Hamoudi A B, Reiner C B, Boles E T, McClung H J, Kerzner B
Arch Pathol Lab Med. 1982 Dec;106(13):670-2.
Increased acetylthiocholinesterase (AchE) reactivity in the rectal lamina propria and lamina muscularis mucosae was used to diagnose Hirschsprung's disease. We processed 131 specimens with the AchE reaction; 43 were suction biopsy specimens and the rest were full-thickness specimens. Of the 68 specimens in which neurocytes were present, none demonstrated a diffuse increase in the number of nerve fibers. However, 15 showed focal increases in the numbers of fibers that were not large enough to be regarded as indicative of Hirschsprung's disease. All patients with a diffuse increase in nerve fibers, regardless of the type of biopsy, were shown to have Hirschsprung's disease. The AchE staining reaction did, however, produce a 29% rate of false-negative reactions (16 of 56 specimens) in patients with Hirschsprung's disease. These data demonstrate that an abnormal pattern of AchE reaction is diagnostic of aganglionic megacolon, whereas a normal pattern does not exclude the disease.
直肠固有层和黏膜肌层中乙酰硫代胆碱酯酶(AchE)反应性增加被用于诊断先天性巨结肠症。我们对131份标本进行了AchE反应处理;其中43份为抽吸活检标本,其余为全层标本。在有神经细胞的68份标本中,没有一份显示神经纤维数量弥漫性增加。然而,有15份标本显示纤维数量局灶性增加,但增加幅度不足以被视为先天性巨结肠症的指征。所有神经纤维弥漫性增加的患者,无论活检类型如何,均被证实患有先天性巨结肠症。然而,在先天性巨结肠症患者中,AchE染色反应确实产生了29%的假阴性率(56份标本中有16份)。这些数据表明,AchE反应的异常模式可诊断无神经节细胞巨结肠,而正常模式并不能排除该疾病。