sacroiliitis

骶髂关节炎
  • 文章类型: Case Reports
    髂腰肌脓肿是一种罕见的疾病,其特征是在髂腰肌隔室中积聚脓液。近年来,随着各种合并症和危险因素的出现,该病的患病率一直在增加。更新的成像方式的可用性也改善了对新病例的检测。沙门氏菌病是髂腰肌脓肿和骶髂关节炎的罕见病因。文献报道的大多数病例与金黄色葡萄球菌有关,链球菌种类,和大肠杆菌。糖尿病,血液恶性肿瘤,艾滋病毒,和其他免疫受损状态是髂腰肌脓肿的重要合并症/危险因素。我们报告了一例18岁男性,有发烧和右髋部疼痛10天的病史。放射显像显示右侧骶髂关节炎和髂腰肌脓肿。血培养显示泛敏感伤寒沙门氏菌。抗生素疗程延长后(静脉注射头孢曲松,然后口服左氧氟沙星),患者病情好转,症状无进一步复发。在排除金黄色葡萄球菌和结核分枝杆菌等常见病因后,伤寒沙门氏菌应该是流行地区髂腰肌脓肿的重要区别。
    Iliopsoas abscess is an infrequent condition characterized by the collection of pus in the iliopsoas compartment. The prevalence of the disease has been increasing in recent years with the emergence of various comorbidities and risk factors. The availability of newer imaging modalities has also improved the detection of new cases. Salmonellosis is an uncommon etiology in iliopsoas abscess and sacroiliitis. Most cases reported in the literature are associated with Staphylococcus aureus, Streptococci species, and Escherichia coli. Diabetes, hematological malignancies, HIV, and other immunocompromised states are important comorbidities/risk factors for iliopsoas abscess. We report a case of an 18-year-old male who presented with a history of fever and right hip pain for 10 days. Radioimaging revealed right sacroiliitis and iliopsoas abscess. Blood culture revealed pan-sensitive Salmonella typhi. After the prolonged course of antibiotics (intravenous ceftriaxone followed by oral levofloxacin), the patient improved with no further relapse in symptoms. Salmonella typhi should be an important differential of iliopsoas abscess in endemic regions after ruling out the common etiology such as S. aureus and Mycobacterium tuberculosis.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    VEXAS综合征是一种最近描述的自身炎症综合征,由髓样前体中UBA1突变的体细胞获得引起,并且通常与血液恶性肿瘤有关。主要是骨髓增生异常综合征。疾病表现可以模拟几种风湿病,延迟诊断。我们描述了一个非典型表现,类似迟发性轴向脊椎关节炎的病例,后来进展为软骨炎的全身性炎症综合征,皮肤血管炎,输血依赖性贫血,需要高剂量的类固醇.Ruxolitinib被用作第一个类固醇保留策略,没有反应。然而,阿扎胞苷显示出控制炎症和突变克隆的活性。该病例提出了阿扎胞苷的抗炎作用是否依赖于或独立于克隆控制的问题。我们讨论了分子缓解在VEXAS综合征中的潜在相关性,并强调了多学科团队对此类复杂患者护理的重要性。
    VEXAS syndrome is a recently described autoinflammatory syndrome caused by the somatic acquisition of UBA1 mutations in myeloid precursors and is frequently associated with hematologic malignancies, chiefly myelodysplastic syndromes. Disease presentation can mimic several rheumatologic disorders, delaying the diagnosis. We describe a case of atypical presentation resembling late-onset axial spondylarthritis, later progressing to a systemic inflammatory syndrome with chondritis, cutaneous vasculitis, and transfusion-dependent anemia, requiring high doses of steroids. Ruxolitinib was used as the first steroid-sparing strategy without response. However, azacitidine showed activity in controlling both inflammation and the mutant clone. This case raises the question of whether azacitidine\'s anti-inflammatory effects are dependent on or independent of clonal control. We discuss the potential relevance of molecular remission in VEXAS syndrome and highlight the importance of a multidisciplinary team for the care of such complex patients.
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  • 文章类型: Case Reports
    化脓性骶髂关节炎是骶髂关节炎的感染性原因之一,很少见。在当前的文学中,到目前为止,已经报道了由几种微生物引起的化脓性骶髂关节炎的病例。该病例报告介绍了第一例由木葡萄球菌引起的化脓性骶髂关节炎,并伴有脓肿形成。
    Septic sacroiliitis is one of the infectious causes of sacroiliitis and it is seen rarely. In current literature, cases of septic sacroiliitis caused by several microorganisms have been reported so far. This case report presents the first case of septic sacroiliitis caused by Staphylococcus xylosus and also complicated with an abscess formation.
