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https://www.readbyqxmd.com/read/29733071/symmetrical-and-bilateral-basal-ganglia-calcification-case-series-and-literature-review
#1
Amado Jiménez-Ruiz, Omar Cárdenas-Sáenz, José Luis Ruiz-Sandoval
Introduction: Symmetric, bilateral basal ganglia calcification is rare finding that sometimes occurs asymptomatically. Its prevalence increases with age, and the most affected site is the globus pallidus. Report of cases: A series of seven cases with clinical and imaging diagnosis of basal ganglia calcification, recorded during the 2012 to 2016 period at the Department of Internal Medicine of the Hospital Civil de Guadalajara "Fray Antonio Alcalde, is presented...
2018: Gaceta Médica de México
https://www.readbyqxmd.com/read/29668961/adult-autoinmune-enteropathy-and-colitis-a-challenge-successfully-treated-with-adalimumab
#2
Lucía Relea, Marta Calvo, Fernando Pons, Clara Salas, Luis Abreu
No abstract text is available yet for this article.
April 13, 2018: Inflammatory Bowel Diseases
https://www.readbyqxmd.com/read/29602447/use-of-tocilizumab-in-systemic-sclerosis-a-brief-literature-review
#3
A Fernández-Codina, J Fernández-Fernández, A Fernández-Pantiga
The available treatments for systemic sclerosis (SS) have limited effectiveness. Treatment with tocilizumab (TCZ), a biological drug that inhibits interleukin 6 (IL-6), has recently been proposed. In this study, we conducted a literature review to assess the safety and efficacy of TCZ in SS. We found 52 articles, 10 of which we selected after evaluating the articles. In a randomised clinical trial, TCZ showed a nonsignificant improvement in the degree of skin induration, while another observational study showed neutral results...
March 27, 2018: Revista Clínica Española
https://www.readbyqxmd.com/read/29469785/p%C3%A3-nfigo-foli%C3%A3-ceo-agravado-por-f%C3%A3-rmacos-en-un-paciente-con-psoriasis-con-buena-respuesta-a-adalimumab
#4
Jimena Sanz-Bueno, Elena Gallo, Dolores Caro-Gutiérrez, Araceli Sánchez-Gilo, Marta Gutiérrez Pascual, Laura Rojas-Scheffer, Francisco Javier Vicente-Martín
El pénfigo foliáceo es una enfermedad autoinmune ampollosa debida a la producción de autoanticuerpos frente a la desmogleína 1. Presentamos el caso de un paciente con psoriasis y pénfigo foliáceo agravado por enalapril y amlodipino, con buena respuesta de ambas patologías a la terapia con adalimumab.Pemphigus foliaceus is a blistering autoimmune disease related to the production of autoantibodies against desmoglein 1. We present a patient with psoriasis and pemphigus foliaceus aggravated by enalapril and amlodipine intake, with successful response of both conditions to adalimumab therapy...
October 15, 2017: Dermatology Online Journal
https://www.readbyqxmd.com/read/28093101/autoinmune-pancreatitis-differential-diagnosis-with-pancreatic-adenocarcinoma
#5
Diego Tristán Enjuto Martínez, Norberto Herrera Merino, Marta Pérez González, Rosa Llorente Lázaro, Pilar Castro Carbajo
No abstract text is available yet for this article.
October 2017: Cirugía Española
https://www.readbyqxmd.com/read/27793331/clinical-characteristics-during-diagnosis-of-a-prospective-cohort-of-patients-with-systemic-lupus-erythematosus-treated-in-spanish-departments-of-internal-medicine-the-reles-study
#6
J Canora, M García, F Mitjavila, G Espinosa, S Suárez, R González-León, B Sopeña, R Boldova, A Castro, G Ruiz-Irastorza
INTRODUCTION: Patient registries are useful tools for assessing rare diseases. Our objective is to present the Spanish registry of patients with systemic lupus erythematosus (Registro español de pacientes con lupus eritematoso sistémico, RELES). PATIENTS AND METHODS: RELES was started in 2008 as an observational, prospective, multicentre cohort registry that included patients from the time they were diagnosed. The registry's objective is to analyse the incidence and noninflammatory complications of systemic lupus erythematosus (SLE)...
