There have been few studies of tracheal agenesis (TA) because it is an extr
emely rare condition and is invariably fatal. However, it is recognised to
be associated with a variety of oesophageal abnormalities, including oesoph
ageal atresia (OA) and communicating bronchopulmonary foregut malformations
(CBPFM). Except for some gross pathological reports, there has been no det
ailed histological investigation of this congenital abnormality. Adriamycin
-induced TA in fetal rats provides a means of studying this uncommon condit
ion, including its relationship to oesophageal abnormalities. TA was induce
d in rat features by intraperitoneal injection of adriamycin (2 mg/kg) into
timed-pregnant rats on days 6-9. Their 33 fetuses were removed by caesarea
n section, cut transversely, and stained after which the slides were examin
ed. OA developed in 27/33 adriamycin-treated fetuses, TA occurred in 5. Fou
r had type III while the 5th had type II TA. The oesophagus of fetuses with
TA acquired tracheal features in the region where both ectopic bronchi ori
ginated. Two fetuses with TA also had OA, and 4 had a CBPFM. Other abnormal
ities detected involved the gastrointestinal, urinary and cardiovascular sy
stems. The association of TA and oesophageal abnormalities suggests that th
ere may be a spectrum of abnormalities comprising a number of variants, whi
ch may have a common aetiology. The other abnormalities co-existing in this
animal model mirror those found in reported cases of human TA. Ultimately,
the rat model of OA and TA may give insight into the embryogenesis of thes
e malformations.