Ulcerative Colitis with Henoch Schonlein Purpura in Pediatric Patient: A Case-Report

Authors

  • Ninung Rose Diana Kusumawati Departement of Pediatrics, Faculty of Medicine, Diponegoro University, Semarang, Indonesia
  • Juwita Pratiwi Departement of Pediatrics, Faculty of Medicine, Diponegoro University, Semarang, Indonesia
  • Sonya Leonardy Low Departement of Pediatrics, Faculty of Medicine, Diponegoro University, Semarang, Indonesia
  • Dyan Ajeng Paramitha Departement of Pediatrics, Faculty of Medicine, Diponegoro University, Semarang, Indonesia
  • Wahyu Aditya Prawirasatra Departement of Pediatrics, Faculty of Medicine, Diponegoro University, Semarang, Indonesia
  • Nindya Riesmania Pratiwi Departement of Pediatrics, Faculty of Medicine, Diponegoro University, Semarang, Indonesia
  • Adinda Ratna Puspita Departement of Pediatrics, Faculty of Medicine, Diponegoro University, Semarang, Indonesia

DOI:

https://doi.org/10.58427/apghn.2.4.2023.30-5

Keywords:

Children, Henoch Schonlein Purpura, Inflammatory Bowel Disease, Ulcerative Colitis

Abstract

Background: Inflammatory bowel disease (IBD) is defined as idiopathic disorder which associated with inflammation of gastrointestinal tract. Ulcerative colitis (UC) and Chron's disease are the predominant forms of IBD. Henoch Schonlein Purpura and UC share some similar symptoms and can mimic each other especially in children. In this case report, we present an eight-year-old boy who had main complaint of recurrent bloody stools and abdominal pain.  Diagnosis was made through history taking, physical examination, laboratory examination and colonoscopy in this patient.

Case: A boy aged 8 years and 1 month had main complaint of bloody stools with fluid consistency. This complaint was accompanied by abdominal pain all over the abdominal region and vomiting. Upon physical examination, the child was in pain. The vital signs were within normal limits. Laboratory examination showed leukocytosis. The routine stool examination showed malabsorption of fat, protein, and carbohydrates, followed with positive erythrocytes, leukocytes, epithelium, bacteria, and yeast cells; but the stool culture was sterile. Gastroscopy and colonoscopy were performed which showed erosive gastritis, duodenitis, and proctitis.

Discussion: The relationship between ulcerative colitis and HSP remains unknown. Recent research showed overproduction of IgA may induce chronic inflammation in the intestinal. While HSP is IgA/immune complex mediated, IBD is thought to be predominantly T-cell driven. Recently, in IBD patients especially those with ulcerative colitis, IgA were found in their histopathologic biopsy result.

Conclusion: The relationship between ulcerative colitis and HSP remains unknown. Recent research has shown that the overproduction of IgA may induce chronic inflammation in the intestinal. As such, symptoms of both diseases may mimic each other as seen in our patients.

References

Sýkora J, Pomahačová R, Kreslová M, Cvalínová D, Štych P, Schwarz J. Current global trends in the incidence of pediatric-onset inflammatory bowel disease. World J Gastroenterol. 2018;24(25):2741-63. https://doi.org/10.3748/wjg.v24.i25.2741 DOI: https://doi.org/10.3748/wjg.v24.i25.2741

Bradley GM, Oliva-Hemker M. Pediatric ulcerative colitis: current treatment approaches including role of infliximab. Biologics. 2012;6:125-34.https://doi.org/10.2147/btt.S31833 DOI: https://doi.org/10.2147/BTT.S31833

Rosen MJ, Dhawan A, Saeed SA. Inflammatory Bowel Disease in Children and Adolescents. JAMA Pediatr. 2015;169(11):1053-60.https://doi.org/10.1001/jamapediatrics.2015.1982 DOI: https://doi.org/10.1001/jamapediatrics.2015.1982

Zeisler B, Lerer T, Markowitz J, Mack D, Griffiths A, Bousvaros A, et al. Outcome following aminosalicylate therapy in children newly diagnosed as having ulcerative colitis. J Pediatr Gastroenterol Nutr. 2013;56(1):12-8.https://doi.org/10.1097/MPG.0b013e31826ac41a DOI: https://doi.org/10.1097/MPG.0b013e31826ac41a

Ruperto N, Ozen S, Pistorio A, Dolezalova P, Brogan P, Cabral DA, et al. EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part I: Overall methodology and clinical characterisation. Ann Rheum Dis. 2010;69(5):790-7.https://doi.org/10.1136/ard.2009.116624 DOI: https://doi.org/10.1136/ard.2009.116624

Louie CY, Gomez AJ, Sibley RK, Bass D, Longacre TA. Histologic Features of Gastrointestinal Tract Biopsies in IgA Vasculitis (Henoch-Schönlein Purpura). Am J Surg Pathol. 2018;42(4):529-33.https://doi.org/10.1097/pas.0000000000001036 DOI: https://doi.org/10.1097/PAS.0000000000001036

Hong JG, Levy J, Stokar E. Henoch-Schönlein purpura and crohn's disease: Expanding the range of association in pediatric patients. Clin J Gastroenterol. 2021;14(5):1392-5.https://doi.org/10.1007/s12328-021-01456-w DOI: https://doi.org/10.1007/s12328-021-01456-w

Published

2023-11-30

How to Cite

1.
Ulcerative Colitis with Henoch Schonlein Purpura in Pediatric Patient: A Case-Report. Arch Pediatr Gastr Hepatol Nutr [Internet]. 2023 Nov. 30 [cited 2024 Oct. 6];2(4):30-5. Available from: https://apghn.com/index.php/journal/article/view/55