Esophageal stricture secondary to candidiasis in a child with glycogen storage disease 1b

Pediatric Gastroenterology, Hepatology and Nutrition

Volumn 19, Issue 1, 2016, Pages 71-75

  Lee, Kyung Jae ^a   Choi, Shin Jie ^a   Kim, Woo Sun ^a   Park, Sung Sup ^a   Moon, Jin Soo ^a   Ko, Jae Sung ^a  

^a Seoul National University College of Medicine   (South Korea)

Author keywords

Candidiasis; Child; Esophageal stenosis; Esophagitis; Glycogen storage disease

Indexed keywords

EID: 84964252140     PISSN: 22348646     EISSN: 22348840     Source Type: Journal    
DOI: 10.5223/pghn.2016.19.1.71     Document Type: Article

References (19)

1. Ismail A, Abdulla S. Post-monilial extensive esophageal stricture. Pediatr Hematol Oncol 1993;10:111-3.
2. Kimura H, Kurachi M, Tsukioka Y, Minami M, Itou M, Fujii H, et al. Esophageal stricture secondary to candidiasis without underlying disease. J Gastroenterol 1995;30:508-11.
3. Dahl C, Fuursted K, Schrøder H. A paediatric case of Candida pericarditis and eosophagus stricture during treatment for acute lymphatic leukaemia. Acta Oncol 2007;46:859-61.
4. Kelly K, Storey L, O' Sullivan M, Butler K, McDermott M, Corbally M, et al. Esophageal strictures during treatment for acute lymphoblastic leukemia. J Pediatr Hematol Oncol 2010;32:124-7.
5. Kim BW, Cho SH, Rha SE, Choi H, Choi KY, Cha SB, et al. Esophagomediastinal fistula and esophageal stricture as a complication of esophageal candidiasis: a case report. Gastrointest Endosc 2000;52:772-5.
6. Hyun JJ, Chun HJ, Keum B, Seo YS, Kim YS, Jeen YT, et al. Candida esophagitis complicated by esophageal stricture. Endoscopy 2010;42 Suppl 2:E180-1.
7. Bartram CR, Przyrembel H, Wendel U, Bremer HJ, Schaub J, Haas JR. Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia. Eur J Pediatr 1981;137:81-4.
8. Andersen LI, Frederiksen HJ, Appleyard M. Prevalence of esophageal Candida colonization in a Danish population: special reference to esophageal symptoms, benign esophageal disorders, and pulmonary disease. J Infect Dis 1992;165:389-92.
9. Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit GP. Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I). Eur J Pediatr 2002;161 Suppl 1:S20-34.
10. Banka S, Newman WG. A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations. Orphanet J Rare Dis 2013;8:84.
11. Han SH, Ki CS, Lee JE, Hong YJ, Son BK, Lee KH, et al. A novel mutation (A148V) in the glucose 6-phosphate translocase (SLC37A4) gene in a Korean patient with glycogen storage disease type 1b. J Korean Med Sci 2005;20:499-501.
12. Chou JY, Jun HS, Mansfield BC. Glycogen storage disease type I and G6Pase-ß deficiency: etiology and therapy. Nat Rev Endocrinol 2010;6:676-88.
13. Kim SY, Jun HS, Mead PA, Mansfield BC, Chou JY. Neutrophil stress and apoptosis underlie myeloid dysfunction in glycogen storage disease type Ib. Blood 2008;111:5704-11.
14. Pierre G, Chakupurakal G, McKiernan P, Hendriksz C, Lawson S, Chakrapani A. Bone marrow transplantation in glycogen storage disease type 1b. J Pediatr 2008;152: 286-8.
15. Calderwood S, Kilpatrick L, Douglas SD, Freedman M, Smith-Whitley K, Rolland M, et al. Recombinant human granulocyte colony-stimulating factor therapy for patients with neutropenia and/or neutrophil dysfunction secondary to glycogen storage disease type 1b. Blood 2001;97:376-82.
16. Martinez-Olmos MA, López-Sanromán A, Martín- Vaquero P, Molina-Pérez E, Bárcena R, Vicente E, et al. Liver transplantation for type Ib glycogenosis with reversal of cyclic neutropenia. Clin Nutr 2001;20:375-7.
17. Adachi M, Shinkai M, Ohhama Y, Tachibana K, Kuratsuji T, Saji H, et al. Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation. Eur J Pediatr 2004;163:202-6.
18. Kasahara M, Horikawa R, Sakamoto S, Shigeta T, Tanaka H, Fukuda A, et al. Living donor liver transplantation for glycogen storage disease type Ib. Liver Transpl 2009;15:1867-71.
19. Yiu WH, Pan CJ, Allamarvdasht M, Kim SY, Chou JY. Glucose-6-phosphate transporter gene therapy corrects metabolic and myeloid abnormalities in glycogen storage disease type Ib mice. Gene Ther 2007;14:219-26.