Abstract:
:Hepatic epithelioid angiomyolipoma (EAML) is a rare type of hepatic tumor. Due to a lack of adequate understanding about this tumor, hepatic EAML is often misdiagnosed as other diseases with similar clinical characteristics such as hepatic cancer. In the present study, 3 cases of hepatic EAML are reported, and the main clinicopathological features of this disease are presented, based on a literature search that included articles published in English between February 2000 and September 2014. A total of 24 hepatic EAML cases were considered, of which, 17 were females and 4 presented multiple liver lesions. Among the patients with single lesions, 2 underwent surgery and relapsed after 5 months and 9 years, respectively. Immunohistochemical staining was positive for human melanoma black-45 in the present 3 cases. The aim of the present study was to focus the attention of clinicians on this type of hepatic tumor in order to improve its diagnosis and treatment.
journal_name
Oncol Lettjournal_title
Oncology lettersauthors
Liu W,Meng Z,Liu H,Li W,Wu Q,Zhang X,E Cdoi
10.3892/ol.2016.4443subject
Has Abstractpub_date
2016-06-01 00:00:00pages
3669-3675issue
6eissn
1792-1074issn
1792-1082pii
OL-0-0-4443journal_volume
11pub_type
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