Davis Georgina, Anderson Lyndal, Pather Selvan
Department of Gynaecology Oncology, Chris O'Brien Lifehouse, Camperdown, New South Wales, Australia.
Department of Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Diagn Cytopathol. 2016 Nov;44(11):931-934. doi: 10.1002/dc.23530. Epub 2016 Jul 7.
A case of Extramammary Paget's Disease (EMPD) involving the cervix mimicking cervical carcinoma on routine cervical cytology in a 66-year-old woman with a history of recurrent multifocal EMPD involving the vulva, perineum, perianal area, and rectum is reported. The patient had undergone multiple excisions and reconstructions of EMPD, however, had a benign cervical smear history and reported no vaginal bleeding. The conventional papanicolaou smear was reported as concerning for carcinoma with abundant, well preserved material illustrating highly atypical cells with anisonucleosis and dense cytoplasm and focal microacini. Gross anatomical distortion from EMPD and previous surgery precluded satisfactory outpatient colposcopic assessment. Examination under anesthesia was performed and colposcopy revealed a four quadrant high grade lesion extending into the vagina with one area suspicious for malignancy on the cervix. Directed biopsies were taken and histopathology confirmed EMPD with diffuse adenocarcinoma in situ cells infiltrating skin and mucosa of all specimens. These large pale cells were seen both a singly and in clusters of nests within the mucosa. Periodic Acid Schiff staining was positive for intracytoplasmic mucin and supportive immunohistochemistry was performed with strong reactivity in atypical cells for CK7, CEA, and Cam 5.2. There was no evidence of invasive malignancy and the patient remains under clinical surveillance. Cervical EMPD is rare but should be considered in women with abnormal cervical cytology and a history of vulval EMPD. Diagn. Cytopathol. 2016;44:931-934. © 2016 Wiley Periodicals, Inc.
报告了一例发生于宫颈的乳腺外佩吉特病(EMPD),该病例在一名66岁女性的常规宫颈细胞学检查中被误诊为宫颈癌。该女性有复发性多灶性EMPD病史,累及外阴、会阴、肛周区域和直肠。患者曾接受多次EMPD切除和重建手术,然而,其宫颈涂片检查既往结果均为良性,且无阴道出血报告。传统巴氏涂片报告显示存在癌细胞,涂片材料丰富且保存良好,可见高度非典型细胞,伴有核大小不均和细胞质致密,以及局灶性微腺泡。EMPD和既往手术导致的大体解剖结构改变,使得门诊阴道镜检查无法获得满意结果。遂在麻醉下进行检查,阴道镜检查发现一个四象限高级别病变延伸至阴道,宫颈有一个区域疑似恶性。进行了定向活检,组织病理学证实为EMPD,所有标本的皮肤和黏膜均有弥漫性原位腺癌细胞浸润。这些大的淡染细胞在黏膜内可见单个或成簇状巢状分布。过碘酸希夫染色显示胞质内黏液呈阳性,并进行了支持性免疫组化检查,非典型细胞对CK7、CEA和Cam 5.2呈强反应性。没有浸润性恶性肿瘤的证据,患者仍在临床监测中。宫颈EMPD很少见,但对于宫颈细胞学异常且有外阴EMPD病史的女性应予以考虑。诊断细胞病理学。2016;44:931 - 934。©2016威利期刊公司。