Rodríguez Herrera María Gabriela, Smith Stephen M, Rosen Cheryl F
Division of Dermatology, Toronto Western Hospital, University of Toronto, ON, Canada.
Department of Laboratory Medicine and Pathobiology, University Health Network, University of Toronto, ON, Canada.
SAGE Open Med Case Rep. 2025 Aug 25;13:2050313X251358992. doi: 10.1177/2050313X251358992. eCollection 2025.
We present a case of a 43-year-old woman with Vogt-Koyanagi-Harada syndrome, on adalimumab, methotrexate, and risedronate, who developed pruritic, skin-colored papules on the dorsal hands. A biopsy revealed features consistent with syringomas. Syringomas are benign eccrine duct tumors that typically appear as small, shiny papules, most often in the periorbital area but can also present in acral regions. Only 14 cases of exclusive acral syringomas have been reported. Eruptive variants may resemble conditions such as lichen nitidus or warts, making dermoscopy and histopathology crucial for diagnosis. Dermoscopically, syringomas may show fine reticulate brown lines and homogenous pigmentation. Histologically, they show small ductal structures and epithelial cords in the dermis. Their exact pathogenesis remains unclear, possibly involving hormonal or inflammatory triggers. Treatment is challenging due to their dermal depth and recurrence risk, with lasers and retinoids among the options. This case highlights the diagnostic complexity of acral eruptive syringomas.
我们报告一例43岁患有Vogt-小柳原田综合征的女性病例,该患者正在使用阿达木单抗、甲氨蝶呤和利塞膦酸盐治疗,其双手背部出现了瘙痒性、肤色丘疹。活检显示其特征与汗管瘤相符。汗管瘤是一种良性小汗腺导管肿瘤,通常表现为小的、有光泽的丘疹,最常见于眶周区域,但也可出现在肢端部位。仅报告过14例单纯性肢端汗管瘤病例。发疹性汗管瘤可能类似光泽苔藓或疣等疾病,因此皮肤镜检查和组织病理学检查对诊断至关重要。在皮肤镜下,汗管瘤可能显示出细网状棕色线条和均匀色素沉着。组织学上,它们在真皮中表现为小导管结构和上皮索。其确切发病机制尚不清楚,可能涉及激素或炎症触发因素。由于其位于真皮的深度和复发风险,治疗具有挑战性,激光和维甲酸类药物是治疗选择之一。该病例突出了肢端发疹性汗管瘤的诊断复杂性。