Hurt M A, Igra-Serfaty H, Stevens C S
Department of Pathology, University of Texas Health Science Center, San Antonio 78284-7750.
Arch Dermatol. 1990 Jul;126(7):945-9.
Two patients with eccrine syringofibroadenomas were studied. The first patient had a 3-year history of asymptomatic, unilateral, linear, moist mosaic plaques of the lower part of the left leg and foot; the second patient had a solitary papule on the back. Histologically, both tumors exhibited superficial elongated strands of eccrine ductal epithelium containing occasional lumina lined by an eosinophilic cuticle. The stroma was loose, myxoid, and fibrovascular. The secretory portions of the eccrine glands were ectatic in the first patient but were not seen in the second patient. We believe these lesions represent acrosyringeal hamartomas (nevi), although some authors interpret them as adenomas. The literature seems to indicate that lesions with similar histologic features may be solitary, multiple, or combined with other neoplasms; in other cases, the lesions may possibly represent an unusual morphologic expression of hidrotic ectodermal dysplasia.
对两名患有小汗腺汗管纤维腺瘤的患者进行了研究。第一名患者有3年病史,表现为左腿和足部下部无症状、单侧、线性、湿润的镶嵌状斑块;第二名患者背部有一个孤立丘疹。组织学上,两个肿瘤均表现为小汗腺导管上皮的浅表细长条索,偶见由嗜酸性角质层衬里的管腔。间质疏松、黏液样且为纤维血管性。第一名患者的小汗腺分泌部扩张,但第二名患者未见。我们认为这些病变代表顶泌汗腺错构瘤(痣),尽管一些作者将其解释为腺瘤。文献似乎表明,具有相似组织学特征的病变可能是孤立的、多发的,或与其他肿瘤合并;在其他情况下,这些病变可能代表出汗性外胚层发育不良的一种不寻常形态学表现。