M. Matossian, Carrie E Crook, Alec Goldberg, A. Stathopoulos, J. Tien, S. Sheth, Osaid Saqqa Christopher Dale Shamburger
{"title":"Domino effect in a patient with Epstein-Barr Virus infection and autoimmunity: A case report","authors":"M. Matossian, Carrie E Crook, Alec Goldberg, A. Stathopoulos, J. Tien, S. Sheth, Osaid Saqqa Christopher Dale Shamburger","doi":"10.37532/1758-4272.2020.15(6).193-197","DOIUrl":"https://doi.org/10.37532/1758-4272.2020.15(6).193-197","url":null,"abstract":"The link between autoimmune diseases and viral infections has been characterized, but specific mechanisms behind this association remain a current area of investigation. Whether viral infections trigger or unmask autoimmunity, or if the pathologies occur concurrently, is not yet completely understood. Specifically, Epstein - Barr virus (EBV) is implicated in several autoimmune disorders, including Systemic Lupus Erythematosus (SLE). It is hypothesized that common immunologic pathways are activated in the two pathologic states. This case report is an example of this confusing presentation, and the importance of recognizing the association between autoimmunity and viral infections. This patient presented with symptoms concerning for SLE and hepatic autoimmunity with serology suggesting a recent infection with EBV. Given this complicated presentation, it is difficult to determine which disease state presented first in patients with evidence of both SLE and EBV infection and whether this information is clinically relevant for ongoing treatment and monitoring. Here, we provide an in-depth discussion of current genomic and immunological research that supports the associations amongst these disease pathologies.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"64 1","pages":"193"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84959354","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Transient Osteoporosis of hip during pregnancy","authors":"K. Nassar, Omar Amriss Saadia Janani","doi":"10.37532/1758-4272.2020.15(6).175-177","DOIUrl":"https://doi.org/10.37532/1758-4272.2020.15(6).175-177","url":null,"abstract":"Transient osteoporosis of pregnancy is a rare condition that causes temporary bone loss. The syndrome is characterized by self-limited course and spontaneous resolution after 6 to 12 months. Several pathogenesis hypotheses have been proposed. Clinical manifestations include sudden onset of pain. MRI is considered the best diagnostic test for this condition in regard to sensitivity and specificity and in monitoring of disease progression. We report a 38-year-old pregnant woman presented during the third trimester of her pregnancy with right hip pain that became progressively severe. Imaging of her bilateral hips with MRI demonstrated increased signal in the bone-marrow of the right femur head and neck with minimal effusion. Repeat MRI performed at five months postpartum revealed resolution of edema.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"11 1","pages":"175"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87065898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Occurrence of cervical spine arthritis with prominent bone edema highly responsive to adalimumab in a patient with psoriatic peripheral arthritis and long-standing remission","authors":"M. C. Miceli, L. Bruno, C. Provenzano","doi":"10.37532/1758-4272.2020.15(3).60-63","DOIUrl":"https://doi.org/10.37532/1758-4272.2020.15(3).60-63","url":null,"abstract":"Cervical spine involvement frequently occurs in patients with psoriatic arthritis (PsA) even in absence of sacroiliitis. Long disease duration, high disease activity in the first five years and presence of peripheral involvement are all predictors of this peculiar articular involvement. We describe the case of a PsA patient, with an initial oligoarthritis pattern of disease highly responsive to etanercept monotherapy and long-standing clinical remission, who developed cervical spine involvement with bone marrow edema of odontoid process and early atlo-axial instability. Notably, he did not exhibit any other clinical symptom or sign of disease activity and was highly responsive to switching to a second anti-TNF drug (adalimumab). The case stresses the importance of strict monitoring PsA patients and considering the possible changing pattern of disease. Early identification of cervical spine involvement requires proper use and interpretation of imaging techniques. Interestingly different articular manifestations of PsA may show different response to therapy even in the same patient.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"6 1","pages":"60"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78526730","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Shaima N. Elgenaid, Z. I. Mahmoud, M. Essa, Shahd H. A. Elwidaa, Latifa M. Elsheikh, A. Abdelhalim, M. Hussein, Mutwaly Defealla Yousif Haron, Ayman Ahmed
