المؤلفون: Adriana Valencia-Herrera, Luciana Ganoza-Granados, Karen Camargo-Sánchez, Yazmín A. Chirino-Barceló, Mirna Toledo-Bahena

المصدر: Acta Dermato-Venereologica, Vol 103 (2023)

مصطلحات موضوعية: Dermatology, RL1-803

الوصف: Abstract is missing (Short communication)

وصف الملف: electronic resource

العلاقة: https://medicaljournalssweden.se/actadv/article/view/3499Test; https://doaj.org/toc/0001-5555Test; https://doaj.org/toc/1651-2057Test

الوصول الحر: https://doaj.org/article/d4919b1ba563463cb6152f842ce134e9Test

المؤلفون: Constanza García-Delgado, Miguel Angel Noriega-Juárez, Alicia Cervantes, José D Abad-Flores, Mirna Toledo-Bahena, Adriana Valencia-Herrera, Carlos A Mena-Cedillos, América Villaseñor-Domínguez, Adriana Sánchez-Boiso, Yumiko Akaki-Carreño, Blanca Del Río-Navarro, Jesús Aguirre-Hernández, Marisol López-López, Marco Cerbón, Verónica F Morán-Barroso, Nancy Monroy-Jaramillo

المصدر: Dermatologica Sinica, Vol 38, Iss 3, Pp 172-175 (2020)

مصطلحات موضوعية: eda gene, heterozygous eda female carriers, hypohidrotic ectodermal dysplasia, penetrance, variable expressivity, Dermatology, RL1-803

الوصف: X-linked hypohidrotic ectodermal dysplasia (XLHED) is caused by EDA pathogenic variants. Female carriers show several clinical manifestations in variable percentages. We studied 11 Mexican heterozygous females with an EDA variant. The most frequent symptoms were similar to previous reports; however, two females (18%) reported dry eye syndrome, data rarely explored in carriers. The penetrance was 91% with clinical variability that might be related to the location of the mutation and/or to a skewed X-inactivation pattern. Our results highlight the importance of offering molecular testing to potential female carriers and support XLHED as an X-linked entity with incomplete penetrance in females.

وصف الملف: electronic resource

العلاقة: http://www.dermsinica.org/article.asp?issn=1027-8117;year=2020;volume=38;issue=3;spage=172;epage=175;aulast=GarcTestía-Delgado; https://doaj.org/toc/1027-8117Test; https://doaj.org/toc/2223-330XTest

الوصول الحر: https://doaj.org/article/483a1ce9046445dbadc08803a0c8a538Test

المؤلفون: Jade Castellanos, Andrea Guillén-Flórez, Adriana Valencia-Herrera, Mirna Toledo-Bahena, Erika Ramírez-Cortés, Sonia Toussaint-Caire, Carlos Mena-Cedillos, Marcela Salazar-García, Alexandro Bonifaz

المصدر: Journal of Fungi; Volume 7; Issue 11; Pages: 929

مصطلحات موضوعية: inflammatory tinea, Majocchi’s granuloma, dermatophytic, Hadida

جغرافية الموضوع: agris

الوصف: Purpose of review. Inflammatory tinea is an uncommon group of dermatophyte entities that predominantly cause fungal infection of the skin and hair. This review intends to present all of the available evidence regarding its epidemiology, etiopathogenesis, clinical features, and diagnostic methods as well as treatments recommended for various inflammatory tinea infections. This article provides a review of Majocchi’s granuloma and dermatophytic or Hadida’s disease. Recent findings. The new phylogenetic classification of dermatophytes includes nine genera, and those that affect humans are Trichophyton, Microsporum, Epidermophyton, and Nannizzia. Furthermore, molecular advancements have revealed impaired antifungal immune responses caused by inflammatory tinea, which are detailed in this article. Summary. The common denominator in these pathologies is the presence of impaired immune responses and, consequently, an impaired inflammatory response by the host. It is necessary to be familiar with these immunological characteristics in order to use the appropriate diagnostic methods and to provide adequate treatment.

