Greenebaum E, Mansukhani M M, Heller D S, Timor-Tristsch I
Department of Surgical Pathology, College of Physicians and Surgeons, New York, NY 10032, USA.
Diagn Cytopathol. 1997 Feb;16(2):143-4. doi: 10.1002/(sici)1097-0339(199702)16:2<143::aid-dc9>3.0.co;2-i.
Cytologic evaluation of second trimester amniotic fluid (AF) is a rapid, inexpensive adjunct to prenatal diagnosis of open neural tube defects (ONTDs). Our goal was to determine whether the neural-appearing cells and/or large foamy macrophages in the AF of anencephalics are indeed of neural and/or glial origin. In two second trimester patients with elevated serum alpha-fetoprotein (AFP) and polyhydramnios, fetal sonogram studies showed anencephaly; amniocentesis was performed for AF-AFP, cytogenetic, and cytologic studies. AF sediment smears were initially Papanicolaou-stained; next, the same smears were immunoperoxidase (IP)-stained for glial fibrillary acidic protein (GFAP). If GFAP negative, slides were restained for synaptophysin (SYN) and neuron-specific enolase (NSE). Both AFs contained small neural-appearing cells (5-10 microns) singly and in clusters, with dense, round, homogeneous nuclei, an occasional nucleolus, and scant cytoplasmic rim. These were GFAP negative and SYN and NSE positive; the large vacuolated, lipid-laden macrophages (20-40 microns) were negative for all three IP stains. In conclusion, positive IP staining for SYN and NSE supports the morphologic impression that small dark cells in AF are of neural origin, while negative IP staining of large foamy macrophages suggests nonneural, nonglial origin.
孕中期羊水(AF)的细胞学评估是开放性神经管缺陷(ONTDs)产前诊断的一种快速、廉价的辅助手段。我们的目标是确定无脑儿羊水中神经样细胞和/或大的泡沫状巨噬细胞是否确实起源于神经和/或神经胶质。在两名血清甲胎蛋白(AFP)升高且羊水过多的孕中期患者中,胎儿超声检查显示无脑儿;进行羊膜穿刺术以进行羊水AFP、细胞遗传学和细胞学研究。羊水沉淀物涂片最初进行巴氏染色;接下来,对相同的涂片进行胶质纤维酸性蛋白(GFAP)的免疫过氧化物酶(IP)染色。如果GFAP为阴性,则对玻片重新进行突触素(SYN)和神经元特异性烯醇化酶(NSE)染色。两份羊水样本均含有单个和成簇的小神经样细胞(5 - 10微米),细胞核致密、圆形、均匀,偶尔有核仁,胞质边缘稀少。这些细胞GFAP为阴性,SYN和NSE为阳性;大的空泡状、富含脂质的巨噬细胞(20 - 40微米)对所有三种IP染色均为阴性。总之,SYN和NSE的阳性IP染色支持了羊水中小的深色细胞起源于神经的形态学印象,而大的泡沫状巨噬细胞的阴性IP染色表明其起源于非神经、非神经胶质。