Results 71 to 80 of about 3,278 (216)

Angeitis necrotizante sistémica no supurativa

Revista de la Facultad de Medicina, 1972
1. Se estudian 3 casos de angeítis necrotizante sistémica no supurativa: un hombre de 36 y una mujer de 58 años con granulomatosis de Wegener y un hombre de 30 años con granulomatosis alérgica del tipo descrito por Churg y Strauss. 2.
Gabriel Toro G., Odilio Méndez S., Hernán Alvarado C., Egon Lichtenberger, Jaime Cantillo G.   +4 more
doaj  

Clinical and Pathological Features of Vasculitic Neuropathy: A Single‐Center Study in China

European Journal of Neurology, Volume 33, Issue 3, March 2026.
Vasculitic neuropathy in mainland China predominantly presents as axonal sensorimotor neuropathy. Systemic VN shows more frequent transmural inflammatory infiltration, whereas EGPA is more common in cases without infiltration. Most treated patients achieved remission, and the overall prognosis was relatively favorable, underscoring the importance of ...
Xiaoyu Zhou, Didi Shan, Bin Wu, Fuchen Liu, Dong Zhang, Pengfei Lin, Wei Li, Yuying Zhao, Chuanzhu Yan, Jingwen Xu   +9 more
wiley   +1 more source

Enfermedades glomerulares durante la gestación: Serie de casos y revisión de la literatura Glomerular disease and pregnancy

Revista Colombiana de Obstetricia y Ginecología, 2008
Objetivos: determinar las glomerulopatías más frecuentes y su curso clínico en mujeres gestantes. Hacer una revisión de la literatura del tema. Materiales y métodos: serie de casos retrospectivos de pacientes gestantes con enfermedad glomerular activa ...
Jorge M Gómez-Jiménez, Luis F Arias
doaj  

Atualização do tratamento das vasculites associadas a anticorpo anticitoplasma de neutrófilos Treatment of antineutrophil cytoplasmic antibody-associated vasculitis: update

Jornal Brasileiro de Pneumologia, 2011
As vasculites antineutrophil cytoplasmic antibody (ANCA, anticorpo anticitoplasma de neutrófilos) associadas (VAAs) são caracterizadas por uma inflamação sistêmica das artérias de pequeno e médio calibre (especialmente no trato respiratório superior e ...
Alfredo Nicodemos Cruz Santana, Viktoria Woronik, Ari Stiel Radu Halpern, Carmen S V Barbas   +3 more
doaj   +1 more source

Granulomatosis de Wegener, una afección poco frecuente

, 2019
Introducción: la granulomatosis de Wegener es una vasculitis sistémica, poco frecuente, cuyo sustrato etiopatogénico es la inflamación de los vasos sanguíneos impidiendo la libre circulación del flujo sanguíneo. Clinicamente se caracteriza por presencia de manifestaciones respiratorias, nasales, auditivas y renales; frecuentemente se asocian trastornos
Latta, Mónica Fabiola Yambay, Vela, Jorge Stalin Solorzano   +1 more
openaire   +1 more source

Animal models of benign airway stenosis: Advances in construction techniques, evaluation systems, and perspectives

Animal Models and Experimental Medicine, Volume 9, Issue 2, Page 280-297, February 2026.
Currently, the animals commonly used to establish animal models of benign airway stenosis (BAS) include mice, rats, pigs, dogs, rabbits, and ferrets. The establishment methods involve one or a combination of two methods such as mechanical injury, tracheal cautery, cuff overpressure intubation, laser injury, and endoscopic silver nitrate cauterization ...
Wusheng Zhang, Yilin Chen, Chengcheng Yang, Yuchao Dong, Haidong Huang, Hui Shi, Chong Bai   +6 more
wiley   +1 more source

Granulomatosis with polyangiitis in children: report of a case with kidney-lung syndrome = Granulomatosis con poliangitis en pediatría: a propósito de un caso con síndrome pulmón-riñón

Iatreia, 2013
Granulomatosis with polyangiitis as a cause of kidney-lung syndrome is uncommon in children. We report the case of a 13 year old patient with alveolar hemorrhage, rapidly progressive glomerulonephritis, episcleritis and anti PR3.
Muñoz Grajales, Carolina, Muñoz Martínez, Laura Carolina, Eraso Garnica, Ruth María   +2 more
doaj  

Anticorpos contra o citoplasma de neutrófilos Antineutrophil cytoplasmic antibodies

Jornal Brasileiro de Pneumologia, 2005
A descoberta do marcador sorológico denominado anticorpo anticitoplasma de neutrófilos revolucionou o diagnóstico e o seguimento das vasculites pulmonares, especialmente da granulomatose de Wegener. Seu padrão pode ser citoplasmático e perinuclear.
Ari Stiel Radu, Mauricio Levi
doaj   +1 more source

Tolosa–Hunt Syndrome Presenting as Painful Unilateral Ophthalmoplegia in a 65‐Year‐Old Woman: A Case Report

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT A 65‐year‐old woman presented to a tertiary care center with a classical clinical scenario—3 months of persistent, right‐sided frontal headache. Over the course of 20 days, a right‐sided frontal headache developed into ptosis of the right upper eyelid.
Saiful Islam Chowdhury, Sumaya Khan Mifty, Tanveer Al Razi Khan, Swagota Roy, Tahmidur Rahman, Faiza Ahmmed, Sharif Mohammad Tawfik Tamim   +6 more
wiley   +1 more source

Granulomatose com poliangeíte inicialmente diagnosticada como cancro do pulmão

Revista Portuguesa de Pneumologia, 2013
Resumo: A granulomatose com poliangeíte (GPA), previamente denominada granulomatose de Wegener, é uma doença sistémica caracterizada por inflamação granulomatosa necrotizante e vasculite que envolve principalmente o trato respiratório superior e inferior,
S. Campainha, M. Gonçalves, V. Tavares, P. Castelões, A. Marinho, S. Neves   +5 more
doaj   +1 more source