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  • 文章类型: Case Reports
    布鲁氏菌病仍然是中东的一种地方性人畜共患病,特别是在黎巴嫩,由于大量食用生肉和未经巴氏消毒的奶酪。在这份报告中,我们介绍了一个21岁女孩的病例,她在持续发烧和盗汗的调查中被诊断出患有布鲁氏菌病,这是由布鲁氏菌的1/160升高的布鲁氏菌凝集滴度证实的。和1/1280的间接库姆斯。不幸的是,由于不遵守规定的抗生素方案,她的病情有所进展,导致梨状肌炎和骶髂关节炎,布鲁氏菌病的不寻常并发症。在包括每日静脉注射庆大霉素5mg/kg和利福平300mgTID的治疗方案后,出现了消退,持续两周,多西环素100mgBID,持续12周。此外,我们进行了文献综述,这表明这种罕见并发症的诊断和成像标准仍不清楚,以及缺乏普遍认可的治疗指南。布鲁氏菌-当患者出现发烧和背痛时,应怀疑肌炎。
    Brucellosis remains an endemic zoonosis in the Middle East, particularly in Lebanon, owing to the high consumption of raw meat and unpasteurized cheese. In this report, we present the case of a twenty-one-year-old girl who was diagnosed with brucellosis during the investigation of persistent fever and night sweats that was confirmed by an elevated Brucella agglutination titer at 1/160 for Brucella melitensis species, and an indirect Coombs at 1/1280. Unfortunately, owing to non-adherence to the antibiotic regimen prescribed, her condition progressed, resulting in piriformis myositis with sacroiliitis, an unusual complication of brucellosis. Resolution occurred following a treatment regimen comprising intravenous gentamycin 5mg/kg daily for two weeks along with rifampin 300mg TID, and doxycycline 100mg BID for 12 weeks. Furthermore, we conducted a literature review, which revealed the diagnostic and imaging criteria for this uncommon complication to be still unclear, as well as the lack of universally approved guidelines for its treatment. Brucella - myositis should be suspected when patients present with fever and back pain.
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  • 文章类型: Case Reports
    梨状肌综合征是一种以髋部为特征的神经肌肉疾病,臀部,和腿部疼痛。轴向脊柱关节炎是主要影响骶髂关节和脊柱的风湿性疾病。由于它们的解剖接近,梨状肌综合征和骶髂关节炎之间的潜在关系已经讨论了一段时间。然而,文献综述显示,在患有轴性脊柱关节炎的个体中,没有关于梨状肌综合征的研究。这里,我们介绍了一个30岁女性患有轴向脊柱关节炎的病例,她出现了严重的下背部,臀部,尽管对轴向脊柱关节炎进行了初步治疗,但臀部疼痛仍然存在。我们首先通过体检重新评估了她的病情,磁共振成像,和梨状肌综合征的注射测试。经过全面评估,患者被诊断为中轴脊柱关节炎和梨状肌综合征。随后,制定了量身定制的治疗计划,解决这两个条件,经过3个月的疗程,我们获得了患者疼痛的显著减轻.这是文献中的首例病例报告,我们使用注射试验来确认轴性脊柱关节炎患者梨状肌综合征的诊断。因此,我们强烈主张将梨状肌综合征视为轴向脊柱关节炎患者疼痛的潜在病因。这种认识很重要,因为梨状肌综合征对非甾体类抗炎药没有足够的反应,并且可能导致不必要地使用生物疾病缓解抗风湿药。及时的识别和干预对于确保最佳的患者护理至关重要。
    Piriformis syndrome is a neuromuscular disorder characterized by hip, buttock, and leg pain. Axial spondyloarthritis is a rheumatic disease primarily affecting the sacroiliac joint and the spine. Due to their anatomical proximity, the potential relationship between piriformis syndrome and sacroiliitis has been discussed for some time. However, literature review revealed that there is no study on piriformis syndrome in individuals with axial spondyloarthritis. Here, we present the case of a 30-year-old female with axial spondyloarthritis who developed severe low back, hip, and buttock pain that persisted despite initial treatment for axial spondyloarthritis. We first re-evaluated her condition through physical examination, magnetic resonance imaging, and an injection test for piriformis syndrome. Following a comprehensive assessment, the patient was diagnosed with both axial spondyloarthritis and piriformis syndrome. Subsequently, a tailored treatment plan was devised, addressing both conditions, and after a 3-month course of treatment, we obtained significant reduction in pain of the patient. This is the first case report in literature, where we used injection test to confirm the diagnosis of the piriformis syndrome in a patient with axial spondyloarthritis. We therefore strongly advocate considering piriformis syndrome as a potential etiology for pain in individuals with axial spondyloarthritis consistently. This recognition is important as piriformis syndrome does not respond adequately to non-steroidal anti-inflammatory drugs and may lead to unnecessary use of biological disease-modifying antirheumatic drugs. Timely identification and intervention are imperative in ensuring optimal patient care.
