Results 1 to 10 of about 409 (135)

Pleural epithelioid hemangioendothelioma mimicking pleural empyema: A case report

open access: yesRespiratory Medicine Case Reports, 2020
Malignant pleural effusion is an important and difficult differential diagnosis to pleural empyema. Epithelioid hemangioendothelioma is an uncommon vascular tumor, which typically occurs in liver, lung or bone.
Katrine Fjaellegaard   +5 more
doaj   +1 more source

Rare epithelioid hemangioendothelioma in the brachiocephalic vein for long-term survival after surgery: A case report

open access: yesSAGE Open Medical Case Reports, 2022
Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor. In this report, we describe the case of a 62-year-old man who presented with pain in the left clavicle and swelling of the left upper limb. Contrast-enhanced computed tomography revealed an
Yasuhito Nakamura   +6 more
doaj   +1 more source

Epithelioid Hemangioendothelioma of the Pisiform [PDF]

open access: yesHAND, 2012
The term epithelioid hemangioendothelioma (EH) was first identified and described in 1982 by Weiss and Enzinger [15] for a rare endothelial vascular neoplasm in soft tissues with a histologic appearance and clinical course between hemangioma and angiosarcoma.
Isidre A, Gracia   +6 more
openaire   +2 more sources

Primary malignant epithelioid hemangioendothelioma of the pleura: A review and report of a novel case

open access: yesClinical Case Reports, 2022
Epithelioid hemangioendothelioma is considered an uncommon tumor originating from vascular tissues. Although this disease is an extremely rare malignant cancer, its pleural subtype is even less common.
Alireza Rezvani   +3 more
doaj   +1 more source

Epithelioid hemangioendothelioma of spine: A case report with review of literatures

open access: yesRadiology Case Reports, 2020
Primary epithelioid hemangioendothelioma of the spine is the extremely rare malignant vascular neoplasm with an unpredictable outcome. A case of epithelioid hemangioendothelioma with multiple lytic lesions of thoracolumbar spine and other bones in a 29 ...
Ping-Kang Chen, MS   +4 more
doaj   +1 more source

Epithelioid hemangioendothelioma in a Child

open access: yesJournal of Cutaneous and Aesthetic Surgery, 2013
Epithelioid hemangioendothelioma (EHE) is a rare tumour arising from the vascular endothelium of soft-tissue, bone and viscera. Skin involvement is rare. The disease has an indolent course, with the potential for recurrence and often associated with multi-systemic localisations.
Madura, C   +3 more
openaire   +2 more sources

Epithelioid Hemangioendothelioma of the Foot [PDF]

open access: yesJournal of Radiology Case Reports, 2021
We describe the case of an 18-year-old male Army reservist presenting with left lower extremity pain for which he was initially diagnosed with a stress injury. After failing conservative treatment, a radiograph was obtained showing a "lacelike" appearance of the medullary bone in the foot and ankle. Magnetic resonance imaging subsequently demonstrated
Christopher, Sardon   +3 more
openaire   +2 more sources

Ambiguous presentations of pulmonary epithelioid hemangioendothelioma: Two case reports of a rare pulmonary malignancy

open access: yesSAGE Open Medical Case Reports, 2016
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 in the Tongue: A Rare Case Report

open access: yesTürk Patoloji Dergisi, 2023
Epithelioid hemangioendothelioma is a rare malignant vascular neoplasm caused by the proliferation of neoplastic endothelial cells. Epithelioid hemangioendothelioma may develop in any organ, but it is commonly observed in the extremities. The tongue is a
Deniz SURMELI CIRKIN   +3 more
doaj   +1 more source

Hepatic epithelioid hemangioendothelioma [PDF]

open access: yesClinics and Research in Hepatology and Gastroenterology, 2016
A 36-year-old woman with no relevant medical or surgical history was referred to our attention for abdominal diffuse pain and mild weight loss. No risk factors such as hepatitis, alcohol abuse, oral contraceptive use, or a family history of carcinoma were reported.
Galletto Pregliasco, Athena   +3 more
openaire   +2 more sources

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