大鼠融合三联体胎盘的组织病理学。

IF 0.9 4区 医学 Q4 PATHOLOGY
Journal of Toxicologic Pathology Pub Date : 2023-10-01 Epub Date: 2023-06-05 DOI:10.1293/tox.2023-0026
FurukawaSatoshi, TsujiNaho, HayashiSeigo, KurodaYusuke, KimuraMasayuki, KojimaChisato, TakeuchiKazuya
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引用次数: 0

摘要

在妊娠第15天,在Wistar Hannover大鼠中观察到融合的三联体胎盘。这种融合胎盘的每个胎盘(称为PL-A、PL-B和PL-C)分别附着在一个胎儿身上,但它们的胎儿重量低于附着在该坝中唯一正常胎盘(也称为PL-N)上的胎儿重量。在组织病理学上,在PL-B和PL-C中观察到滋养层隔膜变薄和迷路区母体血窦扩张,但在PL-A或PL-N中没有观察到。胎盘融合点位于胎盘两侧的交界区,无结缔组织,隔膜由滋养层巨细胞组成。尽管PL-A有一个单独的子宫腺,但PL-B和PL-C共用一个子宫腺,每个迷宫区有一个螺旋动脉末端分支。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Histopathology of fused triplet placenta in rat.

Histopathology of fused triplet placenta in rat.

Histopathology of fused triplet placenta in rat.

Histopathology of fused triplet placenta in rat.

A fused triplet placenta was observed in a Wistar Hannover rat on gestation day 15. Each placenta (referred to as PL-A, PL-B, and PL-C) of this fused placenta was attached to one fetus each, but their fetal weights were lower than that of the fetus attached to the only normal placenta (referred to as PL-N) in this dam. Histopathologically, thinning of the trophoblastic septa and dilatation of the maternal sinusoid in the labyrinth zone were observed in PL-B and PL-C, but not in PL-A or PL-N. The points of placental fusion were at the junctional zone derived from each side of the placenta without connective tissues, and the septum was composed of trophoblastic giant cells. Although PL-A had a solitary metrial gland, PL-B and PL-C shared one metrial gland with one spiral artery terminus branching towards each labyrinth zone.

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来源期刊
Journal of Toxicologic Pathology
Journal of Toxicologic Pathology PATHOLOGY-TOXICOLOGY
CiteScore
2.10
自引率
16.70%
发文量
22
审稿时长
>12 weeks
期刊介绍: JTP is a scientific journal that publishes original studies in the field of toxicological pathology and in a wide variety of other related fields. The main scope of the journal is listed below. Administrative Opinions of Policymakers and Regulatory Agencies Adverse Events Carcinogenesis Data of A Predominantly Negative Nature Drug-Induced Hematologic Toxicity Embryological Pathology High Throughput Pathology Historical Data of Experimental Animals Immunohistochemical Analysis Molecular Pathology Nomenclature of Lesions Non-mammal Toxicity Study Result or Lesion Induced by Chemicals of Which Names Hidden on Account of the Authors Technology and Methodology Related to Toxicological Pathology Tumor Pathology; Neoplasia and Hyperplasia Ultrastructural Analysis Use of Animal Models.
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