Hara K, Mizuno E, Nitta Y, Ikeya T
Department of Pathology, Aichi Medical University, Japan.
Am J Dermatopathol. 1992 Aug;14(4):328-39. doi: 10.1097/00000372-199208000-00008.
The case of a 63-year-old man with acrosyringeal adenomatosis (eccrine syringofibroadenoma of Mascaro) is reported. Asymptomatic papular lesions had appeared on the dorsum of both of his feet 30 years earlier, then extended gradually and symmetrically to his hands, arms, legs, trunk, and auriculae. Although his hair, teeth, and nails were normal, he had glaucoma, chronic sinusitis, chronic otitis media, chronic pancreatitis, and gastrointestinal polyposis. No similar symptoms were found in the family history. Histopathologically, proliferations of pale epithelial cells extended from acrosyringia into the dermis, forming interconnected epithelial cords, within some of which were ductal structures. A syringoma and syringoma-like structures were closely associated with these lesions. Enzyme-histochemical, immunohistochemical, and ultrastructural studies supported the concept that this case represents a benign tumor derived from the acrosyringium, which is different from eccrine poroma. Acrosyringeal adenomatosis seems to be a more appropriate name for such a lesion than does eccrine syringofibroadenoma (Mascaro).
报告了一例63岁患有顶泌汗腺腺瘤病(马氏小汗腺纤维腺瘤)的男性病例。30年前,其双脚背部出现无症状丘疹性病变,随后逐渐对称扩展至双手、双臂、双腿、躯干及耳廓。虽然他的头发、牙齿和指甲正常,但患有青光眼、慢性鼻窦炎、慢性中耳炎、慢性胰腺炎和胃肠道息肉病。家族史中未发现类似症状。组织病理学检查显示,淡色上皮细胞从顶泌汗腺增生延伸至真皮,形成相互连接的上皮索,其中一些含有导管结构。汗管瘤及汗管瘤样结构与这些病变密切相关。酶组织化学、免疫组织化学及超微结构研究支持该病例为源自顶泌汗腺的良性肿瘤这一概念,它与小汗腺汗孔瘤不同。相较于小汗腺纤维腺瘤(马氏型),顶泌汗腺腺瘤病似乎是此类病变更合适的名称。