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原位肠型宫颈腺癌和腺癌表现出部分肠道免疫表型,伴有CDX2的一致性表达。

Intestinal-type cervical adenocarcinoma in situ and adenocarcinoma exhibit a partial enteric immunophenotype with consistent expression of CDX2.

作者信息

McCluggage W G, Shah R, Connolly L E, McBride H A

机构信息

Department of Pathology, Royal Group of Hospitals Trust, Belfast, Ireland.

出版信息

Int J Gynecol Pathol. 2008 Jan;27(1):92-100. doi: 10.1097/pgp.0b013e31815698e7.

Abstract

Most cases of cervical adenocarcinoma in situ (AIS) and adenocarcinoma are of the usual or endocervical type. However, intestinal types of AIS and adenocarcinoma exist. With an intestinal-type adenocarcinoma in the cervix, the question may arise as to whether one is dealing with a primary cervical neoplasm or direct or secondary spread from an intestinal adenocarcinoma. In organs such as the ovary, urinary bladder, esophagus, and gallbladder, intestinal-type glandular epithelium often expresses enteric markers, but this has hardly been studied in the cervix. The purpose of this study was to investigate whether intestinal-type AIS and adenocarcinoma in the cervix express enteric markers and to ascertain whether these antibodies are of value in the distinction from a metastatic intestinal adenocarcinoma. We compared the immunophenotype of these lesions with that of usual-type AIS and adenocarcinomain the cervix. Cases included were AIS of usual type (n = 6), primary cervical adenocarcinoma of usual type (n = 6), AIS of intestinal type (n = 21), primary cervical adenocarcinoma of intestinal type (n = 3), primary cervical adenocarcinoma with signet ring cells (n = 2), and colorectal adenocarcinoma involving the cervix (n = 5). All cases were stained with cytokeratin (CK) 7, CK20, monoclonal carcinoembryonic antigen (CEA), p16, and CDX2. Staining was categorized as negative, focally positive (<50% cells), or diffusely positive (50% or more cells). Usual-type AIS was always diffusely CK7 positive, typically diffusely CEA and p16 positive, and always CK20 negative. CDX2 was positive in 1 case. All usual cervical adenocarcinomas were diffusely CK7 and p16 positive, and all were immunoreactive with CEA. Five and 2 cases were CK20 and CDX2 positive, respectively. Intestinal-type AIS was diffusely CK7 positive (all cases) and typically CK20 negative and diffusely CEA and p16 positive. All but 1 case exhibited diffuse nuclear positivity with CDX2. In addition, usual-type AIS adjacent to intestinal type was CDX2 positive in 13 of 21 cases. The 3 cases of primary cervical intestinal-type adenocarcinoma were diffusely CK7 positive, focally or diffusely positive with CK20 and CDX2, and focally positive with CEA. One case was diffusely p16 positive, 1 focal and 1 negative. The foci of signet ring cells in the 2 primary cervical adenocarcinomas were diffusely CK7 and p16 positive and negative with CK20 and CDX2. Colorectal adenocarcinomas involving the cervix were typically diffusely positive with CK20, CEA, and CDX2; negative with CK7; and negative or focally positive with p16. Intestinal types of cervical AIS and adenocarcinoma exhibit a partial enteric immunophenotype, usually with diffuse expression of CDX2 and, in some cases, staining with CK20. They maintain their CK7 immunoreactivity and are usually p16 positive. Although there is immunophenotypic overlap, focal staining with CK20 together with diffuse CK7 and sometimes p16 positivity helps to distinguish intestinal types of cervical adenocarcinoma from involvement by a colorectal adenocarcinoma; CEA and CDX2 are of no value in this regard. CDX2 positivity in usual-type AIS adjacent to intestinal type and in occasional cases of pure usual-type AIS may be a reflection of early intestinal differentiation before this is morphologically apparent. Using a set of cases of AIS diagnosed in a single institution over a 7-year period (77 usual type; 13 intestinal type), intestinal type was more likely to be associated with early invasive adenocarcinoma than usual type (31% vs 17%), suggesting that intestinal differentiation may be a risk factor for invasion in premalignant cervical glandular lesions.

摘要

大多数宫颈原位腺癌(AIS)和腺癌为常见型或宫颈内膜型。然而,也存在肠型AIS和腺癌。对于宫颈的肠型腺癌,可能会出现这样的问题:所处理的是原发性宫颈肿瘤,还是来自肠腺癌的直接或继发性扩散。在卵巢、膀胱、食管和胆囊等器官中,肠型腺上皮常表达肠道标志物,但在宫颈中对此研究甚少。本研究的目的是调查宫颈肠型AIS和腺癌是否表达肠道标志物,并确定这些抗体在与转移性肠腺癌鉴别诊断中是否有价值。我们将这些病变的免疫表型与宫颈常见型AIS和腺癌的免疫表型进行了比较。纳入的病例包括常见型AIS(n = 6)、常见型原发性宫颈腺癌(n = 6)、肠型AIS(n = 21)、肠型原发性宫颈腺癌(n = 3)、伴有印戒细胞的原发性宫颈腺癌(n = 2)以及累及宫颈的结直肠癌(n = 5)。所有病例均用细胞角蛋白(CK)7、CK20、单克隆癌胚抗原(CEA)、p16和CDX2进行染色。染色分为阴性、局灶阳性(<50%细胞)或弥漫阳性(50%或更多细胞)。常见型AIS总是弥漫性CK7阳性,通常弥漫性CEA和p16阳性,且总是CK20阴性。CDX2在1例中呈阳性。所有常见宫颈腺癌均弥漫性CK7和p16阳性,且均与CEA免疫反应阳性。分别有5例和2例CK20和CDX2阳性。肠型AIS弥漫性CK7阳性(所有病例),通常CK20阴性,弥漫性CEA和p16阳性。除1例以外的所有病例CDX2均呈弥漫性核阳性。此外,在21例中,21例肠型AIS相邻的常见型AIS中有13例CDX2呈阳性。3例原发性宫颈肠型腺癌弥漫性CK7阳性,CK20和CDX2局灶或弥漫性阳性,CEA局灶性阳性。1例弥漫性p16阳性,1例局灶性阳性,1例阴性。2例原发性宫颈腺癌中的印戒细胞灶弥漫性CK7和p16阳性,CK20和CDX2阴性。累及宫颈的结直肠癌通常CK20、CEA和CDX2弥漫性阳性;CK7阴性;p16阴性或局灶性阳性。宫颈肠型AIS和腺癌表现出部分肠道免疫表型,通常CDX2弥漫性表达,在某些情况下,CK20染色阳性。它们保持CK7免疫反应性,通常p16阳性。尽管存在免疫表型重叠,但CK20局灶性染色以及弥漫性CK7和有时p16阳性有助于将宫颈肠型腺癌与结直肠癌累及相鉴别;CEA和CDX2在这方面无价值。在肠型AIS相邻的常见型AIS以及偶尔的纯常见型AIS病例中CDX2阳性,可能反映了在形态学上明显之前的早期肠道分化。利用在单一机构7年期间诊断的一组AIS病例(77例常见型;13例肠型),肠型比常见型更可能与早期浸润性腺癌相关(31%对17%),提示肠道分化可能是宫颈腺性癌前病变浸润的一个危险因素。

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