January 2017: Revista Clínica Española
https://www.readbyqxmd.com/read/27759985/adecuaci%C3%A3-n-de-las-peticiones-de-los-niveles-de-vitamina-d-al-laboratorio
#7
Francisco Javier Valero Chávez, Luis Miguel Luengo Pérez, Javier Cubero Juánez
Introducción: ante las nuevas implicaciones atribuidas a la vitamina D y la asociación con enfermedades tales como el cáncer, diabetes, enfermedades cardiovasculares, autoinmunes y mortalidad, no es de extrañar que se haya defendido la medición de los niveles de vitamina D en la población general. Sin embargo, no existen datos experimentales que demuestren la viabilidad y rentabilidad de la estrategia de cribado en la población y tampoco se ha comprobado la existencia de beneficios para la salud, por lo que en la actualidad solo es aconsejable la medida de 25 (OH) vitamina D en los grupos de personas de alto riesgo como indican las guías clínicas internacionales...
September 20, 2016: Nutrición Hospitalaria: Organo Oficial de la Sociedad Española de Nutrición Parenteral y Enteral
https://www.readbyqxmd.com/read/27384637/-dermatomiositis-and-evans-syndrome-associated-with-htlv-1-infection
#8
David Loja-Oropeza, Ernesto Zavala-Flores, Maricela Vilca-Vasquez
A 55-year-old female patient, born in Ayacucho, with a history of dermatomyositis for 3 years, who received irregular treatment with prednisone. Two months prior to admission, she presented with autoinmune hemolytic anemia and idiopathic thrombocytopenic purpura. The patient received methylprednisolone pulse therapy and packed red blood cells transfusions. Upon admission, she was drowsy, with a poor overall status, marked weight loss, dehydration, with presence of livedo reticularis in her lower extremities, and onychodystrophy and onycholysis on the toes of both feet...
March 2016: Revista Peruana de Medicina Experimental y Salud Pública
https://www.readbyqxmd.com/read/27125615/-autoimmune-pancreatitis-a-case-report
#9
E Valdivielso Cortázar, C Prieto Martínez, I Fernández-Urién, J J Vila Costas, F J Jiménez Pérez, A Guerra Lacunza
Autoimmune pancreatitis (AIP) is an infrequent pathology, although there is a growing incidence in Eastern countries, which might be due to a greater rate of detection. It can be associated with other auto immune pathologies and its association with IgG4-related systemic disease has been described.Its clinical presentation is varied and the normal treatment is medical, using corticoids.A diagnosed clinical case is described.
April 29, 2016: Anales del Sistema Sanitario de Navarra
https://www.readbyqxmd.com/read/26617051/sj%C3%A3-gren-ser-national-registry-of-the-spanish-society-of-rheumatology-of-patients-with-primary-sj%C3%A3-gren-syndrome-objectives-and-methodology
#10
MULTICENTER STUDY
Mónica Fernández Castro, Jose Luis Andreu, Carlos Sánchez-Piedra, Víctor Martínez Taboada, Alejandro Olivé, José Rosas, Fernando Sánchez-Alonso
OBJECTIVE: To describe the objectives and methods of the Spanish Society of Rheumatology primary Sjögren syndrome (pSS) registry (SJOGREN-SER) METHODS: This is a multicenter descriptive transversal study of a cohort of pSS patients fulfilling European/American consensus criteria collected from Rheumatology clinics all over Spain. Patients were included by randomisation from an anonymised list provided by every department. Data were collected by reviewing clinical records and an interviewing the patients...
