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Erschienen in: Journal of Inherited Metabolic Disease 3/2010

01.12.2010 | Case Report

Pulmonary hemorrhage in type 3 Gaucher disease: a case report

verfasst von: Ashok Vellodi, Michael Ashworth, Niamh Finnegan, Colin Wallis

Erschienen in: Journal of Inherited Metabolic Disease | Sonderheft 3/2010

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Abstract

A 2-year-old boy with type 3 Gaucher disease (GD) on treatment with enzyme replacement therapy (ERT) was found dead in bed having been apparently well the night before. At the time of diagnosis, he had significant respiratory symptoms (severe and persistent bouts of coughing) that had been attributed to Gaucher lung infiltration and that were controlled by inhaled and orally administered steroids. These symptoms had begun to reappear just prior to death. Postmortem revealed extensive pulmonary hemorrhage and intra-alveolar collections of Gaucher cells. There was very little evidence of GD elsewhere. Death was ascribed to pulmonary hemorrhage secondary to GD. The pathogenesis was unclear. To the best of our knowledge, this is the first case of isolated pulmonary hemorrhage secondary to GD and may represent a hitherto unrecognized complication of this condition. Given the apparent temporal relationship, we propose that it represented a severe, terminal event in the course of Gaucher lung disease.
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Metadaten
Titel
Pulmonary hemorrhage in type 3 Gaucher disease: a case report
verfasst von
Ashok Vellodi
Michael Ashworth
Niamh Finnegan
Colin Wallis
Publikationsdatum
01.12.2010
Verlag
Springer Netherlands
Erschienen in
Journal of Inherited Metabolic Disease / Ausgabe Sonderheft 3/2010
Print ISSN: 0141-8955
Elektronische ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-010-9176-5

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