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Internal ultraviolet luminescence--internal carcinomas.

The ultraviolet wavelengths in the sun's spectrum are known to be a basic cause of carcinomas of the skin. Since the skin as well as all body cavities, linings, and glands are composed of epithelial cells, it has been suggested that the ultraviolet bioluminescence and chemiluminescence which are emitted by bodily functions may be just as basic a cause of carcinomas within the body. Ninety percent of all human cancers are carcinomas. Bodily functions which emit a "normal" background of ultra-violet emission can be caused to emit higher, more dangerous levels and bursts of radiation by synergistic combinations of foods and chemicals. Damaging effects can also be increased by the sensitization of the epithelia to radiation by foods, dyes, drugs, medications, and prior irradiation. Certain foods and chemicals also produce serious damage at specific sites within the body. If the role of ultraviolet suggested here proves to be correct, an entirely new approach to the knowledge, prevention, and treatment of carcinomas becomes available.

Carcinoma↗

Does stress echocardiography predict the site of future myocardial infarction? A large-scale multicenter study. EPIC (Echo Persantine International Cooperative) and EDIC (Echo Dobutamine International Cooperative) study groups.

OBJECTIVES: We sought to assess whether the site of future myocardial infarction can be predicted on the basis of induced dyssynergy ("area at risk") recognized by stress echocardiography. BACKGROUND: The severity and extent of stress-induced dyssynergy are strong predictors of subsequent major cardiac events. However, high grade stenotic lesions are not strictly associated with the site of future coronary occlusions. METHODS: From the stress echocardiography multicenter trials data bank, we selected 70 patients (56 men; mean age +/- SD 58 +/- 11 years) meeting the following inclusion criteria: 1) dipyridamole (n = 53) or dobutamine (n = 17) stress echocardiography; 2) a spontaneously occurring infarction, with no intercurrent revascularization procedure between the initial study and the infarction; and 3) a follow-up rest echocardiogram obtained 41 +/- 90 days after the infarction. RESULTS: A complete ischemia-infarction mismatch (infarct-related dysfunction in a patient with negative stress test results) occurred in 29 patients (41%). A partial mismatch (ischemic dysfunction in a territory different from the infarct area) occurred in nine patients (13%). A match (ischemia-related and infarction-related dyssynergy involving the same region) occurred in 32 patients (46%). The average time interval between the stress examination and the occurrence of infarction or reinfarction was 144 +/- 160 days in patients with a match and 439 +/- 622 days in patients with a mismatch (p < 0.05). CONCLUSIONS: Induced ischemia (imaged as transient dyssynergy by pharmacologic stress echocardiography) inconsistently identifies the site of future infarction. The majority of spontaneous coronary occlusions leading to infarction are unheralded by induced ischemia. However, most infarctions occurring within 1 year of stress testing are in the area identified as ischemic during testing.

Databases, Factual↗