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首页> 外文期刊>Dermatologica Sinica >Primary invasive triple extramammary Paget's disease with regional lymph node metastasis: A case report and review of the literature
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Primary invasive triple extramammary Paget's disease with regional lymph node metastasis: A case report and review of the literature

机译:原发性浸润性三重乳腺Paget病伴局部淋巴结转移:1例报道并文献复习

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Extramammary Paget's disease (EMPD) is a rare intraepidermal carcinoma and predominantly involves apocrine gland-bearing areas, such as anogenital regions and axillae. EMPD usually involves a solitary area and, less often, two areas in the same patient (double EMPD). The simultaneous involvement of bilateral axillae and anogenital region, called triple extramammary Paget's disease (TEPD), is an extremely rare subgroup of diseases that has been reported mostly from studies conducted in Japan. Because of its rarity, the clinical course, pathology/immunohistochemical staining features, and prognosis of TEPD are still unclear. Herein, to our knowledge, we present the first case of primary invasive TEPD with regional lymph node metastasis in Taiwan, and review the literature.
机译:乳腺Paget病(EMPD)是一种罕见的表皮内癌,主要累及载脂腺的生殖区域,例如肛门生殖器区域和腋窝。 EMPD通常涉及一个单独的区域,在同一患者中很少涉及两个区域(双重EMPD)。双侧腋窝和肛门生殖器区域同时受累,称为三乳腺佩吉特氏病(TEPD),是一种极为罕见的疾病亚类,主要在日本进行的研究中已有报道。由于其稀有性,TEPD的临床病程,病理学/免疫组化染色特征和预后仍不清楚。在此,据我们所知,我们介绍了台湾地区首例伴有区域淋巴结转移的原发性浸润性TEPD,并复习了文献。

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