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1.
Rheumatology (Oxford) ; 60(6): 3004-3011, 2021 06 18.
Artigo em Inglês | MEDLINE | ID: mdl-34144605

RESUMO

OBJECTIVES: Peripheral SpA (pSpA) is comprised of ReA, PsA, enteritis-associated arthritis and undifferentiated pSpA (upSpA). ReA and upSpA share T cell oligotypes and metabolomics in serum and SF. We investigated HLA-B27 subtypes and cytokines in serum and SF that were compared between ReA and upSpA. METHODS: ReA and upSpA were compared in two cohorts. In cohort I (44 ReA and 56 upSpA), HLA-B27 subtyping was carried out. In cohort II (17 ReA and 21 upSpA), serum and SF cytokines were compared using a multiplex cytokine bead assay (27 cytokines). A total of 28 healthy controls with similar age and sex to cohort II were included for comparison of serum cytokine levels. RESULTS: In cohort I, HLA-B27 was positive in 81.8% (36/44) of ReA and 85.71% (48/56) of upSpA patients. HLA-B27 typing was successful in 70 patients (30 ReA and 40 uSpA). HLA-B*2705 was the most common, followed by HLA-B*2704 and HLA-B*2707. Frequencies were the same between ReA and upSpA. In cohort II, 14 cytokines were detectable in the serum of patients. The levels of eight cytokines were higher than in the controls. The cytokine levels of ReA and upSpA were similar. Sixteen cytokines were detectable in the SF of patients. There was no statistical difference in the levels between ReA and upSpA. The cytokine profiles in sera and SF were also similar among HLA-B27-positive and negative patients. CONCLUSION: ReA and upSpA have similar HLA-B27 subtype associations and similar cytokine profiles. They should be considered as a single entity during studies as well as clinical management.


Assuntos
Artrite Reativa/imunologia , Citocinas/imunologia , Antígeno HLA-B27/imunologia , Espondilartrite/imunologia , Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Proibitinas , Adulto Jovem
3.
Indian Pediatr ; 57(1): 75-76, 2020 01 15.
Artigo em Inglês | MEDLINE | ID: mdl-31937708

RESUMO

Juvenile dermatomyositis is a rare systemic autoimmune disease wth calcinosis as its hallmark sequelae. We report three patients with juvenile dermatomyositis with calcinosis, who were treated with pamidronate. There was complete clearance of calcinosis in one child.


Assuntos
Calcinose , Dermatomiosite/complicações , Pamidronato/uso terapêutico , Calcinose/tratamento farmacológico , Calcinose/etiologia , Calcinose/patologia , Criança , Pré-Escolar , Feminino , Dedos/patologia , Humanos , Masculino
4.
World J Orthop ; 6(2): 278-83, 2015 Mar 18.
Artigo em Inglês | MEDLINE | ID: mdl-25793168

RESUMO

The management of rheumatoid arthritis (RA) in the past three decades has undergone a paradigm shift from symptomatic relief to a "treat-to-target" approach. This has been possible through use of various conventional and biologic disease modifying anti-rheumatic drugs (DMARDs) which target disease pathogenesis at a molecular level. Cost and infection risk preclude regular use of biologics in resource-constrained settings. In the recent years, evidence has emerged that combination therapy with conventional DMARDs is not inferior to biologics in the management of RA and is a feasible cost-effective option.

5.
BMJ Case Rep ; 20142014 Nov 14.
Artigo em Inglês | MEDLINE | ID: mdl-25398925

RESUMO

Patients on immunosuppression are at risk of unusual infections. We present a man diagnosed to have adult-onset Still's disease who, on high-dose oral steroid and tacrolimus, developed a cavitating pneumonia due to co-infection with Aspergillus flavus and Nocardia. Timely diagnosis and institution of appropriate therapy resulted in a favourable clinical outcome. Such co-infection in a patient receiving tacrolimus is rare in the published literature. This case serves to emphasise the need to be vigilant for unusual infections in patients who are immunosuppressed, either due to drugs or underlying disease condition.


Assuntos
Aspergilose/diagnóstico , Coinfecção/tratamento farmacológico , Imunossupressores/efeitos adversos , Nocardiose/diagnóstico , Pneumonia/microbiologia , Doença de Still de Início Tardio/imunologia , Adulto , Antibacterianos/uso terapêutico , Antifúngicos/uso terapêutico , Aspergilose/tratamento farmacológico , Aspergilose/imunologia , Coinfecção/imunologia , Coinfecção/microbiologia , Quimioterapia Combinada , Seguimentos , Humanos , Hospedeiro Imunocomprometido , Imunossupressores/administração & dosagem , Masculino , Nocardiose/tratamento farmacológico , Nocardiose/imunologia , Pneumonia/diagnóstico por imagem , Pneumonia/tratamento farmacológico , Radiografia Torácica/métodos , Esteroides/uso terapêutico , Doença de Still de Início Tardio/diagnóstico , Doença de Still de Início Tardio/tratamento farmacológico , Tacrolimo/uso terapêutico , Tomografia Computadorizada por Raios X/métodos , Resultado do Tratamento
6.
Case Reports Immunol ; 2014: 641989, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25580317

RESUMO

Leprosy is a disease typically found in the tropics. Patients with leprosy can have varying presentation with constitutional symptoms, joint pains, skin nodules, and rarely a vasculitis-like picture with skin ulcers and neuropathy. We present a young lady who presented with the rare manifestation of skin infarcts mimicking cutaneous vasculitis, diagnosed on histopathology to have Lucio phenomenon on a background of lepromatous leprosy. With increasing migration and widespread use of biologic response modifiers, clinicians all over the world need to be aware of various presentations of leprosy as well as needing to keep an open mind while considering the differential diagnoses of vasculitis.

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