Mercedes Tello
National University of San Marcos
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Revista Iberoamericana De Micologia | 2015
Vilma Béjar; Mercedes Tello; Ruth García; José M. Guevara; Sofia Gonzales; Germán Vergaray; Esther Valencia; Enma Abanto; Alex G. Ortega-Loayza; Ferry Hagen; Ericson L. Gutierrez
BACKGROUND Cryptococcosis is a fungal infection with a worldwide distribution, mainly caused by Cryptococcus neoformans and Cryptococcus gattii. AIMS To molecularly characterize the mating-types, serotypes, genotypes and antifungal susceptibility profiles of a set of retrospectively isolated C. neoformans strains from Lima, Peru. METHODS A set of 32 Cryptococcus spp. strains from the Institute of Tropical Medicine of the National University of San Marcos, Lima, Peru, were included in this retrospective study. Twenty-four strains were isolated from patients, while the remaining 8 were isolated from the environment. RESULTS Using conventional PCR, 27 (84.4%) of the isolates were identified as C. neoformans var. grubii mating-type alpha and serotype A. Using the AFLP fingerprinting, it was shown that 16 (50%) of the C. neoformans strains were genotype AFLP1, 13 (40.6%) were genotype AFLP1B, 2 (6.3%) were genotype AFLP2, and 1 (3.1%) was found to be a hybrid between both C. neoformans varieties (genotype AFLP3). The antifungal susceptibility profiles for amphotericin B, fluconazole and voriconazole showed that all the 32 C. neoformans are sensitive to these antifungal compounds. CONCLUSIONS In this study we observed that C. neoformans var. grubii (AFLP1 and AFLP1B) and C. neoformans var. neoformans (AFLP2) were the only cryptococcal varieties involved. All strains were found to be sensitive to the antifungals tested, results that are consistent with those found in the international literature.
International Journal of Dermatology | 2010
Ericson L. Gutierrez; Carlos Galarza; Willy Ramos; Mercedes Tello; Gerardo Jiménez; Gerardo Ronceros; Humberto Chía; Jorge Hurtado; Alex G. Ortega-Loayza
Background Dermatologic diseases vary widely as a result of geographic location and may be influenced by environmental factors.
Revista Da Sociedade Brasileira De Medicina Tropical | 2010
Ericson L. Gutierrez; Willi Valqui; Luis Vilchez; Lourdes Evangelista; Sarita Crispin; Mercedes Tello; Marcos Ñavincopa; Vilma Béjar; José Gonzales; Alex G. Ortega-Loayza
We report a case of an immunocompetent Peruvian patient from the Andes with a one-month history of meningoencephalitis. Cryptococcus gattii was identified from a cerebrospinal fluid culture through assimilation of D-proline and D-tryptophan as the single nitrogen source. Initially, the patient received intravenous antifungal therapy with amphotericin B. The patient was discharged 29 days after hospitalization and continued with oral fluconazole treatment for ten weeks. During this period, the patient showed clinical improvement with slight right-side residual weakness. Through this case report, we confirm the existence of this microorganism as an infectious agent in Peru.
Revista Medica De Chile | 2009
Carlos Galarza; Ericson L. Gutierrez; Willy Ramos; Mercedes Tello; Gerardo Ronceros; Sergio Alvizuri; Filda Valverde; Alex G. Ortega-Loayza
Endemic pemphigus foliaceus (EPF) in an autoimmune skin disease present in areas of the Amazonia. We report a 36 year-old woman who presented EPF at 17 weeks of pregnancy. At 29 weeks, she started antimicrobial treatment and steroids. At the moment of delivery, the disease was in remission and cutaneous lesions were not seen in the neonate. Indirect immunofluorescence titers of total IgG in the mother and in the neonate were negative. Sixteen months later, IgG titers in the offspring were 1/20 and remained negative in the mother, who was on low doses of oral corticosteroids.
Australasian Journal of Dermatology | 2010
Ericson L. Gutierrez; Carlos Galarza; Willy Ramos; Mercedes Tello; Patricia Chávez de Paz; Lucia Bobbio; Alicia Barquinero; Gerardo Ronceros; Alex G. Ortega-Loayza
Porokeratosis is a disorder of epidermal keratinization characterized by annular plaques with an atrophic centre and hyperkeratotic edges, and includes a heterogeneous group of disorders that are mostly inherited in an autosomal dominant fashion. Facial porokeratosis is rare and is not well documented. We present six cases of facial porokeratosis seen over a period of 15 years in a hospital in Lima, Peru. In most of the cases, porokeratosis was found in younger women without any significant past medical history. Oral isotretinoin showed moderate improvement in two of our patients.
