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Updated: Jul 3, 2026

Isolation and Expansion of Mesenchymal Stem/Stromal Cells Derived from Human Placenta Tissue
Published on: June 6, 2016
[Placental mesenchymal dysplasia]
Fabienne Allias1, Frédérique Lebreton, Sophie Collardeau-Frachon
1Service d'anatomie et cytologie pathologiques, hôpital de la Croix-Rousse, 93, Grande rue de la Croix-Rousse, 69317 Lyon cedex 04, France. fabienne.allias-montmayeur@chu-lyon.fr
Placental mesenchymal dysplasia (PMD) is a rare placental abnormality. Accurate diagnosis requires detailed microscopic examination, distinguishing it from molar pregnancies for better pregnancy outcomes.
Area of Science:
- Reproductive Medicine
- Obstetrics
- Pathology
Background:
- Placental mesenchymal dysplasia (PMD) is a rare placental abnormality.
- It is often misdiagnosed as a partial mole due to ultrasound and gross placental findings.
- Understanding PMD is crucial for accurate antenatal diagnosis and management.
Purpose of the Study:
- To describe the ultrasonographic, macroscopic, and microscopic features of PMD.
- To review the clinical presentation, pregnancy complications, and fetopathologic associations of PMD.
- To discuss the etiopathogenic hypotheses and differential diagnoses of PMD.
Main Methods:
- Literature review of PMD cases.
- Analysis of personal experience with PMD.
- Integration of ultrasonographic, macroscopic, microscopic, cytogenetic, and molecular data.
Main Results:
- PMD presents with a multicystic placenta and may have an embryo.
- Microscopic examination, cytogenetics, and molecular studies are key to differentiating PMD from molar pregnancies.
- PMD is associated with specific pregnancy complications and fetopathologic findings.
Conclusions:
- Accurate antenatal diagnosis of PMD is achievable through comprehensive evaluation.
- Distinguishing PMD from partial moles is critical for appropriate clinical management.
- Further research into PMD's pathogenesis and long-term implications is warranted.
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