| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4305718 | JPRAS Open | 2014 | 5 Pages |
Abstract
Kaposiform haemangioendothelioma is a rare, but potentially fatal vascular tumour of childhood. We present a case that highlights the diagnostic and management challenges of this condition, particularly when associated with Kasabach–Merritt phenomenon, and supports the use of sirolimus in its treatment.
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Authors
J. May, A. Sadri, L. Shanks, S.H. Liew, B. Pizer,