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Updated: May 30, 2026

Isolation and Expansion of Mesenchymal Stem/Stromal Cells Derived from Human Placenta Tissue
Published on: June 6, 2016
Multiple hepatic mesenchymal hamartomas in a premature associated with placental mesenchymal dysplasia
Birte Mack-Detlefsen1, Thomas M Boemers, Peter Groneck
1Kliniken der Stadt Koeln gGmbH, Kinderkrankenhaus Amsterdamer Strasse, Department of Pediatric Surgery and Urology, 50735 Cologne, Germany. birte.d@gmx.net
Abstract:
Placental mesenchymal dysplasia (PMD) is an uncommon disorder that has to be differentiated histologically from a partial mole. In contrast to a hydatitiform mole, PMD can coexist with a viable fetus. Placental mesenchymal dysplasia is characterized by placentomegaly and dilatation of the chorionic vessels. In our case, multiple hepatic mesenchymal hamartomas in a preterm were associated with PMD. This association is an extremely rare anomaly. Mesenchymal hamartomas occur in 5% of all primary liver tumors in children and are generally benign lesions.
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