胆囊切除术标本的系统选择性取样足以发现偶发胆囊腺癌

A. Akki, Wei Zhang, Kathryn E. Tanaka, S. Chung, Qiang Liu, N. Panarelli
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引用次数: 4

摘要

许多胆囊腺癌(ACs)是在常规胆囊切除术标本中偶然发现的,但当通过常规抽样发现肠化生(IM)或不典型增生时,抽样方法有所不同。我们的做法是当发现IM时提交5个额外的部分,但不典型增生的病例完全提交。当遇到这些发现时,我们试图确定一个适当的抽样方案。我们在26个月的时间里回顾性地发现了具有这些特征的胆囊切除术标本,4059例中有48例(1%)。4名病理学家独立将原始切片(2个纵向切片和1个囊管边缘切片)分为3类(IM、低级别发育不良[LGD]或高级别发育不良[HGD])中的1类;初步发现与最终诊断相关。16例(33%)病例在进一步抽样后发现了其他结果,包括LGD (n=10)或HGD (n=4)和AC (n=2)。HGD常伴有恶性肿瘤。我们前瞻性地分析了3133例(1%)额外胆囊切除术标本中的39例,最初提交了相同的常规切片。我们随机提交了5个IM病例的剖面图。首次检查LGD时,每厘米增加1个切片。在所有这些病例中,所有剩余的组织都被提交并单独审查。HGD的病例全部提交,因为两例HGD的初始切片最终显示为癌。该方案检测到所有HGD和AC病例。囊管边缘清晰的患者没有经历肿瘤进展,即使其他部位存在不典型增生。我们的结论是,有HGD的胆囊应该全部提交,LGD可以有代表性地取样,常规取样对于IM是足够的。
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Systematic Selective Sampling of Cholecystectomy Specimens Is Adequate to Detect Incidental Gallbladder Adenocarcinoma
Many gallbladder adenocarcinomas (ACs) are detected incidentally in routine cholecystectomy specimens, yet sampling practices vary when intestinal metaplasia (IM) or dysplasia are found via routine sampling. Our practice has been to submit 5 additional sections when IM is found, but cases with dysplasia are entirely submitted. We sought to determine an appropriate sampling protocol when encountering these findings. We retrospectively identified cholecystectomy specimens with these features over a 26-month period, yielding 48 of 4059 (1%) cases. Four pathologists independently classified the (2 longitudinal and 1 cystic duct margin) original sections into 1 of 3 categories (IM, low-grade dysplasia [LGD] or high-grade dysplasia [HGD]); initial findings were correlated with final diagnoses. Sixteen (33%) cases had additional findings upon further sampling, including LGD (n=10) or HGD (n=4) and AC (n=2). HGD always accompanied malignancy. We prospectively analyzed 39 of 3133 (1%) additional cholecystectomy specimens, initially submitting the same routine sections. We submitted 5 random sections from cases with IM. Cases with LGD were first examined with 1 additional section per centimeter. All remaining tissue was submitted in all of these cases and separately reviewed. Cases with HGD were entirely submitted as both test cases with HGD in initial sections ultimately showed carcinoma. This protocol detected all cases of HGD and AC. Patients with clear cystic duct margins did not experience neoplastic progression, even if dysplasia was present elsewhere. We conclude gallbladders with HGD should be entirely submitted, LGD may be representatively sampled, and routine sampling is adequate for IM.
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