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Isolation and Analysis of Hematopoietic Stem Cells from the Placenta
Published on: June 24, 2008
Study of placenta in sickle cell disorders
Kalpana B Rathod1, Kirti N Jaiswal, Alok C Shrivastava
1Department of Pathology, I.G.M.C., Nagpur.
Indian Journal of Pathology & Microbiology
|March 1, 2008
Summary
Sickle cell disorders significantly alter placental pathology, leading to fetal complications. This study highlights key placental changes and their association with maternal sickle cell status.
Area of Science:
- Obstetrics and Gynecology
- Hematology
- Pathology
Background:
- Sickle cell disorders present unique challenges during pregnancy.
- Placental examination is crucial for understanding pregnancy outcomes in these patients.
Purpose of the Study:
- To investigate pathological changes in placentas of patients with sickle cell disorders.
- To compare these changes with a control group.
- To assess the impact of maternal sickling on fetal outcomes.
Main Methods:
- A comparative study involving 73 participants: 10 controls and 63 with sickle cell disorders (47 sickle cell trait, 16 sickle cell disease).
- Gross and microscopic examination of placentas.
- Analysis of pregnancy complications such as vaso-occlusive crises, hemolytic crises, pregnancy-induced hypertension, and urinary tract infections (UTI).
Main Results:
- Placentas from sickle cell disorder patients exhibited infarction, calcification, sickled red blood cells, intervillous hemorrhage, increased syncytial knots, fibrinoid necrosis, stromal fibrosis, hyalinized villi, and trophoblastic proliferation.
- Pregnancy complications were observed, including vaso-occlusive/hemolytic crises in SS patients, and increased rates of pregnancy-induced hypertension and UTI in both AS and SS groups compared to controls (implied).
Conclusions:
- Sickle cell disorders are associated with significant placental pathological changes.
- These placental alterations may contribute to adverse pregnancy outcomes and fetal effects.
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