Kobayashi Hiroyuki, Li Zhixin, Yamataka Atsuyuki, Lane Geoffrey J, Miyano Takeshi
Department of Paediatric Surgery, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
Pediatr Surg Int. 2002 Dec;18(8):753-6. doi: 10.1007/s00383-002-0876-2. Epub 2002 Sep 13.
Rectal suction biopsy (RSB) is a well-known diagnostic procedure for disorders of bowel motility such as Hirschsprung's disease (HD). However, there are few reports about the optimal method of obtaining rectal tissue. We introduce a new technique using Gruenwald's nasal cutting forceps (NCF). From 1986 to 1999, we performed 130 sets of rectal biopsies in patients suspected of having HD. In group I (1986 to 1994), 68 sets of three-site biopsies (2, 3, and 5 cm above the dentate line) were performed using a conventional blind RSB technique. In group II (1995 to 1999), 62 sets of one-site biopsies (2 cm above the dentate line) were performed using Gruenwald's NCF after anal dilatation during general anesthesia. Hematoxylin-eosin staining and acetylcholinesterase histochemistry were used to examine all specimens. Biopsy specimens in group II (4.39 +/- 1.07 mm(2)) were larger than in group I (1.59 +/- 0.39 mm(2)) ( P < 0.01). In 18 cases (26 %) in group I, normal and HD bowel could not be differentiated because the specimens were too small to detect ganglion cells (i.e., only lamina propria [9 cases] or a small area of submucosa [9 cases] was present). These cases required repeat biopsy. All cases of HD diagnosed in group I (n = 20) were based on the findings of biopsies taken at 2 cm; biopsies from 3 and 5 cm did not provide additional information. There were 2 cases of post-biopsy hemorrhage in group I. In group II, 18 subjects were diagnosed with HD and 39 were confirmed to have normal bowel. There were no complications and repeating the biopsy was unnecessary. Three cases of hypoganglionosis (1 in group I and 2 in group II) were missed because the myenteric plexus abnormalities could not be detected by RSB. Intestinal neuronal dysplasia (IND) was diagnosed in 5 cases (2 in group I by repeat full-thickness biopsy and 3 in group II by rectal biopsy). We conclude that our new technique is advantageous and safe to differentiate between normal bowel, HD, and even IND on the basis of a single biopsy taken 2 cm above the dentate line. The biopsy can be taken under direct vision and is histopathologically accurate.
直肠吸引活检(RSB)是一种用于诊断诸如先天性巨结肠(HD)等肠道动力障碍的知名诊断方法。然而,关于获取直肠组织的最佳方法的报道很少。我们介绍一种使用格伦瓦尔德鼻咬骨钳(NCF)的新技术。1986年至1999年,我们对疑似患有HD的患者进行了130组直肠活检。在第一组(1986年至1994年)中,使用传统的盲法RSB技术进行了68组三点活检(齿状线以上2、3和5厘米处)。在第二组(1995年至1999年)中,在全身麻醉下肛门扩张后,使用格伦瓦尔德的NCF进行了62组单点活检(齿状线以上2厘米处)。苏木精-伊红染色和乙酰胆碱酯酶组织化学用于检查所有标本。第二组的活检标本(4.39±1.07平方毫米)比第一组(1.59±0.39平方毫米)大(P<0.01)。在第一组的18例(26%)病例中,无法区分正常肠段和HD肠段,因为标本太小无法检测到神经节细胞(即仅存在固有层[9例]或一小片黏膜下层[9例])。这些病例需要重复活检。第一组诊断的所有HD病例(n = 20)均基于在2厘米处获取的活检结果;在3厘米和5厘米处的活检未提供额外信息。第一组有2例活检后出血。在第二组中,18名受试者被诊断为HD,39名被证实肠道正常。没有并发症,无需重复活检。有3例低神经节症(第一组1例,第二组2例)漏诊,因为RSB无法检测到肌间神经丛异常。5例诊断为肠道神经元发育异常(IND)(第一组2例通过重复全层活检诊断,第二组3例通过直肠活检诊断)。我们得出结论,我们的新技术在基于齿状线以上2厘米处的单次活检来区分正常肠段、HD甚至IND方面具有优势且安全。活检可在直视下进行,组织病理学准确。