Drenth J P, Michiels J J, Van Joost T, Vuzevski V D
Department of Medicine, University Hospital St. Radboud, Nijmegen, The Netherlands.
Dermatology. 1995;190(3):232-4. doi: 10.1159/000246692.
A 50-year-old female patient is described with an acquired, persisting and yet incurable erythermalgia featured by symmetric burning pain and red congestion of the extremities secondary to cutaneous vasculitis. A weakly positive antinuclear antibody titer and high titers of antibodies against gastric parietal mucosa cells pointed to an underlying but unclassifiable autoimmune disorder. It is concluded that histopathology of lesional skin contributes to the differential diagnosis of primary and secondary erythermalgia.
本文描述了一名50岁女性患者，其患有后天性、持续性且无法治愈的红斑性肢痛症，其特征为对称性灼痛以及继发于皮肤血管炎的四肢发红充血。抗核抗体滴度弱阳性和抗胃壁粘膜细胞抗体高滴度提示存在一种潜在但无法分类的自身免疫性疾病。得出的结论是，病变皮肤的组织病理学有助于原发性和继发性红斑性肢痛症的鉴别诊断。
