Neurological abnormalities in localized scleroderma of the face and head: a case series study for evaluation of imaging findings and clinical course

被引:12
作者
Lis-Swiety, Anna [1 ]
Brzezinska-Wcislo, Ligia [1 ]
Arasiewicz, Hubert [1 ]
机构
[1] Med Univ Silesia, Sch Med Katowice, Dept Dermatol, Katowice, Poland
关键词
scleroderma en coup de sabre; progressive facial hemiatrophy; neurological pathology; PARRY-ROMBERG-SYNDROME; COUP-DE-SABRE; EN-COUP; LINEAR SCLERODERMA; RETROSPECTIVE ANALYSIS; INVOLVEMENT; CHILDREN; MORPHEA; DISEASE;
D O I
10.1080/00207454.2016.1244823
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Introduction: Localized scleroderma (LoS) of the face and head is often associated with neurological manifestations and/or imaging abnormalities in the central nervous system (CNS). Case series: We present an analysis of 20 cases of LoS affecting the face and head. The CNS symptoms and/or abnormalities in high-resolution computed tomography (HRCT) and/or magnetic resonance imaging (MRI) were observed in 12 patients (60%). In addition to the mild and unspecific disorders (e.g. headaches), serious neurological complications probably in the course of vasculitis were revealed: epilepsy (in two patients), epilepsy and pyramidal sings (in one patient). Neurological disorders and LoS occurred at the same time (in three patients) or at the course of the disease (nine patients) and no later than 29years since the onset of the disease. No link between neurological disorders and the LoS clinical morphology, immunological and other laboratory parameters has been established. Conclusions: CNS involvement is not correlated with the clinical course of the facial and head LoS and may occur years after the disease initial symptomatology. Imaging follow-up is not required if there is not any emerging neurological symptom. In some cases, however, both HRCT and MRI are useful for monitoring disease evolution and addressing therapeutic choices.
引用
收藏
页码:835 / 839
页数:5
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