1.A case of primary hepatic angiosarcoma.
Sang Jin PARK ; Chae Yoon CHON ; Hyun Seung SHIN ; Hee Yong MOON ; Kwang Hyub HAN ; Yung Myung MOON ; Jin Kyung KANG ; In Suh PARK ; Chan Il PARK
Korean Journal of Medicine 1993;45(6):818-823
No abstract available.
Hemangiosarcoma*
2.Angiosarcoma Presenting with a Wide Range of Histopathological Features and Differentiation: A Case Report
Yeongjoo OH ; Hemin LEE ; Sang Kyum KIM ; Sang Ho OH
Korean Journal of Dermatology 2019;57(5):290-291
No abstract available.
Hemangiosarcoma
3.Hepatic and splenic angiosarcoma: A case report
Eun Young KANG ; Chun Hee HAN ; Hae Young SEOL ; Won Hyuck SUH
Journal of the Korean Radiological Society 1986;22(6):1061-1065
Diagnostic radiologic studies for angiosarcoma are usually non-specific, but selective angiography is notablyexceptional, and there had been a few reports of CT or US featurs of hepatic or splenic angiosarcoma. We recentlyexperienced a case of hepatic and splenic angiosarcoma demonstrated by CT, US and selective angiogram in34-year0old man.
Angiography
;
Hemangiosarcoma
4.Angiosarcoma Arising from Chronic Osteomyelitis One Case Report
Sung Kang CHANG ; Suk Woong YOON ; Bern Soo YOUN ; Yong Ju KIM
The Journal of the Korean Orthopaedic Association 1983;18(5):1041-1044
No abstract available in English.
Hemangiosarcoma
;
Osteomyelitis
5.Angiosarcoma of the Distal end of the Clavicle: Report of a Case
Chuong Ill YOO ; Jung Yoon LEE ; Boo Hwan KIM ; Jong Woo LEE
The Journal of the Korean Orthopaedic Association 1976;11(1):127-131
Angiosarcoma is a rare tumor, and it is highly unusual for it to appear in bone as a primary lesion. Review of literature revealed that 38 such lesions have bsen recorded since 1925, when Codman wrote that they had as yet registered no case which could be considered a typical angiosarcoma prior to that date. Recently we encountered one tumor developed in the distal end of a clavicle which was confirmed as angiosarcoma by pathologic study. This case is presented with a review of literature.
Clavicle
;
Hemangiosarcoma
6.Primary Angiosarcoma of the Skin Presenting as Mild Erythema.
Sun Young MOON ; Dong Hyuk EUN ; Yong Hyun JANG ; Seok Jong LEE ; Do Won KIM ; Weon Ju LEE
Annals of Dermatology 2017;29(6):809-810
No abstract available.
Erythema*
;
Hemangiosarcoma*
;
Skin*
7.Cutaneous Metastasis of Renal Angiosarcoma Occurred on the Face.
Jung Eun SEOL ; So Hee PARK ; Wonkyung LEE ; Jeong Nan KANG ; Hyojin KIM
Korean Journal of Dermatology 2017;55(1):77-78
No abstract available.
Hemangiosarcoma*
;
Neoplasm Metastasis*
8.Angiosarcoma of the Breast Masquerading as Hemangioma: Exploring Clinical and Pathological Diagnostic Challenges.
Jordan D FREY ; Pascale G LEVINE ; Farbod DARVISHIAN ; Richard L SHAPIRO
Archives of Plastic Surgery 2015;42(2):261-263
No abstract available.
Breast*
;
Hemangioma*
;
Hemangiosarcoma*
9.Angiosarcoma of the nasal cavity.
Chul Hee LEE ; Tae Hoon JINN ; Ic Tae KIM ; Myung Koo KANG
Korean Journal of Otolaryngology - Head and Neck Surgery 1991;34(2):366-370
No abstract available.
Hemangiosarcoma*
;
Nasal Cavity*
10.Angiosarcoma of the scalp in a 79-year-old male: A case report
Erika Kim R. Chan ; Charlene Marie U. Ang-Tiu ; Mary Elizabeth S. Danga ; Michael Jeff B. Fontano
Journal of the Philippine Dermatological Society 2021;30(1):49-52
Introduction:
Angiosarcoma is a rare head and neck sarcoma of vascular endothelial cell origin. We report a case of angiosar-
coma in an elderly male, and the multidisciplinary approach employed in his treatment.
Case report:
A 79-year-old male presented with a 4-month history of a rapidly enlarging black, soft, immovable tumor surround-
ed by bruise-like patches over the right temporoparietal scalp. There was associated pruritus and bleeding when scratched.
Dermoscopy showed bluish black crusts over the tumor, and surrounding violaceous patches. Wedge biopsy revealed a dermis
with irregular vascular spaces infiltrating dermis, lined by atypical endothelial cells. Immunohistochemistry of the atypical in-
filtrative cells was positive for CD31. These findings were consistent with angiosarcoma. The patient underwent wide excision
with a rotational flap and split thickness skin graft. Postoperatively, the patient was referred to Oncology for adjuvant radiation
therapy.
Conclusion
Even with treatment, the prognosis of angiosarcoma remains poor due to its aggressive nature, with a 5-year sur-
vival rate ranging from 10-54%. However, early detection of the disease may increase patient survival rates. This rare case shows
the importance of maintaining a high level of suspicion for lesions that have an atypical presentation to prevent delays in man-
agement and improve patient outcomes.
Hemangiosarcoma
;
Scalp
;
Neoplasms
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