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4. Unilateral uveitis associated with IgA nephropathy

Author

Rueda-Rueda, T., Sánchez-Vicente, J.L., Moruno-Rodríguez, A., Molina-Socola, F.E., Contreras-Díaz, M., Vizuete-Rodríguez, L., Castilla-Martino, M., Sáez-Ortega, L., Muñoz-Morales, A., Martínez-Borrego, A.C., Parra-Oviedo, E., Medina-Tapia, A., and López-Herrero, F.

Published
2017
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11. Retinopatía Purtscher- like previa a fallo renal agudo

Author

Sánchez Vicente, J.L., primary, Castilla Martino, M., additional, Contreras Díaz, M., additional, Rueda Rueda, T., additional, Molina Socola, F.E., additional, Muñoz Morales, A., additional, López Herrero, F., additional, Moruno Rodríguez, A., additional, Vizuete Rodríguez, L., additional, and Martínez Borrego, A., additional

Published
2018
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13. Uveítis unilateral asociada a nefropatía IgA

Author

Rueda-Rueda, T., primary, Sánchez-Vicente, J.L., additional, Moruno-Rodríguez, A., additional, Molina-Socola, F.E., additional, Contreras-Díaz, M., additional, Vizuete-Rodríguez, L., additional, Castilla-Martino, M., additional, Sáez-Ortega, L., additional, Muñoz-Morales, A., additional, Martínez-Borrego, A.C., additional, Parra-Oviedo, E., additional, Medina-Tapia, A., additional, and López-Herrero, F., additional

Published
2017
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15. Tratamiento quirúrgico en un hamartoma combinado de retina y epitelio pigmentario

Author

Sánchez-Vicente, J.L., primary, Rueda-Rueda, T., additional, Llerena-Manzorro, L., additional, Molina-Socola, F.E., additional, Contreras-Díaz, M., additional, Szewc, M., additional, Vital-Berral, C., additional, Alfaro-Juárez, A., additional, Medina-Tapia, A., additional, López-Herrero, F., additional, González-García, L., additional, and Muñoz-Morales, A., additional

Published
2017
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18. Excavación focal coroidea asociada a membrana neovascular coroidea idiopática

Author

Sánchez-Vicente, J.L., Rueda-Rueda, T., Martínez-Borrego, A.C., Moruno-Rodríguez, A., Molina-Socola, F.E., Contreras-Díaz, M., Medina-Tapia, A., Muñoz-Morales, A., and López-Herrero, F.

Abstract

Presentamos el caso de un varón de 45 años con excavación coroidea asociada a una membrana neovascular coroidea no incluida en el área de la excavación. Se describen las características clínicas mediante retinografía, angiografía fluoresceínica, tomografía de coherencia óptica y angiotomografía. El paciente fue tratado con 3 inyecciones de bevacizumab, consiguiéndose la inactivación de la membrana.

Published
2024
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19. Síndrome de nefritis túbulo-intersticial y uveítis (TINU). Tratamiento con inmunosupresores

Author

Rueda-Rueda, T., Sánchez-Vicente, J.L., Moruno-Rodríguez, A., Castilla-Martino, M., López-Herrero, F., Contreras-Díaz, M., Molina-Socola, F., Sáez-Ortega, L., and Muñoz-Morales, A.

Abstract

Presentamos 2 casos de síndrome de nefritis túbulo-intersticial y uveítis que necesitaron tratamiento con inmunosupresores para lograr el control de la uveítis. Al contrario de lo habitualmente descrito, la uveítis adquirió un carácter crónico, siendo necesario el tratamiento inmunosupresor. La nefritis sí respondió al tratamiento con corticoides.

Published
2024
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20. Uveítis unilateral asociada a nefropatía IgA

Author

Rueda-Rueda, T., Sánchez-Vicente, J.L., Moruno-Rodríguez, A., Molina-Socola, F.E., Contreras-Díaz, M., Vizuete-Rodríguez, L., Castilla-Martino, M., Sáez-Ortega, L., Muñoz-Morales, A., Martínez-Borrego, A.C., Parra-Oviedo, E., Medina-Tapia, A., and López-Herrero, F.

Abstract

Presentamos el caso de un varón de 42 años de edad con varios episodios de uveítis unilateral en su ojo derecho. El examen oftalmológico mostró una uveítis anterior granulomatosa con vitritis. El estudio sistémico puso de manifiesto una proteinuria de rango no nefrótico y microhematuria. La biopsia renal reveló una nefropatía IgA.

Published
2024
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21. Retinopatía Purtscher-likeprevia a fallo renal agudo

Author

Sánchez Vicente, J.L., Castilla Martino, M., Contreras Díaz, M., Rueda Rueda, T., Molina Socola, F.E., Muñoz Morales, A., López Herrero, F., Moruno Rodríguez, A., Vizuete Rodríguez, L., and Martínez Borrego, A.

