| Literature DB >> 10772147 |
C Panow1, C Berger, U Willi, A Valavanis, E Martin.
Abstract
Since the description in 1940 of Kasabach-Merritt syndrome (KMS) in patients with capillary haemangiomas, several other vascular tumours have been recognised as possible causes of this coagulopathy. The literature suggests a specific histological pattern of vascular tumours responsible for KMS, excluding capillary haemangioma [1]. There is an extensive literature on, haemangiomas accompanied by thrombocytopenia, and imaging of thrombosis in the lesion, especially cavernous haemangioma of the liver. However, no report has described a haemangioma of the mandible in the acute stage of the coagulopathy, or serial examinations of such a lesion. We report the features of a mandible lesion with KMS and discusses the interpretations of the changes observed.Entities:
Mesh:
Year: 2000 PMID: 10772147 DOI: 10.1007/s002340050050
Source DB: PubMed Journal: Neuroradiology ISSN: 0028-3940 Impact factor: 2.804