Results 11 to 20 of about 254,719 (146)

Fulminant Hepatic Failure Secondary to Primary Hepatic Angiosarcoma

open access: yesCase Reports in Gastrointestinal Medicine, 2015
Background. Hepatic angiosarcoma is a rare and aggressive tumor that often presents at an advanced stage with nonspecific symptoms. Objective. To report a case of primary hepatic angiosarcoma in an otherwise healthy man with normal liver function tests ...
Ayokunle T. Abegunde   +4 more
doaj   +2 more sources

Diethylnitrosamine (DENA) recapitulates formation of hepatic angiosarcoma in pigs.

open access: yesPLoS ONE, 2019
Background & aimPrimary hepatic angiosarcoma is a rare tumor with poor prognosis. The aim of this study was to generate a new angiosarcoma model to improve research on hepatic angiosarcoma.MethodsPigs sus scrofa were treated with different regimens of ...
Sonja M Kessler   +10 more
doaj   +2 more sources

Paraneoplastic Phenomena of Disseminated Intravascular Coagulopathy in Hepatic Angiosarcoma – Rare, Challenging and Fatal. Case Report and Literature Review [PDF]

open access: yesActa Medica Lituanica, 2021
Background. Hepatic angiosarcoma is an uncommon, malignant, primary liver tumor, comprising 2% of liver cancers and accounting for < 1% of all sarcomas.
Sandra Strainienė   +6 more
doaj   +3 more sources

Hepatic Angiosarcoma Associated with Esophageal Variceal Hemorrhage

open access: yesCase Reports in Gastroenterology, 2016
Primary hepatic angiosarcoma is a very rare malignancy with a poor prognosis. Because patients present with no specific symptoms, the cancer can grow undetected and most cases are diagnosed too late for resection.
Zensho Ito   +12 more
doaj   +2 more sources

Hepatic Angiosarcoma with Kasabach-Merritt Phenomenon: A Case Report and Review of the Literature

open access: yesAnnals of Hepatology, 2018
A 76-year-old woman was referred to our hospital due to massive gingival bleeding following teeth extraction. Laboratory findings suggested disseminated intravascular coagulopathy (DIC).
Fumika Fujii   +7 more
doaj   +2 more sources

Angiosarcoma of the Face: A Case Study and Literature Review of Local and Metastatic Angiosarcoma

open access: yesCase Reports in Oncological Medicine, 2021
Angiosarcomas are vascular malignancies with a tendency to spread extensively both locally and systemically. We report a case of cutaneous angiosarcoma of the face in a 53-year-old man that was originally misdiagnosed as an abscess.
Hugo Lara-Martinez   +5 more
doaj   +2 more sources

Case Report: The value of contrast-enhanced ultrasound and contrast-enhanced computed tomography in the diagnosis of hepatic angiosarcoma [PDF]

open access: yesFrontiers in Oncology, 2023
BackgroundEnhanced imaging techniques have the overwhelming advantages of being noninvasive and sensitive enough to evaluate the microcirculation of lesions, thus making them accurate in the diagnosis of hepatic lesions.
Feiqian Wang   +6 more
doaj   +2 more sources

Advanced diffuse hepatic angiosarcoma treated successfully with TACE and targeted immunotherapy: A case report [PDF]

open access: yesFrontiers in Oncology, 2023
Primary hepatic angiosarcoma (PHA), a rare soft tissue tumor, accounts for only 2% of all liver malignancies. Pathologically challenging, PHA is difficult to be distinguished from other malignancies with ultrasound, Computed Tomography (CT), or Magnetic ...
Yucheng Lin   +6 more
doaj   +2 more sources

Primary hepatic angiosarcoma: A case-based discussion of unique presentations and extrahepatic manifestations

open access: yesCurrent Problems in Cancer: Case Reports, 2020
Hepatic angiosarcoma is a rare and heterogeneous neoplasm that carries with it an especially poor prognosis. Diagnosis is challenging given that patients often present with vague, nonspecific complaints, and early multiorgan dysfunction has the potential
Brandon K.K. Fields   +7 more
doaj   +2 more sources

Hepatic angiosarcoma five years following spontaneous intraperitoneal bleed of a hepatic mass

open access: yesRare Tumors, 2009
Primary hepatic angiosarcoma is a rare and rapidly fatal disease. We present the highly unusual identification of this lesion five years after the initial clinical presentation.
Alexandra N Kalof
exaly   +2 more sources

Home - About - Disclaimer - Privacy