وصف الملف: application/pdf

العلاقة: Fungal Pathogenesis and Disease Control; https://dx.doi.org/10.3390/jof7110929Test

الإتاحة: https://doi.org/10.3390/jof7110929Test

المؤلفون: Catalina Rincón-Pérez, Désirée Larenas-Linnemann, Marco Antonio Figueroa-Morales, Jorge Luna-Pech, Linda García-Hidalgo, Alejandra Macías-Weinmann, Javier Gómez-Vera, José Fernando Barba-Gómez, Juan José Juan José Matta-Campos, Esther Guevara-Sangines, Fermín Jurado-Santacruz, Adriana López Tello-Santillán, José Antonio Ortega-Martell, Nancy Pulido-Díaz, Liliana Guadalupe Serrano-Jaén, Mirna Toledo-Bahena, Guadalupe Villanueva-Quintero, José Luis Mayorga-Butrón

المصدر: Revista Alergia México, Vol 65 suppl 1 (2018)

مصطلحات موضوعية: dermatitis atópica, ciclosporina a, tratamiento biológico, dupilumab, omalizumab, posición de consenso, Immunologic diseases. Allergy, RC581-607

الوصف: Background: The diagnostic approaches and therapeutic strategies of atopic dermatitis (AD) are generally inconsistent among physicians and health institutions. Objective: To develop a consensus statement among experts to reduce the variations in practice regarding the diagnosis and treatment of patients ≥ 12 years with AD to improve their care. Methods: Systematic literature search in PubMed and GREAT. With methodological support and using the Delphi method, a formal consensus was developed among 16 experts in Dermatology and Allergology, based on the current evidence and its applicability in the Mexican context. Apart from intense electronic communication, several issues of disagreement were discussed in two face-to-face meetings. Results: The clinical experts reached consensus on 46 statements related to the definition, classification, diagnostic strategies and treatment of AD. For the diagnosis we suggest the Williams criteria and for severity scoring the SCORAD (by the doctor) and POEM (by the patient). In addition to general care and treatment education (workshops), we suggest four steps for treatment, depending on severity: 1. Topical treatment with anti-inflammatory agents (and systemic: antihistamines/antileukotrienes —low level evidence—) 2. Phototherapy, 3. Cyclosporin A and 4. Dupilumab, with the possibility of managing this biological earlier on if a fast effect is needed. In extrinsic AD we suggest evaluating the addition of allergen immunotherapy or an elimination diet, if there is an IgE-mediated respiratory or food allergy, respectively. Conclusion: The panel of experts reached consensus on relevant aspects of AD with a focus on the transcultural adaptation of recent evidence.

وصف الملف: electronic resource

العلاقة: http://revistaalergia.mx/ojs/index.php/ram/article/view/526Test; https://doaj.org/toc/0002-5151Test; https://doaj.org/toc/2448-9190Test

الوصول الحر: https://doaj.org/article/bd5efcaacd8d4c818c561c37d130c03cTest

المؤلفون: Adriana Valencia-Herrera, Luciana Ganoza-Granados, Karen Camargo-Sánchez, Yazmín A. Chirino-Barceló, Mirna Toledo-Bahena

المصدر: Acta dermato-venereologica.

مصطلحات موضوعية: Dermatology, General Medicine

الوصف: is missing (Short communication)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c8be8db8cb290cfc5efa93e56d45379Test
https://pubmed.ncbi.nlm.nih.gov/36172694Test

المؤلفون: Adriana Valencia-Herrera, Mirna Toledo-Bahena, Mario Duarte-Abdala, Karen Adilene Camargo-Sánchez, Alexandro Bonifaz, Carlos Mena-Cedillos, J. A. López-Gamboa

المصدر: Current Fungal Infection Reports. 15:41-48

مصطلحات موضوعية: 0301 basic medicine, Voriconazole, medicine.medical_specialty, Posaconazole, Itraconazole, business.industry, 030106 microbiology, Cutaneous aspergillosis, Disease, Aspergillosis, medicine.disease, Dermatology, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Infectious Diseases, chemistry, medicine, 030212 general & internal medicine, Caspofungin, Primary cutaneous aspergillosis, business, medicine.drug

الوصف: This is a general review of the disease in this article, especially of the clinical features, diagnosis, new treatments and preventive measures. Diagnostic methods in pediatric population to confirm the diagnosis of aspergillosis and typify the etiologic agent are based on the use of molecular biology through PCR techniques. Currently, the treatment of choice for cases of primary cutaneous aspergillosis is liposomal amphotericin B or itraconazole alone or synergistically, uuse of voriconazole, posaconazole, or caspofungin is recommended as a second-line management. Cutaneous aspergillosis is a rare condition in immunocompetent individuals and is more frequently observed in immunosuppressed patients. Considering the pediatric population as a specific case, it more commonly occurs in individuals suffering from a hemato-oncological disease. Asperillus flavus and A. fumigatus are the main pathogens responsible for primary and secondary (invasive) cutaneous aspergillosis, respectively. The clinical picture develops after direct inoculation of the fungus by contiguity of infected cavities or secondary to the presence of a distant mycotic focus that reaches the skin and its annexes by hematogenous dissemination. Owing to the rapid progression of the disease, a delay in initiating proper management impacts patient mortality. In case of children and adolescents, clinical suspicion in individuals with risk factors should be the main argument for starting pharmacological management in a timely manner.

