Granulomatous Lung Disease
Lung disease could be mild and limiting like the common cold or life-threatening like pneumonia or pulmonary embolism. Granulomatous Lung Disease is a vasculitic syndrome that results due to an increase in ANCAs or antineutrophil cytoplasmic antibodies (abnormal circulating antibodies), affecting the blood vessels in and around the lungs.

Possible Causes
Lung diseases are a common cause of illness and death, with every one out of seven people being affected by some form or the other, worldwide. Chronic lung diseases include the onslaught of pneumonia, pulmonary embolism, asthma and granulomatous lung disease. Granulomas in the lungs cause prolonged lung damage. This vasculitic syndrome is caused due to the increased presence of antineutrophil cytoplasmic antibodies or destructive circulating antibodies that affect small and medium-size blood vessels in and around the lungs. The disease calls for long-term immunosuppression and can result in death, if left untreated. The variable initial manifestations of this disease delays diagnosis, leading to a subsequent delay in treatment. The nonspecific nature of the symptoms makes clinical diagnosis quite difficult. Granulomas in the lung are caused by mycobacterial or fungal infection like aspiration pneumonia, wherein bacteria is inhaled from the oral cavity into the lungs and granulomas form when food particles or pill fragments are aspirated into the lungs. Granulomas are also produced by an infectious disease called histoplasmosis, caused by inhaling spores of the fungal organism Histoplasma capsulatum. Sarcoidosis is another infection that causes lung granulomas.
Signs and Symptoms
This lung disease manifests in the form of:
- Rhinitis or a runny nose, resulting from inflammation of the mucous membrane.
- Nasal congestion.
- Infections of organs in the upper airway, eye and ear.
- Nosebleeds.
- Hearing loss due to dysfunction of the auditory tube.
- Strawberry gingivitis.
- Ulcers throughout the oral mucosa.
- Scleritis
- Subglottic stenosis
- Pulmonary hemorrhage, leading to hemoptysis
- Glomerulonephritis, leading to renal failure
- Arthritis
- Purpura
- Sensory neuropathy
Granulomatous lung disease is usually suspected only after prolonged manifestation of unexplained symptoms. Cytoplasmic staining, microscopy and biopsy are common diagnostic procedures adopted to confirm the condition. The basic criteria of any diagnostic procedure run on this disease demands the presence of a granulomatous inflammation of the respiratory tract and vasculitis of blood vessels in the region affected. It is widely presumed that the disease is the result of inflammation caused by the anti-neutrophil cytoplasmic antibodies. The resultant damage to the endothelium, arterioles and endothelial cells is detected via detailed clinical analysis.
The treatment options to arrest the lung damage triggered by the onset of granulomatous lung disease include:
- Cyclophosphamide in oral and monthly intravenous (IV) doses
- Corticosteroids
- Azathioprine
- Methotrexate
- Mycophenolate mofetil
- 15-deoxyspergualin
- Anti-thymocyte globulin
- Intravenous immunoglobulin
- Rituximab and infliximab
- Plasmapheresis, in the case of pulmonary hemorrhage
- Periodical monitoring of the white blood count
- Tracheotomy
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