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Sabato 27 ottobre 2012 - Pacini Editore

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316<br />

vascular insufficiency pattern was more frequent in the PE group,<br />

although highly represented also among normotensive FGR. Finally,<br />

chronic villitis was more common in normotensive FGR.<br />

Few studies have performed a systematic pathological assessment<br />

of FGR placentas or have correlated histology findings with<br />

clinical outcome and FGR etiology 8 9 . Previous studies were also<br />

limited by small sample size, different inclusion criterion, variability<br />

in clinical and pathologic measures, and lack of multivariate<br />

statistical analysis. Recently, Kovo et al (10) reported a higher<br />

CONGRESSO aNNualE di aNatOmia patOlOGiCa SiapEC – iap • fiRENzE, 25-<strong>27</strong> OttOBRE <strong>2012</strong><br />

Tab. I. placental pathologic findings in 126 pregnancies complicated by fGR according to the presence of pE.<br />

Variables<br />

Variables detected at gross examination<br />

Category<br />

With PE<br />

n 54 (%)<br />

W/o PE<br />

n 72 (%)<br />

p<br />

placental weight (g) mean±ds 266±74 266±96 0.203<br />

Placental maximum diameter (cm) mean±ds 14.0±2.3 14.1±2.4 0.816<br />

Placental minimum diameter (cm) mean±ds 11.1±2.1 11.6±2.2 0.223<br />

placental maximum width (cm) mean±ds 2.6±0.6 2.7±0.8 0.445<br />

placental minimum width (cm) mean±ds 1.5±0.6 1.7±0.6 0.031<br />

Cord length (cm) mean±ds 23.9±10.0 24.5±10.9 0.767<br />

cord diameter (cm) mean±ds 1.0±0.3 1.0±0.3 0.6<strong>27</strong><br />

Retroplacental hematoma Present 4 (7.4) 5 (6.9) 0.920<br />

intervillous thrombus Present 5 (9.2) 12 (16.7) 0.228<br />

Recent infarction Present 11 (20.4) 8 (11.1) 0.151<br />

organized infarction Present 34 (63) 23 (31.9) 0.001<br />

Chronic abruption Present 2 (3.7) 0 0.100<br />

fibrin deposition<br />

Microscopic variables<br />

Mild<br />

Massive<br />

3 (5.5)<br />

1 (1.8)<br />

6 (8.3)<br />

2 (2.8)<br />

0.782<br />

Chorionamnionatis grade<br />

Mild<br />

Moderate-severe<br />

3 (5.5)<br />

0<br />

5 (6.9)<br />

1 (1.4)<br />

0.647<br />

Chorionamnionitis stage<br />

1<br />

2<br />

3 (5.5)<br />

0<br />

3 (4.2)<br />

3 (4.2)<br />

0.301<br />

inflammatory fetal reaction Present 0 1 (1.4) 0.385<br />

acute villitis Present 1 (1.8) 1 (1.4) 0.837<br />

Chronic villitis Present 4 (7.4) 17 (23.6) 0.016<br />

fetal thrombotic vasculopathy Present 2 (3.7) 4 (5.5) 0.629<br />

fVt+ avascular villi Present 15 (<strong>27</strong>.8) 16 (22.2) 0.474<br />

fVt grade<br />

Mild<br />

Moderate-severe<br />

6 (11.1)<br />

9 (16.7)<br />

9 (12.5)<br />

7 (9.7)<br />

0.510<br />

Meconium staining of membranes Present 38 (70.4) 53 (73.6) 0.688<br />

Syncitial knots<br />

< 30%<br />

> 30%<br />

12 (22.2)<br />

38 (70.4)<br />

29 (40.3)<br />

30 (41.7)<br />

0.006<br />

Villous agglutination < 20<br />

> 20<br />

10 (18.5)<br />

7 (13)<br />

13 (18.1)<br />

6 (8.3)<br />

0.685<br />

intervillous fibrin deposition mild-moderate<br />

Marked<br />

30 (55.5)<br />

14 (25.9)<br />

42 (58.3)<br />

22 (30.5)<br />

0.482<br />

Villous hypoplasia Present 13 (24.1) 15 (20.8) 0.665<br />

atherosis of spiral arteries Present 20/51 (39.2) 11/71 (15.5) 0.003<br />

mural arterial hypertrophy Present 31 (57.4) 29 (40.3) 0.065<br />

Muscular arteries in basal plate Present 24/46 (52.2) 23/69 (33.3) 0.044<br />

trophoblastic giant cells Present 38 (70.4) 31/70 (44.3) 0.004<br />

immature intermediate trophoblast<br />

Class of pathological lesions<br />

Present 42 (77.8) 36/70 (51.4) 0.003<br />

Superficial implantation Present 42 (77.8) 37/71 (52.1) 0.003<br />

infection/inflammation Present 3 (5.5) 7 (9.7) 0.392<br />

fetal vascular damage Present 15 (<strong>27</strong>.8) 16 (22.2) 0.474<br />

Maternal vascular damage Present 33 (61.1) 35 (48.6) 0.164<br />

prevalence of maternal vascular lesions in PE-associated FGR<br />

than in normotensive FGR and in PE without FGR; conversely,<br />

fetal vascular anomalies and chronic villitis were more frequent<br />

in normotensive FGR.<br />

The strength points of our study are: a) standardized pathologic<br />

evaluation, including systematic macroscopic examination and<br />

sampling of the placentas, use of validated diagnostic criteria,<br />

semiquantitive scoring of elementary histological features,<br />

analysis of patterns of lesions; b) reproducibility of pathologic

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