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DOI 10.1016/j.rmr.2015.05.005

Медицинская библиотека · Revue des maladies respiratoires · 2015

[Lung disease in adult common variable immunodeficiency].

Hadjadj J, Malphettes M, Fieschi C, Oksenhendler E, Tazi A, Bergeron A

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Аннотация

INTRODUCTION

Common variable immunodeficiency (CVID) is characterized by a defect in antibody production and may be complicated by infectious or non-infectious respiratory disease.

BACKGROUND

In addition to recurrent infectious complications, mainly due to encapsulated bacteria, CVID may be complicated by diffuse infiltrative, non-infectious lung disease. The latter may be related to granulomatosis, lymphoid interstitial pneumonia, follicular bronchiolitis, follicular nodular hyperplasia, organizing pneumonia or lymphoma. Different lymphoid histological lesions can co-exist and form a new entity called GLILD (granulomatous lymphocytic interstitial lung disease), which is associated with a poor prognosis. Replacement of immunoglobulins significantly decreases the frequency and severity of infections but has no impact on the non-infectious complications.

OUTLOOK: Studies are needed to determine the modalities of follow-up and better understand the long-term progress of GLILD. These studies should improve the management of GLILD in the context of immunosuppressive treatments, which increase the risk of infection in CVID.

CONCLUSION

The identification of GLILD, which reflects a variable histological spectrum, rather than a well-defined entity, necessitates revising the approach to diffuse infiltrative lung diseases in CVID.

Для цитирования: Hadjadj J, Malphettes M, Fieschi C, Oksenhendler E, Tazi A, Bergeron A. [Lung disease in adult common variable immunodeficiency].. Revue des maladies respiratoires. 2015. DOI: 10.1016/j.rmr.2015.05.005.

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