Results 51 to 60 of about 1,161,166 (152)

Successful management of Kaposiform Hemangioendothelioma with long-term sirolimus treatment: a case report and review of the literature

Mediterranean Journal of Hematology and Infectious Diseases, 2018
Background: Kaposiform Hemangioendothelioma (KHE) is a rare vascular tumour of the infancy and of the first decade of life. It is locally aggressive and potentially life threatening when associated to consumptive coagulopathy, known as Kasabach-Merritt ...
Matteo Chinello, Daniela Di Carlo, Francesca Olivieri, Rita Balter, Massimiliano De Bortoli, Virginia Vitale, Ada Zaccaron, Elisa Bonetti, Alice Parisi, Simone Cesaro   +9 more
doaj   +1 more source

Extended Right Hepatectomy for Giant Hepatic Hemangioma: A Case Report

Case Reports in Surgery, Volume 2026, Issue 1, 2026.
Liver hemangioma is the most common benign liver tumor, often discovered incidentally. Symptom development and complications underscore the need for surgical intervention. Managing hemangiomas larger than 20 cm is challenging because of the risk of perioperative complications.
Ana Gabriela Cabrera-Lizárraga, Omar Bermúdez-Ferro, Iaarah Montalvo-Gordon, Héctor Rendón-Dosal, Rubén R. Lozano-Salazar, Semonti Nandi   +5 more
wiley   +1 more source

In Utero Sonographic Findings of Giant Hepatic Hemangioma and Associated Perinatal Complications: A Report of Two Cases

Journal of Medical Ultrasound, 2015
It is uncommon to diagnose fetal hepatic hemangioma during the antenatal period. We describe herein two patients with a giant hepatic hemangioma detected antenatally, both with perinatal complications.
Hiromi Imai, Nobuhiro Hidaka, Takeshi Murakami, Saki Kido, Yasuo Yumoto, Kotaro Fukushima, Kiyoko Kato   +6 more
doaj   +1 more source

Surgical intervention for Kasaback-Merritt Syndrome: A case report

Journal of Pediatric Surgery Case Reports, 2015
Kasabach-Merritt Syndrome (KMS) is an uncommon phenomenon characterized by the presence of a vascular tumor in association with thrombocytopenia, consumption coagulopathy and hemodynamic instability. Typically presents in infancy and involve the skin and
Morris Sasson, J. Alford Flippin, Gary Birken, Fuad Alkhoury   +3 more
doaj   +1 more source

Bilateral Ovarian Hemangiomas Presenting With Abnormal Uterine Bleeding: A Rare Case Report

Clinical Case Reports, Volume 13, Issue 6, June 2025.
ABSTRACT Ovarian hemangiomas are rare benign vascular tumors that can present with abnormal uterine bleeding and mimic malignant ovarian lesions. Imaging may be inconclusive, and histopathology remains essential for diagnosis. This case highlights the importance of considering ovarian hemangiomas in the differential diagnosis of pelvic masses to ensure
Ensiyeh Bahadoran, Fatemeh SamieeRad
wiley   +1 more source

Prenatal Ultrasound and Magnetic Resonance Imaging Features and Postnatal Outcomes of Congenital Hepatic Hemangioma: A Retrospective Analysis

iRADIOLOGY, Volume 3, Issue 3, Page 214-221, June 2025.
This study explored the imaging features of congenital hepatic hemangiomas of different sizes. A history of spontaneous regression of congenital hepatic hemangioma was identified at follow‐up. A new type of congenital hepatic hemangioma—the spontaneous regression type after continued proliferation after birth—was also found.
Luyao Yang, Jianbo Teng, Xinhong Wei
wiley   +1 more source

Kaposiform haemangioendothelioma and Kasabach-Merritt syndrome

, 2008
Made available in DSpace on 2019-09-11T20:58:50Z (GMT). No. of bitstreams: 0 Previous issue date: 2008OBJETIVO: Descrever a apresentação e a evolução de um caso de hemangioendotelioma kaposiforme complicado por síndrome de Kasabach-Merritt.
Elias, Chelna Paolichi F., Tutia, Patrícia Cavalcante, Baida, Luciana Lucatto, Marcitelli, Ricardo, Zanlochi, Ana Glenda S., Mukai, Adriana de Oliveira, Rolim, Christine Holtz   +6 more
core   +1 more source

Angiosarcoma of the scalp in the elderly: a case series

Journal of the Egyptian Women’s Dermatologic Society
Cutaneous angiosarcoma (AS) is a rare soft tissue malignancy that often mimics various dermatoses, leading to a delay in diagnosis. The rapid rate of progression portends a poor prognosis.
Carol Lobo, Prathibha J.P, Shubha Bhagavan, Vivek M. Pai   +3 more
doaj   +1 more source

Bleomycin electrosclerotherapy for kaposiform hemangioendothelioma with Kasabach–Merritt phenomenon in an adult

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 4, Page 551-553, April 2026.
Jakob Veeser, Raphael Wilhelm, Janina Dietzel, Yalda Ghoreishi, Nora Laubach, Nora Elspaß, Maike Kaufhold, Beate Weidenthaler‐Barth, Christian Rose, Stephan Grabbe, Henner Stege, Hadrian Nassabi   +11 more
wiley   +1 more source

Transcriptomic Profiling Unveils EDN3+ Meningeal Fibroblasts as Key Players in Sturge‐Weber Syndrome Pathogenesis

Advanced Science, Volume 12, Issue 17, May 8, 2025.
Sturge‐Weber syndrome (SWS) is characterized by leptomeningeal vascular malformations, leading to seizures and stroke. Analysis of 119 446 brain cells from SWS patients uncovered distinct cell heterogeneity and identified an EDN3⁺ meningeal fibroblast cluster, with WNT5A emerging as a potential key driver of SWS progression and a promising therapeutic ...
Daosheng Ai, Tianyue Ming, Xiaoli Li, Shu Wang, Zhanying Bi, Jinyi Zuo, Zizhang Cheng, Weijin Sun, Mingguo Xie, Fengzhi Li, Xiongfei Wang, Xueling Qi, Guoming Luan, Woo‐ping Ge, Yuguang Guan   +14 more
wiley   +1 more source