Hagiwara-Takita Akiko, Fujimura Taku, Kakizaki Aya, Aiba Setsuya
Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Case Rep Dermatol. 2016 Jun 6;8(2):130-5. doi: 10.1159/000445992. eCollection 2016 May-Aug.
Ectopic extramammary Paget's disease (EMPD) is a rare variant of EMPD that develops in nonapocrine regions. Since reports about ectopic EMPD are limited, little is known about the biological and immunological background of ectopic EMPD. In this report, we present a case of ectopic EMPD on the lower abdomen that expressed RANKL but lacked the expression of MMP7. As we previously reported, Paget's cells express RANKL and MMP7, release soluble RANKL in the tumor microenvironment, and stimulate tumor-associated macrophages to produce tumor-loading factors in conventional EMPD. In our present case, both CCL5-expressing cells and MMP25-bearing cells were lacking, whereas substantial numbers of CCL5-expressing cells and MMP25-bearing cells were found in conventional EMPD. Our case suggested that the lack of MMP7 on Paget's cells might be one of the possible explanations for the biology of ectopic EMPD.
异位乳腺外佩吉特病(EMPD)是一种在非顶泌腺区域发生的罕见的EMPD变体。由于关于异位EMPD的报道有限,人们对其生物学和免疫学背景知之甚少。在本报告中,我们展示了一例在下腹部发生的异位EMPD病例,该病例表达核因子κB受体活化因子配体(RANKL)但缺乏基质金属蛋白酶7(MMP7)的表达。正如我们之前所报道的,佩吉特细胞表达RANKL和MMP7,在肿瘤微环境中释放可溶性RANKL,并刺激肿瘤相关巨噬细胞产生肿瘤负荷因子,这在传统EMPD中是常见的。在我们目前的病例中,缺乏表达趋化因子配体5(CCL5)的细胞和携带基质金属蛋白酶25(MMP25)的细胞,而在传统EMPD中发现了大量表达CCL5的细胞和携带MMP25的细胞。我们的病例表明,佩吉特细胞上缺乏MMP7可能是异位EMPD生物学特性的一种可能解释。