Carlos Galarza
National University of San Marcos
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Featured researches published by Carlos Galarza.
International Journal of Dermatology | 2006
Alex Gerardo Ortega Loayza; Willy Ramos; George Elgart; Peter Bouman; Gerardo Jiménez; Jack Avila; Isabel Rojas; María Vilcarromero; Jorge Hurtado; Gisella Lindo; Carlos Galarza
Background Endemic pemphigus foliaceus or fogo selvagem is an autoimmune skin disease characterized by the presence of subcorneal superficial blisters and antibodies of the immunoglobulin G4 (IgG4) class specific for the desmosomal glycoprotein, desmoglein 1. In Peru, no studies have been published on the seroprevalence of antibodies against desmoglein 1 in healthy subjects from endemic foci.
International Journal of Dermatology | 2009
Carlos Galarza; Willy Ramos; Ericson L. Gutierrez; Gerardo Ronceros; Maria Teran; Martha Uribe; Marcos Ñavincopa; Alex G. Ortega-Loayza
Background Cutaneous acanthamebiasis is a rare infection and few patients have been reported worldwide.
Anais Brasileiros De Dermatologia | 2010
Alex G. Ortega-Loayza; Willy Ramos; Ericson L. Gutierrez; Patricia Chávez de Paz; Lucia Bobbio; Carlos Galarza
In a public hospital in Lima, Peru, 24 patients with 16 types of paraneoplastic dermatoses were identified by data collection. The most frequent dermatosis was dermatomyositis (four patients). The other dermatoses were malignant acanthosis nigricans, palmoplantar keratoderma, bullous dermatoses, lymphomatoid papulosis, edematous scarring vasculitic panniculitis, Norwegian scabies, primary systemic amyloidosis, necrolytic migratory erythema, infective dermatitis, pancreatic panniculitis, generalized pruritus, Lesser-Trelat syndrome, and acquired ichthyosis. Most of these paraneoplastic dermatoses were diagnosed before (45.8%) or at the time of (38.5%) the diagnosis of the underlying malignancy. The most frequent underlying malignancies were lymphoma, adenocarcinomas of the upper digestive tract, and malignant neoplasms of the pancreas. The average age of the patients was 47.0 ± 16.9 years and the length of the disease since diagnosis was 13.7 months. The mortality rate was 75%. Paraneoplastic dermatoses are rare dermatologic entities that are difficult to diagnose. Surveillance is also hampered when patients do not have easy access to health care centers due to financial and geographical issues. However, when identified, they might facilitate the early diagnosis of an associated tumor and contribute to increase the surveillance of patients.
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 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 | 2010
Ericson L. Gutierrez; Carlos Galarza; Willy Ramos; Maybbe Mendoza; María E. Smith; Alex G. Ortega-Loayza
Anales de la Facultad de Medicina | 2013
Carlos Galarza; Gerardo Ronceros; Dante Mendoza; Gadwin Sánchez; María Vilcarromero; Ernesto Ráez
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
Acta Médica Peruana | 2007
Willy Ramos; Alex G. Ortega-Loayza; Jorge Hancco; Ericson L. Gutierrez; Jorge Hurtado; Gerardo Jiménez; Gerardo Ronceros; Isabel Rojas; Carlos Galarza