Bilateral corneal perforation and iris prolapse as a complication non-peripheral ulcerative keratitis in a patient with fulminant Granulomatosis with Polyangiitis. A case Report.

Ligia Alejandra Delatorre Cifuentes

doi:10.1186/s12348-020-0195-6

Bilateral corneal perforation and iris prolapse as a complication non-peripheral ulcerative keratitis in a patient with fulminant Granulomatosis with Polyangiitis. A case Report.

Título traducido de la contribución: La perforación corneal bilateral y el prolapso del iris como complicación de queratitis ulcerativa no periférica en un paciente con granulomatosis fulminante con poliangeítis. Un informe de caso.

Ligia Alejandra Delatorre Cifuentes

Producción científica: Contribución a revista › Artículo de Investigación › revisión exhaustiva

Resumen

Propósito: Reportar un caso de granulomatosis con poliangitis (GPA) con un fulminante
fenotipo caracterizado por diversas manifestaciones oculares y sistémicas.
Métodos: Informe de caso y comparación de literatura.
Resultados: reportamos el caso de un paciente masculino de 58 años con diagnóstico de GPA, que presentó manifestaciones oculares atípicas concomitantes con compromiso sistémico que condujeron a progresión severa y fulminante de la enfermedad.
Conclusión: se requiere un diagnóstico precoz y un abordaje interdisciplinario apropiado en pacientes con manifestaciones atípicas de GPA debido a su potencial amenaza a la vida

Título traducido de la contribución	La perforación corneal bilateral y el prolapso del iris como complicación de queratitis ulcerativa no periférica en un paciente con granulomatosis fulminante con poliangeítis. Un informe de caso.
Idioma original	Inglés estadounidense
Número de artículo	2
Páginas (desde-hasta)	3-20
Número de páginas	17
Publicación	Ocular Immunology and Inflammation
Volumen	10
DOI	https://doi.org/10.1186/s12348-020-0195-6
Estado	Publicada - ene 10 2020

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title = "Bilateral corneal perforation and iris prolapse as a complication non-peripheral ulcerative keratitis in a patient with fulminant Granulomatosis with Polyangiitis. A case Report.",

abstract = "Purpose: To report a case of Granulomatosis with Polyangiitis (GPA) with a fulminant phenotype characterized by diverse ocular and systemic manifestations. Methods: Case report and literature comparison. Results: we report the case of a 58 years old male patient with diagnosis of GPA, who presented with atypical ocular manifestations concomitant with systemic compromise thath led to severe and fulminant progression of the disease. Conclusion: early diagnosis and an appropriate interdisciplinary approach are required in patiens with atypical manifestations of GPA dut t its life-threatening potential",

author = "\{Delatorre Cifuentes\}, \{Ligia Alejandra\}",

year = "2020",

month = jan,

day = "10",

doi = "10.1186/s12348-020-0195-6",

language = "English (US)",

volume = "10",

pages = "3--20",

journal = "Ocular Immunology and Inflammation",

issn = "0927-3948",

publisher = "Taylor and Francis Ltd.",

}

Bilateral corneal perforation and iris prolapse as a complication non-peripheral ulcerative keratitis in a patient with fulminant Granulomatosis with Polyangiitis. A case Report. / Delatorre Cifuentes, Ligia Alejandra.
En: Ocular Immunology and Inflammation, Vol. 10, 2, 10.01.2020, p. 3-20.

Producción científica: Contribución a revista › Artículo de Investigación › revisión exhaustiva

TY - JOUR

T1 - Bilateral corneal perforation and iris prolapse as a complication non-peripheral ulcerative keratitis in a patient with fulminant Granulomatosis with Polyangiitis. A case Report.

AU - Delatorre Cifuentes, Ligia Alejandra

PY - 2020/1/10

Y1 - 2020/1/10

N2 - Purpose: To report a case of Granulomatosis with Polyangiitis (GPA) with a fulminant phenotype characterized by diverse ocular and systemic manifestations. Methods: Case report and literature comparison. Results: we report the case of a 58 years old male patient with diagnosis of GPA, who presented with atypical ocular manifestations concomitant with systemic compromise thath led to severe and fulminant progression of the disease. Conclusion: early diagnosis and an appropriate interdisciplinary approach are required in patiens with atypical manifestations of GPA dut t its life-threatening potential

AB - Purpose: To report a case of Granulomatosis with Polyangiitis (GPA) with a fulminant phenotype characterized by diverse ocular and systemic manifestations. Methods: Case report and literature comparison. Results: we report the case of a 58 years old male patient with diagnosis of GPA, who presented with atypical ocular manifestations concomitant with systemic compromise thath led to severe and fulminant progression of the disease. Conclusion: early diagnosis and an appropriate interdisciplinary approach are required in patiens with atypical manifestations of GPA dut t its life-threatening potential

U2 - 10.1186/s12348-020-0195-6

DO - 10.1186/s12348-020-0195-6

M3 - Research Article

C2 - 31925570

SN - 0927-3948

VL - 10

SP - 3

EP - 20

JO - Ocular Immunology and Inflammation

JF - Ocular Immunology and Inflammation

M1 - 2

ER -

Bilateral corneal perforation and iris prolapse as a complication non-peripheral ulcerative keratitis in a patient with fulminant Granulomatosis with Polyangiitis. A case Report.

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