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886 Possible Causes for Langerhans Cell Histiocytosis, Respiratory Failure

  • Interstitial Lung Disease

    This patient was admitted to the emergency department with severe respiratory failure requiring non-invasive ventilation.[] A 10-year-old boy with prolonged cough, and computed tomography of thorax with features suggestive of primary Langerhans's cell histiocytosis.[] Here, we report a 4-year-old girl who suffered from severe progressive respiratory failure.[]

  • Lymphangioleiomyomatosis

    Abstract Aims: To report the first case of respiratory failure due to micronodular type II pneumocyte hyperplasia.[] Lymphangioleiomyomatosis (LAM) and pulmonary Langerhans cell histiocytosis (PLCH) are rare diseases that lead to progressive cystic destruction of the lungs.[] Cystic fibrosis and Langerhans cell histiocytosis (eosinophilic granuloma) share this feature.[]

  • Acute Interstitial Pneumonitis

    respiratory failure, regardless of cause, is quite poor.[] cell histiocytosis.[] Ciprofloxacin can induce interstitial pneumonitis with acute respiratory failure.[]

  • Acute Interstitial Lung Disease

    respiratory failure, regardless of cause, is quite poor.[] Langerhans' cell histiocytosis On the left a chest film of a 19 year old patient with Langerhans cell histiocytosis.[] Mortality is 60%; most patients die within 6 mo of presentation, and death is usually due to respiratory failure.[]

  • Pulmonary Interstitial Glycogenosis

    In this report, we describe changes in successive lung biopsies in a neonate who presented with respiratory failure and pulmonary hypertension.[] 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[] Although some patients improved with age, 7 died of respiratory failure or complications of CHD, suggesting that PIG may be clinically significant when associated with other[]

  • Restrictive Lung Disease

    Multivariate Cox proportional hazard and sensitivity analyses were performed to assess the relationship between restriction and early respiratory failure and nonrelapse mortality[] ' cell histiocytosis Pulmonary alveolar proteinosisConditions specifically affecting the interstitium are called interstitial lung diseases.[] cell histiocytosis; diffuse interstitial fibrosis Clinical SOB, tachypnea, concentric in lung volumes Imaging Interstital and alveolar pattern Functional tests diffusing[]

  • Cystic Lung Disease

    Soon after admission he required conventional mechanical ventilation for respiratory failure.[] MATERIALS AND METHODS: The authors evaluated the size of cystic lesions, as seen on paired inspiratory and expiratory HRCT scans, in 54 patients with Langerhans cell histiocytosis[] PCP is an acquired immunodeficiency syndrome (AIDS)-defining illness and often presents with rapidly deteriorating respiratory failure in the absence of appropriate therapy[]

  • Idiopathic Acute Eosinophilic Pneumonia

    We report a typical case of a 21-year-old male with recent onset of smoking, who presented with acute febrile hypoxemic respiratory failure.[] cell histiocytosis Must exclude drug reactions (antibiotics, cytotoxic or anti-inflammatory drugs), immune disorders (Churg-Strauss syndrome, collagen vascular disease, asthma[] Cell Histiocytosis (LCH) (see Langerhans Cell Histiocytosis, [[Langerhans Cell Histiocytosis]]) Diagnosis : pulmonary pathologic lesions are nodules (with bronchiolocentric[]

  • Desquamative Interstitial Pneumonia

    failure.[] cell histiocytosis (PLCH).[] In rare cases, patients with DIP fail to respond to corticosteroid therapy, and may progress to end-stage fibrotic lung disease with respiratory failure.[]

  • Chronic Interstitial Lung Disease

    respiratory failure, regardless of cause, is quite poor.[] Irregular, thick- and thin-walled cysts and nodules in a patient with pulmonary Langerhans cell histiocytosis.[] cell histiocytosis Wegener's granulomatosis, Churg-Strauss Syndrome RARE ILD alv.proteinosis alv.microlithiasis amyloidosis eosinophilic pneumonia lymphangioleiomyomatosis[]

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