Kaposiform Hemangioendothelioma with Bone Destruction: A 16-Year Follow-Up Cohort Study of the Clinical Characteristics and Prognosis
Abstract
Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular tumor that often occurs in infants and young children. The goal of this study was to analyze the clinical characteristics of KHE patients with bone destruction and provide clinical guidance for diagnosis and treatment.
Keywords
Kaposiform HemangioendotheliomaVascular TumorsPediatric OncologyBone InvolvementKasabach-merritt PhenomenonLong-term OutcomesHashtags
#PediatricOncology#VascularTumors#KHE#RareDiseaseThis article is published on an external journal. Click below to read the full text.
Read full article ↗How to cite: GlobalCastMD. Kaposiform Hemangioendothelioma with Bone Destruction: A 16-Year Follow-Up Cohort Study of the Clinical Characteristics and Prognosis. GlobalCastMD Medical Library. 2023-12-06. https://origin-library.globalcastmd.com/article/8284
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