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2.
Clin Rheumatol ; 39(2): 571-574, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31713735

ABSTRACT

OBJECTIVE: Crowned dens syndrome (CDS) is defined as acute cervical or occipital pain due to a local inflammatory reaction related to calcifications in the ligaments surrounding the odontoid process. Virtually, all previous descriptions of CDS have related to calcium pyrophosphate dehydrate (CPPD) arthropathy. METHODS: We prospectively identified a total of twenty-four consecutive inpatients with Crowned dens syndrome from January 2016 to December 2017 in our institution. RESULTS: All patients (age range 54 to 87 years, 67% females) presented with acute onset pain in the upper neck and/or occiput accompanied with extreme neck stiffness. Most patients (79%) had elevated inflammatory markers. Four patients underwent temporal artery biopsy, which was negative for arteritis in all cases, and one was subjected to lumbar puncture, which was non-contributory. Seventeen patients (71%) had known rheumatic disease on presentation: 10 patients had the diagnosis of calcium pyrophosphate dehydrate arthropathy, 3 patients had ankylosing spondylitis, 2 patients had rheumatoid arthritis, 1 patient had Behcet's disease, and 1 suffered from Familial Mediterranean Fever. In 4 more patients, crowned dens syndrome was the presenting symptom of calcium pyrophosphate dehydrate disease. All patients were treated with glucocorticoids as 0.5 mg/kg prednisone plus colchicine 0.5 mg bid resulting in dramatic improvement in both clinical (head/neck pain alleviated and cervical spinal mobility regained) and laboratory measures. CONCLUSIONS: Crowned dens syndrome should be considered, and craniocervical junction imaged in the context of acute cervical or occipital pain with stiffness and elevated inflammation markers not only in patients previously diagnosed with calcium pyrophosphate dehydrate arthropathy but also in diverse clinical settings.Key Points• This report highlights that crowned dens syndrome should be considered in various clinical setting besides calcium pyrophosphate dehydrate (CPPD) arthropathy.• Vigilance to this syndrome allows rapid treatment and may spare the patient unnecessary invasive procedures (i.e., temporal artery biopsy or lumbar puncture).


Subject(s)
Chondrocalcinosis/diagnosis , Ligaments/diagnostic imaging , Odontoid Process/diagnostic imaging , Rheumatic Diseases/complications , Spinal Diseases/diagnosis , Aged , Aged, 80 and over , Arthritis, Rheumatoid/complications , Behcet Syndrome/complications , Chondrocalcinosis/complications , Chondrocalcinosis/physiopathology , Familial Mediterranean Fever/complications , Female , Humans , Inflammation , Male , Middle Aged , Neck Pain/physiopathology , Occipital Lobe , Spinal Diseases/complications , Spinal Diseases/physiopathology , Spondylitis, Ankylosing/complications , Syndrome , Tomography, X-Ray Computed
3.
Clin Rheumatol ; 38(10): 2825-2833, 2019 Oct.
Article in English | MEDLINE | ID: mdl-30972576

ABSTRACT

Polyarteritis nodosa (PAN) is a necrotizing vasculitis predominantly affecting medium and small size arteries. Cyclophosphamide, a drug with narrow therapeutic range and poor safety profile, constitutes the treatment of choice for PAN vasculitis with major organ involvement. To describe our clinical experience in treating refractory PAN with infliximab (a TNF inhibitor), a drug with good tolerability and better safety profile than cyclophosphamide. Twenty-six PAN patients were admitted to our rheumatology unit between 2006 and 2017, of whom nine patients, with severe and refractory disease, were treated with infliximab after failure of standard treatment. We describe herein the patients' characteristics, clinical manifestations, severity and response to infliximab treatment and review the current literature. Complete remission was defined as the absence of features of active disease and withdrawal of prednisone therapy. Significant improvement was defined as clinical improvement and prednisone dose reduction of at least 50% or a 50% reduction in immune modulatory medications other than prednisone. After 4 months of treatment, 8/9 (89%) patients achieved significant improvement, with two of them achieving complete remission. We suggest that anti-TNF agents, and in particular infliximab, are relatively safe and efficacious treatment options in refractory PAN. A randomized controlled trial should be done in order to objectively evaluate infliximab in PAN.


Subject(s)
Infliximab/therapeutic use , Polyarteritis Nodosa/drug therapy , Polyarteritis Nodosa/immunology , Tumor Necrosis Factor Inhibitors/therapeutic use , Cyclophosphamide/therapeutic use , Disease Progression , Humans , Immunosuppressive Agents/therapeutic use , Patient Safety , Prednisone/therapeutic use , Remission Induction , Treatment Outcome , Vasculitis/drug therapy , Vasculitis/immunology
4.
J Inflamm Res ; 11: 339-344, 2018.
Article in English | MEDLINE | ID: mdl-30237730

ABSTRACT

Sacroiliitis, inflammation of the sacroiliac joint (SIJ), may be associated with many rheumatic and nonrheumatic disorders. The diagnosis of sacroiliitis may be difficult in many patients, and awareness of its typical manifestations along with recognition of its diverse presentations and cognizance of the limitations of today's imaging modalities are critical to good clinical practice. This review presents the didactic approach to the early diagnosis of sacroiliitis in patients with suspected axial spondyloarthritis and other nosologic entities, discussing also differential interpretation of information acquired from patients' histories, physical examination, and imaging.

6.
Fertil Steril ; 99(2): 377-81, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23062734

ABSTRACT

OBJECTIVE: To examine the prevalence, etiology, risk factors, and outcomes of liver abnormality in pregnancy, in a tertiary medical center, and to study the potential impact of artificial reproduction techniques (ART) on the incidence and the outcome of pregnancy-related liver abnormality. DESIGN: A retrospective case-control study using an electronic database and patients' files. SETTING: Tertiary referral center. PATIENT(S): Women in the third trimester of pregnancy who were hospitalized for delivery. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Development of significant elevation of alanine aminotransferase (ALT ≥ 100 IU/L). Secondary outcomes included development of maternal and fetal complications. RESULT(S): The upper limit of normal of ALT was ≥ 1.5 times and it occurred in 440 (1.6%) pregnancies; of those, 228 (0.8%) had ALT ≥ 100 IU/L. The etiology of significant liver test abnormality was idiopathic in 47% of patients. Compared with spontaneous pregnancies (295/23,793), ART was significantly associated with liver test abnormality (145/4, 520). The presence of ALT ≥ 100 IU/L in the third trimester was associated with higher rates of cesarean sections, prematurity, low birthweight, and fetal complications. CONCLUSION(S): A definite etiology was not determined in about half of pregnancy-associated liver test abnormality. The ART was significantly associated with liver test elevation. Significant liver test abnormality in the third trimester may have an impact on maternal and fetal/neonatal outcomes.


Subject(s)
Infertility/epidemiology , Infertility/therapy , Liver Diseases/epidemiology , Pregnancy Complications/epidemiology , Reproductive Techniques, Assisted/statistics & numerical data , Adult , Causality , Female , Humans , Incidence , Israel/epidemiology , Liver Diseases/diagnosis , Liver Function Tests , Middle Aged , Pregnancy , Pregnancy Complications/diagnosis , Retrospective Studies , Statistics as Topic , Young Adult
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