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Sudden fetal death with placental mesenchymal dysplasia complicated by placenta previa

Tanimura, Kenji Shi, Yutoku Imafuku, Hitomi Nakanishi, Takaaki Kanzawa, Maki Terai, Yoshito 神戸大学

2021.11

概要

Placental mesenchymal dysplasia (PMD) is a rare placental abnormality that is closely related to severe pregnancy complications. A 27-year-old woman with fetal growth restriction and placenta previa was referred to a university hospital at 22 gestational weeks (GW). She was suspected of having a twin pregnancy with a complete or partial hydatidiform mole and coexisting normal live fetus, because two separate placentas, an enlarged one with multiple cystic lesions and a normal one, were shown on ultrasound examinations. At 27 GW, she experienced a sudden intrauterine fetal death (IUFD) after bleeding due to placenta previa, despite confirmation of fetal well-being at 2 h before bleeding. After delivery, histopathological examination confirmed the diagnosis of PMD. This is the first documented case of a woman with PMD and placenta previa who had a sudden IUFD after bleeding. Patients with both PMD and placenta previa should be considered at extremely high risk for IUFD.

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Figure legends

Figure 1. Ultrasound and magnetic resonance imaging findings

(A, B) Ultrasound findings at 22+5/7 gestational weeks. (A) Transvaginal sonogram

showed that a placenta with multiple cysts covered the uterine cervix. (B) Abdominal

sonogram demonstrated two placentas, one was an enlarged placenta with multiple

vesicular lesions without blood flow (arrows) and another was a placenta appearing

normal (asterisk). (C, D) Magnetic resonance imaging (MRI) findings at 23+4/7

gestational weeks. (C) Sagittal, T2-weighted MRI showed an enlarged placenta with

multiple cysts. (D) Transverse, T2-weighted MRI indicated the presence of a normal

placenta (sharp sign) and an abnormal one (arrowheads).

Figure 2. Gross appearance of the placenta

(A) The fetal surface of the placenta. Dilated and tortuous vessels were observed (arrows).

(B) The maternal surface of the placenta consisted of grossly normal area (arrow heads)

and grossly abnormal area.

(C) The maternal surface of the placenta. Multiple grape-like vesicles were observed.

Figure 3. Pathological findings of the placenta

(A, B, and C) Hematoxylin and eosin stain; original magnification, 100x objective. (D)

Immunohistochemical staining for p57Kip2; original magnification, 400x objective.

(A) Enlarged hydropic stem villi, (B) no trophoblastic proliferation around the hydropic

stem villi with avascular stroma, and (C) hydropic stem villi with chorangioma-like

vascular proliferations were observed. (D) In immunohistochemical staining for p57Kip2,

positive staining in the villous cytotrophoblasts and no staining in the villous stroma were

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observed.

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