3.Intracranial Epithelioid Hemangioendothelioma.
Seok Kon YEO ; Jeong Hoon KIM ; Chang Jin KIM ; Jung Kyo LEE
Journal of Korean Neurosurgical Society 2007;42(2):129-131
Intracranial epithelioid hemangioendothelioma is extremely rare. We report a case of intracranial epithelioid hemangioendothelioma which developed in a 55-year-old man who presented with dysarthria for two weeks. The brain computed tomography scan and magnetic resonance image showed masses which had fat component at the left frontal convexity and at left posterior parietal area. Excisional biopsy at the left frontal convexity confirmed epithelioid hemangioendothelioma which is immunopositive for CD31, supporting endothelial differentiation, and negative for CD68, SMA and HMB-45.
Biopsy
;
Brain
;
Dysarthria
;
Hemangioendothelioma, Epithelioid*
;
Humans
;
Middle Aged
;
Rabeprazole
4.Epithelioid Hemangioendothelioma of the Liver: A Case Report.
Sung Hoon CHUNG ; Ok Jae LEE ; In Oak AHN ; Sun Ae CHANG ; Sun Young KIRN
Journal of the Korean Radiological Society 1994;30(5):885-887
Hepatic epithelioid hemangioendothelioma is a rare tumor of vascular origin having a intermediate clinical course between benign cavernous hemangioma and malignant anglosarcoma. Patients present nonspecific clinical signs and symptomas. We experienced a case of surgically proven hepatic epithelioid hemangioen-dothelioma. Computed tomography showed multiple nodules with internal calcifications, chiefly in peripheral portion of both lobes of the liver. Ultrasonography showed hypoechoic nodules and tiny calcific foci in peripheral portion. Open biopsy of the liver and the omenrum confirmed epithelioid hemangioendotheliomas.
Biopsy
;
Hemangioendothelioma, Epithelioid*
;
Hemangioma, Cavernous
;
Humans
;
Liver*
;
Ultrasonography
6.Hepatic epithelioid hemangioendothelioma: a case report.
Fu-rong SUN ; Web-heng ZHENG ; Bing-yuan WANG ; Hai WANG ; Ran AO ; Fei WANG ; Ping-ping ZHENG ; Yuan-yuan DING ; Bai-fang WANG
Chinese Journal of Hepatology 2012;20(12):951-952
8.Farber Disease Misdiagnosed as Hemangioendothelioma.
Sang Mok LEE ; Chaeyoun OH ; Sung Eun JUNG ; Hyun Young KIM
Journal of the Korean Association of Pediatric Surgeons 2016;22(2):54-58
Farber disease (FD) is a rare lysosomal storage disorder that shows autosomal recessive inheritance. We report the case of a 58-month-old girl with FD, who was misdiagnosed with epithelioid hemangioendothelioma. The patient had undergone five surgeries for sacrococcygeal masses and three surgeries for scalp masses owing to misdiagnosis. Here, we describe this rare case of FD.
Diagnostic Errors
;
Farber Lipogranulomatosis*
;
Female
;
Hemangioendothelioma*
;
Hemangioendothelioma, Epithelioid
;
Humans
;
Scalp
;
Wills
9.Pulmonary Epithelioid Hemangioendothelioma Association with Subcutaneous Metastasis: Surgical experience of one case.
Hae Young LEE ; Sung Rae CHO ; Sung Ho CHO ; Jung Hun BYUN ; Jong In KIM ; Jin Kyung PARK ; Bong Kwuen CHUN
The Korean Journal of Thoracic and Cardiovascular Surgery 2004;37(12):1025-1028
Epithelioid hemangioendothelioma (HE) is a very rare malignant tumor that is pathologically benign tumor originating from endothelial cell but clinically presents metastasis and recurrence. A 29-year-old asymptomatic man, preoperatively diagnosed as lung cancer in the left lower lung, underwent a lobectomy, a wedge lung resection of left upper lung, and partial resection of diaphragm. Left lower lobar lesion was confirmed as pulmonary epithelioid hemangioendothelioma, but the lesions of the left upper lung and diaphragm were remained calcified by spontaneous regression of HE. We report a case of subcutaneous metastasis that occurred two times at 10 months and 19 months after previous surgical treatment of pulmonary EH.
Adult
;
Diaphragm
;
Endothelial Cells
;
Hemangioendothelioma
;
Hemangioendothelioma, Epithelioid*
;
Humans
;
Lung
;
Lung Neoplasms
;
Neoplasm Metastasis*
;
Recurrence