Herreman G, Huet D, Mundler B, Tamisier J N, Blum F, Wechsler J, Ferme I
Sem Hop. 1982 May 20;58(20):1225-8.
An unusual form of scleroderma, seen in one patient, is described. Clinical and histological examinations demonstrated no dermal changes. Both the subcutaneous tissue and the fascias were involved. This case can be distinguished from Shulman fasciitis, on both histological and biological grounds, as well as from scleroderma, since Raynaud phenomena, sclerodactylia, and visceral involvement were lacking.
本文描述了在一名患者身上发现的一种罕见的硬皮病形式。临床和组织学检查均未发现皮肤变化。皮下组织和筋膜均受累。该病例在组织学和生物学方面均可与舒尔曼筋膜炎以及硬皮病相鉴别,因为患者缺乏雷诺现象、硬指及内脏受累情况。