Zemheri Ebru, Engin Zerk Pinar, Ulukaya Durakbasa Cigdem
Department of Pathology, University of Health Sciences, Umraniye Training and Research Hospital, Istanbul, Turkey.
Department of Pathology, University of Health Sciences, Okmeydani Training and Research Hospital, Istanbul, Turkey.
North Clin Istanb. 2021 Dec 31;8(6):601-606. doi: 10.14744/nci.2020.69376. eCollection 2021.
This study aims to evaluate the results obtained by calretinin staining on tissue samples for diagnosing Hirschsprung's disease (HD) in a single institution, by single expert.
A retrospective evaluation was done for calretinin immunostaining in HD patients for a period of 3 years. Calretinin staining was evaluated in nerve fibers. Calretinin immunohistochemistry was considered positive if any staining was seen in nerve fibers and/or ganglion cells in the lamina propria, muscularis mucosa or submucosa. According to staining intensity, staining was classified as strong, weak or negative. The pathological diagnosis was based on presence or absence of ganglion cells (G0/G1) and nerve hypertrophy (N0/N1). Samples were classified according to the depth (presence of submucosa or intermuscular area), the type (biopsy or resection specimen) and staining intensity of calretinin (strong, weak, or negative staining).
A total of 96 tissue samples from 56 patients were studied. Tissues were from colon (43.8%), rectum (43.8%), stoma (6.2%), ileum (3.1%) and appendix (3.1%). The pathological diagnosis was G0N0 in 14.6%, G1N0 in 54.2%, G0N1 in 25% and G1N1 in 6.2% of cases. Our materials consisted of 92 tissue biopsies and four resection specimens. Intermuscular layer was present in 87.5% of materials and 12.5% of biopsies contained submucosa. Calretinin staining was negative (C0) in 37.5% of cases, strong positive (C1) in 47.9%, and weak positive (C2) in 14.6%. When the C0 category was taken as the reference, the status of calretinin staining as C2 (weak positive) in cases with pathological diagnosis of G1N0 was found to be 37.575 times that of cases with G0N0 (OR [95% CI]: 37.575 [2.928, 482.176], p=0.006) and the status of calretinin staining as C1 (strong positive) in cases with pathologic diagnosis of G1N0 was found to be 131.401 times that of G0N0 (OR [95% CI]: 131.401 [9.263, 1864.082), p<0.001).
Calretinin staining is positive whenever ganglion cells are present independent from presence of nerve hypertrophy, the depth and the site of the biopsy or staining intensity. It is negative in all aganglionic samples. Calretinin staining is a reliable ancillary test in HD diagnosis.
本研究旨在评估在单一机构中,由单一专家对组织样本进行钙视网膜蛋白染色以诊断先天性巨结肠(HD)所获得的结果。
对HD患者进行了为期3年的钙视网膜蛋白免疫染色回顾性评估。在神经纤维中评估钙视网膜蛋白染色。如果在固有层、黏膜肌层或黏膜下层的神经纤维和/或神经节细胞中观察到任何染色,则钙视网膜蛋白免疫组化被认为是阳性。根据染色强度,染色分为强、弱或阴性。病理诊断基于神经节细胞的存在与否(G0/G1)和神经肥大情况(N0/N1)。样本根据深度(黏膜下层或肌间区域的存在)、类型(活检或切除标本)以及钙视网膜蛋白的染色强度(强、弱或阴性染色)进行分类。
共研究了来自56例患者的96个组织样本。组织来自结肠(43.8%)、直肠(43.8%)、造口(6.2%)、回肠(3.1%)和阑尾(3.1%)。病例中病理诊断为G0N0的占14.6%,G1N0的占54.2%,G0N1的占25%,G1N1的占6.2%。我们的材料包括92个组织活检和4个切除标本。87.5%的材料有肌间层,12.5%的活检包含黏膜下层。37.5%的病例钙视网膜蛋白染色为阴性(C0),47.9%为强阳性(C1),14.6%为弱阳性(C2)。以C0类别为参照,病理诊断为G1N0的病例中钙视网膜蛋白染色为C2(弱阳性)的情况是G0N0病例的37.575倍(OR[95%CI]:37.575[2.928,482.176],p = 0.006),病理诊断为G1N0的病例中钙视网膜蛋白染色为C1(强阳性)的情况是G0N0病例的1,31.401倍(OR[95%CI]:131.401[9.263,1864.082],p<0.001)。
只要存在神经节细胞,无论神经肥大情况、活检的深度和部位或染色强度如何,钙视网膜蛋白染色均为阳性。在所有无神经节细胞的样本中染色为阴性。钙视网膜蛋白染色是HD诊断中一项可靠的辅助检查。