20 results match your criteria: "417 Army Share Fund Hospital (NIMTS)[Affiliation]"

Article Synopsis
  • * A unique case is presented where a patient with a long history of AS was diagnosed with FMF after experiencing recurrent symptoms; laboratory tests confirmed the condition.
  • * The patient's treatment with colchicine led to significant improvement, emphasizing the importance of recognizing the relationship between AS and FMF in medical practice.
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Assessment of extra-coronary peripheral arteriopathy in spontaneous coronary dissection: state of the art in non-invasive imaging techniques and future perspectives.

Eur Heart J Imaging Methods Pract

September 2023

Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, National and Heart Lung Institute, Imperial College London, Sydney St, London SW3 6NP, UK.

Article Synopsis
  • Spontaneous coronary artery dissection (SCAD) is a key cause of heart issues for women under 50, especially during pregnancy, connecting it to systemic arterial disorders like Ehlers-Danlos and Marfan syndromes.
  • It often coexists with conditions like fibromuscular dysplasia and other vascular abnormalities, highlighting a genetic link to SCAD.
  • The American Heart Association suggests using advanced imaging, like computed tomography angiography (CTA) and magnetic resonance angiography (MRA), for better diagnosis of related vascular disorders, focusing on the effectiveness of these non-invasive methods.
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Article Synopsis
  • * There are concerns that COVID-19 vaccines might cause autoimmune diseases in previously healthy people, with a case reported of a patient developing anti-MDA5 positive dermatomyositis after receiving the third vaccine dose.
  • * The patient experienced severe symptoms and required multiple treatments, including corticosteroids and rituximab, highlighting the need for further investigation on the rare autoimmune responses potentially linked to COVID-19 vaccines.
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Guest Editors Bio.

Transfus Apher Sci

February 2024

Nephrology Department at Athens, 417 Army Share Fund Hospital (NIMTS), Greece. Electronic address:

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Article Synopsis
  • * A case study of a 66-year-old man showed that his back and knee pain were linked to celiac disease, along with osteoporosis and vitamin D deficiency, discovered through thorough testing.
  • * Following a gluten-free diet and supplements for vitamin D and calcium led to major improvements in his symptoms and bone mineral density after six months, highlighting the need for rheumatologists to recognize the musculoskeletal symptoms associated with CD.
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Cranial giant cell arteritis mimickers: A masquerade to unveil.

Autoimmun Rev

May 2022

Rheumatology Unit, First Department of Propaedeutic Internal Medicine, School of Medicine, Laiko Hospital, National and Kapodistrian University of Athens, Athens, Greece.

Giant cell arteritis (GCA) is a large-vessel vasculitis that affects cranial and extra-cranial arteries. Extra-cranial GCA presents mainly with non-specific symptoms and the differential diagnosis is very broad, while the cranial form has more typical clinical picture and physicians have a lower threshold for diagnosis and treatment. Although temporal artery biopsy (TAB) has an established role, ultrasound (US) is being increasingly used as the first-line imaging modality in suspected GCA.

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Article Synopsis
  • A 55-year-old woman diagnosed with migratory osteoporosis (MO) experienced pain and bone marrow edema in her left ankle, initially treated with non-weight-bearing methods and risedronate.
  • Despite some initial improvement, the condition worsened, affecting her foot and left hip, indicating that the initial treatment was ineffective.
  • Ultimately, a single infusion of zoledronic acid led to complete pain relief and resolution of bone marrow edema, allowing her to return to daily activities, highlighting the need for more robust treatment for MO.
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Article Synopsis
  • - A 63-year-old man initially presented with symptoms resembling giant cell arteritis (GCA) but was later diagnosed with microscopic polyangiitis (MPA) after further evaluation.
  • - His treatment began with corticosteroids for what was thought to be GCA, but after complications arose, tests revealed positive p-ANCA antibodies.
  • - The patient underwent successful treatment with cyclophosphamide, achieving remission from MPA, and has remained symptom-free for two years.
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Article Synopsis
  • Rituximab (RTX) treatment for rheumatoid arthritis (RA) can lead to hypogammaglobulinemia (HGG), a decrease in immunoglobulin levels (IgG, IgM, IgA), affecting patient outcomes and infection rates.
  • In a study of 83 RA patients treated with RTX, nearly 43% experienced HGG, with lower baseline immunoglobulin levels predicting the occurrence of low IgG and low IgM.
  • Interestingly, patients who developed low IgM showed better disease activity outcomes, while the development of HGG did not result in a higher rate of serious infections.*
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Tuberculosis and targeted synthetic or biologic DMARDs, beyond tumor necrosis factor inhibitors.

Ther Adv Musculoskelet Dis

June 2020

Rheumatology Unit, First Department of Propaedeutic Internal Medicine, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Article Synopsis
  • - Patients with autoimmune rheumatic diseases (ARD) have a heightened risk of developing tuberculosis (TB), especially when treated with tumor necrosis factor inhibitors (TNFi) and glucocorticoids, which can lead to latent TB reactivation.
  • - Recent biologic and targeted synthetic DMARDs (like rituximab and JAK inhibitors) seem to show a lower TB risk compared to TNFi, although more real-life data is needed for a clearer understanding.
  • - It's crucial to screen for latent TB before starting any DMARD treatment, and further studies are necessary to compare TB risks among different ARD treatment options.
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Article Synopsis
  • Rheumatoid arthritis (RA) patients may face hematologic issues, but the link between RA and myelodysplastic syndrome (MDS) is not well established.
  • A limited amount of research exists regarding treatment options for RA patients who also develop MDS.
  • This report discusses a case where a patient with RA and worsening MDS was effectively treated using a combination of rituximab and lenalidomide.
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