原发性Sjögren综合征患者多发发疹性皮肤纤维瘤

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
M. Kaya, D. Tecer, S. Yılmaz
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引用次数: 0

摘要

多发发疹性皮肤纤维瘤是一种罕见的肿瘤,被认为与免疫系统紊乱有关。在我们40岁的病例中,4个月内出现了5个结节。患者经皮肤科医生诊断为MEDF,因出现口干、多关节痛等症状转至风湿病门诊。经临床及实验室评估,诊断为原发性Sjögren综合征(SS)。据我们所知,该病例是MEDF与原发性SS关联的首例报道。因此,在诊断MEDF时,SS也应纳入相关疾病的综合评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple Eruptive Dermatofibromas in a Patient with Primary Sjögren’s Syndrome
Multiple eruptive dermatofibromas (MEDF) are rare tumors and thought to be associated with the disturbances in the immune system. In our 40-year-old case, 5 nodules have developed in a 4-month period. The patient was diagnosed by a dermatologist to have MEDF, and referred to rheumatology outpatient clinic because of the symptoms such as dry mouth, and polyarthralgia. After clinical and laboratory evaluation, the diagnosis of primary Sjögren’s syndrome (SS) was made. According to the best of our knowledge, this case is the first reported association between MEDF and primary SS. Therefore, when the diagnosis of MEDF is made, SS should also been included in the comprehensive evaluation of associated diseases.
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来源期刊
European Journal of Therapeutics
European Journal of Therapeutics MEDICINE, GENERAL & INTERNAL-
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