Squamous cell precancerous lesions of the cervix uteri

被引:1
作者
Schmidt, D. [1 ]
机构
[1] Inst Pathol & Zytol Viersen, Gereonstr 14a, D-41747 Viersen, Germany
来源
PATHOLOGE | 2019年 / 40卷 / 01期
关键词
Biomarkers; Cervix uteri; Differential diagnosis; Papillomavirus infections; Squamous intraepithelial lesions of the cervix; BIOMARKERS; DIAGNOSIS; CANCER; RISK; HPV;
D O I
10.1007/s00292-018-0561-4
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
BackgroundThe histological and immunohistochemical evaluation of tissue samples obtained in the course of the investigation and treatment of precancerous squamous lesions of the cervix uteri is an essential task of the pathologist. Given the surprising variety of morphological findings, including the many possible differential diagnoses of dysplastic changes, this is not an easy task.DifferentiationBiologically, only two prognostically different groups can be distinguished, which according to the WHO classification are referred to as low-grade or high-grade squamous intraepithelial lesions (LSILs or HSILs). An additional distinction as CIN1, CIN2 or CIN3 should also be made, in particular because CIN2 lesions represent a heterogeneous group of dysplastic changes.Usage of biomarkersThe p16 biomarker, which has been widely studied, is extremely helpful in the diagnosis and differential diagnosis of these lesions, as regenerative and reparative changes as well as non-HPV-associated squamous cell metaplasia, are p16 negative or show patchy staining only. The indications for its use were clearly defined in the LAST project. In contrast to the diagnostic advantage, the prognostic significance of p16 in the low-grade intraepithelial lesions is controversial. Other markers such as CK7 and HPVE4 may help here. The immunohistochemistry for p16 may also be useful in examining the resection margins of aconization specimen, especially if thermoeffects make it difficult to make an unambiguous assessment. However, for the prognostic assessment of the clinical course after conization, the HPV test is more important because it better captures the risk of persistence or the risk of recurrence.
引用
收藏
页码:7 / 12
页数:6
相关论文
共 22 条
[1]  
[Anonymous], 2012, J LOW GENIT TRACT DI
[2]  
[Anonymous], BESCHL GEM BUND AND
[3]  
[Anonymous], KREBS DEUTSCHL 2013
[4]  
[Anonymous], 2018, DIAGNOSTIC GYNECOLOG, DOI DOI 10.1016/B978-0-323-44732-4.00013-3
[5]   Incomplete excision of cervical precancer as a predictor of treatment failure: a systematic review and meta-analysis [J].
Arbyn, Marc ;
Redman, Charles W. E. ;
Verdoodt, Freija ;
Kyrgiou, Maria ;
Tzafetas, Menelaos ;
Ghaem-Maghami, Sadaf ;
Petry, Karl-Ulrich ;
Leeson, Simon ;
Bergeron, Christine ;
Nieminen, Pekka ;
Gondry, Jean ;
Reich, Olaf ;
Moss, Esther L. .
LANCET ONCOLOGY, 2017, 18 (12) :1665-1679
[6]   Conjunctive p16INK4a Testing Significantly Increases Accuracy in Diagnosing High-Grade Cervical Intraepithelial Neoplasia [J].
Bergeron, Christine ;
Ordi, Jaume ;
Schmidt, Dietmar ;
Trunk, Marcus J. ;
Keller, Thomas ;
Ridder, Ruediger .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2010, 133 (03) :395-406
[7]   Longitudinal evaluation of Interobserver and intraobserver agreement of cervical intraepithelial neoplasia diagnosis among an experienced panel of gynecologic pathologists [J].
Cai, Bing ;
Ronnett, Brigitte M. ;
Stoller, Mark ;
Ferenczy, Alex ;
Kurman, Robert J. ;
Sadow, David ;
Alvarez, Fran ;
Pearson, Jay ;
Sings, Heather L. ;
Barr, Eliav ;
Liaw, Kai-Li .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2007, 31 (12) :1854-1860
[8]  
Curry SJ, 2018, OBSTET GYNECOL SURV, V73, P689, DOI [10.1097/01.ogx.0000549540.69362.81, 10.1001/jama.2018.10897]
[9]   Using Biomarkers as Objective Standards in the Diagnosis of Cervical Biopsies [J].
Galgano, Mary T. ;
Castle, Philip E. ;
Atkins, Kristen A. ;
Brix, William K. ;
Nassau, Sarah R. ;
Stoler, Mark H. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2010, 34 (08) :1077-1087
[10]  
Herfs M, 2013, AM J SURG PATHOL, V37, P1311, DOI 10.1097/PAS.0b013e3182989ee2