[The radiographic report of soft tissue tumor on the legs in a case of cutaneous polyarteritis nodosa].

Ryumachi. [Rheumatism] Pub Date : 2000-02-01
H Yabe, I Sinzato, K Sugimoto, J Saegusa
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Abstract

A 55-year-old male was admitted to our hospital because of arthralgia, rash, and painful tumor in the legs. On admission, skin lesions involving dark erythematous macules and a tender mass of 3 by 5 cm were present. Laboratory findings included hemoglobin of 11.2 g/dl, white blood cell count of 6200/microliter, erythrocyte sedimentation rate (ESR) of 88 mm/hour, and normal results of renal function tests. Hepatitis B surface antigen, anti-nuclear antibody (ANA), and perinuclear pattern antineutrophil cytoplasmic autoantibody (ANCA) were negative. A T 1-weighted magnetic resonance image (MRI) showed iso-intensity areas that increased in intensity on T 2-weighted images of the M. gastrocnemius. The angiographic appearance of tumor staining with some degree of luminal irregularity in the posterior tibial artery suggested a diagnosis of soft tissue neoplasm. Biopsy specimens of the right leg lesion were consistent with necrotizing arteritis of both small and medium-sized vessels. Treatment with prednisolone and cyclophosphamide resulted in the disappearance of the skin lesions and the improvement of laboratory data. At first, classical polyarteritis nodosa was considered histologically. However, lesions were limited to skin, muscles, and joints, and there has been no evidence of systemic disease for 1.5 years; consequently, cutaneous form of polyarteritis nodosa was diagnosed. Reports of soft tissue tumors on the legs of patients with polyarteritis nodosa are quite rare. The interesting radiographic findings of cutaneous polyarteritis nodosa were reported.

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【皮肤结节性多动脉炎1例腿部软组织肿瘤的影像学报告】。
一名55岁男性因关节痛、皮疹和腿部肿瘤疼痛而入院。入院时,皮肤病变包括深色红斑斑和3 × 5厘米的压痛肿块。实验室检查结果包括血红蛋白11.2 g/dl,白细胞计数6200/微升,红细胞沉降率(ESR) 88 mm/小时,肾功能检查结果正常。乙型肝炎表面抗原、抗核抗体(ANA)、核周型抗中性粒细胞胞浆自身抗体(ANCA)均为阴性。t1加权磁共振成像(MRI)显示腓肠肌t2加权图像上的等强度区域强度增加。血管造影显示肿瘤在胫后动脉内有一定程度的腔内不规则,提示软组织肿瘤的诊断。右腿病变活检标本符合中小血管坏死性动脉炎。强的松龙和环磷酰胺治疗导致皮肤病变消失和实验室数据的改善。起初,组织学上认为是典型结节性多动脉炎。然而,病变仅限于皮肤、肌肉和关节,并且在1.5年内没有全身性疾病的证据;因此,确诊为皮肤型结节性多动脉炎。结节性多动脉炎患者的腿部软组织肿瘤的报道是相当罕见的。报告了皮肤结节性多动脉炎的有趣的x线表现。
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