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Types of Pulmonary Fibrosis

A dry Cough
A dry Cough

The cough frequency in IPF is similar to patients with chronic cough presenting to a cough specialist clinic, and higher than in patients with asthma or COPD (asthma median (range) 24-h cough rate 62.4 (0–341), COPD ex-smokers 117.6 (range 14.4–648)) [10, 12].

Aching Muscles and Joints
Aching Muscles and Joints

Home » Aching Muscles and Joints Pulmonary fibrosis is a respiratory condition that causes thick and stiff tissue in the lungs, followed by scarring. It can be developed as a secondary disease to tuberculosis, pneumonia, systemic lupus erythematosus, rheumatoid arthritis, sarcoidosis or scleroderma.

AIP: Acute Interstitial Pneumonia
AIP: Acute Interstitial Pneumonia

Acute interstitial pneumonia (AIP) is an idiopathic version of the acute respiratory distress syndrome . Acute interstitial pneumonia, a form of idiopathic interstitial pneumonia, equally affects apparently healthy men and women, usually those > 40 yr.

Becoming Housebound
Becoming Housebound

End stage pulmonary fibrosis life expectancy is a topic that many would rather avoid, however, it’s vital to understanding one’s options as they navigate the management of their health. Though PF can seem impossible to overcome, changing one’s diet and consistently exercising are among the best lifestyle changes one can do aside from quitting smoking.

Bone Marrow Fibrosis
Bone Marrow Fibrosis

Myelofibrosis, also known as osteomyelofibrosis, is a relatively rare bone marrow cancer. It is currently classified as a myeloproliferative neoplasm, in which the proliferation of an abnormal clone of hematopoietic stem cells in the bone marrow and other sites results in fibrosis, or the replacement of the marrow with scar tissue.

Bothersome Cough
Bothersome Cough

The cough frequency in IPF is similar to patients with chronic cough presenting to a cough specialist clinic, and higher than in patients with asthma or COPD (asthma median (range) 24-h cough rate 62.4 (0–341), COPD ex-smokers 117.6 (range 14.4–648)) [10, 12].

Chest Pain
Chest Pain

Pulmonary rehabilitation is a standard part of treatment for people with pulmonary fibrosis. This can involve an exercise program, breathing exercises, and stress management. This can involve an exercise program, breathing exercises, and stress management.

image: biologos.org
CTD-ILD: Connective Tissue Disease Interstitial Lung Disease
CTD-ILD: Connective Tissue Disease Interstitial Lung Disease

Connective tissue disease associated with interstitial lung disease, or CT-ILD, is a lung condition that affects a small number of patients with a connective tissue disease. Examples of connective tissue diseases — also known as rheumatologic, collagen vascular or autoimmune diseases — include scleroderma, rheumatoid arthritis, Sjogren's syndrome, systemic lupus erythematosus, polymyositis, dermatomyositis and mixed connective tissue disease.

Depression
Depression

Depression is a common problem for patients with pulmonary fibrosis. Common symptoms include feeling blue, loss of interest in activities that you usually enjoy, increased or decreased sleep, irritability, change in appetite, frequent crying, avoiding social situations and thoughts of hurting yourself. The symptoms of depression may be mild, moderate or severe.

Disturbed Sleep Patterns
Disturbed Sleep Patterns

End Stage Pulmonary Fibrosis Life Expectancy: What Is It? ... Disturbed sleep patterns; Need for intensive home support; Frequent flare-ups and hospitalizations ; Increased severity in shortness of breath; Difficulty maintaining a healthy body weight; How Can I Prepare and Improve My Health? Although end-stage pulmonary fibrosis is a difficult position to be in as it pertains to respiratory ...

Fatigue
Fatigue

While the exact reason for fatigue in autoimmune diseases like pulmonary fibrosis is unclear, many experts feel that a lack of oxygen may contribute to the symptom, coupled with the fact that many people living with PF struggle to get quality sleep.

FPF: Familial Pulmonary Fibrosis
FPF: Familial Pulmonary Fibrosis

Individuals with Familial Pulmonary Fibrosis (FPF) have at least one affected first or second-degree relative and account for 0.5-20% of cases.

FVC: Forced Vital Capacity
FVC: Forced Vital Capacity

Rationale: Forced vital capacity (FVC) is an established measure of pulmonary function in idiopathic pulmonary fibrosis (IPF). Evidence regarding its measurement properties and minimal clinically important difference (MCID) in this population is limited.

