{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T23:32:27Z","timestamp":1777937547171,"version":"3.51.4"},"reference-count":17,"publisher":"SAGE Publications","issue":"4","license":[{"start":{"date-parts":[[2022,1,6]],"date-time":"2022-01-06T00:00:00Z","timestamp":1641427200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Pediatr Dev Pathol"],"published-print":{"date-parts":[[2022,7]]},"abstract":"<jats:p>\n                    Maternal floor infarction (MFI) and massive perivillous fibrin deposition (MPFD) are overlapping placental disorders of unknown etiology, associated with adverse obstetric outcome, and a significant risk of recurrence. We describe a 31-year-old mother with asymptomatic thrombocytopenia throughout pregnancy and a positive lupus anticoagulant. She delivered a normal female neonate at term, whose weight was small for gestational age, with a placenta weighing less than the 10\n                    <jats:sup>th<\/jats:sup>\n                    percentile. Placental examination showed MPFD together with excessive subchorionic fibrinoid deposition. The placenta showed diffuse C4d deposition and an immune-mediated reaction was postulated for the pathogenesis of the placental changes. We suggest that excessive subchorionic fibrinoid deposition may be part of the morphologic spectrum of MFI\/MPFD.\n                  <\/jats:p>","DOI":"10.1177\/10935266211069331","type":"journal-article","created":{"date-parts":[[2022,1,6]],"date-time":"2022-01-06T08:12:47Z","timestamp":1641456767000},"page":"466-469","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Excessive Subchorionic Fibrinoid Deposition as a Component of Massive Perivillous Fibrin Deposition: A Case With Maternal Immune Thrombocytopenia"],"prefix":"10.1177","volume":"25","author":[{"given":"Mana","family":"Taweevisit","sequence":"first","affiliation":[{"name":"Department of Pathology, Faculty of Medicine, Chulalongkorn University, Pathumwan, Thailand"},{"name":"King Chulalongkorn Memorial Hospital and Thai Red Cross Society, Pathumwan, Thailand"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Panachai","family":"Nimitpanya","sequence":"additional","affiliation":[{"name":"King Chulalongkorn Memorial Hospital and Thai Red Cross Society, Pathumwan, Thailand"},{"name":"Department of Obstetrics and Gynecology, Faculty of Medicine, ChulalongkornUniversity, Pathumwan, Thailand"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6571-5566","authenticated-orcid":false,"given":"Paul S.","family":"Thorner","sequence":"additional","affiliation":[{"name":"Department of Pathology, Faculty of Medicine, Chulalongkorn University, Pathumwan, Thailand"},{"name":"Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, 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