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diagnosis differential histiocytosis hypertension langerhans lch management phtn
Clinical Classification of Pulmonary Hypertension 1. Pulmonary arterial hypertension from pulmonary vasculopathy Idiopathic pulmonary arterial hypertension Heritable gene mutations
Clinical Classification ... disease Systolic dysfunction ... Diastolic dysfunction ... Langerhans cell ... #Differential #Causes
Langerhans Cell Histiocytosis (LCH) Granulomatous Lesions comprising langerin-positive histiocytes and an inflammatory infiltrate can arise in virtually
• Endocrine Dysfunction ... • Pulmonary Symptoms ... marrow: Organ dysfunction ... Birbeck granules (EM ... is crucial in pulmonary
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