GERD: Gastroesophageal Reflux Disease
GERD: Gastroesophageal Reflux Disease

Background: Gastroesophageal Reflux Disease (GERD) GERD is abnormal movement of stomach contents into the esophagus. This “refluxate” is very acidic and contains digestive enzymes. Background: IPF and GERD. Pulmonary fibrosis was triggered by the insertion of acid into the lungs in animal models, suggesting a relationship between IPF and GERD.

source: cpff.ca
Heart Fibrosis
Heart Fibrosis

Learn what you need to know about pulmonary fibrosis and idiopathic pulmonary fibrosis. What is pulmonary fibrosis? Learn what you need to know about pulmonary fibrosis and idiopathic pulmonary fibrosis, including information about PF types and risk factors, symptoms and diagnosis.

source: lung.org
HRCT: High-Resolution Computed Tomography
HRCT: High-Resolution Computed Tomography

HRCT (high resolution computed tomography) scans of the chest are crucial in the evaluation of idiopathic pulmonary fibrosis. A CT scan of the chest uses X-rays to obtain images of the lung tissue. The images are obtained in “slices” or thin views that are put together to form a picture.

ILD: Interstitial Lung Disease
ILD: Interstitial Lung Disease

Desquamative interstitial pneumonitis: An interstitial lung disease that's partially caused by smoking. Sarcoidosis: A condition causing interstitial lung disease along with swollen lymph nodes, and sometimes heart, skin, nerve, or eye involvement.

source: webmd.com
Increased Anxiety
Increased Anxiety

Depression and anxiety significantly influence the quality of life of people with idiopathic pulmonary fibrosis, although not their hospitalization or death rates, a study found. IPF patients are susceptible to depression and anxiety because it is a chronic disease with no cure.

Liver Fibrosis
Liver Fibrosis

Liver cirrhosis presents areas of scar tissue and nodules that replace the normal liver tissue and alter liver function being caused by alcoholism, hepatitis viruses and fatty liver disease. Pulmonary fibrosis – refers to multiple lung conditions that cause interstitial lung damage and scarring.

image: humpath.com
Lung Fibrosis or Pulmonary Fibrosis
Lung Fibrosis or Pulmonary Fibrosis

Pulmonary fibrosis is a disease marked by scarring in the lungs. The information here can be helpful to anyone facing one of the many types of pulmonary fibrosis, including the most commonly diagnosed idiopathic pulmonary fibrosis (IPF).

source: lung.org
Mediastinal Fibrosis
Mediastinal Fibrosis

mediastinal fibrosis development of hard white fibrous tissue in the upper portion of the mediastinum, sometimes obstructing the air passages and large blood vessels; called also fibrosing or fibrous mediastinitis.

Poor Appetite
Poor Appetite

Idiopathic pulmonary fibrosis is an irreversible, fatal lung disease that plagues adults in their 60s who are otherwise healthy. Fibrotic scar tissue takes over the lungs, progressively decreasing a patient’s ability to transfer oxygen into the bloodstream and causes progressive shortness of breath with activities requiring exertion and, ultimately, while patients are at rest and during conversation.

Reduced Lung Function
Reduced Lung Function

Pulmonary fibrosis describes a group of diseases which produce interstitial lung damage and ultimately fibrosis and loss of the elasticity of the lungs. It is a chronic condition characterised by shortness of breath, diffuse infiltrates on CXR and inflammation and/or fibrosis on biopsy.

source: patient.info
Retroperitoneal Cavity Fibrosis
Retroperitoneal Cavity Fibrosis

retroperitoneal fibrosis deposition of fibrous tissue in the retroperitoneal space, producing vague abdominal discomfort, and often causing blockage of the ureters, with resultant hydronephrosis and impaired renal function, which may result in renal failure.

Scleroderma or Systemic Sclerosis
Scleroderma or Systemic Sclerosis

Our Three-Fold Mission Is Support, Education and Research Pulmonary Fibrosis in Systemic Sclerosis: Diagnosis and Management A publication of Scleroderma Foundation

Shortness of Breath (Dyspnea)
Shortness of Breath (Dyspnea)

Home » Shortness of Breath (Dyspnea) in Pulmonary Fibrosis Along with a persistent cough, shortness of breath is among the most common symptoms associated with Pulmonary Fibrosis (PF). 1 Referred to medically as dyspnea, 2 shortness of breath is symptomatic of a wide range of diseases and conditions, varying from serious pulmonary diseases to simply being out of shape.

Skin Fibrosis
Skin Fibrosis

Scleroderma is named after skin fibrosis, which is one of its most common and recognizable symptoms. Skin fibrosis eventually develops in most patients. Sclero means "hard" and derma means "skin". The diagnosis of skin fibrosis is clinical and it requires no laboratory or special testing.

source: sclero.org
Unexplained Weight Loss
Unexplained Weight Loss

What is Pulmonary Fibrosis? The word “pulmonary” means lung and the word “fibrosis” means scar tissue— similar to scars that you may have on your skin from an old injury or surgery. So, in its simplest sense, pulmonary fibrosis (PF) means scarring in the lungs.