منابع مشابه
Splenomegaly, Cardiomegaly, and Osteoporosis in a Child with Gaucher Disease
A 15-month-old girl, born to the consanguineous parents, was referred with the sign of massive splenomegaly associated with thrombocytopenia and anemia. Plasma Chitotriosidase estimation was carried out as a screening test and was found to be normal with reduced activity of β-glucosidase in leucocytes suggestive of Gaucher disease. At the age of 4 years, severe osteoporosis and cardiomegaly wit...
متن کاملChronic myeloid leukemia with marked splenomegaly and pseudo-Gaucher cells
which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. A 17-year-old boy with no specific medical history presented with abdominal distension. A complete blood analysis revealed a leukocyte count of 151.6×10 9 /L. A contrast-enhanced abdominal computed tomography image showed marked splenomegaly (A) and mildly e...
متن کاملEffect of oral eliglustat on splenomegaly in patients with Gaucher disease type 1: the ENGAGE randomized clinical trial.
IMPORTANCE Gaucher disease type 1 is characterized by hepatosplenomegaly, anemia, thrombocytopenia, and skeletal disease. A safe, effective oral therapy is needed. OBJECTIVE To determine whether eliglustat, a novel oral substrate reduction therapy, safely reverses clinical manifestations in untreated adults with Gaucher disease type 1. DESIGN, SETTING, AND PARTICIPANTS Phase 3, randomized, ...
متن کاملSplenomegaly as a Primary Manifestation of Gaucher Disease in a Young Adult Woman
Gaucher disease is the most common lysosomal storage disease. It is caused by the defective activity of acid β-glucosidase, which results in the accumulation of lipid glucocerebroside in macrophages throughout the body. In this case report we describe the case of a young adult woman with splenomegaly as the primary manifestation of this pathology. This is a case of type 1 Gaucher disease becaus...
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ژورنال
عنوان ژورنال: Journal of the American Medical Association
سال: 1919
ISSN: 0002-9955
DOI: 10.1001/jama.1919.02610010025006