People may have no symptoms or may cough and have difficulty breathing.
Diagnosis requires computed tomography and sometimes analysis of a sample of lung tissue (biopsy).
Whether and which treatments help are unknown, but stopping smoking may help.
(See also Overview of Idiopathic Interstitial Pneumonias Overview of Idiopathic Interstitial Pneumonias Idiopathic interstitial pneumonias are interstitial lung diseases that have no known cause that have some similarities in symptoms and how they affect the lungs. Some types of these diseases... read more .)
Langerhans cell histiocytosis can affect other organs (such as the pituitary gland, bones, and the lymph nodes) as well as the lungs. The cause is unknown, and the disorder is rare. It occurs almost exclusively in White people aged 20 to 40 years who smoke cigarettes.
Pulmonary Langerhans cell histiocytosis starts with infiltration of the lung by histiocytes, which are cells that scavenge for foreign materials, and to a lesser extent by eosinophils, which are cells that are normally involved in allergic reactions.
Symptoms of Pulmonary Langerhans Cell Histiocytosis
About 15% of people have no symptoms and the disorder is first recognized when an imaging study of the chest is done for another reason. The remainder develop coughing, shortness of breath, fever, chest pain worsened by deep breathing, fatigue, and weight loss. Pneumothorax Pneumothorax A pneumothorax is partial or complete collapse of the lung due to the presence of air between the two layers of pleura (thin, transparent, two-layered membrane that covers the lungs and also... read more (a collapsed lung) is a common complication due to rupture of a lung cyst and may be the cause of the first symptoms that develop. Scarring makes the lungs stiff and impairs their ability to transfer oxygen into and out of the blood. A few people cough up blood (hemoptysis).
Some people have pain in certain parts of a bone or a pathologic bone fracture (a fracture that occurs after only a minor injury because the bone has been thinned by a disorder). A few people develop arginine vasopressin deficiency ArginineVasopressin Deficiency (Central Diabetes Insipidus) Argininevasopressin deficiency (central diabetes insipidus) is a lack of the hormone vasopressin (antidiuretic hormone) that causes excessive production of very dilute urine (polyuria). Argininevasopressin... read more (formerly called central diabetes insipidus) when histiocytes also affect the pituitary gland in the brain. The person makes excessive amounts of urine that is dilute. People with arginine vasopressin deficiency probably have a worse prognosis than those who do not.
Diagnosis of Pulmonary Langerhans Cell Histiocytosis
Chest computed tomography
Chest x-rays show nodules, small thick-walled lung cysts, and other changes that are typical of pulmonary Langerhans cell histiocytosis. Computed tomography (CT) may show these changes in enough detail to establish the diagnosis. Pulmonary function testing Pulmonary Function Testing (PFT) Pulmonary function tests measure the lungs' capacity to hold air, to move air in and out, and to absorb oxygen. Pulmonary function tests are better at detecting the general type and severity... read more shows that the amount of air the lungs can hold is below normal.
If CT does not establish the diagnosis, a lung biopsy is required.
X-rays of bones may show that they are also affected.
Treatment of Pulmonary Langerhans Cell Histiocytosis
Corticosteroids or immunosuppressants
Over 90% of people are alive 10 years after diagnosis. Death usually results from respiratory failure Respiratory Failure Respiratory failure is a condition in which the level of oxygen in the blood becomes dangerously low or the level of carbon dioxide in the blood becomes dangerously high. Conditions that block... read more or cor pulmonale (failure of the right side of the heart) Cor Pulmonale Cor pulmonale is enlargement and thickening of the ventricle on the right side of the heart resulting from an underlying lung disorder that causes pulmonary hypertension (high pressures in the... read more .
People with pulmonary Langerhans cell histiocytosis should stop smoking. When people stop smoking Smoking Cessation Most people who smoke want to quit and have tried doing so with limited success. Effective tools to help quit smoking include counseling, nicotine replacement products, and medications. While... read more , improvement occurs in about one third of cases.
Pulmonary Langerhans cell histiocytosis may be treated with corticosteroids and/or immunosuppressants, such as cyclophosphamide, although no therapy is clearly beneficial.