Rhode Island Hospital, Providence, USA.
J Pediatr Gastroenterol Nutr. 2012 Sep;55(3):268-71. doi: 10.1097/MPG.0b013e31824c0acc.
Hirschsprung disease (HD) is defined as the absence of ganglion cells in the Meissner and Auerbach plexuses. Diagnosis depends on demonstrating the absence of ganglion cells in rectal biopsy specimens. Rectal suction biopsy is widely employed as the method of choice in obtaining such specimens. Classically, the diagnosis was made until the 1990s by using the Multipurpose Suction Biopsy Kit, or Rubin Tube. This device was replaced by the Model SBT-100 Suction Biopsy Kit as the exclusive device used to procure rectal tissue. Because the suction devices are known to occasionally yield tissue that is insufficient, the present study was undertaken to determine the efficacy of using this technique to make or exclude the diagnosis of HD.
The last 50 biopsy sessions using the Multipurpose Suction Biopsy Kit and the first 46 sessions using the Model SBT-100 were included for review.
Both groups had similar yields (24%) of biopsy sessions with insufficient tissue to allow meaningful interpretation. The predictive value of rectal suction biopsy in excluding HD at the first biopsy session was 65%.
We conclude that HD can be excluded with a single rectal suction biopsy 65% of the time. A second biopsy session will exclude the diagnosis in an additional 11% of patients. Both devices yield biopsies of comparable quality and are equally useful in excluding the diagnoses of HD.
先天性巨结肠(HD)被定义为 Meissner 和 Auerbach 神经丛中无神经节细胞。诊断取决于直肠活检标本中神经节细胞的缺失。直肠抽吸活检广泛应用于获取此类标本的首选方法。经典上,直到 20 世纪 90 年代,使用多功能抽吸活检试剂盒或 Rubin 管进行诊断。该设备被 Model SBT-100 抽吸活检套件取代,成为唯一用于获取直肠组织的设备。由于抽吸装置偶尔会产生不足的组织,因此进行了本研究以确定使用该技术进行或排除 HD 诊断的功效。
回顾了最后 50 次使用多功能抽吸活检试剂盒和前 46 次使用 Model SBT-100 的活检过程。
两组活检过程中组织不足以进行有意义解释的比例相似(24%)。首次活检时直肠抽吸活检排除 HD 的预测值为 65%。
我们得出结论,HD 可以通过单次直肠抽吸活检排除 65%的时间。第二次活检将使另外 11%的患者排除诊断。两种设备产生的活检质量相当,在排除 HD 的诊断方面同样有用。