Abstract

Presentamos el caso de una mujer de 61 años, con una retinopatía de tipo Purtscher asociada a un fallo renal agudo. La exploración oftalmológica, angiografía fluoresceínica y tomografía de coherencia óptica fueron compatibles con una retinopatía de Purtscher-like. Las manifestaciones oculares precedieron al fracaso renal. El estudio sistémico y de laboratorio descartó su asociación con pancreatitis y otras enfermedades sistémicas. Finalmente se complicó con un glaucoma neovascular.

Published
2018
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22. Clostridium Septicum Endogenous Endophthalmitis as the Initial Manifestation of Colorectal Carcinoma: Clinical Case Report and Literature Review.

Author

Sanchez-Vicente JL, Contreras-Díaz M, López-Herrero F, Martínez-Borrego A, Galván-Ledesma A, Lozano-Bernal O, García-Vazquez M, De Las Morenas-Iglesias J, and Caro-Magdaleno M

Subjects
Humans, Male, Middle Aged, Observational Studies as Topic, Adenocarcinoma complications, Adenocarcinoma diagnosis, Clostridium Infections complications, Clostridium Infections diagnosis, Clostridium Infections microbiology, Clostridium septicum physiology, Colorectal Neoplasms complications, Endophthalmitis microbiology
Abstract

Purpose: To describe the presentation and clinical course of a case of endogenous endophthalmitis caused by Clostridium septicum , an anaerobic and gram positive bacteria., Methods: Observational report of a clinical case presented in Spain., Clinical Case: A 61-year-old male patient was referred to our hospital with a diagnosis of endophthalmitis of his left eye since ten days prior to presentation, and a history of poor response to medical treatment. Evisceration was performed, and C. septicum was isolated from a sample of the vitreous humor. Fourteen days after surgery, the patient returned with orbital cellulitis, and exenteration was performed. Forty-two days after initial presentation, colonoscopy revealed an adenocarcinoma of the proximal colon. Surgical resection of the tumor was performed, and clinical recovery was achieved., Conclusions: iSystemic C. septicum infection without a traumatic cause has been associated with malignancy, although an initial presentation of endophthalmitis has rarely been reported. In cases of clostridial endogenous endophthalmitis, investigation for colorectal carcinoma is indicated.

Published
2022
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24. FOVEAL HYPOPLASIA: DIAGNOSIS USING OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY.

Author

Sánchez-Vicente JL, Contreras-Díaz M, Llerena-Manzorro L, Rueda T, López-Herrero F, Molina-Socola FE, Muñoz-Morales A, and Rodríguez de la Rúa-Franch E

Subjects
Female, Fundus Oculi, Humans, Middle Aged, Retinal Diseases physiopathology, Fluorescein Angiography methods, Fovea Centralis pathology, Retinal Diseases diagnosis, Retinal Vessels pathology, Tomography, Optical Coherence methods, Visual Acuity
Abstract

Purpose: To describe the clinical presentations and image findings of a patient with foveal hypoplasia., Methods: Observational case report of one patient. The clinical presentation of the patient was documented by fluorescein angiography, optical coherence tomography, and optical coherence tomography angiography., Results: A 55-year-old healthy white female with bilateral foveal hypoplasia without nystagmus was presented. There were no signs suggestive of ocular albinism. Absence of foveal depression was noted on both clinical examination and optical coherence tomography. Lack of foveal avascular zone was confirmed on fluorescein angiography and optical coherence tomography angiography., Conclusion: To the best of our knowledge this is the first report of findings in foveal hypoplasia examined by angio-optical coherence tomography. Optical coherence tomography angiography is an easy, rapid, and noninvasive tool that allows imaging of the retinal microvasculature without intravenous dye injection.

Published
2018
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25. Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane.

Author

Sánchez-Vicente JL, Contreras-Díaz M, Rueda T, Rodríguez de la Rúa-Franch E, Molina-Socola FE, Vital-Berral C, Alfaro-Juárez A, López-Herrero F, and Muñoz-Morales A

Abstract

Purpose. To describe the case of spontaneous resolution of epiretinal membrane in a patient with Combined Hamartoma of the Retina and Retinal Pigment Epithelium (CHR-RPE), in the clinical context of Gorlin Syndrome (GS). Methods. Observational case report of a 12-year-old female patient is presented. The diagnosis of CHRRPE was made by OCT and fundus examination, which showed a mound of disorganized tissue originating from retina and retinal pigment epithelium. Epiretinal membrane (EM) was also detected. Genetic study was performed to confirm the diagnosis of GS. Results. The patient was observed for 39 months, showing spontaneous resolution of the traction caused by the EM and improvement in visual acuity (VA), which was 20/80 at initial presentation, rising to 20/40 after follow-up period. Conclusions. The presence of EM in CHR-REP is a cause of reduction of visual acuity. Management of this condition is controversial; however, we would like to highlight that spontaneous resolution of the traction caused by EM is possible, resulting in recovery of VA.

Published
2016
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