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  • Title: Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapy.
    Author: Burrow TA, Cohen MB, Bokulic R, Deutsch G, Choudhary A, Falcone RA, Grabowski GA.
    Journal: J Pediatr; 2007 Feb; 150(2):202-6. PubMed ID: 17236903.
    Abstract:
    A 5-year-old male with Gaucher's disease type 3 developed progressive mesenteric and mediastinal lymphadenopathy over 12 months, despite enzyme replacement therapy, contributing to the development of a protein-losing enteropathy. These complications are unique, indicating poorly accessible, differentially responsive compartments in patients with Gaucher's disease who are receiving enzyme therapy.
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