Alonso-Ruiz A, Zea-Mendoza A C, Salazar-Vallinas J M, Rocamora-Ripoll A, Beltrán-Gutiérrez J
Semin Arthritis Rheum. 1986 Feb;15(3):200-12. doi: 10.1016/0049-0172(86)90017-x.
Thirty-two toxic oil syndrome (TOS) patients were selected because they presented with scleroderma-like changes and were observed during the first 36 months of evolution of the disease. Initially, these patients presented with a noncardiogenic pulmonary edema, eosinophilia, arthralgia/arthritis, peripheral edema, and myositis. Histologic investigations showed a widespread chronic interstitial infiltrate with lymphocytic vasculitis. They subsequently developed peripheral neuropathy, joint contractures, scleroderma-like changes, Raynaud phenomenon, pulmonary hypertension, sicca syndrome, and liver disease. Biopsy studies during this stage showed fibrosis and obliterating arteriopathy. Late features of TOS are musculoskeletal pain, cramps, livedo reticularis, carpal tunnel syndrome, and digital tuft changes. TOS is a new chemically induced scleroderma-like syndrome with features overlapping those of eosinophilic fasciitis, systemic sclerosis, and forms of localized scleroderma.
32名有毒油综合征(TOS)患者被选中,因为他们出现了硬皮病样改变,并在疾病发展的前36个月内接受观察。最初,这些患者表现为非心源性肺水肿、嗜酸性粒细胞增多、关节痛/关节炎、外周水肿和肌炎。组织学检查显示广泛的慢性间质性浸润伴淋巴细胞性血管炎。他们随后出现了周围神经病变、关节挛缩、硬皮病样改变、雷诺现象、肺动脉高压、干燥综合征和肝病。此阶段的活检研究显示有纤维化和闭塞性动脉病变。TOS的晚期特征为肌肉骨骼疼痛、痉挛、网状青斑、腕管综合征和指端改变。TOS是一种新的化学诱导的硬皮病样综合征,其特征与嗜酸性筋膜炎、系统性硬化症及局限性硬皮病的某些类型有重叠。