Stratified mucin-producing intraepithelial lesions of the cervix - Adenosquamous or columnar cell neoplasia?

被引:107
作者
Park, JJ
Sun, DQ
Quade, BJ
Flynn, C
Sheets, EE
Yang, A
McKeon, F
Crum, CP
机构
[1] Brigham & Womens Hosp, Dept Pathol, Div Womens & Perinatal Pathol, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[3] Brigham & Womens Hosp, Dept Obstet & Gynecol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA USA
关键词
cervical intraepithelial neoplasia; cervix neoplasms; adenocarcinoma in situ; p63;
D O I
10.1097/00000478-200010000-00012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
BACKGROUND: Squamous (CIN) and glandular (ACIS) intraepithelial lesions often coexist in the same cervical specimen. However, a less common and little studied Variant consists of a stratified epithelium resembling CIN in which conspicuous mucin production is present (Stratified Mucin-producing Intraepithelial LEsions (SMILE). This report describes the phenotypic characteristics of the SMILE, its associated lesions, and its immunophenotype. METHODS: Eighteen SMILEs were identified by the presence of conspicuous cytoplasmic clearing or vacuoles in lesions otherwise resembling CIN. The morphologic spectrum of SMILEs was detailed; including associated intraepithelial and invasive cervical neoplasms. In addition, selected cases were stained for mucicarmine. markers of squamous cell/reserve cell differentiation (keratin-14 and p63), and proliferative activity (Mib-1). RESULTS: Stratified neoplastic epithelial cells with a high Mib-1 index and a rounded or lobular contour at the epithelial-stromal interface characterized SMILEs. In contrast to CIN, in which mucin droplets are confined to surface cells, mucin was present throughout the epithelium, varying from indistinct cytoplasmic clearing to discrete vacuoles. SMILEs were distinguished from benign metaplasia by nuclear hyperchromasia and a high Mib-1 index. All but three coexisted with either a squamous (CIN) or glandular (ACIS) precursor lesion. Nine of nine coexisting invasive carcinomas contained glandular, adenosquamous differentiation. or both. SMILEs stained negative fur keratin-14 and variably for p63. When present, staining with p63 was confined to basal areas of SMILEs and was absent in areas of columnar differentiation. CONCLUSIONS: SMILEs are unusual cervical intraepithelial lesions best classified as variants of endocervical columnar cell neoplasia based on immunophenotype. The distribution and immunophenotype of SMILEs are consistent with a neoplasm arising in reserve cells in the transformation zone. The coexistence of a wide spectrum of intraepithelial and invasive cell phenotypes suggests that SMILEs are a marker for phenotypic instability, emphasizing the importance of identifying SMILEs and ensuring a complete examination of specimens containing this unusual precursor lesion.
引用
收藏
页码:1414 / 1419
页数:6
相关论文
共 21 条
[11]  
Richart R M, 1973, Pathol Annu, V8, P301
[12]   Do mucin-secreting squamous cell carcinomas of the uterine cervix metastasize more frequently to pelvic lymph nodes? A case-control study [J].
Samlal, RAK ;
Ten Kate, FJW ;
Hart, AAM ;
Lammes, FB .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1998, 17 (03) :201-204
[13]   EPIDEMIOLOGIC CHANGES IN CERVICAL-CARCINOMA WITH PARTICULAR REFERENCE TO MUCIN-SECRETING SUBTYPES [J].
SHORROCK, K ;
JOHNSON, J ;
JOHNSON, IR .
HISTOPATHOLOGY, 1990, 17 (01) :53-57
[14]  
SMEDTS F, 1992, AM J PATHOL, V140, P601
[15]  
SMOTKIN D, 1986, OBSTET GYNECOL, V68, P241
[16]  
STEINER G, 1965, CANCER, V18, P807, DOI 10.1002/1097-0142(196507)18:7<807::AID-CNCR2820180705>3.0.CO
[17]  
2-N
[18]   SMALL-CELL NEUROENDOCRINE CARCINOMA OF THE CERVIX - A HUMAN PAPILLOMAVIRUS TYPE-18 ASSOCIATED CANCER [J].
STOLER, MH ;
MILLS, SE ;
GERSELL, DJ ;
WALKER, AN .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1991, 15 (01) :28-32
[19]   MUCOEPIDERMOID CARCINOMA OF UTERINE CERVIX STAGE IB - LONG-TERM FOLLOW-UP, HISTOCHEMICAL AND IMMUNOHISTOCHEMICAL STUDY [J].
THELMO, WL ;
NICASTRI, AD ;
FRUCHTER, R ;
SPRING, H ;
DIMAIO, T ;
BOYCE, J .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1990, 9 (04) :316-324
[20]  
WRIGHT TC, 1994, BLAUSTEINS PATHOLOGY, P279