2006
DOI: 10.1007/s00431-006-0254-5
|View full text |Cite
|
Sign up to set email alerts
|

Henoch-Schonlein purpura presenting duodenal involvement similar to superior mesenteric artery syndrome in a girl

Abstract: Henoch-Schonlein purpura (HSP) is an inflammatory vasculitis involving the skin, joints, gastrointestinal (GI) tract, and kidneys. This is the first case report describing a 5-year-old girl with HSP presenting duodenal involvement which might be associated with superior mesenteric artery syndrome (SMAS).

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
5
0
1

Year Published

2006
2006
2022
2022

Publication Types

Select...
6
3

Relationship

2
7

Authors

Journals

citations
Cited by 13 publications
(6 citation statements)
references
References 4 publications
(3 reference statements)
0
5
0
1
Order By: Relevance
“…We read with great interest the recent contribution by Harada et al in Eur J Pediatr [1]. They reported a 5-year old girl with Henoch-Schonlein purpura (HSP) presenting duodenal involvement which might be associated with superior mesenteric artery syndrome (SMAS).…”
Section: Sirmentioning
confidence: 90%
“…We read with great interest the recent contribution by Harada et al in Eur J Pediatr [1]. They reported a 5-year old girl with Henoch-Schonlein purpura (HSP) presenting duodenal involvement which might be associated with superior mesenteric artery syndrome (SMAS).…”
Section: Sirmentioning
confidence: 90%
“…1a). 9 The exclusion criteria were: past history of HSP, and past history of abdominal surgery. For controls, we prospectively recruited consecutive children who presented to the department and who underwent screening on abdominal ultrasound due to hematuria and/or proteinuria on urinalysis.…”
Section: Methodsmentioning
confidence: 99%
“…Some researchers have proposed that nutcracker should be defined only when the clinical symptoms are present along with compatible radiologic findings, [4] because asymptomatic dilatation of LRV frequently shown on ultrasound or computed tomography has been regarded as a finding of a normal variant [5] . However, LRV entrapment has been reported to coexist with some idiopathic glomerular disease in some case reports, among which coexistence with IgAN were the most commonly reported ones [6–11] . The combination increases the difficulty of differentiating the primary cause of renal manifestations and influences the choice of therapy.…”
Section: Introductionmentioning
confidence: 99%