【以水疱及口腔溃疡为表现的淀粉性皮肌炎1例】。

Ryumachi. [Rheumatism] Pub Date : 1999-12-01
A Seno, M Tokuda, H Yamasaki, K Akiyama
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引用次数: 0

摘要

一名84岁男性因进行性不适和双眼睑水肿(日光性红斑)住进三代总医院。他还注意到脖子上有水泡,手指关节伸面有红斑(Gottron氏征),肘部和膝盖也有红斑。入院时体格检查未发现其近端肌肉无力或疼痛。血检显示炎症阳性体征(ESR轻度升高,CRP阳性),肌酶值未升高。肌电图显示正常。肌组织活检未见炎性细胞浸润。根据这些观察结果,诊断为“肌肌炎”。胸部电脑断层显示间质性肺炎在双肺下野扩散。结肠纤维镜检查示降结肠息肉,细胞学检查为I组。患者给予2组甲基强的松龙(mPSL)脉冲治疗(500 mg/天,连续3天,静脉注射),随后口服强的松龙(PSL) 30 mg/天。他的皮肤病变对上述治疗反应良好,口服PSL的剂量逐渐减少。开始治疗一个月后,他的舌头下出现严重的口腔炎和大溃疡,并伴有顽固性疼痛。粘膜活检显示溃疡底部中动脉坏死性血管炎。另一组mPSL脉冲治疗使他的症状迅速缓解,并阻止了口腔病变的复发。值得注意的是,我们的患者由于缺乏肌肉症状而不符合糖尿病的诊断标准,而他有特征性的皮肤病变。针对在诊断amyopathic DM时可能遇到的挫折,我们研究了皮肤病变对DM诊断的敏感性和特异性。此外,还讨论了水疱作为糖尿病皮肤表现的罕见性。
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[A case of amyopathic dermatomyositis presenting blister and oral ulcer].

An 84-year old man was admitted to Mitoyo General Hospital because of progressive malaise and edematous erythema on both eyelids (Heliotrope erythema). He also noted blister on his neck as well as erythema on the extensor surface of finger joints (Gottron's sign), elbows and knees. Neither weakness nor pain of his proximal muscle was elicited on physical examination on admission. His blood test disclosed positive inflammatory signs (i.e., mild elevation of ESR and positive CRP) without elevated value of muscle enzymes. Electromyogram showed normal pattern. Infiltration of inflammatory cells was not revealed by histological examination of biopsied muscle. A diagnosis of 'amyopathic dermatomyositis' was made based on these observations. Computed tomography of his chest disclosed interstitial pneumonia spreading over both lower lung fields. Colon fiberscopy revealed a polyp in his descending colon, which was classified into group I on cytological examination. He was treated with two sets of methylprednisolone (mPSL) pulse therapy (500 mg/day, 3 consecutive days, intravenously) followed by 30 mg/day of oral prednisolone (PSL). His skin lesions responded well to the above treatment and the dose of oral PSL was tapered. One month after the initiation of treatment, severe stomatitis as well as a large ulcer beneath his tongue developed accompanying an intractable pain. Mucosal biopsy revealed necrotizing vasculitis in medium-sizedartery at the bottom of ulcer. Another set of mPSL pulse therapy brought a prompt relief of his symptom and prohibited the recurrence of oral lesion. It should be noted that our patient did not fulfill the diagnostic criteria for DM because of the lack of muscular symptoms whereas he had characteristic skin lesions. Regarding the frustration possibly encountered at the time of diagnosing amyopathic DM, both sensitivity and specificity of the skin lesion for the diagnosis of DM were investigated. Moreover, the rarity of blister as a skin manifestation of DM was discussed as well.

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