Hypersensitivity pneumonitis in a cystic fibrosis patient

被引：5

作者：

Bellanger, A. P. ^{[1
,2
]}

Morisse-Pradier, H. ^{[2
]}

Reboux, G. ^{[1
,2
]}

Scherer, E. ^{[1
]}

Pramil, S. ^{[3
]}

Dominique, S. ^{[3
]}

Millon, L. ^{[1
,2
]}

机构：

[1] Jean Minjoz Univ Hosp, Parasitol Mycol Dept, 2 Blvd Fleming, F-25000 Besancon, France

[2] Univ Bourgogne Franche Comte, Chronoenvironm UMR CNRS 6249, F-25000 Besancon, France

[3] Rouen Univ Hosp, Pneumol Dept, F-76000 Rouen, France

来源：

OCCUPATIONAL MEDICINE-OXFORD | 2019年 / 69卷 / 8-9期

关键词：

Cystic fibrosis; metalworking fluid; hypersensitivity pneumonitis; Pseudomonas oleovorans; serodiagnosis; METALWORKING FLUIDS; SERODIAGNOSIS;

D O I：

10.1093/occmed/kqz115

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

Hypersensitivity pneumonitis (HP) is a chronic inflammatory lung disease caused by repeated inhalation of antigenic substances. We present a case of metalworking fluids (MWFs)-HP sensitized to Pseudomonas oleovorans in a cystic fibrosis patient. This case illustrates that HP diagnosis remains challenging, especially in patients with another pulmonary disease, and that serodiagnosis contributes to identifying the precise microorganism involved. It also demonstrates that P. oleovorans is an important secondary aetiological agent in MWF-HP, less known than Mycobacterium immunogenum.

引用

页码：632 / 634

页数：3

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