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743 Possible Causes for Langerhans Cell Histiocytosis, Pulmonary Hypertension

  • Interstitial Lung Disease

    A 10-year-old boy with prolonged cough, and computed tomography of thorax with features suggestive of primary Langerhans's cell histiocytosis.[] BACKGROUND AND OBJECTIVE: In interstitial lung disease (ILD), pulmonary hypertension (PH) is a major adverse prognostic determinant.[] cell histiocytosis.[]

  • Pulmonary Histiocytosis X

    Pulmonary Langerhans Cell Histiocytosis (PLCH) Eosinophilic Granuloma of the Lung Pulmonary Langerhans Cell Granulomatosis Pulmonary Histiocytosis X Uncommon ILD Young adults[] Articles include: Epidemiology of Pulmonary Arterial Hypertension, Pathology of Pulmonary Hypertension, Genetics of Pulmonary Arterial Hypertension, Diagnosis of Pulmonary[] Pulmonary haemodynamics in LCH-related PH are similar to those in idiopathic pulmonary arterial hypertension, are unrelated to lung function variables 3, 7 and are associated[]

  • Chronic Interstitial Lung Disease

    Irregular, thick- and thin-walled cysts and nodules in a patient with pulmonary Langerhans cell histiocytosis.[] Patients affected with histiocytosis X, even with higher degrees of pulmonary hypertension, had a better survival rate (p 0.0005) compared with patients with idiopathic pulmonary[] cell histiocytosis Wegener's granulomatosis, Churg-Strauss Syndrome RARE ILD alv.proteinosis alv.microlithiasis amyloidosis eosinophilic pneumonia lymphangioleiomyomatosis[]

  • Restrictive Lung Disease

    ' cell histiocytosis Pulmonary alveolar proteinosisConditions specifically affecting the interstitium are called interstitial lung diseases.[] There is limited literature on restrictive lung disease and pulmonary hypertension with regards to their management during pregnancy.[] cell histiocytosis; diffuse interstitial fibrosis Clinical SOB, tachypnea, concentric in lung volumes Imaging Interstital and alveolar pattern Functional tests diffusing[]

  • Pulmonary Interstitial Glycogenosis

    cell histiocytosis J84.83 Surfactant mutations of the lung J84.84 Other interstitial lung diseases of childhood J84.841 Neuroendocrine cell hyperplasia of infancy J84.843[] Abstract A neonate with pulmonary interstitial glycogenosis, pulmonary hypertension, and hypertrophic cardiomyopathy is described.[] cell histiocytosis J84.83 Surfactant mutations of the lung J84.84 Other interstitial lung diseases of childhood J84.841 Neuroendocrine cell hyperplasia of infancy J84.842[]

  • Secondary Pulmonary Interstitial Fibrosis

    cell histiocytosis (EG) – Langerhans cell histiocytosis (EG) – Respiratory bronchiolitis-ILD – Respiratory bronchiolitis-ILD Subacute hypersensitivity pneumonitis Subacute[] Pulmonary Hypertension Associated With Pulmonary Fibrosis Pulmonary hypertension (PH) occurs when mean pulmonary arterial pressure (PAP) is elevated more than 20-25 mm Hg[] […] and or granulomas Predominantly bronchiolocentric distribution Features of other defined diseases such as: Langerhans cell histiocytosis Sarcoidosis Marked inflammation Marked[]

  • Hemangiomatosis

    Congenital self-healing reticulohistiocytosis (CSRH), a rare benign variant of Langerhans cell histiocytosis (LCH), is characterized by (a). congenital skin lesions, (b).[] Abstract Pulmonary capillary hemangiomatosis is a rare cause of pulmonary hypertension characterized by extensive proliferation of pulmonary capillaries within alveolar septae[] Articles include: Lymphangioleiomyomatosis, Pulmonary Lymphangiomatosis, Langerhans Cell Histiocytosis and other Histiocytic Diseases of the Lung, Pulmonary Alveolar Proteinosis[]

  • Interstitial Pulmonary Fibrosis of the Newborn

    Cell Histiocytosis (LCH) is a rare disease 2008-2018 MeDitorial ISSN 1803-6597 Last update: 25.3.2018 Statement[] Lastly, patients with idiopathic pulmonary fibrosis often have pulmonary hypertension as their disease progresses.[] Connective-tissue diseases (also called collagen vascular disease) Pulmonary hemorrhage syndromes including capillaritis, Goodpasture’s syndrome or vasculitis Langerhans cell[]

  • Lung Biopsy showing Centrilobular Emphysema

    Introduction Pulmonary Langerhans cell histiocytosis (PLCH) is an isolated form of Langerhans cell histiocytosis characterised by granulomatous infiltration of the distal[] […] and impact of pulmonary arterial hypertension therapies.[] The patient died 5 months after the diagnosis of pulmonary hypertension from acute respiratory failure.[]

  • Autoimmune Interstitial Lung Disease - Arthritis Syndrome

    Examples include: granulomatous diseases, e.g. sarcoidosis, Langerhans cell histiocytosis neoplasia primary, e.g. lymphoma, other lymphoproliferative diseases secondary, e.g[] Pulmonary vasculitis can cause pulmonary hypertension.[] cell histiocytosis, silicosis, coal workers pneumoconiosis, carmustine related pulmonary fibrosis, respiratory broncholitis associated with interstitial lung disease.[]

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