Publications by authors named "Debashis Maikap"

Article Synopsis
  • The review examines whether biologic therapies are effective for treating reactive arthritis (ReA), an inflammatory joint condition caused by infections.
  • Recent studies highlight that biologics like anti-TNF agents, anti-IL17, and anti-IL6 are effective and generally safe for patients with refractory ReA, showing significant clinical improvement.
  • The authors emphasize the necessity for controlled trials to enhance the scientific understanding and clinical decision-making for patients not responding to standard treatments.
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Article Synopsis
  • The study aimed to compare nailfold capillaroscopy (NFC) findings and lung function between patients with Mixed Connective Tissue Disease associated Interstitial Lung Disease (MCTD-ILD) and those with Systemic Sclerosis associated Interstitial Lung Disease (SSc-ILD).
  • The results indicated that significant capillaroscopic changes were more common in SSc-ILD patients (92%) compared to MCTD-ILD patients (72.3%), with SSc-ILD patients also showing greater lung function restrictions.
  • The findings suggest that NFC can effectively identify lung damage severity, as more severe capillary abnormalities correlate with worse lung function in these conditions.
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Tofacitinib, a Janus kinase inhibitor, has been recently investigated as a potential therapy for refractory scleritis. Despite treatment with systemic immunosuppressive agents, scleritis is refractory to conventional therapy in a significant number of patients. Hereby, we report the use of tofacitinib as a steroid-sparing immunomodulatory agent in three patients with refractory scleritis who were either recalcitrant or intolerant to conventional therapy.

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Objective: To study the clinical effectiveness and safety of Tofacitinib in refractory Takayasu arteritis (TAK).

Methods: This study was conducted from September 2021 to June 2022. Ten cases of refractory TAK patients were enrolled.

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Musculoskeletal manifestations of systemic sclerosis (SSc) are frequent and may be one of the early manifestations of the disease. However, arthralgia, pain and stiffness without frank arthritis usually constitute the clinical picture, while overlap syndromes such as rheumatoid-like polyarthritis can dominate when the arthritis is erosive. Hereby, we report a case of primary SSc presenting as frank erosive arthritis involving small and large joints mimicking rheumatoid arthritis, unresponsive to methotrexate, which was successfully treated with tofacitinib.

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Systemic lupus erythematosus (SLE) is a multi-system autoimmune disease with varied dermatological manifestations that are almost universal. Overall, lupus disease has a major effect on the quality of life in these patients. We assessed the extent of cutaneous disease in early lupus and correlated it with the SLE quality-of-life (SLEQoL) index and disease activity measures.

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Article Synopsis
  • - Neuropsychiatric issues, including rare movement disorders like Parkinsonism, can affect up to 50% of systemic lupus erythematosus (SLE) patients, but only a small fraction experience Parkinsonism symptoms.
  • - A detailed case study of a 50-year-old woman showed symptoms like slowed movements and speech, alongside laboratory results indicating active SLE, including high anti-dsDNA levels and proteinuria; she responded well to treatment with steroids and cyclophosphamide.
  • - The low prevalence of Parkinsonism in SLE cases highlights the need for clinicians to be vigilant; immunosuppressive therapy can lead to significant improvement and recovery for affected patients.
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Introduction: Restless leg syndrome (RLS) is a neurological disorder characterized by an uncontrollable desire to move legs along with abnormal sensations, particularly at night, which can lead to sleep disturbance. RLS may mimic rheumatic diseases or can be associated with them, hence their identification and treatment are important to improve sleep quality and overall quality of life in rheumatic diseases.

Methods: We conducted a search of the PubMed, SCOPUS, and EMBASE databases to identify studies reporting a prevalence of RLS in patients with rheumatic disease.

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Article Synopsis
  • Lupus can impact vision mainly through conditions like vasculitic retinopathy and ischemic optic neuropathy, often linked to antiphospholipid syndrome.
  • Severe anemia and thrombocytopenia can lead to anaemic retinopathy, which may cause decreased visual acuity due to various retinal issues.
  • A case is presented where a lupus patient experienced vision loss from anaemic retinopathy, but her vision improved within a month after treating her anemia and lupus.
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Background: Trigeminal neuralgia, also known as tic doloureaux, refers to a sudden onset of unilateral or bilateral facial numbness with or without pain or paraesthesia. Trigeminal neuralgia is rare in connective tissue diseases (CTD); however, it is the most common neurologic manifestation of mixed connective tissue (MCTD) and maybe the only presenting symptom in various CTDs.

Patients And Methods: Here, we describe a series of four cases of various autoimmune connective tissue diseases where trigeminal neuralgia was the presenting complaint.

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Reactive arthritis is an immune-mediated aseptic arthritis resulting from either genitourinary or gastrointestinal tract in a genetically susceptible host. It commonly presents as oligoarthritis of the lower limbs with or without extra-articular features such as urethritis and non-purulent conjunctivitis. Therapies include non steroidal anti inflammatory drugs (NSAIDs), conventional disease modifying anti-rheumatic drugs (DMARDs) and, rarely, biologics in severe cases.

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Cogan's syndrome (CS) is a rare autoimmune vasculitis of unknown aetiology characterised by non-syphilitic interstitial keratitis, audiovestibular symptoms, sometimes systemic symptoms, and multi-organ involvement. Atypical CS has other ocular features, such as scleritis, episcelritis, retinitis, and optic neuritis. Diagnosis of CS is purely clinical without a confirmatory test.

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Reactive arthritis (ReA) is an immune-mediated aseptic synovitis resulting either from genitourinary or gastrointestinal tract, commonly presenting as oligoarthritis of the lower limbs and rarely urethritis and conjunctivitis. The treatment options include nonsteroidal anti-inflammatory drugs, conventional disease-modifying antirheumatic drugs, and biologics in severe cases. We report successful use of secukinumab in two cases of chronic severe ReA who initially failed to treatment with tumour necrosis factor inhibitor.

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Background: Neurological involvement has been found in many autoimmune diseases, with psychiatric abnormalities such as anxiety, depression, psychosis, and cognitive dysfunction.

Patients And Methods: Here, we describe a series of 5 consecutive cases of autoimmune diseases presenting with psychiatric symptoms as the predominant manifestation.

Result: Our case series suggests that psychiatric symptoms, mainly depression, can be one of the presenting symptoms of several autoimmune diseases that often cause a significant delay in diagnosis.

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Chronic obstructive pulmonary disease (COPD) is a lung disease that can affect various extra-pulmonary organs; one being the musculoskeletal system. Skeletal muscle dysfunction and osteoporosis are two important musculoskeletal disorders that have an impact on the quality of life in COPD patients in terms of morbidity and mortality. Treatment related adverse effects of COPD such as steroid-induced myopathy and osteoporosis are well recognised.

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