Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome
Eosinophilic gastroenteritis is a rare disease characterized by prominent eosinophilic tissue infiltration of the gastrointestinal tract. Here, we report a case of eosinophilic gastroenteritis in an 18-year-old patient with prolonged nephrotic syndrome who presented with abdominal pain and periphera...
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doaj-6f41ba0827cd441d8f3b18eca3c27d2c2020-11-24T20:45:58ZengKorean Pediatric SocietyKorean Journal of Pediatrics1738-10612092-72582016-11-0159Suppl 1S72S7510.3345/kjp.2016.59.11.S7220125553440Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndromeDa Min Choi0Jung Eun Pyun1Hyung Eun Yim2Kee Hwan Yoo3Jung Ok Shim4Eun Jung Lee5Nam Hee Won6Department of Pediatrics, Korea University College of Medicine, Seoul, Korea.Department of Pediatrics, Korea University College of Medicine, Seoul, Korea.Department of Pediatrics, Korea University College of Medicine, Seoul, Korea.Department of Pediatrics, Korea University College of Medicine, Seoul, Korea.Department of Pediatrics, Korea University College of Medicine, Seoul, Korea.Department of Pathology, Korea University College of Medicine, Seoul, Korea.Department of Pathology, Korea University College of Medicine, Seoul, Korea.Eosinophilic gastroenteritis is a rare disease characterized by prominent eosinophilic tissue infiltration of the gastrointestinal tract. Here, we report a case of eosinophilic gastroenteritis in an 18-year-old patient with prolonged nephrotic syndrome who presented with abdominal pain and peripheral hypereosinophilia. During the previous 2 years, he had visited local Emergency Department several times because of epigastric pain and nausea. He had been treated with steroid-dependent nephrotic syndrome since 3 years of age. Tests ruled out allergic and parasitic disease etiologies. Gastroduodenoscopy with biopsy revealed marked eosinophilic infiltration in the duodenum. Renal biopsy findings indicated minimal change disease spectrum without eosinophilic infiltration. The oral deflazacort dosage was increased, and the patient was discharged after abdominal pain resolved. To our knowledge, this is the first report of eosinophilic gastroenteritis in a patient with minimal change disease.http://kjp.or.kr/upload/pdf/kjped-59-S72.pdfNephrotic syndromeEosinophilic enteropathyEosinophilia |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Da Min Choi Jung Eun Pyun Hyung Eun Yim Kee Hwan Yoo Jung Ok Shim Eun Jung Lee Nam Hee Won |
spellingShingle |
Da Min Choi Jung Eun Pyun Hyung Eun Yim Kee Hwan Yoo Jung Ok Shim Eun Jung Lee Nam Hee Won Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome Korean Journal of Pediatrics Nephrotic syndrome Eosinophilic enteropathy Eosinophilia |
author_facet |
Da Min Choi Jung Eun Pyun Hyung Eun Yim Kee Hwan Yoo Jung Ok Shim Eun Jung Lee Nam Hee Won |
author_sort |
Da Min Choi |
title |
Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome |
title_short |
Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome |
title_full |
Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome |
title_fullStr |
Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome |
title_full_unstemmed |
Eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome |
title_sort |
eosinophilic gastroenteritis in an 18-year-old male with prolonged nephrotic syndrome |
publisher |
Korean Pediatric Society |
series |
Korean Journal of Pediatrics |
issn |
1738-1061 2092-7258 |
publishDate |
2016-11-01 |
description |
Eosinophilic gastroenteritis is a rare disease characterized by prominent eosinophilic tissue infiltration of the gastrointestinal tract. Here, we report a case of eosinophilic gastroenteritis in an 18-year-old patient with prolonged nephrotic syndrome who presented with abdominal pain and peripheral hypereosinophilia. During the previous 2 years, he had visited local Emergency Department several times because of epigastric pain and nausea. He had been treated with steroid-dependent nephrotic syndrome since 3 years of age. Tests ruled out allergic and parasitic disease etiologies. Gastroduodenoscopy with biopsy revealed marked eosinophilic infiltration in the duodenum. Renal biopsy findings indicated minimal change disease spectrum without eosinophilic infiltration. The oral deflazacort dosage was increased, and the patient was discharged after abdominal pain resolved. To our knowledge, this is the first report of eosinophilic gastroenteritis in a patient with minimal change disease. |
topic |
Nephrotic syndrome Eosinophilic enteropathy Eosinophilia |
url |
http://kjp.or.kr/upload/pdf/kjped-59-S72.pdf |
work_keys_str_mv |
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