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971 Possible Causes for Cough, Langerhans Cell Histiocytosis

  • Respiratory Bronchiolitis Interstitial Lung Disease

    Cell Histiocytosis (PLCH) Discussion Background Respiratory bronchiolitis ( RB ) ( smoker’s bronchiolitis ) is a common but incidental histologic finding in asymptomatic[] The onset is usually insidious with exertional dyspnea and persistent cough, which may be non-productive, developing over a course of weeks or months.[] Children with ILD usually present with failure to thrive, dry cough, dyspnea, and tachypnea and rales.[]

  • Desquamative Interstitial Pneumonia

    cell histiocytosis (PLCH).[] He noticed a dry cough and shortness of breath on exertion when the pigment of other colors was added at the age of 27.[] Cough, difficulty in breathing, cyanosis, and failure to gain weight appeared during the first month of life; progressive hypoxia followed, and the three infants died in respiratory[]

  • Pulmonary Histiocytosis X

    Pulmonary Langerhans Cell Histiocytosis (PLCH) Eosinophilic Granuloma of the Lung Pulmonary Langerhans Cell Granulomatosis Pulmonary Histiocytosis X Uncommon ILD Young adults[] It primarily affects young smokers and usually presents with symptoms of cough, dyspnea, and chest pain.[] History A 36-year-old Caucasian woman presented to her primary care physician complaining of approximately 12 months of nonproductive cough.[]

  • Secondary Pulmonary Interstitial Fibrosis

    cell histiocytosis (EG) – Langerhans cell histiocytosis (EG) – Respiratory bronchiolitis-ILD – Respiratory bronchiolitis-ILD Subacute hypersensitivity pneumonitis Subacute[] Estimates of GERD as the primary cause of chronic cough range from 10% to 40%, but the literature linking GERD to chronic cough varies by the population being tested and the[] […] and or granulomas Predominantly bronchiolocentric distribution Features of other defined diseases such as: Langerhans cell histiocytosis Sarcoidosis Marked inflammation Marked[]

  • Lymphangioleiomyomatosis

    Lymphangioleiomyomatosis (LAM) and pulmonary Langerhans cell histiocytosis (PLCH) are rare diseases that lead to progressive cystic destruction of the lungs.[] A 32-year-old primigravida presented with cough and dyspnea at 16 weeks' gestation.[] Cystic fibrosis and Langerhans cell histiocytosis (eosinophilic granuloma) share this feature.[]

  • Acute Interstitial Lung Disease

    Langerhans' cell histiocytosis On the left a chest film of a 19 year old patient with Langerhans cell histiocytosis.[] Symptoms of acute interstitial pneumonia consist of the abrupt onset of fever, cough, and shortness of breath, which in most patients increase in severity over 7 to 14 days[] […] year-old female with a history of idiopathic pulmonary fibrosis and pulmonary hypertension (prednisone, sildenafil, and bosentan therapy) presents with a three day history of cough[]

  • Chronic Interstitial Lung Disease

    Irregular, thick- and thin-walled cysts and nodules in a patient with pulmonary Langerhans cell histiocytosis.[] […] evaluation can have cough caused by these other more common causes of chronic cough.[] cell histiocytosis Wegener's granulomatosis, Churg-Strauss Syndrome RARE ILD alv.proteinosis alv.microlithiasis amyloidosis eosinophilic pneumonia lymphangioleiomyomatosis[]

  • Langerhans-Cell Histiocytosis

    Langerhans cell histiocytosis (LCH), also called Histiocytosis X, is a rare disease characterized by the proliferation and accumulation of Langerhans cells in various tissues[] A 2-year-old boy presented with generalized lymphadenopathy, fever, and cough. The patient had hepatosplenomegaly, anemia, and lytic lesions in the skull.[] A 50-year-old man was referred for dry cough and exertional dyspnea of more than 1 week.[]

  • 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.[] We describe a case with chronic interstitial lung disease and chronic cough that was attributed to P. jirovecii.[] cell histiocytosis.[]

  • Acute Interstitial Pneumonitis

    cell histiocytosis.[] The most common symptoms of acute interstitial pneumonitis are highly productive cough with expectoration of thick mucus, fever, and difficulties breathing.[] Abstract We report a case of a previously healthy 41-year-old man who was admitted for progressive dyspnea and cough, which culminated in respiratory failure, shock, and death[]

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