Journal Basic Info
- Impact Factor: 0.285**
- H-Index: 6
- ISSN: 2638-4558
- DOI: 10.25107/2638-4558
Major Scope
- Neonatology
- Cardiovascular Medicine
- Microbiology
- Gastric Cancer
- Otolaryngology
- Tuberculosis
- Genetics
- Renal Disease
Abstract
Citation: Clin Case Rep Int. 2022;6(1):1330.DOI: 10.25107/2638-4558.1330
Adult Kasabach-Merritt Syndrome: A Case Report and Review of Literature
Msheik Aliand Bitar Nizar
Department of Internal Medicine, Lebanese University, Lebanon
*Correspondance to: Msheik Ali
PDF Full Text Case Report | Open Access
Abstract:
The most common benign liver tumors are cavernous Hemangioma. They can reach enormous sizes and cause varied complications. Kasabach-Merritt syndrome is a constellation of a hemangioma inclusive of endothelial abnormalities, which lead to a consumptive coagulopathy and subsequent thrombocytopenia. Although rare, serious complications are present yielding a mortality rate of 10% to 37%. 80% of cases occur in the first year of life with 0.3% of infants with hemangiomas affected. The treatment aims to control the coagulopathy and thrombocytopenia as well as eradicate the hemangioma. Different treatment approaches are present inclusive of surgical and non-surgical techniques of which systemic corticosteroids, irradiation and immune-suppressors are an option. Surgery is limited to cases of symptomatic and complicated presentations. Although not simple, enucleation is curative usually. Here, we present a 53-year-old man with giant hemangiomas causing KMS.
Keywords:
Hemangiomas; Liver; Kasabach-Merritt Syndrome (KMS)
Cite the Article:
Ali M, Nizar B. Adult Kasabach-Merritt Syndrome: A Case Report and Review of Literature. Clin Case Rep Int. 2022; 6: 1330.