{"title":"Rheumatoid arthritis and gouty arthritis in an adult patient with Down's syndrome","authors":"Shaima N. Elgenaid, Z. I. Mahmoud, M. Essa, Shahd H. A. Elwidaa, Latifa M. Elsheikh, A. Abdelhalim, M. Hussein, Mutwaly Defealla Yousif Haron, Ayman Ahmed","doi":"10.37532/1758-4272.2019.15(2).18-20","DOIUrl":"https://doi.org/10.37532/1758-4272.2019.15(2).18-20","url":null,"abstract":"Down’s syndrome is a chromosomal disorder caused by trisomy of chromosome 21. It presents with different phenotypes including autoimmune diseases and arthritis. The aim of this case report is to describe and document rheumatoid arthritis and gouty arthritis in patient with Down's syndrome. Here we are reporting a case of 44 year-old female with Down's syndrome who was diagnosed with epilepsy 10 months ago. She presented with a one-year history of swelling of knees, bilateral big toes and the metacrpopharyngal joints. In addition, on examination she had ulnar deviation of her hands, limited range of motion and severe tenderness of the noted joints, hair loss and scoliosis. Her serum uric acid, ESR and CRP levels were elevated and rheumatoid factor was strongly positive; however, ANA profile and anti CCP antibodies were negative. Therefore, she was diagnosed with rheumatoid arthritis and gouty arthritis. Currently she is on hydroxychoroquine, allopurinl, baclofen, methotrexate, folic acid and sodium valproate.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"23 1","pages":"18"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76734564","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Pregabalin-induced focal myositis: A report of two cases and review of literature","authors":"S. Manohar","doi":"10.37532/1758-4272.2020.15(4).114-118","DOIUrl":"https://doi.org/10.37532/1758-4272.2020.15(4).114-118","url":null,"abstract":"Background: Drug-induced myopathy should be on the differential diagnosis in patients with non-traumatic muscle pain. It is important to consider the diagnosis as symptoms typically abate with removal of the offending agent. Case: Two elderly females presented separately with complaint of lower extremity pain and swelling. There was no elevation in inflammatory markers or muscle enzymes in either case. MRI revealed inflammatory changes on T2-weighted sequences. Both patients experienced rapid improvement of symptoms with discontinuation of pregabalin. Discussion: Medication-induced myositis should be considered in patients presenting with muscle complaints. Due to the overall high prevalence of pregabalin in the management of chronic pain, it is important to consider its role in the pathogenesis of focal myositis.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"768 1","pages":"114"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77525749","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kathlyn Camargo, A. Chawla, Ashwini Komarla Sujatha Vuyyuru
{"title":"Relapsing polychondritis presenting in a patient with cryptogenic organizing pneumonia","authors":"Kathlyn Camargo, A. Chawla, Ashwini Komarla Sujatha Vuyyuru","doi":"10.37532/1758-4272.2020.15(5).140-142","DOIUrl":"https://doi.org/10.37532/1758-4272.2020.15(5).140-142","url":null,"abstract":"Relapsing Polychondritis (RP) is an autoimmune disease that affects cartilaginous tissues in the body, including lower respiratory tract. Involvement of the pulmonary interstitium is very rare. We present a 67-year-old Caucasian man presented to the clinic with one-year of recurrent dyspnea and dry cough along with worsening anemia and thrombocytopenia. CT of the chest demonstrated diffuse, bilateral (left > right) multifocal peribronchovascular ground glass opacities with mediastinal lymphadenopathy. All rheumatologic serology workup was negative as well as infectious workup. Lung biopsy of the left lower lobe consolidation showed plugs of fibroblastic tissue incorporated into alveolar walls and airspaces consistent with COP. No features of malignancy or granulomatous process were seen. Oral prednisone was started and tapered over the next 3 months with improvement of his respiratory symptoms. Two weeks later, he developed bilateral ear pain/redness and conjunctivitis. CT of the sinuses revealed mild prominence in the left nasopharyngeal soft tissue. Biopsy of this lesion showed inflammatory infiltrative changes and RP was diagnosed. Adalimumab was started. However, the patient developed worsening dyspnea that required supplemental oxygen and hospitalization. High dose steroids were again added, along with oral cyclophosphamide. The patient had significant clinical and radiological improvement over the next 6 months. Interstitial lung disease has been rarely associated with RP. Most of the lower respiratory track involvement is in the trachea. We present a case of cryptogenic organizing pneumonia in association with relapsing polychondritis.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"10 1","pages":"140"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74283833","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. Boussaid, N. B. Ayed, M. Bani, Takoua Issaoui, S. Jammali, E. Hannech, H. Sahli, E. Cheour, S. Elleuch
