Person J R, Su W P
Br J Dermatol. 1979 Apr;100(4):371-80. doi: 10.1111/j.1365-2133.1979.tb01636.x.
Sixteen patients had biopsy-proved inflammatory sclerosis of the panniculus or fascia, which usually was seen in a generalized distribution. Although the sclerosis involved the digits of five patients, it was the result of centrifugal spread of the sclerosis and was not accompanied by ulcers, calcinosis, distal phalangeal resorption or telangiectasia. Four patients may have had digital vasopasm in the extremities involved in the sclerotic process. Five patients also had cutaneous lesions of dermal morphoea or lichen sclerosus et atrophicus. Four patients had a reduced carbon monoxide diffusing capacity, and one of these had roentgenographic evidence of pulmonary fibrosis. In three patients, oesophageal motility or barium swallow studies showed evidence of sclerodermatous changes. The sclerotic process was a contributory cause of the death of one patient. Five patients had peripheral eosinophilia. Six patients seemed to have responded to anti-inflammatory agents. We believe that subcutaneous morphoea is generally more inflammatory than generalized morphoea of the dermal type and may be more likely to progress to mild systemic sclerosis. We suggest that response of subcutaneous morphoea to anti-inflammatory agents is simply a reflection of the degree of inflammation present.
16例患者经活检证实为脂膜或筋膜的炎性硬化,通常呈全身性分布。虽然5例患者的硬化累及手指,但这是硬化离心性扩散的结果,且不伴有溃疡、钙质沉着、远端指骨吸收或毛细血管扩张。4例患者在硬化过程累及的肢体可能出现了手指血管痉挛。5例患者还患有真皮硬斑病或萎缩性硬化性苔藓的皮肤病变。4例患者一氧化碳弥散能力降低,其中1例有肺纤维化的X线证据。3例患者的食管动力或吞钡检查显示有硬皮病样改变。硬化过程是1例患者死亡的一个促成因素。5例患者有外周血嗜酸性粒细胞增多。6例患者似乎对抗炎药有反应。我们认为皮下硬斑病通常比真皮型全身性硬斑病炎症更重,可能更易进展为轻度系统性硬化症。我们认为皮下硬斑病对抗炎药的反应仅仅反映了当前的炎症程度。