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  • 文章类型: Case Reports
    急性阑尾炎是世界上最常见的腹部外科急症,通常需要手术干预。阑尾炎的并发症之一是脓肿形成。在极少数情况下,局部脓肿可以发生在相邻的器官中,如髂肌和腰大肌。继发于,或者伴随着,急性阑尾炎极为罕见。然而,漏诊其中一种或两种情况都可能导致严重的并发症,包括死亡率。
    方法:一名27岁男性患者就诊于急诊科,有急性严重右髋部疼痛病史,该疼痛因运动而加重,并伴有恶心和呕吐。CT提示急性单纯性阑尾炎,无局部污染。他接受了紧急腹腔镜检查,显示阑尾轻度炎症,并进行了阑尾切除术。手术后几小时他就出现了败血症,导致入院高度依赖护理单位进行密切观察。在第二天的审查中,他报告了持续的右髋部疼痛和下背部疼痛,新发作不能负重。进行了MRI扫描,显示右骶髂关节周围有感染特征,金黄色葡萄球菌在他的血液培养物中生长。然后诊断为急性化脓性骶髂关节炎。患者接受静脉抗生素治疗共四周,随后口服抗生素两周。
    急性化脓性骶髂关节炎是可以模拟急腹症的罕见病症之一,在这种情况下,急性阑尾炎。MRI是骶髂关节炎的最佳诊断方式,与阑尾炎的CT相比。在大多数急性阑尾炎病例中,血液培养中可见混合细菌,包括需氧菌和厌氧菌,而金黄色葡萄球菌主要见于急性化脓性骶髂关节炎。据报道,金黄色葡萄球菌引起的阑尾炎的病例不到3.7%。早期诊断其中一种或两种情况可以显着减少并发症,更重要的是,加快实施适当的治疗。
    结论:在我们的案例中,我们提出了一种联合急性阑尾炎,急性骶髂关节炎和金黄色葡萄球菌败血症,并证明急性化脓性骶髂关节炎可能是急性阑尾炎的罕见并发症。因此,在适当的临床方案中,应考虑高临床怀疑指数.
    UNASSIGNED: Acute appendicitis is the most common abdominal surgical emergency in the world and often requires surgical intervention. One of the complications of appendicitis is abscess formation. In rare cases, a localised abscess can occur in the adjacent organs, such as the iliac and psoas muscles. Sacroiliitis occurring secondary to, or concomitant with, acute appendicitis is extremely rare. However, a missed diagnosis of either or both conditions can lead to serious complications, including mortality.
    METHODS: A 27-year-old male patient presented to the emergency department with a history of acute severe right hip pain that was aggravated by movement and associated with nausea and vomiting. CT suggested acute uncomplicated appendicitis with no localised contamination. He underwent an emergent laparoscopy which showed mild appendiceal inflammation and appendicectomy was performed. He became septic a few hours after the operation, resulting in admission to the high dependency care unit for close observation. On review the following day, he reported ongoing right hip pain and lower back pain with a new onset inability to weight-bear. An MRI scan was performed which showed features of infection around the right sacroiliac joint and Staphylococcus aureus grew in his blood culture. A diagnosis of acute pyogenic sacroiliitis was then made. The patient was treated with IV antibiotics for a total of four weeks, followed by two weeks of oral antibiotics.
