Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere digital illustration

Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere Save


ICD-10 code: J84.178

Disease category: None

Other Interstitial Pulmonary Diseases with Fibrosis in Diseases Classified Elsewhere

Interstitial pulmonary diseases with fibrosis can manifest in various forms, including those classified elsewhere. These conditions, while less commonly discussed, are crucial to understand for a comprehensive understanding of respiratory health. In this article, we will explore some of these interstitial pulmonary diseases, excluding their treatments.

  1. Hypersensitivity pneumonitis: This condition occurs when the lung tissue becomes inflamed due to an allergic reaction to inhaled substances such as dust, mold, or chemicals. Common symptoms include coughing, shortness of breath, and fatigue. Diagnosis involves a thorough medical history, physical examination, and imaging tests like chest X-rays or CT scans.
  2. Eosinophilic pneumonia: Eosinophils are a type of white blood cell that plays a role in allergic reactions. Eosinophilic pneumonia occurs when these cells accumulate in the lungs, leading to inflammation and fibrosis. Symptoms may include fever, cough, and difficulty breathing. Diagnosis involves blood tests, imaging studies, and sometimes a lung biopsy.
  3. Sarcoidosis: Sarcoidosis is a multisystem inflammatory disease that can affect various organs, including the lungs. In this condition, abnormal collections of inflammatory cells form in different parts of the body, leading to fibrosis. Symptoms vary depending on the affected organs, but pulmonary involvement often presents as cough, shortness of breath, and chest pain. Diagnosis involves physical examination, blood tests, imaging studies, and sometimes a biopsy.
  4. Lymphangioleiomyomatosis (LAM): LAM is a rare lung disease that primarily affects women. It causes the growth of abnormal smooth muscle cells, leading to the formation of cysts in the lungs. Symptoms may include shortness of breath, coughing, and chest pain. Diagnosis involves lung function tests, imaging studies, and sometimes a biopsy.
  5. Desquamative interstitial pneumonia (DIP): DIP is a form of interstitial lung disease primarily associated with smoking. It is characterized by the accumulation of macrophages (a type of immune cell) in the lungs, leading to tissue damage and fibrosis. Symptoms include cough, shortness of breath, and fatigue. Diagnosis involves physical examination, imaging tests, and sometimes a lung biopsy.

These are just a few examples of interstitial pulmonary diseases with fibrosis that are classified elsewhere. It's important to consult a healthcare professional for an accurate diagnosis and appropriate treatment options if you suspect any respiratory issues. Understanding these conditions can help individuals and their loved ones make informed decisions regarding their health and well-being.

Treatment of Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere:

Treatment Options for 'Other Interstitial Pulmonary Diseases with Fibrosis in Diseases Classified Elsewhere'

Interstitial pulmonary diseases with fibrosis in diseases classified elsewhere refer to a group of respiratory conditions that involve the scarring of lung tissue, resulting in difficulty breathing and reduced lung function. While treatment options may vary depending on the ...

To see full information about treatment please Sign up or Log in