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Leukocytoclastic Vasculitis in a Patient with Ankylosing Spondylitis

机译:强直性脊柱炎患者的白细胞碎裂性血管炎

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A 26-year-old male patient presented to our rheumatology clinic with pain, swelling and limitation of movement in his right ankle, and also purpuric skin lesions in the lower extremity pretibial region. He was asked questions, and he said that he had been having chronic low back pain and morning stiffness for the last few years. His physical examination revealed that he had arthritis in his right ankle, purpuric skin lesions in pretibial regions of both legs, and bilateral FABERE/FADIR positivity. The sacroiliac joint imaging and MRI revealed bilateral sacroiliitis findings, and the lateral heel imaging revealed enthesitis. HLA-B27 was positive. Skin biopsy from lower skin lesions was reported to be consistent with leukocytoclastic vasculitis. Based on clinical, laboratory, radiological, and pathological examinations, the patient was diagnosed with ankylosing spondylitis and leukocytoclastic vasculitis. Administration of corticosteroid, salazopyrin, and nonsteroid anti-inflammatory medications was started. Notable clinical and laboratory regression was observed during his checks 3 months later.
机译:一位26岁的男性患者因风湿病,右脚踝疼痛,肿胀和活动受限,以及下肢前胫骨区域的紫癜性皮肤病而出现在我们的风湿病诊所。有人问他,他说过去几年来他一直患有慢性腰背痛和晨僵。体格检查发现他的右脚踝患有关节炎,双腿胫前区有紫癜性皮肤病变,双侧FABERE / FADIR阳性。 sa关节成像和MRI显示双侧ili肌炎的发现,而外侧足跟成像则显示出脑炎。 HLA-B27为阳性。据报道,来自下部皮肤病变的皮肤活检与白细胞碎裂性血管炎一致。根据临床,实验室,放射学和病理学检查,该患者被诊断出患有强直性脊柱炎和白细胞碎裂性血管炎。开始给予皮质类固醇,Salazopyrin和非甾体抗炎药。三个月后的检查期间,观察到明显的临床和实验室回归。

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