Behçet's disease with multiple splenic abscesses in a child
We report the case of a 5-year-old male patient with multiple aseptic splenic abscesses associated with Behçet's disease. The patient visited Gachon University Gil Hospital with fever, abdominal pain, and acute watery and bloody diarrhea, and reported a 2-year history of chronic abdominal pain...
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Format: | Article |
Language: | English |
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Korean Association for the Study of Intestinal Diseases
2017-07-01
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Series: | Intestinal Research |
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Online Access: | https://doi.org/10.5217/ir.2017.15.3.422 |
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author | Kyung In Lim Dong Hwa Yang Eell Ryoo |
author_facet | Kyung In Lim Dong Hwa Yang Eell Ryoo |
author_sort | Kyung In Lim |
collection | DOAJ |
description | We report the case of a 5-year-old male patient with multiple aseptic splenic abscesses associated with Behçet's disease. The patient visited Gachon University Gil Hospital with fever, abdominal pain, and acute watery and bloody diarrhea, and reported a 2-year history of chronic abdominal pain and intermittent watery diarrhea. He was treated with antibiotics at a local clinic for fever and cervical lymph node swelling. Additionally, he had recurrent stomatitis. A colonoscopy showed multiple well-demarcated ulcerations throughout the colon, and abdominal computed tomography showed multiple splenic abscesses. Pathergy and HLA-B51 tests were positive. Investigations did not reveal any infectious organisms in the aspirate obtained via ultrasound-guided fine needle aspiration. After steroid treatment, all symptoms and multiple aseptic splenic abscesses resolved. However, oral ulcers, genital ulcers, and abdominal pain recurred after tapering the steroids. Infliximab treatment improved the patient's symptoms. However, 5 months after the treatment, the symptoms recurred. The treatment was changed to include adalimumab. Subsequently, the patient's symptoms resolved and colonoscopic findings improved. No recurrence was noted after 3 months of follow-up. |
first_indexed | 2024-12-10T21:02:24Z |
format | Article |
id | doaj.art-63abb2ae322d468bab025700bab85706 |
institution | Directory Open Access Journal |
issn | 1598-9100 |
language | English |
last_indexed | 2024-12-10T21:02:24Z |
publishDate | 2017-07-01 |
publisher | Korean Association for the Study of Intestinal Diseases |
record_format | Article |
series | Intestinal Research |
spelling | doaj.art-63abb2ae322d468bab025700bab857062022-12-22T01:33:45ZengKorean Association for the Study of Intestinal DiseasesIntestinal Research1598-91002017-07-0115342242810.5217/ir.2017.15.3.422ir.2017.15.3.422Behçet's disease with multiple splenic abscesses in a childKyung In Lim0Dong Hwa Yang1Eell Ryoo2Department of Pediatrics, Gachon University Gil Hospital, Incheon, Korea.Department of Pediatrics, Gachon University Gil Hospital, Incheon, Korea.Department of Pediatrics, Gachon University Gil Hospital, Incheon, Korea.We report the case of a 5-year-old male patient with multiple aseptic splenic abscesses associated with Behçet's disease. The patient visited Gachon University Gil Hospital with fever, abdominal pain, and acute watery and bloody diarrhea, and reported a 2-year history of chronic abdominal pain and intermittent watery diarrhea. He was treated with antibiotics at a local clinic for fever and cervical lymph node swelling. Additionally, he had recurrent stomatitis. A colonoscopy showed multiple well-demarcated ulcerations throughout the colon, and abdominal computed tomography showed multiple splenic abscesses. Pathergy and HLA-B51 tests were positive. Investigations did not reveal any infectious organisms in the aspirate obtained via ultrasound-guided fine needle aspiration. After steroid treatment, all symptoms and multiple aseptic splenic abscesses resolved. However, oral ulcers, genital ulcers, and abdominal pain recurred after tapering the steroids. Infliximab treatment improved the patient's symptoms. However, 5 months after the treatment, the symptoms recurred. The treatment was changed to include adalimumab. Subsequently, the patient's symptoms resolved and colonoscopic findings improved. No recurrence was noted after 3 months of follow-up.https://doi.org/10.5217/ir.2017.15.3.422Behcet syndromeSpleenAbscessPediatrics |
spellingShingle | Kyung In Lim Dong Hwa Yang Eell Ryoo Behçet's disease with multiple splenic abscesses in a child Intestinal Research Behcet syndrome Spleen Abscess Pediatrics |
title | Behçet's disease with multiple splenic abscesses in a child |
title_full | Behçet's disease with multiple splenic abscesses in a child |
title_fullStr | Behçet's disease with multiple splenic abscesses in a child |
title_full_unstemmed | Behçet's disease with multiple splenic abscesses in a child |
title_short | Behçet's disease with multiple splenic abscesses in a child |
title_sort | behcet s disease with multiple splenic abscesses in a child |
topic | Behcet syndrome Spleen Abscess Pediatrics |
url | https://doi.org/10.5217/ir.2017.15.3.422 |
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