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Spectrum of changes in anogenital mammary-like glands in primary extramammary (Anogenital) paget disease and their possible role in the pathogenesis of the disease

机译:原发性乳房外(肛门生殖器)Paget疾病肛门生殖器样乳腺的变化谱及其在疾病发病机理中的可能作用

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摘要

To determine whether a subset of primary extramammary Paget disease (EMPD) may originate in anogenital mammary-like glands (AGMLG), the authors studied 181 specimens of EMPD, detailing alterations in AGMLG. The latter were identified in 33 specimens from 31 patients. All patients were women, ranging in age from 38 to 93 years (median, 65 y). In all cases, lesions involved the vulva and in 1 patient the perianal skin was affected. Histopathologically, AGMLG manifested changes identical to columnar cell change (CCC) (87.1%), usual ductal hyperplasia (22.6%), columnar cell hyperplasia (CCH) (9.7%), oxyphilic (apocrine) metaplasia (6.5%), and atypical duct hyperplasia (3.2%). Four cases (12.9%), in addition to intraepidermal carcinoma, harbored invasive carcinoma. In all 4 of these, AGMLG displayed a range of alterations including ductal carcinoma in situ, CCC, and CCH. Three further cases (9.7%) showed ductal carcinoma in situ without any definite invasive carcinoma. Colonization of AGMLG by neoplastic Paget cells was noted in 6 cases. As CCC and CCH may be encountered in normal AGMLG, these alterations are unlikely to play a significant role in the pathogenesis of the disease. However, by analogy with mammary Paget disease, rare cases of primary EMPD may originate in AGMLG with a subsequent upward migration of the neoplastic cells into the epidermis and possible later breach through the basal membrane. Usual ductal hyperplasia and atypical duct hyperplasia can then be regarded as earlier precursor lesions, linking both ends of the spectrum.
机译:为了确定原发性乳腺Paget疾病(EMPD)的子集是否可能起源于肛门生殖器样乳腺(AGMLG),作者研究了181个EMPD标本,详细介绍了AGMLG的改变。后者是在来自31位患者的33个标本中鉴定出来的。所有患者均为女性,年龄从38岁至93岁(中位数为65岁)。在所有情况下,皮损均累及外阴,其中1位患者的肛周皮肤受到影响。在组织病理学上,AGGMG表现出与柱状细胞变化(CCC)(87.1%),常见的导管增生(22.6%),柱状细胞增生(CCH)(9.7%),嗜氧性(顶泌性)增生(6.5%)和非典型导管相同的变化增生(3.2%)。除表皮内癌外,还有4例(12.9%)患有浸润性癌。在所有这四个方面,AGGMG表现出一系列改变,包括原位导管癌,CCC和CCH。另外三例(9.7%)显示为原位导管癌,无任何明确的浸润性癌。在6例中注意到肿瘤性Paget细胞对AMGMG的定殖。由于正常AGMLG中可能会遇到CCC和CCH,因此这些改变不太可能在疾病的发病机理中起重要作用。然而,通过与乳腺Paget疾病类似,罕见的原发性EMPD病例可能起源于AGMLG,随后肿瘤细胞向上迁移至表皮,并可能随后穿透基底膜。然后,通常的导管增生和非典型导管增生可被认为是较早的前体病变,连接频谱的两端。

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