000 01658nam a22002537a 4500
999 _c8234
_d8234
003 MED20100007
005 20240720152621.0
008 160505b2010 xxu||||| |||| 00| 0 eng d
040 _cFEU-NRMF MEDICAL LIBRARY
041 _aEnglish
050 _aMED20100007
100 _aNavarro, Kate Leslie Ann C., MD.
_eauthor
245 _aCase report gastrointestinal stromal tumor /
_cKate Leslie Ann C. Navarro.
260 _aFairview, Quezon City
_bDepartment of Medicine, FEU-NRMF,
_c2010
300 _c(in folder)
336 _atext
_2rdacontent
337 _aunmediated
_2rdamedia
338 _avolume
_2rdacarrier
504 _aIncludes appendices and bibliographical references.
520 _aABSTRACT: Gastrointestinal stromal tumor is a rare type of soft tissue carcinoma that is usually found in the stomach. It can present as gastrointestinal bleeding, abdominal pain, abdominal fullness or abdominal mass. Endoscopy aids in the diagnosis of this rare type of tumor, Moreover, biopsy is confirmatory of the diagnosis. Surgery with adequate margin is the only treatment. Imatinib, a c-kit tyrosine inhibitor, is recently used now as adjuvant. Follow-up consult is necessary for monitoring response to treatment.This is a case of E.C., 73 year old, female, who presented with melena and abdominal pain with secondary anemia. Endoscopy was done and showed a mass on the stomach. Excision and biopsy of the mass was made thereafter validating the initial impression of gastrointestinal stromal tumor. Patient was discharged improved. Follow-up consult was suggested for monitoring.
521 _aRESDM
887 _aRC0003
942 _2lcc
_cRE