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Peutz-Jeghers syndrome-associated atypical mucinous proliferation of the uterine cervix: A case of minimal deviation adenocarcinoma ('adenoma malignum') in situ

机译:Peutz-Jeghers综合征相关的子宫颈非典型黏液性增生:原位最小偏差腺癌('Adenoma malignum')一例

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摘要

We describe a case of a non-invasive precursor of minimal deviation adenocarcinoma (MDA) of the uterine cervix, associated with Peutz-Jeghers syndrome (PJS). A 27-year-old woman, who had been followed for PJS, was referred to the gynecology clinic. Colposcopic examination demonstrated a small polypoid lesion in the transformation zone. Microscopic examination of the biopsy specimen demonstrated papillary proliferation of the mucinous epithelium with bland nuclear morphology. Conization revealed lobular endocervical glandular hyperplasia (LEGH) with distinct nuclear anaplasia, as well as papillary proliferation of the mucinous epithelium with mild to moderate nuclear abnormalities. This case suggests that the incipient phase of PJS-associated MDA is related to atypical LEGH (" MDA in situ"), and indicates the importance of early screening and surveillance by gynecologists in cases of PJS to detect cervical adenocarcinomas.
机译:我们描述了一种非侵入性的子宫颈最小偏差腺癌(MDA)前体,与Peutz-Jeghers综合征(PJS)相关。一名接受PJS随访的27岁妇女被转诊至妇科诊所。阴道镜检查显示在转化区有一个小的息肉样病变。活检标本的显微镜检查表明粘液上皮的乳头状增生具有温和的核形态。锥切显示小叶宫颈腺体增生(LEGH)具有明显的核增生,以及粘液上皮的乳头状增生,伴轻度至中度核异常。该病例表明,与PJS相关的MDA的初始阶段与非典型LEGH(“原位MDA”)有关,并表明在PJS病例中,由妇科医生进行早期筛查和监视对于检测宫颈腺癌的重要性。

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