浅表浸润性肛门鳞状细胞癌一致组织学诊断的挑战。

Faruk Erdem Kombak, Qingqing Liu, John D Paulsen, Xintong Wang, Fatemeh Ghazanfari Amlashi, Pei Hui, Wenxin Zheng, Alexandros D Polydorides, Yuxin Liu
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摘要

上下文。-:浅表浸润性肛门鳞状细胞癌(scisca)是一种深度小于3mm,水平扩散小于7mm的微创性癌症。其细微的形态学改变对组织学诊断提出了重大挑战。-:评估病理学家对SISCCA的诊断一致性,并确定潜在的改进领域。-: 4名胃肠道(GI)和4名妇科(GYN)病理学家独立审查了20例疑似早期侵袭的肛门高级鳞状上皮内病变的数字化苏木精-伊红图像。参与者将每个病变分为侵入性或非侵入性,并从主要教科书编制的列表中选择指示侵入的特征。计算Cohen κ系数以评估观察者间的一致性。-:在20个病变中,8个(40%)得到一致诊断,而12个(60%)有差异。总体一致性中等(κ = 0.46;95% CI, 0.29-0.48), GI之间的水平相似(κ = 0.53;95% CI, 0.45-0.74)和GYN (κ = 0.46;95% CI, 0.25-0.48)组(P < 0.01)。GYN组诊断为侵袭性病变的数量高于GI组(中位数,14.5 vs 10.5;P < 0.01)。在一致的SISCCA诊断中,最常见的特征是存在不规则的小肿瘤巢,其次是结缔组织增生反应和矛盾成熟。-:识别早期侵袭组织学特征的差异导致SISCCA诊断的可重复性较差。努力应集中在改进诊断标准和整合已被证明在其他解剖部位有效识别早期浸润性癌症的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Challenges in Consistent Histologic Diagnosis of Superficially Invasive Anal Squamous Cell Carcinoma.

Context.—: Superficially invasive squamous cell carcinoma of the anus (SISCCA) is defined as a minimally invasive cancer measuring less than 3 mm in depth and less than 7 mm in horizontal spread. Its subtle morphologic alterations pose a significant challenge for histologic diagnosis.

Objective.—: To evaluate the diagnostic agreement among pathologists for SISCCA and to identify potential areas for improvement.

Design.—: Four gastrointestinal (GI) and 4 gynecologic (GYN) pathologists independently reviewed digitized hematoxylin-eosin images of 20 anal high-grade squamous intraepithelial lesions with suspected early invasion. Participants classified each lesion as either invasive or noninvasive and selected features indicative of invasion from a list compiled from major textbooks. Cohen κ coefficient was calculated to assess interobserver agreement.

Results.—: Of the 20 lesions, 8 (40%) received unanimous diagnoses, while 12 (60%) had discrepancies. Overall agreement was moderate (κ = 0.46; 95% CI, 0.29-0.48), with similar levels between the GI (κ = 0.53; 95% CI, 0.45-0.74) and GYN (κ = 0.46; 95% CI, 0.25-0.48) groups (P > .01). The GYN group diagnosed a higher number of lesions as invasive than did the GI group (median, 14.5 versus 10.5; P > .01). In consensus SISCCA diagnoses, the most commonly noted feature was the presence of small irregular tumor nests, followed by desmoplastic response and paradoxical maturation.

Conclusions.—: Variability in recognizing histologic features indicative of early invasion contributed to the poor reproducibility in the diagnosis of SISCCA. Efforts should focus on refining diagnostic criteria and integrating features that have proved effective in identifying early invasive cancer at other anatomic sites.

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