Results 121 to 130 of about 12,136 (174)

An extremely rare case of epithelioid hemangioendothelioma presumed metastasis to the pineal body. [PDF]

Surg Neurol Int
Miyauchi K, Inoue A, Ono T, Suehiro S, Watanabe H, Kitazawa R, Kunieda T.   +6 more
europepmc   +1 more source

A Rare Case of Solitary Primary and Recurrent Hepatic Epithelioid Hemangioendothelioma Undergoing Repeat Liver Resections. [PDF]

Surg Case Rep
Yoshizaki Y, Inagaki F, Nakamura M, Kokudo T, Mihara F, Takemura N, Kokudo N.   +6 more
europepmc   +1 more source

An adult case of thrombocytopenia associated with posterior mediastinal hemangioma suggestive of Kasabach-Merritt phenomenon with uncertain diagnosis. [PDF]

J Int Med Res
Zhang Y, Zhu K, Wang X, Zhao Y, Liu Z, Shi J.   +5 more
europepmc   +1 more source

Trichiasis as a clinical manifestation of subconjunctival epithelioid hemangioendothelioma: a rare case report. [PDF]

Front Oncol
Hu M, Wang J, Zhou S, Chen Y, Luo T, Guo J, Wang Z, Sun Y.   +7 more
europepmc   +1 more source

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Hemangioendothelioma

Seminars in Diagnostic Pathology, 2013
Hemangioendothelioma is the term used to name those vascular neoplasms that show a borderline biological behavior, intermediate between entirely benign hemangiomas and highly malignant angiosarcomas. Although originally spindle cell hemangioendothelioma was proposed as a specific clinicopathologic variant of hemangioendothelioma, currently, it is ...
Luis, Requena, Heinz, Kutzner
exaly   +3 more sources

Kaposiform hemangioendothelioma

European Journal of Internal Medicine, 2009
Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular neoplasm that mainly occurs during childhood. It generally originates on the skin, usually affecting deeper tissue by infiltrative growth. It appears as one or multiple masses, and in most cases is associated to consumptive coagulopathy (Kasabach-Merritt syndrome), and ...
Máximo Bernabeu-Wittel, José-Salvador García-Morillo   +1 more
exaly   +3 more sources

Epithelioid Hemangioendothelioma

2020
We describe herein the inaugural manifestations, the radiological and histological diagnosis criteria for and the outcome of epithelioid hemangioendothelioma (EHE). Most of EHE (90%) display a specific reciprocal chromosomic translocation t(1;3)(p36;q23-25), which is associated with the synthesis of fusion protein WWTR1/CAMTA1.
Sophie, Cousin, François, Le Loarer, Amandine, Crombé, Marie, Karanian, Véronique, Minard-Colin, Nicolas, Penel   +5 more
openaire   +2 more sources

MALIGNANT HEMANGIOENDOTHELIOMA

International Journal of Dermatology, 1995
Abstract Background. The administration of interleukin‐2 (il‐2) has recently been reported to be favorable for treating malignant hemangioendothelioma (mhe). Methods. Two patients with mhe responded well to intra‐lesional injections of recombinant il‐2 (ril‐2) without major side effects.
H, Ihda, Y, Tokura, M, Fushimi, R, Yokote, H, Hashizume, S, Shirahama, K, Iwatsuki, K, Murakami, M, Takigawa   +8 more
openaire   +2 more sources

Polymorphous hemangioendothelioma

The Annals of Thoracic Surgery, 1999
Polymorphous hemangioendothelioma is a rare vascular tumor; only 5 patients have been previously described. Half of all cases described have occurred in the thoracic cavity, all being discovered on chest radiologic studies obtained for other reasons. This report presents the case of a female patient with polymorphous hemangioendothelioma and a brief ...
T F, Rehring, A, Deutchman, J S, Cross
openaire   +2 more sources

Infantile hemangioendothelioma

The Indian Journal of Pediatrics, 2001
Primary hepatic tumors are uncommon in children and account for only three per cent of the tumors in children. Infantile hemangioendothelioma is a rare benign hepatic tumor arising from mesenchymal tissue. Most of the cases present before six months. An unusual presentation and progression of infantile hemangioendothelioma is reported in a 19-month-old
R C, Parmar, S B, Bavdekar, S S, Borwankar, M N, Muranjan, A, Shenoy   +4 more
openaire   +2 more sources