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Dive into the research topics where Diana Andrea Herrera-Sánchez is active.

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Featured researches published by Diana Andrea Herrera-Sánchez.


robotics, automation and mechatronics | 2018

Síndrome látex-papaya: una asociación poco frecuente

Victoria Rojas-Mandujano; Kitzia González-Juárez; Cecilia Hernández-Fernández; Patricia María O’Farrill-Romanillos; Leonel Del Rivero; Diana Andrea Herrera-Sánchez

BACKGROUND Latex-fruit syndrome (LFS) is characterized by allergy to latex and plants. Papain, chymopapain, caricaine and class I chitinases are papayas most allergenic proteins. The similarity between latex hevein epitopes and papaya class I chitinases might explain the latex-papaya syndrome (LPS). OBJECTIVE To describe the clinical characteristics of patients with LPS. METHODS Cross-sectional, observational, descriptive study where 11 patients diagnosed with latex allergy by skin prick test and clinically diagnosed with papaya-induced anaphylaxis were included. The results were analyzed with descriptive statistics. RESULTS Out of 11 patients with LPS, 72.7% were females (7 to 46 years), all with a history of papaya-induced anaphylaxis, identified by medical history and medical notes plus latex-positive skin prick tests, with 63.3% exhibiting anaphylaxis in the skin prick tests. Risk factors included multiple surgeries, another allergic disease, and being employed in the field of health; 63.6% were allergic to to other foods, 45.4% to medications, 45.4% had allergic rhinitis and 27.3% had asthma. CONCLUSIONS Hypersensitivity to papaya increases the risk of anaphylaxis in patients with latex allergy and, therefore, mortality. Clinical data is the main diagnostic tool. Education for the management of anaphylaxis with adrenaline self-administration is essential.


robotics, automation and mechatronics | 2018

Severidad de bronquiectasias en pacientes adultos con inmunodeficiencia común variable

Irving Jesús Vivas-Rosales; Mariana Hernández-Ojeda; Patricia María O'Farrill-Romanillos; Diana Andrea Herrera-Sánchez; Abril Helena Maciel-Fierro; Juan Carlos Núñez-Enríquez

BACKGROUND Common variable immunodeficiency (CVID) is the most common primary symptomatic humoral immunodeficiency in adults. Antibody deficiency entails higher susceptibility to sinopulmonary infections and bronchiectasis formation, which is related to increased mortality. Scales have been established to assess the degree of severity of bronchiectasis in order to predict outcomes such as mortality, exacerbations and hospitalizations. OBJECTIVE To determine bronchiectasis severity in adult patients with common variable immunodeficiency using the Brief Symptom Inventory scale. METHOD Cross-sectional study in adult population diagnosed with common variable immunodeficiency and attended to at the Mexican Institute of Social Security National Medical Center Siglo XXI Specialty Hospital. RESULTS Bronchiectasis severity according to the Brief Symptom Inventory was mild in 60% of patients and moderate in 40%. Statistically significant differences were found for body mass index, number of affected lobes and type of bronchiectasis (p < 0.001). CONCLUSIONS Using bronchiectasis severity scales in patients with common variable immunodeficiency is indispensable for clinical and therapeutic decision making; however, determining the most appropriate instrument to assess bronchiectasis severity in this population is necessary.


Revista alergia Mexico | 2015

Infection due to Mycobacterium bovis in common variable immunodeficiency

Diana Andrea Herrera-Sánchez; Castilla-Rodríguez Jl; Castrejón-Vázquez Mi; Vargas-Camaño Me; Medina-Torres Ea; Blancas-Galicia L; Sara Elva Espinosa-Padilla


robotics, automation and mechatronics | 2017

Inmunodeficiencia común variable en adultos

Patricia María O’Farrill-Romanillos; Diana Andrea Herrera-Sánchez; Cecilia Hernández-Fernández; Eunice Giselle López-Rocha


robotics, automation and mechatronics | 2017

Trasplante de médula ósea en pacientes con inmunodeficiencia común variable, ¿es una opción terapéutica?

Julio César Cambray-Gutiérrez; Diana Andrea Herrera-Sánchez; Patricia López-Pérez; Aurora Alejandra Chávez-García; Marco Antonio Yamazaki-Nakashimada


robotics, automation and mechatronics | 2017

Síndrome de Good. Reporte de un caso

Diana Andrea Herrera-Sánchez; José Israel León-Pedroza; María Eugenia Vargas-Camaño; María Isabel Castrejón-Vázquez


Revista alergia Mexico | 2017

Hematopoietic stem cells transplant in patients with common variable immunodeficiency. Is a therapeutic option

Cambray-Gutiérrez Jc; Diana Andrea Herrera-Sánchez; López-Pérez P; Chávez-García Aa; Marco Antonio Yamazaki-Nakashimada


robotics, automation and mechatronics | 2016

Clínica de inmunodeficiencias primarias en adultos. Experiencia en un hospital de tercer nivel

Julio César Cambray-Gutiérrez; Diana Andrea Herrera-Sánchez; Lizbeth Blancas-Galicia; Patricia María O’Farrill-Romanillos


robotics, automation and mechatronics | 2016

Identificación de microorganismos asociados con rinosinusitis crónica en pacientes adultos con inmunodeficiencia común variable

Gabriela Angulo-Pérez; Eulalio Vivar-Acevedo; Diana Andrea Herrera-Sánchez


Revista alergia Mexico | 2016

Clinic of humoral primary immunodeficiencies in adults. Experience in a tertiary hospital

Cambray-Gutiérrez Jc; Diana Andrea Herrera-Sánchez; Blancas-Galicia L; O'Farrill-Romanillos Pm

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Marco Antonio Yamazaki-Nakashimada

National Autonomous University of Mexico

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Sara Elva Espinosa-Padilla

National Autonomous University of Mexico

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Abril Helena Maciel-Fierro

Mexican Social Security Institute

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Eulalio Vivar-Acevedo

Mexican Social Security Institute

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Eunice Giselle López-Rocha

Mexican Social Security Institute

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Gabriela Angulo-Pérez

Mexican Social Security Institute

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