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Diagnosis and treatment of adult mixed-type Henoch-Schönlein purpura
AIM OF THE STUDY: The purpose of this study was to investigate the clinical manifestations and outcomes of patients with adult mixed-type Henoch-Schönlein purpura (HSP) and imaging characteristics of the disease, and to evaluate the efficacy of combined therapy in treating symptoms of HSP. MATERIAL...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Polish Society of Experimental and Clinical Immunology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745548/ https://www.ncbi.nlm.nih.gov/pubmed/31530983 http://dx.doi.org/10.5114/ceji.2019.87064 |
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author | Cui, Jun Huang, Liu-Ye Guo, Juan Wu, Cheng-Rong Zhang, Bo |
author_facet | Cui, Jun Huang, Liu-Ye Guo, Juan Wu, Cheng-Rong Zhang, Bo |
author_sort | Cui, Jun |
collection | PubMed |
description | AIM OF THE STUDY: The purpose of this study was to investigate the clinical manifestations and outcomes of patients with adult mixed-type Henoch-Schönlein purpura (HSP) and imaging characteristics of the disease, and to evaluate the efficacy of combined therapy in treating symptoms of HSP. MATERIAL AND METHODS: From January 2008 to October 2015, 23 patients with adult mixed-type HSP were enrolled. Abdominal contrast-enhanced computed tomography (CT) examination and small intestinal enteroscopy were performed for all the patients. For patients with positive urine protein, ultrasonic guided renal needle biopsy with 18G biopsy needle was performed; immunofluorescence and pathologic examinations were performed. Combined therapy with antihistamine drugs, gastric acid suppressants and glucocorticoids was used to relieve abdominal pain, gastrointestinal tract bleeding and urine protein. RESULTS: The typical skin manifestation of HSP is distributed purpura in dependent areas. Abdominal contrast-enhanced CT examination exhibited the intestinal canal wall thickening and edema. Small intestinal endoscopy showed diffused hyperemia, dropsy, and erosion. All the patients with positive urine protein showed significantly higher IgA levels. With the use of combined therapy, abdominal pain and gastrointestinal tract bleeding disappeared, and urine protein decreased gradually. CONCLUSIONS: Higher IgA levels with multiorgan involvement (gastrointestinal, kidney and skin) should make one consider the diagnosis. The combined examination of abdominal contrast-enhanced CT, small intestinal endoscopy and renal needle biopsy is a valuable method for the early diagnosis of adult mixed-type HSP. |
format | Online Article Text |
id | pubmed-6745548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Polish Society of Experimental and Clinical Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-67455482019-09-17 Diagnosis and treatment of adult mixed-type Henoch-Schönlein purpura Cui, Jun Huang, Liu-Ye Guo, Juan Wu, Cheng-Rong Zhang, Bo Cent Eur J Immunol Clinical Immunology AIM OF THE STUDY: The purpose of this study was to investigate the clinical manifestations and outcomes of patients with adult mixed-type Henoch-Schönlein purpura (HSP) and imaging characteristics of the disease, and to evaluate the efficacy of combined therapy in treating symptoms of HSP. MATERIAL AND METHODS: From January 2008 to October 2015, 23 patients with adult mixed-type HSP were enrolled. Abdominal contrast-enhanced computed tomography (CT) examination and small intestinal enteroscopy were performed for all the patients. For patients with positive urine protein, ultrasonic guided renal needle biopsy with 18G biopsy needle was performed; immunofluorescence and pathologic examinations were performed. Combined therapy with antihistamine drugs, gastric acid suppressants and glucocorticoids was used to relieve abdominal pain, gastrointestinal tract bleeding and urine protein. RESULTS: The typical skin manifestation of HSP is distributed purpura in dependent areas. Abdominal contrast-enhanced CT examination exhibited the intestinal canal wall thickening and edema. Small intestinal endoscopy showed diffused hyperemia, dropsy, and erosion. All the patients with positive urine protein showed significantly higher IgA levels. With the use of combined therapy, abdominal pain and gastrointestinal tract bleeding disappeared, and urine protein decreased gradually. CONCLUSIONS: Higher IgA levels with multiorgan involvement (gastrointestinal, kidney and skin) should make one consider the diagnosis. The combined examination of abdominal contrast-enhanced CT, small intestinal endoscopy and renal needle biopsy is a valuable method for the early diagnosis of adult mixed-type HSP. Polish Society of Experimental and Clinical Immunology 2019-07-30 2019 /pmc/articles/PMC6745548/ /pubmed/31530983 http://dx.doi.org/10.5114/ceji.2019.87064 Text en Copyright: © 2019 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Immunology Cui, Jun Huang, Liu-Ye Guo, Juan Wu, Cheng-Rong Zhang, Bo Diagnosis and treatment of adult mixed-type Henoch-Schönlein purpura |
title | Diagnosis and treatment of adult mixed-type Henoch-Schönlein purpura |
title_full | Diagnosis and treatment of adult mixed-type Henoch-Schönlein purpura |
title_fullStr | Diagnosis and treatment of adult mixed-type Henoch-Schönlein purpura |
title_full_unstemmed | Diagnosis and treatment of adult mixed-type Henoch-Schönlein purpura |
title_short | Diagnosis and treatment of adult mixed-type Henoch-Schönlein purpura |
title_sort | diagnosis and treatment of adult mixed-type henoch-schönlein purpura |
topic | Clinical Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745548/ https://www.ncbi.nlm.nih.gov/pubmed/31530983 http://dx.doi.org/10.5114/ceji.2019.87064 |
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