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Langerhans Cell Histiocytosis Treatment (PDQ®): Treatment - Health Professional Information [NCI] | Cigna

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Langerhans cell histiocytosis - very high mag.jpg

The skeleton is the most commonly involved organs system in Langerhans cell histiocytosis (LCH) and is by far the most common location for single lesion, often referred to as eosinophilic granuloma (EG) (the terms are used interchangeably in this article). For a general discusion of this disease please refer to the article on Langerhans cell histiocytosis (LCH). Read more: http://radiopaedia.org/articles/skeletal-manifestations-of-langerhans-cell-histiocytosis

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Research on rare blood disorder leads to diagnostic test, potential new therapies

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from Odyssey

Lessons From Langerhans Cell Histiocytosis

Langerhans Cell Histiocytosis,Lch,Odyssey Online,Rare Disease,Teachings,Learned,Warrior,Lessons,Books Worth

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Langerhans Cell Histiocytosis: Emerging Insights and Clinical Implications | Cancer Network

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Figure 5. Model of Langerhans Cell Histiocytosis Pathogenesis

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Langerhans cell histiocytosis (LCH) is a rare multi-system disease with a wide and heterogeneous clinical spectrum. Skull solitary or multiple punched out lytic lesions without sclerotic rim double contour or beveled edge appearance may be seen due to greater involvement of the inner than the outer table (hole within a hole) sign button sequestrum representing residual bone geographic skull http://radiopaedia.org/articles/langerhans-cell-histiocytosis-skeletal-manifestations

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