July 2016: Reumatología Clinica
https://www.readbyqxmd.com/read/26234085/-autoimmune-diseases-of-digestive-system
#11
REVIEW
V T Ivashkinl, A F Sheptulina, K L Raĭkhelson, E A Losik, K V Ivashkin, A V Okhlobystin, E K Baranskaia, E A Polouvektova, O S Shifrin
Autoimmune diseases of digestive system refer to pathological conditions, caused by autoimmune mechanisms, and their etiology remains unknown. This is a group of relatively rare diseases, however, during the last years a marked tendency towards the raise in incidence andprevalence is observed, which led to an increase in number of clinical investigations on etiology, pathogenesis, and, accordingly, development of new diagnostic methods and therapies. Results of such trials shown, for example, that the pathogenesis of chronic cholestatic liver diseases is associated with nuclear receptors function, while the main etiological and pathogenic factor of inflammatory bowel diseases represents gut microbiota...
2015: Vestnik Rossiĭskoĭ Akademii Meditsinskikh Nauk
https://www.readbyqxmd.com/read/25958373/-orofacial-clinical-manifestations-in-adult-patients-with-variable-common-immunodeficiency
#12
Aurora Alejandra Chávez-García, Miguel Ángel Moreno-Alba, Martín Elizalde-Monroy, Nora Hilda Segura-Méndez, Jovita Romero-Flores, Julio César Cambray-Gutiérrez, Patricia López-Pérez, Leonel Gerardo Del Rivero-Hernández
BACKGROUND: Common variable immunodeficiency is the primary immunodeficiency (CVID) frequently found in adults. Its prevalence is estimated from 1:25,000 to 75,000 alive newborns; there are variations by ethnic groups, it is estimated about 50-70% in Caucasian patients. Oral cavity lesions are rarely found in adult patients with CVID, there are reports about lesions on pediatric patients mostly caused by infections. OBJECTIVE: To describe the orofacial lesions (oral, maxillofacial and neck area) affecting adults with CVID...
April 2015: Revista Alergia Mexico: Organo Oficial de la Sociedad Mexicana de Alergia e Inmunología, A.C
https://www.readbyqxmd.com/read/25639457/clinical-practice-guidelines-for-the-management-of-pregnancy-in-women-with-autoimmune-rheumatic-diseases-of-the-mexican-college-of-rheumatology-part-i
#13
Miguel Ángel Saavedra Salinas, Antonio Barrera Cruz, Antonio Rafael Cabral Castañeda, Luis Javier Jara Quezada, C Alejandro Arce-Salinas, José Álvarez Nemegyei, Antonio Fraga Mouret, Javier Orozco Alcalá, Mario Salazar Páramo, Claudia Verónica Cruz Reyes, Lilia Andrade Ortega, Olga Lidia Vera Lastra, Claudia Mendoza Pinto, Antonio Sánchez González, Polita Del Rocío Cruz Cruz, Sara Morales Hernández, Margarita Portela Hernández, Mario Pérez Cristóbal, Gabriela Medina García, Noé Hernández Romero, María Del Carmen Velarde Ochoa, José Eduardo Navarro Zarza, Verónica Portillo Díaz, Angélica Vargas Guerrero, María Victoria Goycochea Robles, José Luis García Figueroa, Eduardo Barreira Mercado, Mary Carmen Amigo Castañeda
BACKGROUND: Pregnancy in women with autoimmune rheumatic diseases is associated with several maternal and fetal complications. The development of clinical practice guidelines with the best available scientific evidence may help standardize the care of these patients. OBJECTIVES: To provide recommendations regarding prenatal care, treatment, and a more effective monitoring of pregnancy in women with lupus erythematosus (SLE), rheumatoid arthritis (RA) and antiphospholipid antibody syndrome (APS)...
September 2015: Reumatología Clinica
https://www.readbyqxmd.com/read/25601124/-igg4-related-disease-extrapancreatic-manifestations-in-autoinmune-pancreatitis
#14
LETTER
Zoltán Berger, Carla Mancilla A
No abstract text is available yet for this article.
October 2014: Revista Médica de Chile
https://www.readbyqxmd.com/read/25582871/latent-autoimmune-diabetes-in-adults-are-we-paying-sufficient-attention
#15
EDITORIAL
Marta Hernández, Dídac Mauricio
No abstract text is available yet for this article.
