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1.
Neurosurgery ; 44(6): 1207-23; discussion 1223-4, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10371620

ABSTRACT

OBJECTIVE: In the treatment of patients with cranial base tumors, unclippable aneurysms, or medically intractable ischemia, it may be necessary to use high-flow bypass grafts. The indications, surgical techniques and complications are discussed. METHODS: During a 10-year period, 99 saphenous vein grafts and 3 radial artery grafts were performed for 101 patients, i.e., 72 with neoplasms, 23 with aneurysms, and 6 with ischemia. Clinical follow-up monitoring of the patients was by direct examination or telephone interview, with a mean follow-up period of 41.2 months (range, 5-147 mo). Radiological follow-up monitoring was by magnetic resonance imaging, magnetic resonance angiography, or three-dimensional computed tomographic angiography, with a mean follow-up period of 32 months (range, 1-120 mo). During the follow-up period, there was one late graft occlusion and one graft stenosis. RESULTS: The use of intraoperative angiography improved the patency rate from 90 to 98% and reduced the incidence of perioperative stroke from 13 to 9.5%. Ninety-two percent of the patients were in excellent or good neurological condition at the time of discharge from the hospital, compared with 95% before surgery. The perioperative mortality rate was 2%. Other complications included three intracranial hematomas, rupture of a vein graft in a patient with Marfan's syndrome, and five tumor resection-related problems. The long-term survival rates for patients who received grafts were excellent for patients with benign tumors, fair to poor for patients with malignant tumors, good for patients with aneurysms, and excellent for patients with ischemia. CONCLUSION: The results of saphenous vein and radial artery grafting have been greatly improved by the use of intraoperative angiography, improvements in surgical techniques, and improved perioperative treatment.

2.
Cancer Control ; 5(2): 138-149, 1998 Mar.
Article in English | MEDLINE | ID: mdl-10761025

ABSTRACT

BACKGROUND: Due to their involvement with critical neurovascular structures, tumors located in the cranial base present challenges to neurosurgeons and are associated with high morbidity and mortality. METHODS: Rates of tumor control, complications, patient outcomes, and recurrences were extracted and summarized from two decades of our surgical and radiological treatment follow-up and review of the medical literature. RESULTS: Recent advances in surgical techniques involving cranial base approaches have made surgical intervention safer and curative resection more likely. In managing benign tumors, surgical resection is the gold standard for treatment. While immediate complications are still significant, long-term outcomes in most cases are excellent. Focused radiosurgery using a gamma knife or linear accelerator has produced favorable outcomes, and it improves the management of small or minimally symptomatic cranial base tumors. For slow-growing malignant tumors, extensive surgery followed by radiotherapy achieves the best outcome. In managing highly malignant tumors, outcome is determined by the effects of chemotherapy and radiotherapy. On some occasions, surgery is needed to obtain greater control of highly malignant tumors. CONCLUSIONS: Skull base tumors are relatively common, and management of these tumors is rapidly evolving. The combination of surgical excision using cranial base techniques, radiosurgery, fractionated radiotherapy, and chemotherapy should be individually tailored based on the location and pathological aggressiveness of the tumor and the symptomatology of the patient.

3.
Phys Rev B Condens Matter ; 42(13): 8517-8536, 1990 Nov 01.
Article in English | MEDLINE | ID: mdl-9995028
4.
Phys Rev B Condens Matter ; 41(15): 10498-10502, 1990 May 15.
Article in English | MEDLINE | ID: mdl-9993457
5.
Phys Rev B Condens Matter ; 37(14): 8145-8149, 1988 May 15.
Article in English | MEDLINE | ID: mdl-9944146
6.
Phys Rev Lett ; 59(2): 221-224, 1987 Jul 13.
Article in English | MEDLINE | ID: mdl-10035483
9.
Phys Rev Lett ; 56(19): 2068-2071, 1986 May 12.
Article in English | MEDLINE | ID: mdl-10032849
11.
Phys Rev A Gen Phys ; 31(5): 3498-3500, 1985 May.
Article in English | MEDLINE | ID: mdl-9895917
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