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c6875a30e2a479f9b462c9bcbc33ff77Test
https://doi.org/10.1007/s12281-021-00410-0Test

المؤلفون: Adriana Valencia-Herrera, Alexandro Bonifaz, Mario Duarte-Abdala, Mirna Toledo-Bahena, Carlos Mena-Cedillos, A. P. Sánchez-Padilla, Marcela Salazar-García

المصدر: Current Fungal Infection Reports. 13:175-180

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, medicine.diagnostic_test, biology, business.industry, 030106 microbiology, Direct examination, Disease, medicine.disease, biology.organism_classification, Dermatology, Congenital cutaneous candidiasis, 03 medical and health sciences, 0302 clinical medicine, Infectious Diseases, Premature newborn, Skin biopsy, Etiology, medicine, 030212 general & internal medicine, Candida albicans, business

الوصف: We have created a general review of the disease in this article, especially of the clinical features, diagnosis, new treatments and preventive measures. Congenital cutaneous candidiasis is a vertically transmitted fungal infection which affects term and premature newborn. It is considered as an underdiagnosed pathology, and infection caused by Candida albicans is considered the most common aetiology. Clinically characterized by erythematous papular lesions and pustules with collarette scale. It can also affect other organs and systems by causing an invasive fungal infection. Diagnosis is clinical, and the agent can be isolated; other tools of diagnosis include direct examination and skin biopsy. Regarding the treatment, this infection can be self-limiting in a majority of cases and topical antifungals constitute the treatment of choice. However, in the case of a systemic condition, the first-line treatment is amphotericin B. Prognosis is good, although it is unfavourable in the case of a systemic condition.

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::6d58be6a89b39851e3d6e9198094b771Test
https://doi.org/10.1007/s12281-019-00359-1Test

المؤلفون: Sonia Toussaint-Caire, Erika Ramirez-Cortes, Mirna Toledo-Bahena, Alexandro Bonifaz, Marcela Salazar-García, Carlos Mena-Cedillos, Adriana Valencia-Herrera, Karen Adilene Camargo-Sánchez

المصدر: Current Fungal Infection Reports. 13:157-168

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, business.industry, 030106 microbiology, Pityriasis, Disease, Diagnostic tools, medicine.disease, Dermatology, Superficial mycosis, Tinea versicolor, 03 medical and health sciences, 0302 clinical medicine, Infectious Diseases, Epidemiology, Etiology, Medicine, 030212 general & internal medicine, business

الوصف: Pityriasis versicolor (PV) is a superficial mycosis that it can occur at any age, even in newborns. In this review, we will describe epidemiological data, mycological characteristics of yeast, pathogenesis and clinical characteristics of the disease, different diagnostic resources, and the current recommendations for treatment. The typical morphology and topography of PV allow us to make a quick diagnosis, but atypical presentations have been described. Diagnostic tools, such as dermoscopy, can also reveal patterns that allow the evaluation of characteristics of scales and pigment in lesions. The discovery of new species and new mechanisms of interaction with the host has broadened the panorama of aetiological possibilities. Although PV is a common disorder, extensive research is necessary to better understand the pathophysiology of the disease, immunological characteristics of the pathogen-host relationship and resources needed to precisely diagnose the disease, treat the disease, and avoid its chronic and recurrent course.

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::59de547e4e35b44ef96eea6330f897a6Test
https://doi.org/10.1007/s12281-019-00360-8Test

المؤلفون: Erika Ramirez-Cortes, Alexandro Bonifaz, Sonia Toussaint-Caire, Jade Castellanos, Adriana Valencia-Herrera, Marcela Salazar-García, Andrea Guillén-Flórez, Carlos Mena-Cedillos, Mirna Toledo-Bahena

المصدر: Journal of Fungi
Journal of Fungi, Vol 7, Iss 929, p 929 (2021)

مصطلحات موضوعية: Microbiology (medical), medicine.medical_specialty, QH301-705.5, Plant Science, Disease, Review, medicine.disease_cause, Immune system, medicine, Trichophyton, Epidermophyton, Biology (General), inflammatory tinea, Ecology, Evolution, Behavior and Systematics, Hadida, dermatophytic, biology, business.industry, Majocchi’s granuloma, biology.organism_classification, medicine.disease, Dermatology, Granuloma, Dermatophyte, Tinea Infection, business, Microsporum

الوصف: Purpose of review. Inflammatory tinea is an uncommon group of dermatophyte entities that predominantly cause fungal infection of the skin and hair. This review intends to present all of the available evidence regarding its epidemiology, etiopathogenesis, clinical features, and diagnostic methods as well as treatments recommended for various inflammatory tinea infections. This article provides a review of Majocchi’s granuloma and dermatophytic or Hadida’s disease. Recent findings. The new phylogenetic classification of dermatophytes includes nine genera, and those that affect humans are Trichophyton, Microsporum, Epidermophyton, and Nannizzia. Furthermore, molecular advancements have revealed impaired antifungal immune responses caused by inflammatory tinea, which are detailed in this article. Summary. The common denominator in these pathologies is the presence of impaired immune responses and, consequently, an impaired inflammatory response by the host. It is necessary to be familiar with these immunological characteristics in order to use the appropriate diagnostic methods and to provide adequate treatment.

