Jiang Maolin, Xiang Mei, Li Jing, et al. Clinical Analysis of Abdominal Henoch-Schönlein Purpura Complicated with Protein-Losing Enteropathy in Children[J]. 2022,28(12):43-47.
Jiang Maolin, Xiang Mei, Li Jing, et al. Clinical Analysis of Abdominal Henoch-Schönlein Purpura Complicated with Protein-Losing Enteropathy in Children[J]. 2022,28(12):43-47. DOI: 10.13407/j.cnki.jpp.1672-108X.2022.12.012.
Objective: To probe into the clinical characteristics of abdominal Henoch-Schönlein purpura (HSP) complicated with protein-losing enteropathy (PLE) in children
and to compare the differences with the abdominal HSP with normal albumin. Methods: Nineteen children diagnosed with abdominal HSP complicated with PLE admitted into Chengdu Women’s and Children’s Central Hospital
School of Medicine
University of Electronic Science and Technology of China from Jan. 2015 to Feb. 2020 were extracted. Nineteen children with abdominal HSP and normal albumin who were hospitalized during the same period were selected as the control group by 1∶1 propensity score matching. Case-control study method was performed to analyze the clinical manifestations
biochemical indicators
imaging examination
endoscopic changes and pathological results of two groups. Results: There were 19 cases in the PLE group
including 10 males and 9 females
the male/female ratio was 1.1︰1.0. The average age of onset was (6.2±2.0) years. The main clinical manifestations were abdominal pain and rash
partly accompanied by hematochezia
vomiting
hypoprotein edema and joint swelling. In PLE group
significant increases were found in white blood cells
neutrophils
C-reactive protein (CRP)
platelets
neutrophils/lymphocytes (NLR)
and decreases were found in albumin and immunoglobulin G
statistically different from those in the control group (P<0.05). Imaging changes indicated intestinal wall thickening and ascites. Results of gastroscopy showed congestion and edema of gastric and duodenal mucosa
and some lesions such as erosion and ulcer. Pathological changes mainly suggested mucosal epithelial cell swelling
submucosal vasodilation
vascular wall necrosis
interstitial edema
perivascular inflammatory changes
neutrophil
lymphocyte and eosinophil infiltration. The length of stay in the PLE group were longer than that in the control group
with statistically significant difference (P<0.05). Conclusion: The clinical manifestations of abdominal HSP complicated with PLE are significantly increased inflammatory indicators such as white blood cells
neutrophils
CRP and NLR
severe intestinal mucosal injury and long length of stay. Therefore
active and effective treatment measures should be taken.