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Your search keyword '"Vázquez‐Osorio, I."' showing total 152 results
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152 results on '"Vázquez‐Osorio, I."'

10. Mixed vascular naevus syndrome: report of three children with somatic GNA11 mutation and new systemic associations.

Author

Beteta‐Gorriti, V., Vázquez‐Osorio, I., de Dios‐Velázquez, Á., Rodriguez‐Laguna, L., Viana‐Huete, V., García Torrijos, C., Martinez‐Glez, V., and Rodríguez‐Díaz, E.

Subjects
*SOMATIC mutation, *HUMAN abnormalities, *MUSCULOSKELETAL system diseases, *HEART abnormalities, *CUTANEOUS manifestations of general diseases, *NEVUS, *HYPOPLASTIC left heart syndrome
Abstract

Summary: Mixed vascular naevus (MVN) is characterized by the co‐occurrence of telangiectatic capillary malformation and naevus anaemicus, which can appear as a pure cutaneous phenotype or be combined with systemic manifestations such as brain malformations, neurological abnormalities and musculoskeletal disorders. Recently, GNA11 and GNAQ somatic mutations have been reported in some patients with isolated and syndromic MVN. We report three children with MVN syndrome with generalized cutaneous manifestations and a number of systemic associations not reported to date, including ophthalmological anomalies, musculoskeletal abnormalities such as Sprengel deformity and posterior vertebral fusion anomalies, and septal heart defects. We also confirm a somatic mutation of GNA11 in both telangiectatic naevus and naevus anaemicus in two of our patients and discuss a possible common pathogenic mechanism underlying the different manifestations of the syndrome. Currently, there are no guidelines for the evaluation of patients with MVN syndrome, but according to the different known aspects of the disease, a complete clinical examination should be made, and complementary laboratory and imaging tests should be considered. [ABSTRACT FROM AUTHOR]

Published
2022
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11. Reply to 'Comment on 'Interruption of oral clindamycin plus rifampicin therapy in patients with hidradenitis suppurativa: an observational study to assess prevalence and causes' '

Author

Schneller-Pavelescu L, Vergara-de Caso E, Martorell A, Romaní J, Lázaro M, Vilarrasa E, Díaz-Ley B, Vázquez-Osorio I, Segura Palacios JM, Azaña JM, González-López MA, Cañueto J, Molina-Leyva A, Leiva-Salinas M, Navarro-Triviño FJ, Sanchez-Paya J, and Pascual J

Subjects
acne inversa, adverse events, clindamycin, compliance, hidradenitis suppurativa, observational, retrospective, rifampicin, safety, therapy
Published
2019

12. Lipoedematous scalp

Author

Fernández‐Canga, P., primary, Rodríguez‐Díaz, E., additional, Carvajal‐Álvarez, M., additional, Gonzalvo‐Rodríguez, P., additional, and Vázquez‐Osorio, I., additional

Published
2019
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13. Multiple Perianal Ulcers Related to Use of a Hemorrhoidal Ointment With the Active Ingredients Triamcinolone Acetonide, Lidocaine, and Pentosan Polysulfate Sodium: A Series of 11 Spanish Patients

Author

Marín-Piñero, D., Iglesias-Sancho, M., Company-Quiroga, J., Martínez-Moran, C., Perez-Feal, P., Vazquez-Osorio, I., Rodriguez-Jiménez, P., Sánchez-Estella, J., Suárez-Valle, A., Buzón-Martín, L., Martín-Saez, E., García-Rodiño, S., Sáez-Vicente, A., Arranz-Sánchez, D.M., Cervigón-González, I., and del Rio, E.

Published
2021
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37. Skin ultrasound features of Merkel cell carcinoma.

Author

Hernández ‐ Aragüés, I., Vázquez ‐ Osorio, I., Alfageme, F., Ciudad ‐ Blanco, C., Casas ‐ Férnandez, L., Rodríguez ‐ Blanco, M.I., and Suárez ‐ Fernández, R.

Subjects
*MERKEL cell carcinoma, *ULTRASONIC imaging, *SKIN cancer diagnosis, *TUMORS, *COLOR Doppler ultrasonography
Abstract

The article discusses the skin ultrasound features of Merkel cell carcinoma (MCC) and focuses on several patients related to it. Topics discussed include the important role of ultrasound imaging in diagnosis of skin cancers, the tumors that were found through ultrasound in several patients, and the intense vascularization in the intratumoural region by MCC in colour Doppler mode.

