Increased Prevalence of IgG-lnduced Sensitization and Hypersensitivity Pneumonitis (Humidifier Lung) in Nonsmokers Exposed to Aerosols of a Contaminated Air Conditioner

Respiration ◽  
1992 ◽  
Vol 59 (4) ◽  
pp. 211-214 ◽  
Author(s):  
X. Baur ◽  
G. Richter ◽  
A. Pethran ◽  
A.B. Czuppon ◽  
M. Schwaiblmair
Respirology ◽  
2021 ◽  
Author(s):  
Masafumi Shimoda ◽  
Kozo Morimoto ◽  
Yoshiaki Tanaka ◽  
Koji Furuuchi ◽  
Takeshi Osawa ◽  
...  

2021 ◽  
Vol 2 (4) ◽  
pp. 96-100
Author(s):  
N. A. Karoli ◽  
V. E. Kharlamov ◽  
O. T. Zarmanbetova

Humidifier lung syndrome is a rare phenotype of hypersensitive pneumonitis (HP) caused by inhalation of fumes from contaminated climate appliances such as a humidifier and air conditioner. Since the described syndrome is rarely found in the Russian Federation, the practitioner should be wary of this pathology, carefully collect an anamnesis from the patient, and also carry out differential diagnostics with lung lesions of autoimmune, drug, infectious genesis. HP therapy includes exclusion of contact with the etiological factor and the appointment of systemic hormonal therapy. 


CHEST Journal ◽  
1976 ◽  
Vol 69 (2) ◽  
pp. 294-296 ◽  
Author(s):  
Peter F. Kohler ◽  
Gary Gross ◽  
John Salvaggio ◽  
June Hawkins

2020 ◽  
Vol 174 ◽  
pp. 106196
Author(s):  
Susumu Sakamoto ◽  
Marie Furukawa ◽  
Hiroshige Shimizu ◽  
Muneyuki Sekiya ◽  
Shion Miyoshi ◽  
...  

2020 ◽  
pp. 4244-4256
Author(s):  
S. J. Bourke ◽  
G.P. Spickett

Hypersensitivity pneumonitis is an immune-mediated lung disease in which the repeated inhalation of certain antigens provokes a hypersensitivity response, with granulomatous inflammation in the distal bronchioles and alveoli of susceptible people. A diverse range of antigens including bacteria (Thermophilic actinomycetes), fungi (Trichosporon cutaneum), animal proteins (bird antigens), mycobacteria, and chemicals may cause the disease. The commonest forms are bird fancier’s lung, farmer’s lung, humidifier lung, and metal-working fluid pneumonitis. In some cases no antigen is identified. Acute disease is characterized by recurrent episodes of breathlessness, cough, fevers, malaise, and flu-like symptoms occurring 4–8 hours after antigen exposure. Fever and basal crackles are the main physical signs. Chronic disease is characterized by the insidious development of dyspnoea and persistent pneumonitis, sometimes progressing to lung fibrosis. Clinical features are similar to those of other varieties of pulmonary fibrosis, but clubbing is uncommon.


CHEST Journal ◽  
1976 ◽  
Vol 69 (2) ◽  
pp. 294-296 ◽  
Author(s):  
P. F. Kohler ◽  
G. Gross ◽  
J. Salvaggio ◽  
J. Hawkins

1970 ◽  
Vol 283 (6) ◽  
pp. 271-276 ◽  
Author(s):  
Edward F. Banaszak ◽  
Walter H. Thiede ◽  
Jordan N. Fink

2020 ◽  
Vol 31 ◽  
pp. 101267
Author(s):  
Masafumi Shimoda ◽  
Kozo Morimoto ◽  
Yoshiaki Tanaka ◽  
Ohta Ken ◽  
Kozo Yoshimori

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