Results 31 to 40 of about 12,136 (174)

Hemangioendothelioma of orbit [PDF]

open access: yesIndian Journal of Otolaryngology and Head and Neck Surgery, 1999
Hemangioendothelioma of the orbit is a rare condition which usually occurs in young adult with mean age group of 24 years. Very few cases had been reported in the literature. We describe here a case of hemangioendothelioma in a female of 30 years who came with history of pen-etrating foreign body entering into right eye and fluctuating painful swelling
N, Misra   +3 more
openaire   +2 more sources

Dermoscopy of kaposiform hemangioendothelioma: a case report

open access: yesDermatology Reports
Kaposiform hemangioendothelioma (KHE) is a rare vascular tumor of infancy, characterized by an infiltrative, firm, and ill-defined plaque that may be associated with Kasabach-Merritt phenomenon.
Filomena Barbato   +5 more
doaj   +1 more source

A Rare Tumor that Mimicked Metastasis in a Patient with Breast Cancer: Epithelioid Hemangioendothelioma

open access: yesEuropean Journal of Breast Health, 2016
A woman aged 50 years was diagnosed as having an invasive ductal carcinoma in the right breast and ductal carcinoma in situ in the left breast and underwent bilateral mastectomy eight years ago. A mass was identified during follow-up in positron-emission
Fatmagül Kuşku Çabuk   +5 more
doaj   +1 more source

Kaposiform hemangioendothelioma: Diagnosis and treatment

open access: yesPediatric Investigation, EarlyView.
Vascular endothelial growth factor‐C (VEGF‐C)/vascular endothelial growth factor receptor‐3 (VEGFR‐3) and angiopoietin‐2 (Ang‐2)/tyrosine kinase with immunoglobulin‐like and EGF‐like domain 2 (TIE2) signaling pathways play an important role in lymphangiogenesis.
Yi Tian   +5 more
wiley   +1 more source

Epitheloid hemangioendothelioma of urinary bladder

open access: yesIndian Journal of Urology, 2008
Epitheloid hemangioendothelioma is an uncommon vascular neoplasm and has an unpredictable clinical behavior. It is characterized by round or spindle-shaped endothelial cells with cytoplasmic vacuolation.
Narmada P Gupta   +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

Hepatic Epithelioid Hemangioendothelioma [PDF]

open access: yesArchives of Pathology & Laboratory Medicine, 2018
Epithelioid hemangioendothelioma is a rare vascular tumor, composed of epithelioid and histiocytoid vascular endothelial cells in myxoid or fibrotic stroma, which can arise in multiple locations throughout the body. In the liver, this neoplasm usually presents on imaging as an incidental finding of multifocal, heterogeneously enhancing nodules in both ...
Lynette L, Studer, Dale M, Selby
openaire   +2 more sources

Epithelioid hemangioendothelioma of the temporal artery presenting as temporal arteritis: Case report and literature review

open access: yesRare Tumors, 2009
Hemangioendotheliomas are classified as epithelioid hemangioendothelioma(EHE), retiform hemangioendothelioma, composite hemanioendothelioma, Kaposiform hemangioendothelioma (with or without Kasabach-Merritt syndrome), and Spindle cell ...
Salem Alowami   +2 more
doaj   +1 more source

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

Oral Angiolymphoid Hyperplasia With Eosinophilia Exhibiting Cutaneous‐Type Histopathologic Features: Clinical Regression Following Hormonal Withdrawal and a 50‐Year Review

open access: yesJournal of Cutaneous Pathology, EarlyView.
Case report of a 30‐year‐old female. Asymptomatic, red‐purple hyperplastic lesion extending from teeth 21 to 25, with bleeding upon manipulation. Differential diagnosis included: inflammatory gingival hyperplasia, plasma cell gingivitis, leukemia, and Wegener's granulomatosis.
Pedro Vinícius Santos de Jesus   +8 more
wiley   +1 more source

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