Kershisnik M M, Kaplan C, Craven C M, Carey J C, Townsend J J, Knisely A S
Department of Pathology, University of Utah Medical Center, Salt Lake City 84132.
Arch Pathol Lab Med. 1992 Oct;116(10):1043-6.
Nonteratomatous intrapulmonary neuroglial heterotopia not associated with birth trauma or frank vascular embolization has been described rarely. This article briefly reviews the literature, and presents two additional cases of intrapulmonary neuroglial heterotopia. We found 14 cases in the literature. Twelve of these cases had central nervous system disruption, where neuroglial elements were in direct contact with amniotic fluid. Several hypotheses have been proposed, including fetal aspiration of detached neural fragments within amniotic fluid, neural crest migration defects, and vascular embolization with implantation. Of our two cases, one represents the first occurrence where central nervous system abnormalities were secondary to mechanical disruption, rather than to a primary neural tube defect. Our second case represents the youngest documented occurrence (17 weeks gestation) of intrapulmonary neuroglial heterotopia. Additionally, immunohistochemical studies were performed on these lesions, the results of which favor their neural origin. We present these findings and suggest they support the aspiration mechanism for neuroglial heterotopia in lung tissue.
非畸胎瘤性肺内神经胶质异位症,若不伴有出生创伤或明显的血管栓塞,鲜有报道。本文简要回顾相关文献,并报告另外两例肺内神经胶质异位症病例。我们在文献中发现了14例。其中12例存在中枢神经系统破坏,神经胶质成分与羊水直接接触。已经提出了几种假说,包括胎儿吸入羊水中分离的神经碎片、神经嵴迁移缺陷以及血管栓塞伴植入。在我们的两例病例中,一例是首次出现中枢神经系统异常继发于机械性破坏,而非原发性神经管缺陷。我们的第二例病例代表了有记录的肺内神经胶质异位症最年轻的发病情况(妊娠17周)。此外,对这些病变进行了免疫组化研究,结果支持它们起源于神经。我们展示这些发现,并表明它们支持肺组织中神经胶质异位症的吸入机制。