Patch-Type Granuloma Annulare with Clinical and Histological Features of Morphea: A True Overlap?

Carlie Reeves, L. Falcone, Collen J Beatty, V. Kazlouskaya, Joseph C English Iii
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引用次数: 0

Abstract

A 67-year-old woman was evaluated for a worsening asymptomatic rash located on her torso, back, and legs. She denied any chills or fevers, and reported feeling otherwise well. Clinically, large brownish, slightly atrophic plaques were seen on the torso suggestive of either morphea or a granulomatous condition. Histopathologic examination revealed an increase in interstitial histiocytes infiltrating between altered collagen fibers, palisaded granulomas with increased mucin, suggestive of granuloma annulare (GA), as well as dermal sclerosis, perineural infiltrates with plasma cells and diminished CD34 counts, that are more typical for localized scleroderma/morphea. Morphea and patch-type GA may be indistinguishable clinically and share some histopathological features. This case demonstrates similarities between these conditions and features of both conditions in the same patient.
具有吗啡临床和组织学特征的斑块型环状肉芽肿:真正的重叠?
一名67岁的女性被评估为躯干、背部和腿部出现了恶化的无症状皮疹。她否认有任何寒战或发烧,并表示感觉良好。临床上,躯干上可见大的褐色轻度萎缩斑块,提示有变形或肉芽肿。组织病理学检查显示,间质组织细胞浸润在胶原纤维改变之间增加,栅栏状肉芽肿伴粘蛋白增加,提示环状肉芽肿(GA),以及真皮硬化、带浆细胞的神经周浸润和CD34计数减少,这在局限性硬皮病/变形症中更为典型。吗啡和GA型贴片在临床上可能无法区分,并且有一些共同的组织病理学特征。该病例证明了这些情况与同一患者的两种情况的特征之间的相似性。
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