Results 1 to 10 of about 254,719 (146)

An Autopsy Case of Ruptured Hepatic Angiosarcoma Treated by Transcatheter Arterial Embolization [PDF]

Case Reports in Gastroenterology, 2023
An 80-year-old Japanese man presented to our hospital with intra-abdominal hemorrhage due to a ruptured liver tumor. Transcatheter arterial embolization (TAE) temporarily achieved hemostasis, but he died following re-rupture 4 days later.
Toshiki Entani, Kazuto Tajiri, Akira Noguchi, Aiko Murayama, Nozomu Muraishi, Yuka Hayashi, Ichiro Yasuda   +6 more
doaj   +4 more sources

Acute rupture of primary hepatic angiosarcoma with Kasabach-Merritt syndrome: a rare case report and literature review [PDF]

World Journal of Surgical Oncology
Background Primary hepatic angiosarcoma (PHA) is an extremely rare malignant tumor originating from vascular endothelial cells, accounting for only 0.1-2% of primary liver malignancies. Kasabach-Merritt syndrome (KMS) is a rare complication characterized
Lin Ye, Wanrong Yue, Hao Shi, Renjian Li, Jun Weng, Haozhe Zhou, Yaqun Yu   +6 more
doaj   +3 more sources

An exceedingly rare case of de novo hepatic angiosarcoma in a transplanted liver [PDF]

Radiology Case Reports
De novo primary hepatic angiosarcoma is an exceedingly rare malignancy in transplanted livers. Only 1 previous case has been reported in the literature.
Howard Chow, MD, Samer Ghattas, MD, Joshua Liu, MD, David Bowen, PhD   +3 more
doaj   +3 more sources

Hepatic angiosarcoma: A challenging diagnosis [PDF]

Radiology Case Reports
Primary hepatic angiosarcoma (PHA) is a rare and aggressive malignancy, accounting for roughly 2% of primary hepatic cancers. It is characterized by rapid progression and nonspecific clinical symptoms, making early diagnosis challenging. This case report
Charles K. Crawford, BS, Hajra Arshad, MD, Linda C. Chu, MD, Elliot K. Fishman, MD   +3 more
doaj   +3 more sources

Hepatic angiosarcoma: Pitfalls in establishing a diagnosis [PDF]

SAGE Open Medical Case Reports, 2021
Hepatic angiosarcomas are rare, deceptive and aggressive malignancies that remain notoriously difficult to diagnose and treat. This case report discusses some of the common challenges faced by clinicians, and potential clinical, radiological and ...
Deborah Chaves Gomes, Katerina Flabouris, Patrick Russell   +2 more
exaly   +3 more sources

Clinical characteristics and surgical treatments of primary hepatic angiosarcoma [PDF]

BMC Gastroenterology, 2021
Purpose Primary hepatic angiosarcoma is a very rare and highly malignant tumor with poor prognosis. It is difficult to diagnose because of the lack of typical clinical features, and the treatment protocols for PHA are also not clear.
Lei Jiang, Lijun Xie, Ge Li, Hang Xie, Zhao Fang, Xinran Cai, Yanling Chen   +6 more
doaj   +2 more sources

Hepatic Angiosarcoma with eosinophilia: A Case Report and Literature Review [PDF]

International Journal of Women's Health
Meiqin Chen,1 Xiguo Chen,2 Shun Wang,1 Dan Lei,1 Chunxian Peng1 1Department of Infectious Diseases, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou, People’s Hospital, Quzhou, People’s Republic of China; 2Department of ...
Chen M, Chen X, Wang S, Lei D, Peng C
doaj   +2 more sources

Primary Hepatic Angiosarcoma: Distinct Imaging Phenotypes Mirroring Histopathologic Growth Patterns in a Retrospective Human Study [PDF]

Diagnostics
Background/Objectives: To date, no studies have examined radiologic findings by histologic patterns of primary hepatic angiosarcoma; this study clarified radiologic findings of primary hepatic angiosarcoma according to distinct histologic patterns ...
Byoung Je Kim, Jung Hee Hong, Hye Won Lee   +2 more
doaj   +2 more sources

Case of Primary Hepatic Angiosarcoma Presenting With Jaundice and Infiltrative Liver Masses [PDF]

Journal of Investigative Medicine High Impact Case Reports, 2022
Primary hepatic angiosarcoma (PHA) is a rare and aggressive mesenchymal liver tumor with a poor prognosis and high mortality. Treatment options are limited to palliative chemotherapy with surgical resection reserved for the few cases that present early ...
Adnan Shaaban MD, Chimaobi Anugwom MBBS, Alma Habib MD, Tetyana Mettler MD, Shahid Jaffer MD, Mary Thomson MD   +5 more
doaj   +2 more sources

Primary hepatic angiosarcoma with noncirrhotic portal hypertension: A case report [PDF]

Frontiers in Oncology, 2023
BackgroundPrimary hepatic angiosarcoma (PHA) is a rare malignant tumor of mesothelial tissue origin in the liver. The diagnosis of PHA relies on pathology, and it is frequently misdiagnosed as multiple hepatic hemangioma. Noncirrhotic portal hypertension
Xuwei Wu, Xia Yu, Qiaorong Gan, Bin Wang, Zhaowang Lin, Yu Shi, Zuxiong Huang   +6 more
doaj   +2 more sources