Lee Julia Yu-Yun, Lin Ming-Hsien
Department of Dermatology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
J Cutan Pathol. 2006 Oct;33(10):705-8. doi: 10.1111/j.1600-0560.2006.00508.x.
Pigmented variant of malignant hidroacanthoma simplex (PMHS) is very rare. We are aware of only two reported cases, all arising in pigmented hidroacanthoma simplex (HS). We report the third case of PMHS arising in a pigmented HS. A 71-year-old-woman presented with a well-demarcated pigmented hyperkeratotic tumor on the right knee resembling irritated seborrheic keratosis. Histopathologic examination of the excised tumor revealed intraepidermal proliferation of atypical polygonal poroid cells forming large, sharply demarcated nests with colonization of dendritic melanocytes. In addition, there were focal changes of a benign pigmented HS and syringofibroadenoma. The key diagnostic features of ductal structures and intracytoplasmic lumina were highlighted by carcinoembryonic antigen and epithelial membrane antigen immunostaining. PMHS should be differentiated from irritated seborrheic keratosis, melanoacanthoma, Bowen's disease and malignant melanoma both clinically and pathologically.
恶性单纯性汗腺棘皮瘤色素沉着变异型(PMHS)非常罕见。我们仅知晓两例报道病例,均发生于色素沉着性单纯性汗腺棘皮瘤(HS)。我们报告了第三例发生于色素沉着性HS的PMHS。一名71岁女性右膝出现一个边界清晰的色素沉着性角化过度肿瘤,类似刺激性脂溢性角化病。切除肿瘤的组织病理学检查显示,非典型多边形汗孔样细胞在表皮内增生,形成大的、边界清晰的巢状结构,并伴有树突状黑素细胞浸润。此外,还有良性色素沉着性HS和汗腺纤维腺瘤的局灶性改变。癌胚抗原和上皮膜抗原免疫染色突出了导管结构和胞质内腔的关键诊断特征。PMHS在临床和病理上均应与刺激性脂溢性角化病、黑素棘皮瘤、鲍温病和恶性黑色素瘤相鉴别。