Five Cases of Hepatic Mesenchymal Tumors Diagnosed by Endoscopic Ultrasound-Guided Tissue Acquisition. [PDF]
ABSTRACT Percutaneous biopsy remains the gold standard for diagnosing focal liver lesions; however, endoscopic ultrasound‐guided tissue acquisition (EUS‐TA) has recently emerged as a promising alternative. Although its diagnostic performance is favorable, most available evidence has focused on epithelial tumors, and reports on mesenchymal tumors are ...
Takano Y +9 more
europepmc +2 more sources
Epithelioid Hemangioendothelioma With a Novel Chromosomal Deletion and an Aggressive Clinical Course: A Case Report and Literature Review. [PDF]
Epithelioid hemangioendothelioma (EHE) is a rare neoplastic process arising from the endothelial lining of virtually any blood vessel, with varying degrees of metastatic spread. In the following case report, the clinical course and treatment stratification are detailed for a 59‐year‐old female who originally presented with cervical radiculopathy and ...
Thor DC, Hussain N, de Leon AB.
europepmc +2 more sources
Pseudomyogenic Hemangioendothelioma of the Femur Treated by Intercalary Resection and Massive Allograft Reconstruction: A Case Report. [PDF]
Pseudomyogenic hemangioendothelioma (PHME) is a very rare vascular tumor that usually arises in the extremities, mainly cutaneous or subcutaneous, but also occurs in deeper locations, such as muscles and bone. Less than 200 cases have been reported so far, and primary intraosseous PHMEs are further infrequent.
Martín Cocilova FN +6 more
europepmc +2 more sources
The Diagnostic Dilemma of Incidentally Detected Pulmonary Nodules: A Fatal Case of Pulmonary Epithelioid Hemangioendothelioma. [PDF]
Pulmonary epithelioid hemangioendothelioma (PEH) is a rare, low‐ to intermediate‐grade malignant vascular tumour. We present an illustrative case of PEH, aiming to contribute to the ongoing clinical characterisation of this rare malignancy. ABSTRACT Pulmonary epithelioid hemangioendothelioma (PEH) is a rare, low‐ to intermediate‐grade malignant ...
Yao Q, Jiang H, Fu D.
europepmc +2 more sources
Two Cases of Hepatic Epithelioid Hemangioendothelioma Misdiagnosed With Hepatic Veno‐Occlusive Disease [PDF]
Hepatic epithelioid hemangioendothelioma (HEHE) is a rare tumor of vascular origin with an incidence of < 0.1/100,000. The disease is easily misdiagnosed. The aim of this article is to increase public awareness and vigilance of HEHE. We report two cases presenting with fever, abdominal discomfort, abnormal liver function, and jaundice.
Zhu B +6 more
europepmc +2 more sources
Pulmonary epithelioid hemangioendothelioma is an uncommon lung malignancy of endothelial origin. Besides demonstrating unpredictable presentation features and prognosis, the paucity of established treatment guidelines remains a challenge in managing ...
Chun Ian Soo +3 more
doaj +1 more source
Epithelioid hemangioendothelioma is a rare tumor of endothelial differentiation most commonly arising in soft tissue, liver, and lung, following a variable clinical course.
Landon J. Kunzelman +3 more
doaj +1 more source
A Case Report of Prostatic and Peritoneal Hemangioendothelioma
Epithelioid hemangioendothelioma is a rare endothelial neoplasm that is uncommonly described in the urinary system. To date, only one case has been described as originating from the prostate.
Michael Lao +3 more
doaj +1 more source
Pseudomyogenic Hemangioendothelioma (Epithelioid Sarcoma-Like Hemangioendothelioma) [PDF]
Pseudomyogenic hemangioendothelioma (PMH) is a rare vascular tumor that presents more frequently in young adults and has a male predominance. It is usually located in the superficial or deep soft tissues of the extremities, but concurrent bone involvement can be present.
Gustavo A, Caballero, Pablo D, Roitman
openaire +2 more sources
Primary Renal Epithelioid Hemangioendothelioma
Epithelioid hemangioendothelioma is a rare vascular tumor with intermediate biologic behavior and metastatic potential. Primary renal epithelioid hemangioendothelioma is extremely rare and we present the second report of this rare tumor in an interesting
S. Roy, A. V. Parwani
doaj +1 more source

