Results 71 to 80 of about 254,719 (146)

Hepatic angiosarcoma: Presentation of two cases

, 2009
Hepatic angiosarcoma is a rare primary tumor of the liver with a mesenchymal origin. Diagnosis is difficult because clinical manifestations and imaging studies are inconclusive.
Carballo Álvarez,F., Pérez Fuenzalida,F. J., López Poveda,M. J., Martínez Barba,E., Egea Valenzuela,J., Garre Sánchez,C.   +5 more
core   +1 more source

Angiosarcoma of the Gallbladder: Case Report and Review of the Literature

Canadian Journal of Gastroenterology, 2005
A 62-year-old white woman with an unremarkable past medical history presented with acute cholecystitis. A cholecystectomy was performed, revealing an acute hemorrhagic and chronic cholecystitis associated with cholelithiasis.
Alexandre N Odashiro, Patricia Rusa Pereira, Luciana N Odashiro Miiji, Gia-Khanh Nguyen   +3 more
doaj   +1 more source

Postoperative Outcomes and Risk Profiles in Dual Liver–Lung Transplantation: A Single‐Center Retrospective Analysis

Journal of Transplantation, Volume 2026, Issue 1, 2026.
Background Dual liver–lung transplantation (DLLT) is an uncommon but definitive therapy for carefully selected patients with concurrent end‐stage hepatic and pulmonary disease. The combined operative complexity and dual‐organ immunosuppressive burden may predispose recipients to early morbidity and graft‐threatening complications [1–4].
Abdulmalik Saleem, Omar Ilyas, Mark Obri, Ahmad Alomari, Muhammad Saad Faisal, Haya Omeish, Ammad Chaudhary, Yara Dababneh, Uthman Shukairy, Shunji Nagai, Domingo Franco-Palacios, Deepak Venkat, Adarsh Varma, Syed-Mohammed Jafri, Reut Hod-Dvorai   +14 more
wiley   +1 more source

sj-pdf-4-sco-10.1177_2050313X211046726 – Supplemental material for Hepatic angiosarcoma: Pitfalls in establishing a diagnosis

, 2021
Supplemental material, sj-pdf-4-sco-10.1177_2050313X211046726 for Hepatic angiosarcoma: Pitfalls in establishing a diagnosis by Katerina Flabouris, Suzanne McKeen, Deborah Chaves Gomes, Debajyoti Chaudhuri and Patrick Russell in SAGE Open Medical Case ...
Patrick Russell (6806306), Deborah Chaves Gomes (11451968), Debajyoti Chaudhuri (11451971), Suzanne McKeen (11451965), Katerina Flabouris (841081)   +4 more
core   +1 more source

sj-pdf-3-sco-10.1177_2050313X211046726 – Supplemental material for Hepatic angiosarcoma: Pitfalls in establishing a diagnosis

, 2021
Supplemental material, sj-pdf-3-sco-10.1177_2050313X211046726 for Hepatic angiosarcoma: Pitfalls in establishing a diagnosis by Katerina Flabouris, Suzanne McKeen, Deborah Chaves Gomes, Debajyoti Chaudhuri and Patrick Russell in SAGE Open Medical Case ...
Patrick Russell (6806306), Deborah Chaves Gomes (11451968), Debajyoti Chaudhuri (11451971), Suzanne McKeen (11451965), Katerina Flabouris (841081)   +4 more
core   +1 more source

Surgical therapy of primary hepatic angiosarcoma

BMC Surgery, 2019
Background Primary hepatic angiosarcoma (PHA) is a rare tumor entity. Radical surgical resection is currently considered the best treatment choice. The aim of this analysis is to report our experience with surgery for PHA.
Verena Tripke, Stefan Heinrich, Tobias Huber, Jens Mittler, Maria Hoppe-Lotichius, Beate K. Straub, Hauke Lang   +6 more
doaj   +1 more source

Hepatic angiosarcoma and liver transplantation: case report and literature review [PDF]

, 2015
BackgroundHepatic angiosarcoma is a rare vascular malignancy that accounts for 2% of all hepatic primary tumours. The diagnosis is difficult, especially if the patient does not have history of exposure to carcinogens, which are considered as risk factors.
Leonher-Ruezga, Karla Lisseth, Huerta-Orozco, Lorena Denisse, Hermosillo-Sandoval, José Manuel, Morán-Galaviz, Rubén Eduardo, Sandoval-Alvarado, José de Jesús, Ramírez-González, Luis Ricardo   +5 more
core   +1 more source

Long term survival in pediatric hepatic angiosarcoma (PHAS): A case report and review of the literature

Journal of Pediatric Surgery Case Reports, 2015
Pediatric hepatic angiosarcoma (PHAS) is extremely rare, with only five reported tumor-free survivors. Aggressive surgical resection and chemotherapy have been the management in all documented survivors of this disease, however no specific treatment ...
Kristina M. Potanos, Nicole Hodgkinson, Nora M. Fullington, Anupama Narla, Karen Albritton, Harry Kozakewich, Heung Bae Kim   +6 more
doaj   +1 more source

Case Report: Adult-onset diffuse hepatic hemangiomatosis with rapid progression: an autopsy case with diagnostic difficulty

Frontiers in Medicine
Diffuse hepatic hemangiomatosis (DHH) in adults is a rare benign vascular tumor of the liver that histologically resembles a hepatic hemangioma but is characterized by an infiltrative growth pattern despite the absence of cytologic atypia typical of ...
Takahiro Sugie, Takahiro Sugie, Rieko Nishimura, Yuya Urano, Yuya Urano, Akari Iwakoshi, Yoshiko Murakami, Mariko Sato, Chiyoe Kitagawa, Kenichi Harada   +9 more
doaj   +1 more source

A First Case of Hepatic Angiosarcoma Treated with Recombinant Interleukin-2 [PDF]

, 2011
A 60 year-old woman was admitted to our hospital because of management of multiple liver tumors. According to image findings and liver biopsy, she was diagnosed as having epithelioid hemangioendothelioma of the liver accompanied by metastases in the ...
Hashimoto, Yoshimasa, Katamura, Yoshio, Arihiro, Koji, Tsuge, Masataka, Imamura, Michio, Kimura, Yuki, Aikata, Hiroshi, Hiramatsu, Akira, Waki, Koji, Mitsui, Fukiko, Takaki, Shintaro, Takahashi, Shoichi, Chayama, Kazuaki, Nagaoki, Yuko, Kawakami, Yoshiiku, Kawaoka, Tomokazu, Hiraga, Nobuhiko   +16 more
core