2005
DOI: 10.1016/j.jpedsurg.2005.02.018
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Congenital hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta: case report

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Cited by 30 publications
(22 citation statements)
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“…In our review, the incidence of BWS was 19%, close to the 23% risk reported in the literature. There are multiple case reports in the literature describing the co‐existence of PMD with fetal hepatic mesenchymal tumors, suggesting a common pathogenetic origin for the two anomalies. Carta et al .…”
Section: Discussionsupporting
confidence: 81%
“…In our review, the incidence of BWS was 19%, close to the 23% risk reported in the literature. There are multiple case reports in the literature describing the co‐existence of PMD with fetal hepatic mesenchymal tumors, suggesting a common pathogenetic origin for the two anomalies. Carta et al .…”
Section: Discussionsupporting
confidence: 81%
“…Table 2 shows a comparison of outcomes of reported cases. Of the eight cases found in the literature, there were two fetal demises, one neonatal death, four postnatal surgically resections (two immediately postnatal, one at 3 months and one at 11 months of age), and one had serial postnatal percutaneous decompression with full resolution [3][4][5][6][7][8][9][10]. HMH should always be considered a likely diagnosis in cases of PMD with an associated abdominal mass seen antenatally on ultrasonography.…”
Section: Discussionmentioning
confidence: 94%
“…Placental mesenchymal dysplasia may be associated with chromosomal abnormalities such as trisomy 13, Klinefelter syndrome, triploidy and Xp deletion [6,7]. Rare cases of fetal congenital adrenal hyperplasia, vascular hamartoma, and hepatic mesenchymal hamartoma have been described [8].…”
Section: Discussionmentioning
confidence: 99%