January 2015: Endocrinología y Nutrición: órgano de la Sociedad Española de Endocrinología y Nutrición
https://www.readbyqxmd.com/read/24584802/-linear-iga-bullous-dermatosis-of-childhood-case-report
#16
Francisco Reyes-Baraona, Romina Andino, Juan Eduardo Carrasco, Camila Arriagada, Silvia Guerrero
Linear IgA bullous dermatosis is a rare acquired autoinmune vesiculobullous disease characterized by linear IgA deposit on the dermo-epidermal basement membrane observed with direct inmunofluorescence. The characteristic lesions are vesicles and tense serous bullae, which most often are grouped giving a "cluster of jewels" appearance. Differential diagnosis must be established with other autoimmune dermatosis, such as dermatitis herpetiformis and bullous pemphigoid. Dapsone is the first line therapy, with excellent response in a short period...
April 2014: Archivos Argentinos de Pediatría
https://www.readbyqxmd.com/read/23871155/national-registry-of-patients-with-systemic-lupus-erythematosus-of-the-spanish-society-of-rheumatology-objectives-and-methodology
#17
MULTICENTER STUDY
Iñigo Rúa-Figueroa, Francisco Javier López-Longo, Jaime Calvo-Alén, María Galindo-Izquierdo, Estíbaliz Loza, M Jesús García de Yebenes, José M Pego-Reigosa
OBJECTIVE: To describe the objectives, design and methods of the Spanish Society of Rheumatology systemic lupus erythematosus (SLE) registry (RELESSER). METHODS: Multicenter, hospital-based registry, with retrospective collection of data from a large representative sample of adult patients with SLE (1997 ACR criteria) attending Spanish rheumatology services. The registry includes demographic data, frequent and infrequent (<1%) clinical manifestations, information about activity, damage, severity, comorbidity, treatments and mortality, collecting 359 variables per patient, with highly standardized definitions...
January 2014: Reumatología Clinica
https://www.readbyqxmd.com/read/23565550/-belimumab-in-systemic-lupus-erythematosus-a-guide-for-its-use-in-the-daily-practice
#18
M Ramos-Casals, G Ruiz-Irastorza, J Jiménez-Alonso, M A Khamashta
No abstract text is available yet for this article.
January 2013: Revista Clínica Espanõla
https://www.readbyqxmd.com/read/23518639/autoimmunity-related-neutrophilic-dermatosis-a-newly-described-entity-that-is-not-exclusive-of-systemic-lupus-erythematosus
#19
Marcela Saeb-Lima, Yann Charli-Joseph, Elva Dalia Rodríguez-Acosta, Judith Domínguez-Cherit
Neutrophilic dermatoses have long been known to be associated with autoinmune systemic diseases. Recently, a small number of cases of a disorder distinct from Sweet syndrome or bullous lupus erythematosus (LE) have been described as specifically related to systemic LE under diverse terms, including nonbullous neutrophilic dermatosis, nonbullous neutrophilic LE, and Sweet-like neutrophilic dermatosis. We describe 7 patients that developed urticarial lesions in the context of a known or concurrently diagnosed autoimmune connective tissue disease...
August 2013: American Journal of Dermatopathology
https://www.readbyqxmd.com/read/23266125/-recommendations-on-the-use-of-belimumab-in-systemic-lupus-erythematosus-geas-semi-clinical-practice-guide
#20
M Ramos-Casals, G Ruiz-Irastorza, J Jiménez-Alonso, M A Khamashta
Biological therapies are based on the administration of various types of synthetic molecules related to the immune response. Their use has spread in recent years to the field of systemic autoimmune diseases, particularly to systemic lupus erythematosus (SLE). Until 2011, these diseases were not included in the therapeutic indications approved by international regulatory agencies. Therefore, the use of biological therapies was restricted to clinical trials and to compassionate use for cases refractory to standard treatments (off-label use), which require the approval of the Health Ministry...
January 2013: Revista Clínica Espanõla
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