000			02072nam a22002537a 4500
001			R000772
003			PILC
005			20240720153335.0
008			240717b |||||||| |||| 00| 0 eng d
040			_beng _cFEU-NRMF MEDICAL LIBRARY _drda
041			_aeng
050			_aMED 2024 0005
245			_aA 58-year-old FILIPINO male with multiple cutaneous masses and diagnosed with angiosarcoma: a case report / _b[author]: Argante, Shiela Ann A.
260			_aFairview, Quezon City: _bDepartment od Internal Medicine, FEU-NRMF, _c2024
300			_c(in folder) _ewith flash drive (soft copy)
336			_2rdacontent _atext
337			_2rdamedia _aunmediated
338			_2rdacarrier _avolume
504			_aIncludes bibliographical references.
520			_aABSTRACT: Angiosarcoma is a rare oncologic disease that affects the lining of blood vessels and lymph vessels. It can occur in any part of the body but it mostly affects the skin.1 It presents as bruised, purplish area of the skin. They grow larger in time and the skin around the area can bruise as well. It is diagnosed through imaging scans and confirmed through biopsy and immunohistochemistry stains. It can be misdiagnosed as other oncologic diseases that present with masses as well. For this paper, it aims to present a 58-year-old male whose initial complaint was generalized body weakness accompanied with multiple masses on his nape, scalp, left eye, abdomen and chest. The positive immunohistochemical result of Ki-67 antigen (30-9), CD 31 (JC70)/ (JC70 A), CD34 endothelium (OBEnd/10) was confirmatory and led to the initiation of chemotherapy instead of removal of the masses. This paper aims to discuss the approach and management of patients with angiosarcoma and its chemotherapy protocol. OBJECTIVES: 1. To present a case of a 58-year-old male diagnosed with Angiosarcoma. 2. To discuss the incidence, clinical presentation of Angiosarcoma. 3. To discuss the management of Angiosarcoma on our patient.
521			_aRESDM
700			_aArgante, Shiela Ann A. _eauthor
942			_2lcc _cRU
999			_c12736 _d12736