Logan Suzanna J, Yin Hong, Rogers Beverly, Arva Nicoleta, Conces Miriam R, Cope-Yokoyama Sandy, Dehner Louis P, Galliani Carlos, Garg Shipra, He Mai, Husain Aliya N, Keisling Matthew, Krishnan Chandra, Puscasiu Elena, Rossi Christopher, Siddiqui Faiza, Sutton Lisa, Terry Jefferson, Thaker Ameet I, Huang Yuan, Zhang Jie, McCracken Courtney, Rytting Heather
Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
Department of Pathology, Children's Healthcare of Atlanta, Atlanta, GA, USA.
Pediatr Dev Pathol. 2022 Nov-Dec;25(6):645-655. doi: 10.1177/10935266221132602. Epub 2022 Nov 21.
The absence of submucosal ganglion cells does not reliably distinguish Hirschsprung disease from non Hirschsprung disease in anorectal line biopsies. Calretinin staining might be helpful in these biopsies. To determine its value, we analyzed calretinin positive mucosal neurites in anorectal line biopsies.
Two pediatric pathologists, without access to patient data, evaluated calretinin positive mucosal neurites in anorectal line junctional mucosa in archival rectal biopsies contributed by 17 institutions. A separate investigator compiled patient information and sent data for statistical analysis.
Biopsies with anorectal junctional mucosa from 115 patients were evaluated for calretinin positive mucosal neurites. 20/20 Hirschsprung disease biopsies were negative. 87/88 non Hirschsprung disease biopsies and 7/7 post pullthrough Hirschsprung disease neorectal biopsies were positive. Statistical analysis of the 108 non pullthrough biopsies yielded an accuracy of 99.1% (sensitivity 100%, specificity 98.9%). Age range was preterm to 16 years. Biopsy size was less than 1 mm to over 1 cm.
Absence of calretinin positive mucosal neurites at the anorectal line was highly accurate in distinguishing Hirschsprung disease from non Hirschsprung disease cases in this blinded retrospective study. Calretinin staining is useful for interpreting biopsies from the physiologic hypoganglionic zone up to the anorectal line.
在直肠肛管活检中,黏膜下神经节细胞的缺失并不能可靠地将先天性巨结肠病与非先天性巨结肠病区分开来。钙视网膜蛋白染色可能有助于这些活检。为了确定其价值,我们分析了直肠肛管活检中钙视网膜蛋白阳性的黏膜神经突。
两名儿科病理学家在无法获取患者数据的情况下,对17个机构提供的存档直肠活检标本中直肠肛管交界黏膜的钙视网膜蛋白阳性黏膜神经突进行评估。另一名研究人员收集患者信息并发送数据进行统计分析。
对115例患者的直肠肛管交界黏膜活检标本进行了钙视网膜蛋白阳性黏膜神经突评估。20例先天性巨结肠病活检标本均为阴性。88例非先天性巨结肠病活检标本中的87例以及7例先天性巨结肠病拖出术后新直肠活检标本均为阳性。对108例未进行拖出术的活检标本进行统计分析,准确率为99.1%(敏感性100%,特异性98.9%)。年龄范围为早产儿至16岁。活检标本大小从小于1毫米到超过1厘米不等。
在这项盲法回顾性研究中,直肠肛管处无钙视网膜蛋白阳性黏膜神经突在区分先天性巨结肠病与非先天性巨结肠病病例方面具有高度准确性。钙视网膜蛋白染色有助于解释从生理性神经节减少区直至直肠肛管的活检标本。