Since the introduction of the National Health Service Breast Screening Prog
ramme (NHSBSP), the number of ductal carcinoma in situ (DCIS) cases has inc
reased considerably. Despite its increased incidence, some NHS leaflets and
reports do not mention it, and the general public seems largely unaware of
its existence. There are numerous biological studies dealing with this con
dition, but its psychosocial aspects seem to have been neglected. We have o
nly been able to locate two British studies (Farmer, A. 1996. Unpublished P
hD thesis, University of Southampton; Webb, C. and Koch, T. 1997. J. Adv. N
urs., 25, 154-525) that address some of the psychosocial issues associated
with DCIS.
This paper starts by defining DCIS and explaining its usual presentation, n
atural history and epidemiology. The treatment options for DCIS are describ
ed, together with the great deal of confusion and lack of agreement that ac
companies them. The psychological issues that women with screen-detected DC
IS have to deal with are different from those affecting women diagnosed wit
h symptomatic breast cancer, and a summary of these issues is given. Finall
y, some suggestions for future psychosocial research are provided. Because
the UK as a whole was not covered by the NHSBSP until 1990 (Baum, M. 1995.
Lancet, 346, 436; Gage and Fouquet, 1997), the main focus will be on papers
published from that year onwards, although some key papers published befor
e then will also be included. The papers reviewed here were found in MEDLIN
E, EMBASE and BIDS (ISI). Copyright (C) 1999 John Wiley & Sons, Ltd.