Anais Brasileiros De Dermatologia | 2018
Ericson L. Gutierrez; Willy Ramos; Lucia Seminario-Vidal; Mercedes Tello; Gerardo Ronceros; Alex G. Ortega-Loayza
BACKGROUND Previous studies have shown oxidative stress in pemphigus vulgaris and pemphigus foliaceus, nevertheless, it remains unknown whether a similar response is characteristic of endemic pemphigus foliaceus in Peru. OBJECTIVES To determine the oxidative stress response in endemic pemphigus foliaceus patients and subjects with positive for anti-desmoglein1 antibodies (anti-dsg1) from endemic areas of Peru. SUBJECTS AND METHODS This is a cross-sectional study. The study population included 21 patients with Endemic Pemphigus foliaceus and 12 healthy subjects with anti-dsg1 antibodies from the Peruvian Amazon (Ucayali), as well as 30 healthy control subjects. Malondialdehyde, an indicator of lipid peroxidation by free radicals, was measured in serum. RESULTS We collected 21 cases of endemic pemphigus foliaceus, 15 of them with active chronic disease and 6 in clinical remission. Serum malondialdehyde values in patients with chronic active evolution and healthy subjects with anti-dsg1 antibodies were statistically higher than those of healthy controls (p<0.001). There was no significant difference between serum values of localized and generalized clinical forms. STUDY LIMITATIONS The main limitation of this present study is the small number of patients with endemic pemphigus and healthy subjects positive for desmoglein 1 antibodies. CONCLUSIONS The increased serum levels of malondialdehyde in patients with chronic active endemic pemphigus foliaceus and healthy subjects from endemic areas with anti-dsg1 antibodies may suggest a contribution of systemic lipid peroxidation in the pathogenesis of endemic pemphigus foliaceus.Background Previous studies have shown oxidative stress in pemphigus vulgaris and pemphigus foliaceus, nevertheless, it remains unknown whether a similar response is characteristic of endemic pemphigus foliaceus in Peru. Objectives To determine the oxidative stress response in endemic pemphigus foliaceus patients and subjects with positive for anti-desmoglein1 antibodies (anti-dsg1) from endemic areas of Peru. Subjects and Methods This is a cross-sectional study. The study population included 21 patients with Endemic Pemphigus foliaceus and 12 healthy subjects with anti-dsg1 antibodies from the Peruvian Amazon (Ucayali), as well as 30 healthy control subjects. Malondialdehyde, an indicator of lipid peroxidation by free radicals, was measured in serum. Results We collected 21 cases of endemic pemphigus foliaceus, 15 of them with active chronic disease and 6 in clinical remission. Serum malondialdehyde values in patients with chronic active evolution and healthy subjects with anti-dsg1 antibodies were statistically higher than those of healthy controls (p<0.001). There was no significant difference between serum values of localized and generalized clinical forms. Study limitations The main limitation of this present study is the small number of patients with endemic pemphigus and healthy subjects positive for desmoglein 1 antibodies. Conclusions The increased serum levels of malondialdehyde in patients with chronic active endemic pemphigus foliaceus and healthy subjects from endemic areas with anti-dsg1 antibodies may suggest a contribution of systemic lipid peroxidation in the pathogenesis of endemic pemphigus foliaceus.
Dermatol. peru | 2009
Willy Ramos; Carlos Galarza; Ericson L. Gutierrez; Gerardo Jiménez; Isabel Rojas; Jorge Hancco; Gerardo Ronceros; Leopoldo Munive; Mercedes Tello; María Vilcarromero; Nancy Rojas; Alex G. Ortega-Loayza
Dermatol. peru | 2009
Carlos Galarza; Mercedes Tello; Ericson L. Gutierrez; Patricia Güere; Willy Ramos
Dermatol. peru | 2009
Ericson L. Gutierrez; Carlos Galarza; Willy Ramos; Mercedes Tello; Isabel Rojas; Humberto Chía; Gerardo Ronceros; Alex G. Ortega-Loayza
Dermatol. peru | 2009
Carlos Galarza; Willy Ramos; Ericson L. Gutierrez; Jesús Díaz; Judith Munive; Gerardo Ronceros; Jorge Hurtado; Jack Avila; Mercedes Tello; Alex G. Ortega-Loayza