Misago N, Toda S, Hikichi Y, Iyadomi M, Kohda H
Department of Internal Medicine, Saga Medical School, Japan.
Am J Dermatopathol. 1992 Dec;14(6):553-9. doi: 10.1097/00000372-199212000-00014.
A unique case of extramammary Paget's disease is reported that may have derived from eccrine porocarcinoma. A palm-sized erythematous plaque on the patient's pubis spread to the lower abdominal wall. The center of the lesion contained a reddish tumor. Histologic findings of the erythematous plaque showed features of extra-mammary Paget's disease. Those of the reddish tumor, however, corresponded most closely to eccrine porocarcinoma, though we could not entirely rule out that the changes corresponded to larger nests of less differentiated Paget cells. The two distinct neoplastic areas showed continuity both clinically and histologically; our case differed from epidermotropic eccrine porocarcinoma in several clinicopathologic respects. Our case suggests the possibility that extramammary Paget's disease could arise from preexisting porocarcinoma.
报告了一例可能源于小汗腺汗孔癌的乳腺外佩吉特病的独特病例。患者耻骨上有一个手掌大小的红斑性斑块,蔓延至下腹壁。病变中心有一个红色肿瘤。红斑性斑块的组织学表现显示为乳腺外佩吉特病的特征。然而,红色肿瘤的组织学表现与小汗腺汗孔癌最为相符,尽管我们不能完全排除这些变化对应于分化程度较低的佩吉特细胞的较大巢团。这两个不同的肿瘤区域在临床和组织学上均显示连续;我们的病例在几个临床病理方面与亲表皮性小汗腺汗孔癌不同。我们的病例提示乳腺外佩吉特病可能起源于先前存在的汗孔癌。