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Published in: Journal of Inherited Metabolic Disease 3/2010

01-12-2010 | Case Report

Pulmonary hemorrhage in type 3 Gaucher disease: a case report

Authors: Ashok Vellodi, Michael Ashworth, Niamh Finnegan, Colin Wallis

Published in: Journal of Inherited Metabolic Disease | Special Issue 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.
Literature
go back to reference Banjar H (1998) Pulmonary involvement of Gaucher's disease in children: a common presentation in Saudi Arabia. Ann Trop Paediatr 18:55–59PubMed Banjar H (1998) Pulmonary involvement of Gaucher's disease in children: a common presentation in Saudi Arabia. Ann Trop Paediatr 18:55–59PubMed
go back to reference Beutler E, Grabowski GA (2001) Gaucher disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 3635–3638 Beutler E, Grabowski GA (2001) Gaucher disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 3635–3638
go back to reference Burrow TA, Cohen MB, Bokulic R, Deutsch G, Choudhary A, Falcone RA Jr, Grabowski GA (2007) Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapy. J Pediatr 150:202–206PubMedCrossRef Burrow TA, Cohen MB, Bokulic R, Deutsch G, Choudhary A, Falcone RA Jr, Grabowski GA (2007) Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapy. J Pediatr 150:202–206PubMedCrossRef
go back to reference Goitein O, Elstein D, Abrahamov A, Hadas-Halpern I, Melzer E, Kerem E, Zimran A (2001) Lung involvement and enzyme replacement therapy in Gaucher's disease. QJM 94:407–415PubMedCrossRef Goitein O, Elstein D, Abrahamov A, Hadas-Halpern I, Melzer E, Kerem E, Zimran A (2001) Lung involvement and enzyme replacement therapy in Gaucher's disease. QJM 94:407–415PubMedCrossRef
go back to reference Hoffmann B, Schwahn B, Knobbe CB, Vogel M, Blohm M, Mayatepek E, Wendel U (2006) Acute neuronopathic Gaucher disease complicated by fatal gastrointestinal bleeding. Neuropediatrics 37:163–165PubMedCrossRef Hoffmann B, Schwahn B, Knobbe CB, Vogel M, Blohm M, Mayatepek E, Wendel U (2006) Acute neuronopathic Gaucher disease complicated by fatal gastrointestinal bleeding. Neuropediatrics 37:163–165PubMedCrossRef
go back to reference Kerem E, Elstein D, Abrahamov A, Bar ZY, Hadas-Halpern I, Melzer E, Cahan C, Branski D, Zimran A (1996) Pulmonary function abnormalities in type I Gaucher disease. Eur Respir J 9:340–345PubMedCrossRef Kerem E, Elstein D, Abrahamov A, Bar ZY, Hadas-Halpern I, Melzer E, Cahan C, Branski D, Zimran A (1996) Pulmonary function abnormalities in type I Gaucher disease. Eur Respir J 9:340–345PubMedCrossRef
go back to reference Kim JH, Park CH, Pai MS, Hahn MH, Kim HJ (1999) Hepatopulmonary syndrome in Gaucher disease with right-to-left shunt: evaluation and measurement using Tc-99 m MAA. Clin Nucl Med 24:164–166PubMedCrossRef Kim JH, Park CH, Pai MS, Hahn MH, Kim HJ (1999) Hepatopulmonary syndrome in Gaucher disease with right-to-left shunt: evaluation and measurement using Tc-99 m MAA. Clin Nucl Med 24:164–166PubMedCrossRef
go back to reference Lee RE (2007) Pathological anaomy of Gaucher disease: a pictorial essay. In: Futerman AH, Zimran A (eds) Gaucher disease. Taylor & Francis, Boca Raton, pp 197–224 Lee RE (2007) Pathological anaomy of Gaucher disease: a pictorial essay. In: Futerman AH, Zimran A (eds) Gaucher disease. Taylor & Francis, Boca Raton, pp 197–224
go back to reference Mistry PK, Sirrs S, Chan A, Pritzker MR, Duffy TP, Grace ME, Meeker DP, Goldman ME (2002) Pulmonary hypertension in type 1 Gaucher's disease: genetic and epigenetic determinants of phenotype and response to therapy. Mol Genet Metab 77:91–98PubMedCrossRef Mistry PK, Sirrs S, Chan A, Pritzker MR, Duffy TP, Grace ME, Meeker DP, Goldman ME (2002) Pulmonary hypertension in type 1 Gaucher's disease: genetic and epigenetic determinants of phenotype and response to therapy. Mol Genet Metab 77:91–98PubMedCrossRef
go back to reference Pastores GM (2010) Recombinant glucocerebrosidase (imiglucerase) as a therapy for Gaucher disease. BioDrugs 24:41–47PubMedCrossRef Pastores GM (2010) Recombinant glucocerebrosidase (imiglucerase) as a therapy for Gaucher disease. BioDrugs 24:41–47PubMedCrossRef
go back to reference Poll LW, Maas M, Terk MR, Roca-Espiau M, Bembi B, Ciana G, Weinreb NJ (2002) Response of Gaucher bone disease to enzyme replacement therapy. Br J Radiol 75(Suppl 1):A25–A36PubMed Poll LW, Maas M, Terk MR, Roca-Espiau M, Bembi B, Ciana G, Weinreb NJ (2002) Response of Gaucher bone disease to enzyme replacement therapy. Br J Radiol 75(Suppl 1):A25–A36PubMed
go back to reference Schneider EL, Epstein CJ, Kaback MJ, Brandes D (1977) Severe pulmonary involvement in adult Gaucher's disease. Report of three cases and review of the literature. Am J Med 63:475–480PubMedCrossRef Schneider EL, Epstein CJ, Kaback MJ, Brandes D (1977) Severe pulmonary involvement in adult Gaucher's disease. Report of three cases and review of the literature. Am J Med 63:475–480PubMedCrossRef
go back to reference Vellodi A, Bembi B, de Villemeur TB, Collin-Histed T, Erikson A, Mengel E, Rolfs A, Tylki-Szymanska A (2001) Neuronopathic gaucher dis task for management of neuronopathic Gaucher disease: a European consensus. J Inherit Metab Dis 24:319–327PubMedCrossRef Vellodi A, Bembi B, de Villemeur TB, Collin-Histed T, Erikson A, Mengel E, Rolfs A, Tylki-Szymanska A (2001) Neuronopathic gaucher dis task for management of neuronopathic Gaucher disease: a European consensus. J Inherit Metab Dis 24:319–327PubMedCrossRef
Metadata
Title
Pulmonary hemorrhage in type 3 Gaucher disease: a case report
Authors
Ashok Vellodi
Michael Ashworth
Niamh Finnegan
Colin Wallis
Publication date
01-12-2010
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue Special Issue 3/2010
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-010-9176-5

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