    UNASSIGNED: Acute pyogenic sacroiliitis is one of the rarer conditions seen that can mimic the acute abdomen, in this case acute appendicitis. MRI is the best diagnostic modality in sacroiliitis, in comparison to CT for appendicitis. In most cases of acute appendicitis, mixed bacteria including aerobes and anaerobes are seen in the blood culture while staphylococcus aureus is seen mostly in acute pyogenic sacroiliitis. Staphylococcus aureus-induced appendicitis is reported in less than 3.7 % of cases. An early diagnosis of either or both conditions can significantly reduce complications and, more importantly, expedite implementation of appropriate treatment.
    CONCLUSIONS: In our case we present a combination acute appendicitis, acute sacroiliitis and staphylococcus aureus septicaemia and provide proof that acute pyogenic sacroiliitis can be a rare complication of acute appendicitis. Thus, a high clinical index of suspicion should be considered in the appropriate clinical scenario.
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  • 文章类型: Case Reports
    家族性地中海热和强直性脊柱炎的关联很少见,但对于有FMF病史且出现背痛或其他风湿病症状的患者,必须考虑这种诊断。
    家族性地中海热(FMF)是一种遗传性炎症性疾病,以反复发热为特征,腹痛,和关节痛.强直性脊柱炎(AS)是一种影响脊柱关节的慢性炎症性疾病。FMF和AS的关联是罕见的。我们报告了一名22岁的男性患者,其父亲有FMF病史和FMF家族史,出现炎症性背痛的人。MRI发现病人有骶髂关节炎,这是AS的特征。患者的HLA-B27阴性,这是一种通常与AS相关的遗传标记。此病例报告强调了在有FMF病史且出现背痛症状或其他风湿病的患者中考虑AS的重要性。
    UNASSIGNED: The association of familial Mediterranean fever and ankylosing spondylitis is rare, but it is essential to consider this diagnosis in patients with a history of FMF who develop symptoms of back pain or other rheumatologic conditions.
    UNASSIGNED: Familial Mediterranean fever (FMF) is an inherited inflammatory disorder characterized by recurrent fever episodes, abdominal pain, and arthralgia. Ankylosing spondylitis (AS) is a chronic inflammatory disease that affects the spine\'s joints. The association of FMF and AS is rare. We report the case of a 22-year-old male patient with a history of FMF and a positive family history of FMF in his father, who presented with inflammatory back pain. The patient was found to have sacroiliitis on MRI, which is a characteristic feature of AS. The patient was negative for HLA-B27, a genetic marker often associated with AS. This case report highlights the importance of considering AS in patients with a history of FMF who develop back pain symptoms or other rheumatologic conditions.
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  • 文章类型: Review
    背景:C1-C2半脱位是附着性关节炎(ERA)的一种罕见并发症。如果不及时治疗,它可能导致功能障碍或颈脊髓压迫。本研究旨在强调ERA中C1-C2半脱位的管理要点。
    方法:我们介绍了2例C1-C2半脱位:一个8岁的ERA男孩和16岁的ERA男孩伴双侧骶髂关节炎。对文献中的10例ERA进行了回顾。C1-C2半脱位的诊断主要基于X线片和颈椎计算机断层扫描。所有患者均接受非甾体抗炎药治疗。对6例ERA患者进行了手术治疗,以进行宫颈融合。大多数患有骶髂关节炎的ERA患者具有颈领保护。未报告治疗后的神经系统异常。尽管使用了颈圈,在两名未经手术治疗的ERA患者中发现了宫颈融合和持续强直。
    结论:应优先考虑保护颈椎和排除脊髓压迫,除了控制ERA的潜在炎症。在排除严重的宫颈炎症后,可以应用宫颈露背牵引。为了降低并发症的风险,ERA中C1-C2半脱位的早期识别和适当治疗至关重要.
    BACKGROUND: C1-C2 subluxation is a rare complication of enthesitis-related arthritis (ERA). If left untreated, it may lead to functional impairment or cervical spinal cord compression. This study aims to highlight key points regarding the management of C1-C2 subluxation in ERA.
    METHODS: We present two cases of C1-C2 subluxation: an 8-year-old boy with ERA and 16-year-old boy with ERA with bilateral sacroiliitis. Ten cases of ERA in the literature were reviewed. The diagnosis of C1-C2 subluxation is mostly based on radiographs and cervical spine computed tomography. All patients were treated with non-steroidal anti-inflammatory drugs. Six ERA patients were treated surgically for cervical fusion. Most ERA patients with sacroiliitis had cervical collar protection. Neurologic abnormalities after treatment were not reported. Despite the use of cervical collar, cervical fusion and persisting ankylosis were found in two ERA patients with sacroiliitis without surgical treatment.