{"title":"Impact of Rheumatoid Arthritis and disease activity on work productivity and quality of life","authors":"S. Boussaid, N. B. Ayed, M. Bani, Takoua Issaoui, S. Jammali, E. Hannech, H. Sahli, E. Cheour, S. Elleuch","doi":"10.37532/1758-4272.2020.15(5).123-127","DOIUrl":"https://doi.org/10.37532/1758-4272.2020.15(5).123-127","url":null,"abstract":"Introduction: Rheumatoid Arthritis (RA) physical disability can impair the Quality of Life (QoL) and professional activity. Aim of the work: to assess the impact of RA on work productivity and functional impairment in Tunisian patients. Relation to the disease activity was also considered. Patients and mehods: The study included 25 RA patients having a professional occupation at the time of disease onset. The Disease Activity Score (DAS28), Health Assessment Questionnaire (HAQ) and 'Work Productivity and Activity Impairment' (WPAI) questionnaire were assessed. Results: The mean age of the patients was 50.4 ± 8.3 years with a female: male ratio of 1.08. The mean age at onset was 40.6 ± 9.8 years and the mean disease duration was 9.8 ± 9.68 years. The patients' occupation involved a manual job in 84% of cases. The mean of DAS28 was 4.3 ± 1.6; 72% had moderate to severe disease activity. The mean HAQ was 1.4 ± 0.7 and 76% had moderate to severe disability. The evaluation of the work productivity and activity impairment objectified an absenteeism of 30.7 ± 39.4%, presenteeism of 46.7 ± 26.4%, work productivity loss of 60.4 ± 33.8% and an activity impairment of 57.2 ± 25.4%. A significant correlation was noted between WPAI parameters and HAQ (p<0.0001) and of the decline in productivity and daily activity with DAS28 (p=0.01). Conclusion: Functional impairment and disease activity affected productivity and work ability in Tunisian RA patients. Absenteeism, increase of presenteeism, decline of productivity and daily activity were associated with the HAQ and the latter 2 with the disease activity but not with the age of patients or disease duration.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"60 1","pages":"123"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88016379","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Sonographic detection of sacroiliitis - An appraisal","authors":"Plamen Todorov Anastas Batalov","doi":"10.37532/1758-4272.2020.15(3).43-47","DOIUrl":"https://doi.org/10.37532/1758-4272.2020.15(3).43-47","url":null,"abstract":"In the last decade, rheumatology saw an exponential rise in the use of Musculoskeletal Ultrasound (MSUS) as a diagnostic imaging modality. The ability of MSUS to detect inflammation of the sacroiliac joints (SIJ) in Spondyloarthritis (SpA) was also tested. Studies on sacroiliitis utilized different MSUS technologies: B-Mode US (BM US) to search for intraarticular effusion, synovitis, and measure the joint width; color Doppler (CD US) to detect low velocity blood flow as a marker for inflammation and Contrast-Enhanced US (CE US), able to show increased vascularity in the deeper part of the SIJ. Though, in general, most of these studies have promising results in the ability of MSUS to detect sacroiliitis, there are some important limitations of this method due to both anatomical and technological reasoning. The aim of this narrative review is to briefly outline the new data on US application to diagnose sacroiliitis and to discuss it in relation with SIJ anatomy. In addition, some important pitfalls that could be encountered when scanning these joints are noted. Plamen Todorov*1,2 & Anastas Batalov1,2","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"7 1","pages":"43"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83602244","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"B-mode ultrasound in the uveitis in the psoriatic arthritis without skin lesion","authors":"J. Alex, R. Mendonça, V. Le, Rosaria Aquino","doi":"10.37532/1758-4272.2020.15(3).64-66","DOIUrl":"https://doi.org/10.37532/1758-4272.2020.15(3).64-66","url":null,"abstract":"Introduction: The involvement of inflammatory ocular and joint manifestations can be better evaluated by ultrasound, but the application of this image method in the eyes is a universe that is still very little explored in inflammatory joint diseases. Objective: The aim of this case report was to detect inflammatory ocular and joint changes by ultrasound with a high frequency linear probe in patients without prior established diagnosis. Case report: This case describes a caucasoid patient of the female sex, 32 years of age, without diagnosis. The patient referred red eyes when using a computer, with weak nails and left ankle arthritis, for 6 months. An ultrasound with 12 MHz high frequency linear probe was used to evaluate the eyes and a frequency of 15 to 18 MHZ for joint investigates. Discussion: The ultrasound showed in eyes the following findings: floating hypoecogenic images in vitreous humor more intensely to the left, characterizing vitritis, in all of the distal interphalangicas evaluated, with loss of the plate nail pattern trilaminar, effusion tibio - talar, tenosynovitis peroneus longus tendon and entesopathy Achilles tendon, without the presence of power Doppler. Conclusion: B-mode ultrasound can an important adjunct to the clinical evaluation in patients with arthritis e uveitis. Future studies will better signal the intensity of these findings of vitreous humor alterations, and also define this relationship with the subclinical and inflammatory, ocular and joint activity condition.","PeriodicalId":13740,"journal":{"name":"International Journal of Clinical Rheumatology","volume":"77 1","pages":"64"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79288363","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}