LaChance A, Phelps A, Finch J, Lu J, Elaba Z, Rezuke W, Murphy M J
Division of Dermatopathology, Department of Dermatology, University of Connecticut Health Center, Farmington, CT, USA.
Clin Exp Dermatol. 2014 Apr;39(3):344-7. doi: 10.1111/ced.12305.
Primary cutaneous amyloidosis describes a group of disorders in which amyloid is deposited in the skin without evidence of systemic involvement. Nodular localized primary cutaneous amyloidosis (NLPCA) is a rare form of these skin-restricted amyloidoses. We present an unusual case of NLPCA in a 51-year-old man, who had clinical and histopathological evidence of subepidermal bullous formation, a unique feature in NLPCA. The possible pathogenesis of this change is discussed.
原发性皮肤淀粉样变是指一组疾病,其中淀粉样蛋白沉积于皮肤,而无系统性受累的证据。结节性局限性原发性皮肤淀粉样变(NLPCA)是这些皮肤局限性淀粉样变的一种罕见形式。我们报告了一例51岁男性的不寻常NLPCA病例,该患者有表皮下大疱形成的临床和组织病理学证据,这是NLPCA的一个独特特征。本文讨论了这种变化可能的发病机制。