Evidence map›Paper›PMID 41438152›Full record

ArticleFrontiers in medicine2025

Intra-abdominal multi-organ involvement of kaposiform hemangioendothelioma in a child with Kasabach-Merritt phenomenon and contrast-enhanced ultrasound findings: a case report.

Shu Luo, Anjie Chen, Jiaojiao Zhou, Yi Ji, Shuguang Jin, Juxian Liu

Abstract readCase Reports
In one paragraph

Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Shu Luo *Division of Ultrasound, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Anjie Chen *Division of Ultrasound, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Jiaojiao ZhouDivision of Ultrasound, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Yi JiDivision of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Shuguang JinDivision of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Juxian LiuDivision of Ultrasound, West China Hospital of Sichuan University, Chengdu, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular tumor that occurs in infancy and early childhood and is associated with significant morbidity. A severe complication of KEH is Kasabach-Merritt phenomenon (KMP), a life-threatening consumptive coagulopathy accompanied by thrombocytopenia. Case presentation: We report a rare case of KHE complicated by KMP, with multifocal involvement of the pancreatic head, liver, biliary tract, and duodenal papilla. Contrast-enhanced ultrasound (CEUS) revealed characteristic imaging features of the pancreatic head lesion, demonstrating inhomogeneous hypoenhancement during the arterial and portal phases, followed by complete washout and absence of enhancement in the late phase. Conclusion: After the failure of multiple therapeutic interventions, the patient successfully underwent a pancreatoduodenectomy. This case underscores that surgical resection should be considered for KHE when it is feasible and safe. Furthermore, recognizing the distinctive CEUS features of pancreatic KHE is crucial for accurate diagnosis and avoiding diagnostic pitfalls.

Indexed as

childcontrast-enhanced ultrasoundKaposiform hemangioendotheliomaKasabach-Merritt phenomenonpancreatic neoplasms

Identifiers

PMID41438152
PMCPMC12719487

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