| Li CC |
------>authors3_c=??? ------>paper_class1=1 ------>Impact_Factor=None ------>paper_class3=1 ------>paper_class2=2 ------>vol=43 ------>confirm_bywho=fplee ------>insert_bywho=tsaistella ------>Jurnal_Rank=None ------>authors4_c=??? ------>comm_author=1 ------>patent_EDate=None ------>authors5_c=??? ------>publish_day=1 ------>paper_class2Letter=None ------>page2=119 ------>medlineContent= ------>unit=E0114 ------>insert_date=20081008 ------>iam=7 ------>update_date=None ------>author=??? ------>change_event=4 ------>ISSN= ------>authors_c=??? ------>score=333 ------>journal_name=??????????? ------>paper_name=Sinonasal Hemangiopericytoma ------>confirm_date=20081201 ------>tch_id=092065 ------>pmid=18761848 ------>page1=115 ------>fullAbstract=Sinonasal-type hemangiopericytomas are rare tumors believed to derive from perivascular modified smooth muscle cells. They have a predilection for the nasal cavity and paranasal sinuses, where they grow as polypoid masses. Affected patients experience epistaxis, nasal obstruction, sinusitis and bone erosion along with a wide array of other nonspecific findings. The overall excellent survival is achieved with complete surgical excision. Up to 30% of the cases develop recurrence, often many years after initial surgery. Malignant behavior is uncommon. A case of a 59 year old woman is presented. ------>tmu_sno=None ------>sno=18869 ------>authors2=Li CR ------>authors3=Hon CS ------>authors4=Yer YH ------>authors5=Lee UC ------>authors6=Pan ST, Tsai SC ------>authors6_c=???,??? ------>authors=Li CC ------>delete_flag=0 ------>SCI_JNo=None ------>authors2_c=??? ------>publish_area=0 ------>updateTitle=[Sinonasal-type hemangiopericytoma] ------>language=1 ------>check_flag=None ------>submit_date=None ------>country=None ------>no= ------>patent_SDate=None ------>update_bywho=None ------>publish_year=2008 ------>submit_flag=None ------>publish_month=10 |