J Korean Soc Ther Radiol.  1991 Dec;9(2):303-310.

Ultrastructural Effects of Irradiation on Squamous Cell Carcinoma of the Uterine Cervix

Affiliations
  • 1Department of Therapeutic Radiology, Keimyung university, School of Medicine, Taegu, Korea.
  • 2Department of Pathology, Keimyung university, School of Medicine, Taegu, Korea.
  • 3Department of Gynecology, Keimyung university, School of Medicine, Taegu, Korea.

Abstract

Nineteen patients with previously untreated invasive squamous cell carcinoma of the uterine cervix were treated by irradiation alone at the Keimyung University Hospital from January, 1990 to July, 1991. The serial samplings of the tissue taken before and during radiation of the uterine cervix were studied by light and electron microscopic examination. Radiation-induced cellular changes, particularly nuclear degeneration was pronounced. The tumor invasion pattern remained unchanged but the number of mitosis and tumor cells decreased. The number of infiltrating inflammatory cells, multinucleated giant cells and karyolitic cells were increased with radiation. Fibrosis was also increased. Electron microscopically, the amount of tonofilament in the tissue samplings was increased in the postirradiated state, but the desmosomes were decreased in numbers. Fibroblasts began to appear after an irradiation dose of 2700cGy. After an irradiation dose of 3600cGy or more, tumor cells were nearly completely degenerated and displaced with mature fibrotic tissue. There was an increase of activated fibroblasts and collagen fibers but a decrease of inflammatory cells in the interstitial tissue. Swelling of the mitochondria and endoplasmic reticulum, loss of intercellular bridges and an increased number of secondary lysosomes were also found with radiation.

Keyword

Ultrastructural effect; Radiation; Squamous cell carcinoma; Uterine cervix

MeSH Terms

Carcinoma, Squamous Cell*
Cervix Uteri*
Collagen
Desmosomes
Endoplasmic Reticulum
Female
Fibroblasts
Fibrosis
Giant Cells
Humans
Intermediate Filaments
Lysosomes
Mitochondria
Mitosis
Collagen
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