ArticleCancer imaging : the official publication of the International Cancer Imaging Society2026
Primary osseous kaposiform hemangioendothelioma confined to long bones: a retrospective imaging analysis of 12 pediatric cases.
Article in Cancer imaging : the official publication of the International Cancer Imaging Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundKaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular tumor predominantly affecting infants and children. While musculoskeletal involvement is common, cases originating in and confined exclusively to bone are exceptionally rare, and their specific imaging characteristics are not well-defined. This study aims to characterize the clinical and detailed radiological features of primary, intraosseous KHE in a pediatric cohort.
methodsWe conducted a retrospective review of pediatric patients with biopsy-proven KHE admitted to our institution between January 2016 and December 2024. Inclusion criteria stipulated that lesions must be confined entirely within the bone on initial diagnostic imaging. The clinical data, computed tomography (CT), and magnetic resonance imaging (MRI) scans of 12 eligible patients were systematically analyzed by two senior musculoskeletal radiologists. Ki-67 proliferation index was analyzed to correlate with imaging patterns.
resultsThe cohort included 12 patients (11 males, 1 female) with a median age of 5 years (range, 2–12 years). Common presenting symptoms were chronic pain, limping, and muscle atrophy. Notably, no patients presented with Kasabach-Merritt phenomenon (KMP) or cutaneous lesions. Two distinct and recurring radiological patterns were identified. The first, a permeative/moth-eaten pattern (n = 7/12), was characterized by dotted, infiltrative osteolytic lesions involving both the epiphysis and metaphysis, often with associated tubular formations. The second, a cortical excavation pattern (n = 5/12), presented as well-defined, saucer-like erosions of the bone cortex, primarily in the metaphysis. No cases exhibited significant periosteal reaction or a discrete soft-tissue mass. Histopathology confirmed infiltrative nodules of spindled endothelial cells forming slit-like vascular channels. The Ki-67 proliferation index was significantly higher in Pattern 1 compared to Pattern 2 (18.7% vs. 9.2%, P < 0.001, excluding one mixed-pattern case).
conclusionPrimary KHE confined to bone presents with two distinct imaging patterns: permeative/moth-eaten infiltration and cortical excavation. These patterns correlate with biological aggressiveness as indicated by Ki-67 expression. Recognition of these specific features, particularly in the absence of KMP or skin changes, is crucial for radiologists and clinicians. These findings likely represent the earliest detectable stage of osseous KHE and should prompt consideration of this rare entity in the differential diagnosis of pediatric lytic bone lesions, facilitating timely diagnosis and intervention.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.