Paper
1 June 2001 Partial in-vitro resistance to direct cryothermic injury in human leiomyomata and myometrium
Christopher C. Rupp, David J. Swanlund, Pragati Bhowmick, John C. Bischof, James E. Coad M.D.
Author Affiliations +
Abstract
Uterine leiomyomata are the most common pelvic tumor in women. Minimally invasive cryosurgery is being investigated as a therapeutic option for symptomatic women. Direct cryothermic cell injury thresholds for leiomyomata and the adjacent myometrium are not well quantified. Using a directional solidification stage to simulate in-vivo cryothermic cooling, tissue sections (3 mm) from ten leiomyomata and six portions of myometrium were cooled (5°C/min) to -20°C, -40°C, -60°C, and - 80°C, held for 15 minutes, and then rapidly thawed to 21°C. In conjunction with tissue culturing and appropriate controls, cell death was assessed using a viability dye (ethidium homodimer/Hoechst) and routine histology. After normalizing to controls, leiomyomata cell death (LCD) increased from -20 to -80°C by histology (12 to 27 percent LCD) and dye assay (26 to 38 percent LCD). Myometrial cell death (MCD) from -20 to -80°C was 10 to 12 percent by histology and 4 to 20 percent by dye assay. In contrast to LCD from -40 to -80°C, MCD was significantly less and plateaued over this range (p<0.05). The dye assay appears to be more sensitive for detecting cell death than histology. This study suggests that both leiomyomata and myometrium are moderately resistant to direct cryothermic injury, with leiomyomata somewhat more susceptible.
© (2001) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Christopher C. Rupp, David J. Swanlund, Pragati Bhowmick, John C. Bischof, and James E. Coad M.D. "Partial in-vitro resistance to direct cryothermic injury in human leiomyomata and myometrium", Proc. SPIE 4247, Thermal Treatment of Tissue: Energy Delivery and Assessment, (1 June 2001); https://doi.org/10.1117/12.427862
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Cited by 2 scholarly publications.
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KEYWORDS
Cell death

Tissues

Injuries

Control systems

Liquids

Nitrogen

In vitro testing

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