Results 31 to 40 of about 14,994 (170)

Multifocal Epithelioid Hemangioma With FOSB Overexpression

open access: yesJournal of Cutaneous Pathology, EarlyView.
ABSTRACT Epithelioid hemangioma (EH) is a benign vascular tumor that most commonly arises on the skin but may also occur in other anatomical locations, including deep soft tissue, bone, visceral organs, penis, and mucosal sites. A hallmark of EH is overexpression of FOS and FOSB, often resulting from various gene fusions.
Phuong Daniels   +6 more
wiley   +1 more source

Uterine polypoid hemangioendothelioma: Conservative treatment

open access: yes, 1996
Background and Objective A polypoid uterine hemangioendothelioma was treated by conservative means. Study Design/Materials and Methods The diagnosis of hemangioendothelioma was confirmed by histopathology and angiography.
Shapiro, Arthur   +4 more
core   +1 more source

A rare hepatic tumor; hepatic epithelioid hemangioendothelioma

open access: yes, 2013
Primary sarcomas of the liver account for about 1% of all liver tumors. Two basic histological forms of these sarcomas are hepatic epithelioid hemangioendothelioma and angiosarcoma.
Adım, Şaduman Balaban   +4 more
core   +1 more source

Epithelioid hemangioendothelioma of the larynx.

open access: yes, 1999
Epithelioid hemangioendothelioma is an uncommon vascular tumor of the soft tissues. Several reports have described this tumor in visceral locations such as liver, lung, and brain.
Tornillo L   +6 more
core   +2 more sources

Pseudomyogenic Hemangioendothelioma Involving the Esophagus: A Case Report

open access: yesJournal of Chest Surgery, 2021
Herein, we describe the case of a 20-year-old woman who presented with dysphagia of 2 months’ duration associated with vomiting, moderate abdominal pain, decreased oral intake, and significant weight loss.
Abdul-Rahman Fadi Diab   +3 more
doaj   +1 more source

Optimal dosing for vascular anomalies paediatric patients with population pharmacokinetic model of sirolimus

open access: yesBritish Journal of Clinical Pharmacology, Volume 92, Issue 9, Page 3115-3123, September 2026.
Abstract Aim Sirolimus is currently used off‐label for paediatric patients with vascular anomalies. However, the optimal dosage regimen for paediatric patients remains controversial. This study aimed to determine the optimal dosing regimen of sirolimus in these patients using a population pharmacokinetic (PK) model.
Seongmee Jeong   +13 more
wiley   +1 more source

Epithelioid Hemangioendothelioma of Cavernous Sinus

open access: yesIndian Journal of Neurosurgery, 2017
Epithelioid hemangioendothelioma is an uncommon vascular neoplasm. It is rare in the intracranial location. Its occurrence in the region of cavernous sinus is reported only once.
Raj S. Chandran   +3 more
doaj   +1 more source

Thoracic composite hemangioendothelioma with neuroendocrine marker expression

open access: yesSurgical Case Reports, 2021
Background Composite hemangioendothelioma is an extraordinarily rare form of vascular neoplasm which develops predominantly in the skins and soft tissues of the adults.
Ei Miyamoto   +7 more
doaj   +1 more source

Application of Three‐Dimensionally Printed Surgical Guides in Precise Sacral Tumor Excision and Defect Reconstruction

open access: yesOrthopaedic Surgery, Volume 18, Issue 9, Page 1847-1860, September 2026.
Patient‐specific 3D‐printed guiding templates significantly improve surgical precision and efficiency in complex sacral tumor resection and reconstruction compared to conventional freehand techniques. This computer‐assisted workflow reduces operative time, intraoperative blood loss, and fluoroscopy frequency, providing a safer, highly reproducible ...
Yansong Liu   +7 more
wiley   +1 more source

Chondroid Soft Tissue Tumors With FOS::PABPN1 Fusion: A New Entity? About Two Cases

open access: yesGenes, Chromosomes and Cancer, Volume 65, Issue 8, August 2026.
ABSTRACT Soft tissue tumors with chondroid matrix represent a heterogeneous group with persistent diagnostic challenges. Advances in molecular diagnostics have identified recurrent gene fusions in several chondroid neoplasms, predominantly involving FN1. Here, we report two cases of chondroid tumors harboring a novel FOS::PABPN1 fusion.
Jinane Kharmoum   +7 more
wiley   +1 more source

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