肠壁结构分析:发现克罗恩病儿童患者的纤维化。

Andrew S Phelps
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摘要

在这期的文章中,“磁共振肠造影增强的纹理分析可以检测克罗恩病狭窄中的纤维化”,Tabari和同事证明了计算机比人类放射科医生具有更高的诊断准确性(1)。使用组织学作为纤维化的金标准,计算机区分无纤维化和轻度纤维化,从中度到重度纤维化,曲线下面积(AUC)为0.995。为了理解这篇文章和AUC的重要性,回顾一下自Burrill Crohn博士的开创性论文以来的87年里,成像技术取得了多大的进步将会有所帮助。在被诊断为克罗恩病的患者中,几乎一半会在首次确诊后的10年内发展为纤维化狭窄,通常需要手术切除(2)。诊断纤维化的金标准是胶原沉积,通过全层肠切除术在组织学上检测到。由于胶原沉积位于粘膜下和浆膜下,纤维化可能难以通过内镜可视化或部分厚度内镜活检来判断。通过影像学检查,纤维化狭窄典型地表现为3个解剖特征:管腔狭窄、管壁增厚和狭窄扩张(3)。然而,这3个解剖特征单独为晚期特征且非特异性,因为无纤维化的活动性炎症可能具有类似的外观。在克罗恩1932年的原始文章中,他承认了解剖成像的前景和局限性:“然而,当仔细解释钡餐时,给出了明确的积极结果. ...虽然只有在晚期或狭窄阶段才会出现明显的延迟。除了细心的x线医生外,任何人都很容易忽视回肠袢中中等程度的瘀滞和淤积。”又过了50年,横断成像(包括计算机断层扫描、磁共振成像和超声波)才显示出与传统的透视“钡餐”或我们现在所说的“小肠跟随检查”相比的诊断优势。然而,解剖细节的改进只能使诊断的准确性提高到目前为止。什么
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intestinal Wall Texture Analysis: Finding Fibrosis in Pediatric Patients with Crohn Disease.
n this issue’s article, ‘‘Texture analysis of magnetic resonance enterography contrast enhancement can detect fibrosis in Crohn I disease strictures,’’ Tabari and co-workers demonstrated that a computer had greater diagnostic accuracy than a human radiologist (1). Using histology as the gold standard for fibrosis, the computer distinguished no fibrosis and mild fibrosis from moderate-to-severe fibrosis with an impressive area under the curve (AUC) of 0.995. To appreciate the significance of this article and that AUC, it will be helpful to review how far imaging has advanced in the 87 years since Dr Burrill Crohn’s seminal paper. In patients diagnosed with Crohn disease, almost half will develop a fibrotic stricture within 10 years of first receiving their diagnosis, often requiring surgical resection (2). The gold standard for diagnosing fibrosis is the deposition of collagen, detected histologically from full-thickness bowel resection. Due to the submucosal and subserosal location of the collagen deposition, fibrosis may be difficult to appreciate by endoscopic visualization or partial-thickness endoscopic biopsy. By imaging, a fibrotic stricture classically demonstrates 3 anatomic features: luminal narrowing, wall thickening, and prestenotic dilation (3). However, these 3 anatomic features alone are late features and are nonspecific, as active inflammation without fibrosis can have a similar appearance. In Crohn’s original 1932 article, he acknowledged the promise and limitations of anatomic imaging: ‘‘The barium meal, however, when carefully interpreted, gives definite positive findings. ... though only in the late or stenotic stages is the delay striking. The midler degrees of stasis and puddling in the ileal loops may easily be overlooked by any but a careful roentgenologist’’(4). It would be another 50 years before cross-sectional imaging (including computed tomography, magnetic resonance imaging ‘‘MRI,’’ and ultrasound) demonstrated diagnostic superiority compared with the traditional fluoroscopic ‘‘barium meal,’’ or what we would now call a ‘‘small bowel follow through’’(5). However, improvements in anatomic detail would only take diagnostic accuracy so far. What
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