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A pediatric patient with glycogen storage disease type IA and Castleman disease

  • Published:2016-12-30 Issue:8 Volume:64 Page:e26431
  • ISSN:1545-5009
  • Container-title:Pediatric Blood & Cancer
  • language:en
  • Short-container-title:Pediatr Blood Cancer

Author:

Cuglievan Branko1,Menegaz Brian A.2,DePombo April1,Morani Ajaykumar C.3,Miranda Roberto N.4,Rytting Michael1

Affiliation:

1. Department of Pediatric Oncology; The University of Texas MD Anderson Cancer Center; Houston Texas

2. Department of Sarcoma Medical Oncology; The University of Texas MD Anderson Cancer Center; Houston Texas

3. Department of Diagnostic Radiology; The University of Texas MD Anderson Cancer Center; Houston Texas

4. Department of Hematopathology; The University of Texas MD Anderson Cancer Center; Houston Texas

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Malignant Transformation of Hepatic Adenoma in Glycogen Storage Disease Type-1a: Report of an Exceptional Case Diagnosed on Surveillance Imaging;Baheti;J Clin Imaging Sci.,2015

2. Hepatocellular glycogenosis and hepatocarcinogenesis;Bannasch;Biochimica Et Biophysica Acta.,1980

3. Hepatocellular adenoma and metabolic balance in patients with type Ia glycogen storage disease;Di Rocco;Mol Genet Metab.,2008

4. Embryonal Hepatoblastoma with Co-existent Glycogen Storage Disease in a Seven-month-old Child;Shirazi;J. Clin Diagn Res: JCDR.,2016

5. Type 1a glycogen storage disease with hepatoblastoma in siblings;Ito;Cancer.,1987

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