Pedro Herranz Pinto
Hospital Universitario La Paz
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Publication
Featured researches published by Pedro Herranz Pinto.
European Journal of Dermatology | 2011
Cristina Gómez-Fernández; Pedro Herranz Pinto; Beatriz Casado Verrier; Elena Sendagorta Cudós; María Beato-Merino; Mariano Casado Jiménez
Auteur(s) : Cristina GOMEZ-FERNANDEZ1 [email protected], Pedro HERRANZ PINTO1, Beatriz CASADO VERRIER1, Elena SENDAGORTA CUDOS1, Maria Jose BEATO-MERINO2, Mariano CASADO JIMENEZ1 1 University Hospital La Paz, Department of Dermatology, Paseo de la Castellana, 261, 28046. Madrid, Spain 2 University Hospital La Paz, Department of Pathology, Madrid, Spain Bupropion hydrochloride is a psychotropic drug with significant antidepressant effects through the inhibition of re-uptake of norepinephrine [...]
International Journal of Dermatology | 2015
Ana Isabel Rodríguez Bandera; Cristina Gómez Fernández; K. Vorlicka; Elena Ruiz‐Bravo Burguillo; Pedro Herranz Pinto
Panitumumab is a fully human monoclonal antibody that inhibits the epidermal growth factor receptor (EGFR). It was approved by the Food and Drug Association in 2006, and it is currently considered a useful option in patients with wild-type KRAS tumors when used in combination with chemotherapy for the firstor second-line treatment of metastatic colorectal cancer or as monotherapy for the treatment of metastatic colorectal cancer refractory to chemotherapy. Panitumumab has an acceptable tolerability profile with less systemic toxicities than traditional cytotoxic agents and with lower immunogenetic power than cetuximab, a chimerical monoclonal antibody anti-EGFR. Hypomagnesemia has been reported in a third of patients. Other common systemic adverse events have been described such as fatigue, abdominal pain, anorexia, nausea, diarrhea, constipation, and vomiting. However, the most frequent reported adverse events are cutaneous reactions, experienced by nearly 100% of patients treated with panitumumab. Like other EGFR inhibitors, panitumumab is associated with papulopustular rash, xerosis, pruritus, and nail, hair, and mucosal changes. The severity of dermatologic side effects is associated with the efficacy of treatment, but when they impair life quality, they can hamper compliance and lead to treatment refusal. We present a case of severe folliculitis in the scalp with secondary impetiginization in a 76-year-old woman with metastatic colorectal cancer treated with panitumumab that forced treatment to be withdrawn.
Actas Dermo-Sifiliográficas | 2001
Marta Ruano del Salado; Pedro Herranz Pinto; Julio García; Silvia Salinas; Elena Naz Villalba; Mariano Casado Jiménez
Resumen —Presentamos el caso de un varon de 37 anos VIH positivo, con nodulos subcutaneos faciales, sin historia previa de infeccion micotica superficial. El estudio histologico mostraba granulomas en dermis centrados por estructuras fungicas. En cultivos repetidos se identifico Microsporum canis. (Actas Dermosifiliogr 2001;92:364-366).
Journal of Dermatological Treatment | 2017
Mariano Ara-Martín; Pedro Herranz Pinto; Dora Pascual-Salcedo
Abstract Purpose: This study was conducted to examine the relationship between loss of clinical response to anti-tumor necrosis factor (TNF) therapy and the production of anti-drug antibodies (ADAs) and the potential effects of biologic immunogenicity. Materials and methods: This observational, non-interventional, cross-sectional study included patients with moderate-to-severe plaque psoriasis and secondary failure of adalimumab, etanercept and infliximab who were seen in the clinical practice setting. Clinical data and blood samples were collected after patient enrollment at the time that next doses of anti-TNF therapy were scheduled. ADA and serum drug concentrations were detected at a central reference laboratory using ELISA. Results: Among 137 enrolled patients, ADA were identified in 31/65 (48%), 0/47 and 8/19 (42%) of patients treated with adalimumab, etanercept and infliximab, respectively. The presence of ADA was associated with a slightly worse clinical response in adalimumab-treated patients (Physician Global Assessment score: 3.7 vs. 3.2, ADA-positive vs. ADA-negative patients [p < .05]; correlation between serum ADA titer and body surface area: r = .292 [p = .019]). Concomitant DMARDs were not associated with anti-TNF immunogenicity in any treatment group. Conclusions: Additional evidence is needed from studies of anti-TNF therapy in psoriasis for clinicians to gain a better understanding of the impact of immunogenicity on clinical response.
Revista Clínica de Medicina de Familia | 2011
Paola Maldonado Cid; Elena Sendagorta Cudós; Lucero Noguera Morel; Pedro Herranz Pinto
Abstract es: Presentamos el caso de un paciente con lesiones purpuricas en regiones acrales. El diagnostico diferencial de este tipo de lesiones incluye patologias mu...
Journal of The American Academy of Dermatology | 2012
Paola Maldonado Cid; Ricardo Moreno-Alonso de Celada; Pedro Herranz Pinto; Lucero Noguera Morel; Rosa Feltes Ochoa; María José Beato Merino; Elena Collantes Bellido; Mónica López Rodríguez; Mariano Casado Jiménez
International Journal of Dermatology | 2015
Ander Mayor Ibarguren; Cristina Gómez Fernández; Antonio Tallón Barranco; Mireya Fernández Fournier; Jéssica González Ramos; María Pilar Romero Gómez; Pedro Herranz Pinto
European journal of clinical pharmacy: atención farmacéutica | 2015
M. A. González Fernández; Francisco Moreno Ramos; Adolfo Varela Hugo; C. Plasencia; Dora Pascual-Salcedo; Pedro Herranz Pinto; Alicia Herrero Ambrosio
European Journal of Dermatology | 2010
Cristina Gómez-Fernández; Marta Feito Rodríguez; Beatriz Casado Verrier; Pedro Herranz Pinto; María Beato-Merino; Mariano Casado Jiménez
Medicina cutánea ibero-latino-americana | 2005
Eduardo López de Ayala Casado; Yolanda Prats Caelles; Dulce María Arranz Sánchez; Miriam Corral La Calle; Mariano Casado Jiménez; Pedro Herranz Pinto