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Case Reports

Intrauterine Fetal Demise Associated with Vascular Malperfusion and Multiple Uterine Leiomyomata: A Report of Two Cases

ORCID Icon, ORCID Icon & ORCID Icon
Pages 83-92 | Received 30 Dec 2021, Accepted 24 Feb 2022, Published online: 04 Mar 2022
 

Abstract

Background

Uterine leiomyomata have been loosely associated with intrauterine fetal demise (IUFD), largely attributed to fetal growth restriction from cavitary distortion. We present two cases of IUFD in patients with non-distorting leiomyomata and pathologic placental findings of maternal vascular malperfusion (MVM) and fetal vascular malperfusion (FVM).

Case Report

Case 1 details a 28w3d IUFD associated with large leiomyomata (largest 11.9 × 7.6 × 9.7 cm), post-partum deep vein thrombosis, and severe pre-eclampsia histologic features. Case 2 details a 25w2d IUFD associated with smaller leiomyomata (largest 3.1 × 3.0 × 3.3 cm). Both placentas demonstrated MVM, including parenchymal thrombi and accelerated villous maturity, and FVM, including avascular stem villi.

Discussion

As the placentas in both cases demonstrated findings consistent with altered placental perfusion, we posit that leiomyomata in these cases may have been associated with both maternal and fetal vascular malperfusion, ultimately contributing to fetal demise.

Acknowledgements

Linh Tran, PA-C, assisted in the curation and editing of ultrasonic images.

Disclosure statement

The authors have no financial or other conflicts of interest to disclose.

Funding

The author(s) reported there is no funding associated with the work featured in this article.

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