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Case Report

Placental Chorioangioma Cellular Histological Subtype: A Rare Primary Benign Tumor of Placenta

Sunil V. Jagtap, Shashwita S. Jagtap, Neha N. Ghadge, Manasi R. Bhade, Pooja Pandey, Abhilasha S. Jadhav

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Indian Journal of Pathology: Research and Practice 13(3):p 107-110, July- September 2024. | DOI: https://doi.org/10.21088/ijprp.2278.148X.13324.3

How Cite This Article:

Sunil V. Jagtap, Shashwita S. Jagtap, Neha N. Ghadge et al. Placental Chorioangioma Cellular Histological Subtype: A Rare Primary Benign Tumor of Placenta. Ind Jr of Path: Res and Practice 2024;13(3)107-110.

Timeline

Received : July 12, 2024         Accepted : August 31, 2024          Published : September 30, 2024

Abstract

Background: Placental chorangioma is a benign angioma arising from chorionic tissue. These are well demarcated placental mass composed of capillaries, stromal cells and surrounding trophoblast arising in a stem villus. Case report: A 28-year-old, gravida 2 para 1, L1 was admitted for abdominal pain, vaginal bleeding and foul smelling discharge. She had history of normal vaginal delivery at home two month back. On per vaginal examination cervix dilated, foul smelling discharge was noted. Clinically suspected of retained placenta, placenta increta. USG abdomen and pelvis showed an enlarged uterus with a focal heterogeneously hyperechoic lesion measures 44x23x34mm noted in the upper endometrial cavity. Moderate increase vascularity in color doppler examination. The findings likely placental remains (? Placenta increta) / retained product of conceptions. No pelvic mass was seen. Hysterecscopy with dilation and curettage were done for removal of retained products. On gross pathological examination single, rounded, well demarcated placental mass was seen. It was firm, reddish brown in color with localization on the fetal side of the placental disk. On histopathology reported as placental chorangioma cellular subtype. Chorioamnitis was noted. Areas of degenerative changes, necrosis, focal calcification, and hyalinization was noted. Conclusion: Placental chorioangioma is a rare benign tumor of the placenta. Early diagnosis, close prenatal checkup and monitor with appropriate intervention may prevent severe fetal and maternal complications and perinatal mortality related to chorioangioma.


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Data Sharing Statement

There are no additional data available. All raw data and code are available upon request.

Funding

This research received no funding.

Author Contributions

All authors contributed significantly to the work and approve its publication.

Ethics Declaration

This article does not involve any human or animal subjects, and therefore does not require ethics approval.

Acknowledgements

We would like to express our gratitude to the patients, their families, and all those who have contributed to this study.

Conflicts of Interest

No conflicts of interest in this work.


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Cite this article

Sunil V. Jagtap, Shashwita S. Jagtap, Neha N. Ghadge et al. Placental Chorioangioma Cellular Histological Subtype: A Rare Primary Benign Tumor of Placenta. Ind Jr of Path: Res and Practice 2024;13(3)107-110.


Licence:

Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.


Received Accepted Published
July 12, 2024 August 31, 2024 September 30, 2024

DOI: https://doi.org/10.21088/ijprp.2278.148X.13324.3

Keywords

HemangiomaTumors of placentaNon-trophoblastic tumorsPlacental Chorioangioma Placenta

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Received July 12, 2024
Accepted August 31, 2024
Published September 30, 2024

licence


Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.


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