Abstract
s / Placenta 35 (2014) A1eA112 A14 (80-100%) and specificity (98.5-100%) for all inflammatory and non-inflammatory lesions. Conclusion: Our study demonstrates a reliable approach to electronically integrate placental pathology and delivery data. These linked data provide a platform to identify risk factors associated with placental lesions. They also set the stage for linkage to other biologic and clinical data enabling large-scale studies of offspring and maternal health sequelae associated with placental measures. P1.11-N. IMAGING ANALYSIS AND PATHOLOGICAL FEATURES OF PLACENTAL MESENCHYMAL DYSPLASIA (PMD) Akiko Tanuma , Rie Kawaguchi , Haruka Yanagisawa , Tomohiro Tanemoto , Nozomu Yanaihara , Aikou Okamoto a Department of Obstetrics and Gynecology, The Jikei University School of Medicine, Tokyo, Japan; Department of Pathology, The Jikei University School of Medicine,
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