    CONCLUSIONS: Cervical spine protection and ruling out spinal cord compression should be prioritized, in addition to controlling the underlying inflammation in ERA. Cervical halter traction may be applied after severe cervical inflammation is excluded. To reduce the risk of complications, early recognition and appropriate treatments of C1-C2 subluxation in ERA are essential.
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  • 文章类型: Review
    目的:骶髂关节(SIJ)功能障碍是背痛的重要原因。尽管最近在微创(MIS)SIJ融合方面取得了进展,融合率仍然存在争议。这项研究旨在证明MISSIJ融合中的导航剥脱和直接关节固定术技术将获得令人满意的融合率和患者报告的结果(PRO)。
    方法:作者回顾性回顾了2018年至2021年连续接受MISSIJ融合的患者。使用圆柱形螺纹植入物进行SIJ融合,并使用O形臂手术成像系统和StealthStation进行SIJ脱皮。主要结果是融合,术后6、9和12个月使用CT进行评估。次要结果包括翻修手术,翻修手术的时间,背痛的视觉模拟量表(VAS)评分,和Oswestry残疾指数(ODI),术前和术后6个月和12个月测量。还收集了患者的人口统计学和围手术期数据。随着时间的推移,使用方差分析进行分析,然后进行事后分析。
    结果:本研究纳入118例患者。平均(±SD)患者年龄为58.56±13.12岁,大多数患者为女性(68.6%vs31.4%男性)。有19名吸烟者(16.1%),平均BMI为29.92±6.73。112例患者(94.9%)在CT上成功融合。ODI从基线到6个月(Δ7.73,95%CI2.43-13.03,p=0.002)和从基线到12个月(Δ7.54,95%CI1.65-13.43,p=0.008)显着改善。同样,VAS背痛评分从基线到6个月(Δ2.31,95%CI1.07-3.56,p<0.001)和从基线到12个月(Δ1.63,95%CI0.25-3.00,p=0.015)显着改善。
    结论:MISSIJ融合结合导航剥脱术和直接关节固定术与高融合率和残疾和疼痛评分的显著改善相关。有必要对这种技术进行进一步的前瞻性研究。
    Sacroiliac joint (SIJ) dysfunction is a significant cause of back pain. Despite recent advances in minimally invasive (MIS) SIJ fusion, the fusion rate remains controversial. This study sought to demonstrate that a navigated decortication and direct arthrodesis technique in MIS SIJ fusion would result in satisfactory fusion rates and patient-reported outcomes (PROs).
    The authors retrospectively reviewed consecutive patients who underwent MIS SIJ fusion from 2018 to 2021. SIJ fusion was performed using cylindrical threaded implants and SIJ decortication employing the O-arm surgical imaging system and StealthStation. The primary outcome was fusion, evaluated using CT at 6, 9, and 12 months postoperatively. Secondary outcomes included revision surgery, time to revision surgery, visual analog scale (VAS) score for back pain, and the Oswestry Disability Index (ODI), measured preoperatively and 6 and 12 months postoperatively. Patient demographics and perioperative data were also collected. PROs over time were analyzed using ANOVA followed by a post hoc analysis.
    One hundred eighteen patients were included in this study. The mean (± SD) patient age was 58.56 ± 13.12 years, and most patients were female (68.6% vs 31.4% male). There were 19 smokers (16.1%) with an average BMI of 29.92 ± 6.73. One hundred twelve patients (94.9%) underwent successful fusion on CT. The ODI improved significantly from baseline to 6 months (Δ7.73, 95% CI 2.43-13.03, p = 0.002) and from baseline to 12 months (Δ7.54, 95% CI 1.65-13.43, p = 0.008). Similarly, VAS back pain scores improved significantly from baseline to 6 months (Δ2.31, 95% CI 1.07-3.56, p < 0.001) and from baseline to 12 months (Δ1.63, 95% CI 0.25-3.00, p = 0.015).
    MIS SIJ fusion with navigated decortication and direct arthrodesis was associated with a high fusion rate and significant improvement in disability and pain scores. Further prospective studies examining this technique are warranted.
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