Results 131 to 140 of about 12,136 (174)
Some of the next articles are maybe not open access.
International Journal of Dermatology, 2000
A 32‐year‐old white woman presented with a 2‐year history of a gradually enlarging, asymptomatic, cutaneous and subcutaneous, 3 Ï 5‐cm plaque with a nodular surface on the left upper thigh ( Fig. 1). There were no other complaints or physical signs.
M, El Darouti +3 more
openaire +2 more sources
A 32‐year‐old white woman presented with a 2‐year history of a gradually enlarging, asymptomatic, cutaneous and subcutaneous, 3 Ï 5‐cm plaque with a nodular surface on the left upper thigh ( Fig. 1). There were no other complaints or physical signs.
M, El Darouti +3 more
openaire +2 more sources
Ossifying Epithelioid Hemangioendothelioma
The American Journal of Dermatopathology, 1996A case of small epithelioid hemangioendothelioma encapsulated by an egg‐shaped bony shell composed of newly formed mature lamellar bone is presented. A nodule measuring 10 × 5 × 5 mm was excised from inside of the right cheek muscle of a 46‐year‐old man.
H, Kiryu, H, Hashimoto, Y, Hori
openaire +2 more sources
Surgical Neurology, 1983
A case of hemangioendothelioma encountered in the lumbar region of a child is presented. Clinically, the tumor could not be differentiated from a dermoid cyst. This lesion must be included in the differential diagnosis of benign lumbar tumors.
openaire +2 more sources
A case of hemangioendothelioma encountered in the lumbar region of a child is presented. Clinically, the tumor could not be differentiated from a dermoid cyst. This lesion must be included in the differential diagnosis of benign lumbar tumors.
openaire +2 more sources
Hepatic Epithelioid Hemangioendothelioma
Journal of Clinical Gastroenterology, 2001Epithelioid hemangioendothelioma (EHE) is a rare neoplasm of vascular origin with unpredictable malignant potential. We describe two patients with primary EHE of the liver and review 34 cases previously published in Japan and compare them with those in Western countries.
K, Uchimura +7 more
openaire +2 more sources
Intracranial epithelioid hemangioendothelioma
Child's Nervous System, 2008Epithelioid hemangioendothelioma (EHE) is an uncommon soft-tissue vascular neoplasm. Although a well-defined entity outside the neuraxis, its intracranial occurrence is rare. Literature review revealed 35 reported cases till date.The authors report a case of intracranial EHE in a 15-year-old girl, who presented with a short history and unusual ...
Murali, Mohan S +4 more
openaire +2 more sources
Pulmonary epithelioid hemangioendothelioma
Arkhiv patologii, 2022The article describes the clinical, radiological and pathological features of epithelioid hemangioendothelioma (EHE) in 27 adult patients, mainly female. In all cases, with the exception of one, there was a benign course of the disease over many years with a tendency to stabilize growth, the morphological sign of which was the development of widespread
I.V. Dvorakovskaya +4 more
openaire +2 more sources
Oropharyngeal Kaposiform Hemangioendothelioma
Acta Otorrinolaringologica (English Edition), 2008The kaposiform hemangioendothelioma is a very infrequent tumor proceeding from the endothelial-derived spindle cells, more often found on the limbs, although peritoneal, retroperitoneal and sacrum locations are also prevailing. Head and neck are exceptional locations. The kaposiform hemangioendothelioma is almost exclusively found in children and early
Eduardo, Maseda +3 more
openaire +2 more sources
Infantile cardiac hemangioendothelioma
Pediatric Cardiology, 1992A 4-month-old infant with cardiac hemangioendothelioma presented with thrombocytopenia, and pericardial effusion, as well as signs and symptoms of heart failure. This is the first reported case of infantile cardiac hemangioma successfully treated with steroids.
J S, Chang +3 more
openaire +2 more sources
Mediastinal epithelioid hemangioendothelioma
The Annals of Thoracic Surgery, 1990An epithelioid hemangioendothelioma arising from the innominate vein in the anterior superior mediastinum of a 62-year-old man was treated by wide local excision followed by radiotherapy. This clinicopathologic entity is a rare cause of mediastinal mass and is characterized by an intermediate malignant potential.
B, Toursarkissian +2 more
openaire +2 more sources
INFANTILE HEPATIC HEMANGIOENDOTHELIOMA
American Journal of Roentgenology, 1969A case of infantile hemangioendothelioma of the liver without associated cutaneous hemangiomas is reported. The infant died from high output congestive heart failure secondary to the massive arteriovenous shunting of blood through the neoplasm.The diagnosis was established before death by the presence of hepatic calcifications and by abdominal ...
A C, Selke, S H, Cornell
openaire +2 more sources

