An instance of clinical radiation morbidity and cellular radiosensitivity, not associated with ataxia-telangiectasia

PN Plowman, BA Bridges, CF Arlett… - The British journal of …, 1990 - birpublications.org
PN Plowman, BA Bridges, CF Arlett, A Hinney, JE Kingston
The British journal of radiology, 1990birpublications.org
A 14-year-old boy received standard induction chemotherapy for acute lymphoblastic
leukaemia followed by standard dose cranial radiation prophylaxis (18 Gy). Severe
chemosensitivity and acute radiation reactions occurred and he died at 8 months from late
radiation damage. In vitro radiobiological studies of the boy's fibroblasts in culture
demonstrated an enhanced radiosensitivity indistinguishable from ataxia-telangiectasia (AT)
cells. However, unlike AT cells, DNA synthesis following irradiation was inhibited in a normal …
Abstract
A 14-year-old boy received standard induction chemotherapy for acute lymphoblastic leukaemia followed by standard dose cranial radiation prophylaxis (18 Gy). Severe chemosensitivity and acute radiation reactions occurred and he died at 8 months from late radiation damage. In vitro radiobiological studies of the boy's fibroblasts in culture demonstrated an enhanced radiosensitivity indistinguishable from ataxia-telangiectasia (A-T) cells. However, unlike A-T cells, DNA synthesis following irradiation was inhibited in a normal manner. This patient represents yet another example of extreme radiosensitivity, and the possibility of clinical prediction in the future is discussed.
British Institute of Radiology