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胎盘慢性绒毛间炎

Chronic intervillositis of the placenta.

作者信息

Jacques S M, Qureshi F

机构信息

Department of Pathology, Hutzel Hospital, Detroit, MI 48201.

出版信息

Arch Pathol Lab Med. 1993 Oct;117(10):1032-5.

PMID:8215826
Abstract

We report six cases of chronic intervillositis, an infrequently recognized placental lesion that is characterized by a prominent mononuclear inflammatory cell infiltrate in the intervillous space and that is associated with poor fetal outcome. In all six placentas, the inflammatory infiltrate was essentially limited to the intervillous space: chronic villitis was present focally only in one and absent in the other five. Additional placental histopathologic findings included increased villous fibrinoid material in all six, infarcts in two, atherosis in decidual vessels in two, and acute chorioamnionitis in two. Results of immunohistochemical staining confirmed the predominantly histiocytic nature of the intervillous infiltrate. Two mothers had a history of severe preeclampsia, one had elevated blood pressure at the time of delivery, two had a history of substance abuse, two had a history of systemic lupus erythematosus treated with prednisone, and one of these last two also had diabetes. Five of the six pregnancies resulted in perinatal death. One fetus was nonviable, one was anencephalic, one died in utero, and two died of complications of prematurity shortly after birth; one of the premature infants was small for gestational age. The mononuclear nature of the inflammatory cell infiltrate and its association with increased villous fibrinoid material and atherosis suggests an immunological origin, although the possibility that this lesion may have an infectious cause cannot be excluded.

摘要

我们报告了6例慢性绒毛间隙炎,这是一种较少被认识的胎盘病变,其特征是绒毛间隙有显著的单核炎性细胞浸润,并与不良胎儿结局相关。在所有6个胎盘中,炎性浸润基本局限于绒毛间隙:仅1个胎盘局灶性存在慢性绒毛炎,其他5个胎盘无慢性绒毛炎。胎盘的其他组织病理学发现包括:6个胎盘均有绒毛纤维蛋白样物质增多,2个胎盘有梗死灶,2个胎盘的蜕膜血管有动脉粥样硬化,2个胎盘有急性绒毛膜羊膜炎。免疫组化染色结果证实绒毛间隙浸润主要为组织细胞性质。2位母亲有重度子痫前期病史,1位母亲在分娩时血压升高,2位母亲有药物滥用史.2位母亲有系统性红斑狼疮病史且用泼尼松治疗,这最后2位母亲中的1位还患有糖尿病。6次妊娠中有5次导致围产期死亡。1例胎儿无法存活,1例为无脑儿,1例死于宫内,2例出生后不久死于早产并发症;其中1例早产儿为小于胎龄儿。炎性细胞浸润的单核性质及其与绒毛纤维蛋白样物质增多和动脉粥样硬化的关联提示其起源于免疫反应,尽管不能排除该病变由感染引起的可能性。

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