[Granulomatous lymphocytic interstitial lung disease (GLILD) as a manifestation of pulmonary changes in common variable immunodeficiency (CVID) – case report].
Elżbieta Marciszewska, Anna Szaflarska, Anna Pituch-Noworolska
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引用次数: 0
Abstract
Common variable immunodeficiency
(CVID) comprise different kinds of
primary hypogammaglobulinemias of
mostly unknown etiology. The onset of
the disease and its clinical symptoms
may appear as well in children as in
adults. Apart from susceptibility to
bacterial, viral and fungal infections,
other clinical signs (autoimmunization,
non-infectious lung and gastrointestinal
diseases, neoplasm) are frequently
observed. About 58% of patients with
CVID develops granulomatous and
lymphocytic interstitial lung disease
(GLILD) associated with early mortality.
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