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0f0747047c0f90c752c791e6b0a1726Test
http://europepmc.org/articles/PMC8617809Test

المؤلفون: Mario Duarte-Abdala, Carlos Mena-Cedillos, Mirna Toledo-Bahena, Juan A Godínez-Chaparro, Adriana Valencia-Herrera

المصدر: Boletín Médico del Hospital Infantil de México, Vol 78, Iss 5 (2021)

مصطلحات موضوعية: Male, medicine.medical_specialty, Skin Neoplasms, Acute myeloblastic leukemia, Mucocutaneous zone, Disease, Pediatrics, RJ1-570, Cohort Studies, Epidemiology, medicine, Humans, Child, Retrospective Studies, Skin, business.industry, Myeloid leukemia, Leukemia cutis, Retrospective cohort study, Hyperplasia, medicine.disease, Dermatology, Leukemia cutis. Cutaneous leukemia. Pediatric cutaneous leukemia. Acute myeloid leukemia, Leukemia, Myeloid, Acute, Pediatrics, Perinatology and Child Health, Public aspects of medicine, RA1-1270, medicine.symptom, business

الوصف: Leukemia cutis (LC) is the infiltration of neoplastic leukocytes into the skin, causing skin lesions. In children, it appears more frequently in patients with acute myeloblastic leukemia (AML), particularly in subtypes with a monocytic component.We studied a retrospective cohort including all AML cases from the Hospital Infantil de México Federico Gómez between January 2009 to December 2019 and described the clinical characteristics of those who presented LC and other mucocutaneous manifestations. The information was collected from clinical records and analyzed using SPSS software (version 17).We identified 54 AML cases: 53.7% were males, and 75.9% of the patients presented at least one dermatosis in the course of the disease. LC was clinically present in 14.8% of patients and was histologically confirmed in 9.2% of them; two congenital leukemia cases were identified. Among these patients, LC was more frequent in males. LC patients were younger than those without LC, the most frequent AML subtype was M2 (37.5%), and the most frequent clinical manifestations were plaques, chloromas, and gingival hyperplasia. None of the patients presented LC before AML diagnosis.Currently, only a few studies about LC on pediatric populations have been reported, and the existing ones have small sample sizes. We found clinical and epidemiological similarities with other populations in the studied sample.La leucemia cutis (LC) es la infiltración de leucocitos neoplásicos a la piel que provoca lesiones cutáneas. En la población infantil aparece con más frecuencia en pacientes con leucemia mieloblástica aguda (LMA), principalmente en los subtipos con componente monocítico.Se estudió una cohorte retrospectiva en el Hospital Infantil de México Federico Gómez entre enero de 2009 y diciembre de 2019 para conocer las características clínicas de los pacientes con LMA que cursaron con LC y otras manifestaciones mucocutáneas. La información se recabó de los expedientes clínicos y se analizó con el programa estadístico SPSS versión 17.Se identificaron 54 casos de LMA: el 53.7% en el sexo masculino y el 46.3% en el sexo femenino. El 75.9% de los pacientes presentaron alguna dermatosis durante el curso de su enfermedad. La LC se presentó clínicamente en el 14.8% de los pacientes y se confirmó histológicamente en el 9.2% de ellos; dos casos correspondieron a leucemia congénita. De estos pacientes, la LC fue más frecuente en el sexo masculino, los pacientes fueron más jóvenes que el grupo sin LC, el subtipo de LMA más frecuente fue el M2 (37.5%) y las principales manifestaciones clínicas fueron placas infiltradas, cloromas e hiperplasia gingival. Ninguno de los pacientes presentó LC antes del diagnóstico de LMA.Hasta ahora existen pocos estudios de LC en las diferentes variedades de leucemia en la población infantil, y los existentes cuentan con un tamaño de muestra pequeño. En este estudio se reportan estadísticas descriptivas y se encuentran similitudes clínico-epidemiológicas con otras poblaciones.

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee250b2d20e410254052c04827423dabTest
https://pubmed.ncbi.nlm.nih.gov/34571521Test