Esophageal Stricture Secondary to Candidiasis in a Child with Glycogen Storage Disease 1b
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Esophageal candidiasis is commonly seen in immunocompromised patients; however, candida esophagitis induced stricture is a very rare complication. We report the first case of esophageal stricture secondary to candidiasis in a glycogen storage disease (GSD) 1b child. The patient was diagnosed with GSD type 1b by liver biopsy. No mutation was found in the G6PC gene, but SLC37A4 gene sequencing revealed a compound heterozygous mutation (p.R28H and p.W107X, which was a novel mutation). The patient’s absolute neutrophil count was continuously under 1,000/µLwhen he was over 6 years of age. He was admitted frequently for recurrent fever and infection, and frequently received intravenous antibiotics, antifungal agents. He complained of persistent dysphagia beginning at age 7 years. Esophageal stricture and multiple whitish patches were observed by endoscopy and endoscopic biopsy revealed numerous fungal hyphae consistent with candida esophagitis. He received esophageal balloon dilatation four times, and his symptoms improved.
Abstract
Esophageal candidiasis is commonly seen in immunocompromised patients; however, candida esophagitis induced stricture is a very rare complication. We report the first case of esophageal stricture secondary to candidiasis in a glycogen storage disease (GSD) 1b child. The patient was diagnosed with GSD type 1b by liver biopsy. No mutation was found in the G6PC gene, but SLC37A4 gene sequencing revealed a compound heterozygous mutation (p.R28H and p.W107X, which was a novel mutation). The patient’s absolute neutrophil count was continuously under 1,000/µLwhen he was over 6 years of age. He was admitted frequently for recurrent fever and infection, and frequently received intravenous antibiotics, antifungal agents. He complained of persistent dysphagia beginning at age 7 years. Esophageal stricture and multiple whitish patches were observed by endoscopy and endoscopic biopsy revealed numerous fungal hyphae consistent with candida esophagitis. He received esophageal balloon dilatation four times, and his symptoms improved.
참고문헌 (19)
- Ismail A, "Post-monilial extensive esophageal stricture", Pediatr Hematol Oncol, 10, pp.111~113 (1993)
- Kimura H, "Esophageal stricture secondary to candidiasis without underlying disease", J Gastroenterol, 30, pp.508~511 (1995)
- Dahl C, "A paediatric case of Candida pericarditis and eosophagus stricture during treatment for acute lymphatic leukaemia", Acta Oncol, 46, pp.859~861 (2007)
- Kelly K, "Esophageal strictures during treatment for acute lymphoblastic leukemia", J Pediatr Hematol Oncol, 32, pp.124~127 (2010)
- Kim BW, "Esophagomediastinal fistula and esophageal stricture as a complication of esophageal candidiasis: a case report", Gastrointest Endosc, 52, pp.772~775 (2000)
- Hyun JJ, "Candida esophagitis complicated by esophageal stricture", Endoscopy, 42(Suppl 2), pp.E180~E181 (2010)
- Bartram CR, "Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia", Eur J Pediatr, 137, pp.81~84 (1981)
- Andersen LI, "Prevalence of esophageal Candida colonization in a Danish population: special reference to esophageal symptoms, benign esophageal disorders, and pulmonary disease", J Infect Dis, 165, pp.389~392 (1992)
- Rake JP, "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, 161(Suppl 1), pp.S20~S34 (2002)
- Banka S, "A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations", Orphanet J Rare Dis, 8, pp.84~ (2013)
- Han Sung Hee, "A Novel Mutation (A148V) in the Glucose 6-phosphate Translocase (SLC37A4) Gene in a Korean Patient with Glycogen Storage Disease Type 1b", Journal of Korean Medical Science, 20(3), pp.499~501 (2005), 대한의학회
- Chou JY, "Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy", Nat Rev Endocrinol, 6, pp.676~688 (2010)
- Kim SY, "Neutrophil stress and apoptosis underlie myeloid dysfunction in glycogen storage disease type Ib", Blood, 111, pp.5704~5711 (2008)
- Pierre G, "Bone marrow transplantation in glycogen storage disease type 1b", J Pediatr, 152, pp.286~288 (2008)
- Calderwood S, "Recombinant human granulocyte colony-stimulating factor therapy for patients with neutropenia and", or neutrophil dysfunction secondary to glycogen storage disease type 1b, 2001, pp.97, 376~382
- Martinez-Olmos MA, "Liver transplantation for type Ib glycogenosis with reversal of cyclic neutropenia", Clin Nutr, 20, pp.375~377 (2001)
- Adachi M, "Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation", Eur J Pediatr, 163, pp.202~206 (2004)
- Kasahara M, "Living donor liver transplantation for glycogen storage disease type Ib", Liver Transpl, 15, pp.1867~1871 (2009)
- Yiu WH, "Glucose-6-phosphate transporter gene therapy corrects metabolic and myeloid abnormalities in glycogen storage disease type Ib mice", Gene Ther, 14, pp.219~226 (2007)