Published
2017
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38. Cutaneous collagenous vasculopathy: a case series.

Author

Vicente Basanta E, Vázquez-Osorio I, Figueroa-Silva O, Blanco Bellas M, and Suárez-Peñaranda JM

Subjects
Humans, Female, Male, Middle Aged, Adult, Aged, Collagen Diseases pathology, Collagen Diseases diagnosis, Skin Diseases, Vascular pathology, Skin Diseases, Vascular diagnosis
Published
2024
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39. Granulomatous rosacea: a clue to the diagnosis of STAT1 gain of function in a child with immunodeficiency.

Author

Buján Bonino C, Moreiras Arias N, López-Pardo Rico M, López Franco M, Loidi L, Suárez Peñaranda JM, and Vázquez Osorio I

Subjects
Humans, Gain of Function Mutation, Male, Child, Female, Rosacea diagnosis, Rosacea pathology, STAT1 Transcription Factor genetics, STAT1 Transcription Factor metabolism
Abstract

Competing Interests: Conflicts of interest The authors declare no conflicts of interest.

Published
2024
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40. Reply to: "Comment on 'Interruption of oral clindamycin plus rifampicin therapy in patients with hidradenitis suppurativa: An observational study to assess prevalence and causes'".

Author

Schneller-Pavelescu L, Vergara-de Caso E, Martorell A, Romaní J, Lázaro M, Vilarrasa E, Díaz-Ley B, Vázquez-Osorio I, Segura Palacios JM, Azaña JM, González-López MA, Cañueto J, Molina-Leyva A, Leiva-Salinas M, Navarro-Triviño FJ, Sánchez-Payá J, and Pascual JC

Subjects
Humans, Rifampin therapeutic use, Prevalence, Anti-Bacterial Agents therapeutic use, Clindamycin adverse effects, Hidradenitis Suppurativa drug therapy, Hidradenitis Suppurativa chemically induced
Published
2023
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43. Silicone Granulomas at the Peripheral Intravenous Cannula Puncture Site.

Author

Gil-Pallares P, Vázquez-Osorio I, Pérez-Feal P, and Suárez-Peñaranda JM

Subjects
Cannula adverse effects, Humans, Punctures adverse effects, Silicones adverse effects, Cosmetic Techniques adverse effects, Granuloma, Foreign-Body etiology, Granuloma, Foreign-Body pathology
Abstract

Abstract: Different adverse reactions to silicone present in cosmetic fillers, implants, or medical devices have been reported. The granulomatous reaction on the injection site due to catheters' silicone coating is an infrequent complication, which may be clinically difficult to suspect. Although the definitive diagnosis requires identification of the silicone with techniques such as X-ray spectroscopy, the possibility of involvement of silicone, as well as the histopathologic demonstration of granulomas with refractile, nonpolarizable, and nonstainable material strongly suggests this diagnosis. Moreover, the use of a low-diaphragm aperture or phase-contrast microscopy could be useful to demonstrate the presence of this, otherwise almost transparent, foreign body., Competing Interests: The authors declare no conflicts of interest. The authors declare no conflicts of interest., (Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.)

Published
2022
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45. Scabies in a 14-year-old girl with superficial epidermolytic ichthyosis.

Author

Vázquez-Osorio I, Moreiras-Arias N, Pérez-Feal P, Sainz-Gaspar L, Ortiz-Cabrera NV, and Hernández-Martín A

Subjects
Adolescent, Animals, Female, Humans, Infant, Keratin-2 genetics, Sarcoptes scabiei genetics, Hyperkeratosis, Epidermolytic diagnosis, Hyperkeratosis, Epidermolytic drug therapy, Hyperkeratosis, Epidermolytic genetics, Keratosis, Scabies complications, Scabies diagnosis, Scabies drug therapy
Abstract

A 14-year-old girl who reported generalized scaling and hyperkeratosis since age 1 year presented with severe pruritus of several months' duration. Scabies mites were detected, and molecular genetic analysis subsequently revealed a rare pathogenic variant in the keratin 2 (KRT2) gene, confirming a diagnosis of superficial epidermolytic ichthyosis. Treatment with oral ivermectin led to complete remission of symptoms. Disorders of keratinization can mimic clinical signs of scabies, leading to a delay in diagnosis., (© 2021 Wiley Periodicals LLC.)

Published
2022
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