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Primary hepatic leiomyosarcoma: a case report and review of the literature
T. Feretis, ID. Kostakis, C. Damaskos, N. Garmpis, D. Mantas, A. Nonni, G. Kouraklis, D. Dimitroulis
Language English Country Czech Republic
Document type Case Reports, Journal Article, Review
Digital library NLK
Source
NLK
Directory of Open Access Journals
from 1997
Free Medical Journals
from 1997
Open Access Digital Library
from 1997-01-01
Medline Complete (EBSCOhost)
from 2012-06-01
ROAD: Directory of Open Access Scholarly Resources
from 1997
- MeSH
- Chemotherapy, Adjuvant MeSH
- Fatal Outcome MeSH
- Leiomyosarcoma diagnostic imaging drug therapy pathology surgery MeSH
- Humans MeSH
- Magnetic Resonance Imaging MeSH
- Liver Neoplasms diagnostic imaging drug therapy pathology surgery MeSH
- Tomography, X-Ray Computed MeSH
- Aged MeSH
- Check Tag
- Humans MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Review MeSH
BACKGROUND/AIM: Primary hepatic leiomyosarcoma is an extremely rare type of liver sarcoma with relatively poor prognosis, with about 50 cases having been reported in the literature. Potential origins of this tumor in the liver are the smooth muscle cells in the round ligament, intrahepatic blood vessels and intrahepatic bile ducts. There is no apparent sex predilection and there is a wide age range. The clinical presentation is not specific and the diagnosis depends on the expression of markers such as smooth muscle actin, desmin and vimentin by tumor cells. PATIENTS AND METHODS: Herein, we present a case of a bulky primary hepatic leiomyosarcoma in a 68-year-old female patient. The patient underwent resection of the exophytic mass en block with the hepatic segments III and IVB. CONCLUSION: Surgical resection is the most effective among the treatment options.
References provided by Crossref.org
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