FDG PET/CT in Type I Glycogen Storage Disease - Université de Lorraine
Journal Articles Clinical Nuclear Medicine Year : 2016

FDG PET/CT in Type I Glycogen Storage Disease

Abstract

Type I glycogen storage disease (GSD) is a rare autosomal recessive disorder caused by glucose-6-phosphatase deficiency. We report herein the particular pattern provided by FDG PET imaging in a 33-year-old patient with type Ib GSD. PET images yielded evidence of a pulmonary infectious focus as well as of: (1) a dramatically enlarged liver leading to a high global FDG uptake, (2) increased bone marrow activity, (3) splenomegalia leading to a high global spleen uptake, (4) a diffuse enhancement in muscle FDG uptake.
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Dates and versions

hal-01734818 , version 1 (15-03-2018)

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Chloé Manca, Marine Claudin, Arthur Belle, Pierre Yves Marie, Antoine Verger. FDG PET/CT in Type I Glycogen Storage Disease. Clinical Nuclear Medicine, 2016, 41 (4), pp.e200 - e201. ⟨10.1097/RLU.0000000000001103⟩. ⟨hal-01734818⟩
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