Portal Cavernoma in Children: Rare Pathology with Complex Management about 3 Cases
S. Aithmadouch, A. Radi, K. Larbiouassou, R. Abikassem
Asian Journal of Advanced Research and Reports · pp. 175–179 · Published 28 Nov 2024
10.9734/ajarr/2024/v18i12815Abstract
We report 03 cases of portal cavernoma hospitalized in pediatric department. Through these observations, we will try to describe the different clinical and biological aspects and discuss the diagnostic and therapeutic approaches through a literature review. Somatic examination revealed a distended abdomen and hepatosplenomegaly, presence of collateral venous circulation. The diagnostic approach to portal cavernoma in children is based on careful clinical examination, including identification of symptoms such as gastrointestinal bleeding, hepatomegaly and signs of liver disease. The biological work-up showed bicytopenia (microcytic hypochromic anaemia with thrombocytopenia) with a normal blood and liver count. The long-term course of portal cavernoma in children depends on various factors, such as the presence of complications, response to treatment and medical and surgical management. The prognosis is generally better in children who receive regular medical follow-up and appropriate treatment in the event of complications.
Cited by 0
No indexed citations yet.
Related research
- Management of Abdominal Trauma at Three Hospitals in the Western Cameroon — shares topic coverage
Article metrics
Real usage data collected on this platform.
0
Page views
0
PDF downloads
0
Outbound clicks
0
Citations
Views by country
Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".
No views recorded yet.
Traffic sources
Referring site, by host.
No traffic recorded yet.
Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.