中华内科杂志
中華內科雜誌
중화내과잡지
CHINESE JOURNAL OF INTERNAL MEDICINE
2013年
11期
924-927
,共4页
王炎焱%赵征%张江林%朱剑%冯莉霞%黄烽
王炎焱%趙徵%張江林%硃劍%馮莉霞%黃烽
왕염염%조정%장강림%주검%풍리하%황봉
骶髂关节炎%脊柱炎,强直性%回顾性研究
骶髂關節炎%脊柱炎,彊直性%迴顧性研究
저가관절염%척주염,강직성%회고성연구
Sacroiliitis%Spondylitis,ankylosing%Retrospective studies
目的 探讨骶髂关节炎的临床特点及鉴别诊断.方法 回顾性分析2007-2012年解放军总医院门诊和住院有腰背痛和骶髂关节炎患者509例的临床资料.结果 509例患者中,男性406例,女性103例,其中强直性脊柱炎/脊柱关节炎436例,致密性骨炎36例,骶髂关节退行性病变10例,骶髂关节感染10例,弥漫性特发性骨肥厚4例,掌趾脓疱病性关节炎4例,代谢性骨病4例,骶髂关节痛风l例,肿瘤性疾病4例.强直性脊柱炎/脊柱关节炎患者HLA-B27阳性率86.9%.强直性脊柱炎/脊柱关节炎患者红细胞沉降率、C反应蛋白轻中度升高,骶髂关节感染和肿瘤性疾病患者红细胞沉降率、C反应蛋白升高较明显.强直性脊柱炎/脊柱关节炎影像学特点主要表现为骶髂关节骨破坏,磁共振成像显示为骶髂关节骨髓水肿,但范围不超出解剖结构.结论 非强直性脊柱炎引起的骶髂关节炎并不少见,应提高警惕,防止遗漏,尤其是HLA-B27阴性者,以免误诊、误治.
目的 探討骶髂關節炎的臨床特點及鑒彆診斷.方法 迴顧性分析2007-2012年解放軍總醫院門診和住院有腰揹痛和骶髂關節炎患者509例的臨床資料.結果 509例患者中,男性406例,女性103例,其中彊直性脊柱炎/脊柱關節炎436例,緻密性骨炎36例,骶髂關節退行性病變10例,骶髂關節感染10例,瀰漫性特髮性骨肥厚4例,掌趾膿皰病性關節炎4例,代謝性骨病4例,骶髂關節痛風l例,腫瘤性疾病4例.彊直性脊柱炎/脊柱關節炎患者HLA-B27暘性率86.9%.彊直性脊柱炎/脊柱關節炎患者紅細胞沉降率、C反應蛋白輕中度升高,骶髂關節感染和腫瘤性疾病患者紅細胞沉降率、C反應蛋白升高較明顯.彊直性脊柱炎/脊柱關節炎影像學特點主要錶現為骶髂關節骨破壞,磁共振成像顯示為骶髂關節骨髓水腫,但範圍不超齣解剖結構.結論 非彊直性脊柱炎引起的骶髂關節炎併不少見,應提高警惕,防止遺漏,尤其是HLA-B27陰性者,以免誤診、誤治.
목적 탐토저가관절염적림상특점급감별진단.방법 회고성분석2007-2012년해방군총의원문진화주원유요배통화저가관절염환자509례적림상자료.결과 509례환자중,남성406례,녀성103례,기중강직성척주염/척주관절염436례,치밀성골염36례,저가관절퇴행성병변10례,저가관절감염10례,미만성특발성골비후4례,장지농포병성관절염4례,대사성골병4례,저가관절통풍l례,종류성질병4례.강직성척주염/척주관절염환자HLA-B27양성솔86.9%.강직성척주염/척주관절염환자홍세포침강솔、C반응단백경중도승고,저가관절감염화종류성질병환자홍세포침강솔、C반응단백승고교명현.강직성척주염/척주관절염영상학특점주요표현위저가관절골파배,자공진성상현시위저가관절골수수종,단범위불초출해부결구.결론 비강직성척주염인기적저가관절염병불소견,응제고경척,방지유루,우기시HLA-B27음성자,이면오진、오치.
Objective To study the clinical features of sacroiliitis and differential diagnosis.Methods Totally 509 patients with chief complaints of back pain and diagnosed as sacroiliitis from January 2007 to January in Chinese PLA General Hospital were enrolled.The clinical manifestations,laboratory examinations,imaging and pathological data of the 509 patients were retrospectively analyzed.Results There were totally 406 male patients and 103 female patients.Among all 509 patients,436 were diagnosed as ankylosing spondylitis (AS)/ spondyloarthropathy (SpA),including 385 men.Thirty-six cases were diagnosed as sclerosing osteitis.Ten cases were diagnosed as sacroiliac joint degeneration.Ten cases were diagnosed as pyogenic sacroiliitis or sacroiliac joint tuberculosis.Four cases were diagnosed as diffuse idiopathic bone hypertrophy.Four cases were diagnosed as palmoplantar pustulosis arthritis.Four cases were diagnosed as metabolic bone disease.One case was diagnosed as sacroiliac joint gout.Four cases were diagnosed as neoplastic disease.HLA-B27 positive rate was 86.9% in AS/SpA.Erythrocyte sedimentation rate and C-reactive protein were increased mildly-to-moderately in AS/SpA patients.Erythrocyte sedimentation rate and C-reactive protein increased obviously in sacroiliac joint infection and tumor diseases.Imaging characteristics were sacroiliac joint bone destruction.Magnetic resonance imaging showed sacroiliac joint bone marrow edema,but range was not beyond anatomical structure in AS/SpA.Conclusions Based on disease distribution of sacroiliitis,AS/SpA is predominant while non-ankylosing spondylitis is not uncommon.Differential diagnoses of sacroiliitis should be considered to avoid malpractice,especially in patients with negative HLA-B27.