Cm. Salafia et Fs. Cowchock, PLACENTAL PATHOLOGY AND ANTIPHOSPHOLIPID ANTIBODIES - A DESCRIPTIVE STUDY, American journal of perinatology, 14(8), 1997, pp. 435-441
We described placental pathology in antiphospholipid antibody (APL) sy
ndrome, APL and no history of recurrent pregnancy loss, and in treated
and untreated pregnancies of APL syndrome. Thirty-nine pregnancies of
28 patients were studied: 23 placentas delivered from 23 women with A
PL (13 with APL syndrome and 10 with serological APL); 8 untreated mis
carriages before APL diagnosis from 6 of the 13 patients with APL synd
rome and 1 of 10 with serological APL; and 8 miscarriages by 5 additio
nal women before APL syndrome diagnosis. Histopathology was reviewed b
y a pathologist blinded except to gestational age. Contingency tables
and analysis of variance (ANOVA) considered p < 0.05 significant. Comp
aring the placentas delivered at >18 weeks' gestation, excessive periv
illous coagulation, avascular terminal villi, and ch ron ic villitis/u
teroplacental vasculitis tended to be more com mon in treated APL synd
rome than serological APL cases ip = 0.07). Oi the 16 miscarriages bef
ore diagnosis of APL, 11 were lost at <18 weeks' gestation. None had p
athology typical of APL, but 4 of 11 (36%) had chronic intervillositis
. Five of 16 miscarriages before the diagnosis of APL were miscarried
between 18-22 weeks. Three oi 5 (60%) miscarried after 18 weeks had mu
ltifocal uteroplacental thromboses, compared to 6 of 13 (46%) treated
pregnancies with APL syndrome and 0 of 10 cases with serological APL.