PPT-INTERSTITIAL AND INFILTRATIVE PULMONARY DISEASES

DIFFUSE PARENCHYMAL LUNG DISEASE Restrictive pulmonary Diseases INTRODUCTION Restrictive lung diseases Intrinsic lung diseases alteration in lung parenchyma Extrinsic lung diseases. Paul Swift. What the?. Extrinsic Allergic . alveolitis. Idiopathic pulmonary fibrosis. Industrial dust disease. Organic dust disease. Sarcoidosis. What’s important. Pathophysiology. Clinical features. Diagnosis and Monitoring. Kevin R. Flaherty, MD, . MS.  . Associate Professor. Pulmonary and Critical Care Medicine. University of Michigan Health System. Ann Arbor, Michigan. Faculty Disclosure. . PULMONARY FIBROSIS. 1. By: . Dr.Bidhi. . Chand. Junior Resident Pulmonary Medicine. INTERSTITIAL PULMONARY FIBROSIS. ATS Definition. . Interstitial Pulmonary Fibrosis is defined as a specific form of chronic . Diagnosing Idiopathic Pulmonary Fibrosis. FACULTY. Title. Affiliation. Learning Objectives. Explain the considerations associated with . clinical evaluation, imaging, and . biopsy. , in terms of differentially diagnosing . Robert . Schilz. DO, PhD. University Hospitals Case Medical Center. Cleveland, OH. Outline of Discussion: Scleroderma Lung Concerns. Lung Problems. Interstitial Lung Disease. Pulmonary Vascular Disease. Dr. . Heyam. . Awad. FRCPath. Restrictive lung diseases. - Are . a group of disorders characterized by bilateral, patchy, chronic involvement of the lung connective tissue, mainly the . interstitium. Bahman Saatian, M.D.. Pulmonary Critical Care Medicine. UC Irvine Medical Center. September 8 2014. OBJECTIVES. Review the spectrum of ILD. Identify the clues on presentation to make the diagnosis. Diagnosing Idiopathic Pulmonary Fibrosis. FACULTY. Title. Affiliation. Learning Objectives. Explain the considerations associated with . clinical evaluation, imaging, and . biopsy. , in terms of differentially diagnosing . Paul Swift. What the?. Extrinsic Allergic . alveolitis. Idiopathic pulmonary fibrosis. Industrial dust disease. Organic dust disease. Sarcoidosis. What’s important. Pathophysiology. Clinical features. m. att.velkey@duke.edu. 454A Davison, Duke South, Green Zone. Atelectasis (collapse). Resorption. Obstruction (e.g. infection or inflammation or mucous plug in CF patients): air downstream of blockage is slowly resorbed. Past History. ILD risk factors:. . Other. :. . Presenting . History. Symptom . duration:. . Dyspnoea:. . Cough:. . Other:. . Systemic . symptoms:. . Symptom progression. Pattern: . [improving, stable, relapsing/remitting, worsening]. Dr. Marwa . majid. Aladhab. Homework. Case 1. Case 2. Case 3. Objectives . Anatomically, functionally and radiologically the lungs may be divided into two compartments:. 1. The interstitium: . soft tissue structures between the alveoli, and includes branching distal bronchi and bronchioles, accompanying arteries, veins and lymphatics, plus supporting connective tissue.. ) Pulmonary . Diseases. DR. NISHI. Assistant Professor. Department of Pathology. SKMCH, . Muzaffarpur. Obstructive versus Restrictive Pulmonary Diseases. Chronic . noninfectious. diffuse pulmonary diseases. hypoxia. :. including COPD and interstitial lung disease. Chronic . thromboembolic pulmonary . hypertension. Pulmonary . hypertension with unclear or . multifactorial mechanisms. Pathogenesis. Chronic obstructive or interstitial lung diseases.