Current Treatment Strategy in Langerhans Cell Histiocytosis

Langerhans cell histiocytosis (LCH) is a rare disorder described as three different entities including eosinophilic granulomaof bone, the Hand-Schuller-Christian syndrome, and Letterer-Siwe disease. LCH is currently classified into singlesystem LCH, and multisystem LCH. Patients with single system LCH have an excellent prognosis, and are mostlytreated with local therapy. Multisystem LCH is subd...

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Herpes Simplex Virus and Langerhans Cell Histiocytosis

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ژورنال

عنوان ژورنال: QJM

سال: 2011

ISSN: 1460-2725,1460-2393

DOI: 10.1093/qjmed/hcr006