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Recurrent diffuse lung disease due to surfactant protein C deficiency.

Identifieur interne : 000C18 ( Main/Exploration ); précédent : 000C17; suivant : 000C19

Recurrent diffuse lung disease due to surfactant protein C deficiency.

Auteurs : Brigitte Kazzi [États-Unis] ; David Lederer [États-Unis] ; Emilio Arteaga-Solis [États-Unis] ; Anjali Saqi [États-Unis] ; Wendy K. Chung [États-Unis]

Source :

RBID : pubmed:30094155

Abstract

Surfactant protein C (SP-C) deficiency causes diffuse lung disease with variable prognosis and severity that usually presents in infancy. We present the case of a patient with diffuse lung disease who was successfully treated with hydroxychloroquine and steroids in infancy, who presented again as a young adult with respiratory symptoms. Exome sequencing identified a novel de novo SFTPC mutation (c.397A > C p.S133R). Mutated SP-C accumulates and leads to injury of alveolar type II cells, which normally replenish alveolar type I cells after injury. This may explain the symptom recurrence after lung injury in young adulthood. Although hydroxychloroquine has been hypothesized to interfere with mutated SP-C accumulation, data on long term outcome remains limited.

DOI: 10.1016/j.rmcr.2018.07.003
PubMed: 30094155


Affiliations:


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mutation (c.397A > C p.S133R). Mutated SP-C accumulates and leads to injury of alveolar type II cells, which normally replenish alveolar type I cells after injury. This may explain the symptom recurrence after lung injury in young adulthood. Although hydroxychloroquine has been hypothesized to interfere with mutated SP-C accumulation, data on long term outcome remains limited.</div>
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