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1.
Cureus ; 16(5): e59565, 2024 May.
Article in English | MEDLINE | ID: mdl-38826967

ABSTRACT

Terra firma-forme dermatosis is an acquired and idiopathic disorder with an underestimated incidence. It is characterized by brownish skin pigmentation, forming asymptomatic plaques that give a soiled skin appearance. Soap and water have a minor effect; however, friction with 70% ethyl or isopropyl alcohol immediately eliminates plaques to a normal skin appearance, thus being the ideal method for diagnosis and treatment. The lack of familiarity with this disease possibly contributes to an alarming underdiagnosis. In this report, the authors present a case of terra firma-forme occurring in a 14-year-old Mexican patient who presented with a heart-shaped pigmented lesion in the pubic area.

2.
Article in English | MEDLINE | ID: mdl-38747851

ABSTRACT

Microsporum canis, one of the most widespread dermatophytes worldwide, is a zoonotic microorganism that transmits infection from reservoirs such as cats and dogs to humans. This microorganism is associated with Tinea corporis and other clinical manifestations; however, few studies have used genetic surveillance to determine and characterize the process of zoonotic transmission. In this study, we show a clear example of zoonotic transmission from a cat to an intrafamilial environment, where it caused Tinea corporis by infection with M. canis. Molecular characterization using the b-tubulin gene and Random Amplified Polymorphic DNA analysis made it possible to determine that the six isolates of M. canis obtained in this study belonged to the same genetic variant or clone responsible for reservoir-reservoir or reservoir-human transmission.


Subject(s)
Cat Diseases , Microsporum , Tinea , Zoonoses , Microsporum/isolation & purification , Microsporum/genetics , Microsporum/classification , Cats/microbiology , Animals , Tinea/microbiology , Tinea/transmission , Tinea/veterinary , Cat Diseases/microbiology , Cat Diseases/transmission , Zoonoses/microbiology , Zoonoses/transmission , Pets/microbiology , Humans , Dogs , Random Amplified Polymorphic DNA Technique , Male , Female , Dog Diseases/microbiology , Dog Diseases/transmission , DNA, Fungal/genetics
3.
Gac Med Mex ; 158(Suplement 2): 1-116, 2023 Jan 20.
Article in Spanish | MEDLINE | ID: mdl-36763412

ABSTRACT

With the advancement of knowledge in relation to the physiopathogenesis of atopic dermatitis (AD), several new therapeutic forms have been developed. There are also new guidelines for self-care. On the other hand, there is still an underdiagnosis of AD in Mexico. Thus, the need was seen to develop a national guide, with a broad base among the different medical groups that care for patients with AD. The Atopic Dermatitis Guidelines for Mexico (GUIDAMEX) was developed with the ADAPTE methodology, with the endorsement and participation of ten national medical societies, from physicians in Primary Healthcare to allergists and dermatologists. Throughout the manuscript, key clinical questions are answered that lead to recommendations and suggestions for the diagnosis of AD (including differential diagnosis with immunodeficiency syndromes), the recognition of comorbidities and complications, non-pharmacological treatment including therapeutic education, treatment of flares and maintenance therapy. The latter encompasses general measures to avoid triggering factors, first-line treatment focussed on repair of the skin barrier, second-line treatment (topical proactive therapy), and third-line phototherapy or systemic treatment, including dupilumab and JAK inhibitors.


Con el avance de los conocimientos en relación con la fisiopatogenia de la dermatitis atópica (DA) se han desarrollado varias formas terapéuticas nuevas. Asimismo, existen nuevos lineamientos para el autocuidado. Por otro lado, aún existe un subdiagnóstico de la DA en México. Así, se vio la necesidad de desarrollar una guía nacional, con base amplia entre las diferentes agrupaciones médicos que atienden pacientes con DA. Se desarrolló la Guía de DA para México (GUIDAMEX) con la metodología ADAPTE, con el aval y la participación de diez sociedades médicas nacionales, desde médicos del primer contacto hasta alergólogos y dermatólogos. A lo largo del escrito se contestan preguntas clínicas clave que llevan a recomendaciones y sugerencias para el diagnóstico de la DA (incluyendo diagnóstico diferencial con síndromes de inmunodeficiencia), el reconocer de las comorbilidades y complicaciones, las medidas generales (tratamiento no farmacológico) incluyendo la educación terapéutica, el tratamiento de los brotes y el tratamiento de mantenimiento. Este último abarca las medidas generales de evitar agravantes, el tratamiento de primera línea reparador de la barrera cutánea, de segunda línea (manejo proactivo tópico), hasta la fototerapia y el tratamiento sistémico de la tercera línea, incluyendo dupilumab y los inhibidores de la cinasa de Jano.


Subject(s)
Dermatitis, Atopic , Humans , Dermatitis, Atopic/therapy , Dermatitis, Atopic/drug therapy , Mexico , Comorbidity , Diagnosis, Differential , Phototherapy/methods
4.
Cureus ; 15(12): e49806, 2023 Dec.
Article in English | MEDLINE | ID: mdl-38161568

ABSTRACT

A 63-year-old woman with light skin and a history of chronic sun damage presented with a painless, pale macule on her nasal tip. A punch biopsy was performed due to concerns about skin conditions like vitiligo or morpheaform basal cell carcinoma (BCC). The biopsy confirmed a micronodular BCC, an unusual presentation, as these typically manifest as an erythematous macule or thin papule/plaque. This report highlights the importance of considering various factors and differential diagnoses to ensure the best patient care and the need for vigilance in diagnosing rare presentations of BCC.

5.
An Bras Dermatol ; 93(4): 562-565, 2018.
Article in English | MEDLINE | ID: mdl-30066765

ABSTRACT

Fox-Fordyce disease is a relatively infrequent pathology of the apocrine glands that affects almost exclusively young women. The disease is characterized by the presence of pruritic follicular papules mainly in the armpits that respond poorly to treatment and severely affect the patient's quality of life. We report two cases with clinical diagnosis and histopathological confirmation, presenting perifollicular xanthomatosis on histological examination, recently described as a distinctive, consistent, and specific feature of this disease.


Subject(s)
Fox-Fordyce Disease/pathology , Xanthomatosis/pathology , Adult , Female , Fox-Fordyce Disease/complications , Humans , Immunohistochemistry , Xanthomatosis/etiology , Young Adult
6.
An. bras. dermatol ; 93(4): 562-565, July-Aug. 2018. graf
Article in English | LILACS | ID: biblio-949904

ABSTRACT

Abstract: Fox-Fordyce disease is a relatively infrequent pathology of the apocrine glands that affects almost exclusively young women. The disease is characterized by the presence of pruritic follicular papules mainly in the armpits that respond poorly to treatment and severely affect the patient's quality of life. We report two cases with clinical diagnosis and histopathological confirmation, presenting perifollicular xanthomatosis on histological examination, recently described as a distinctive, consistent, and specific feature of this disease.


Subject(s)
Humans , Female , Adult , Young Adult , Xanthomatosis/pathology , Fox-Fordyce Disease/pathology , Immunohistochemistry , Xanthomatosis/etiology , Fox-Fordyce Disease/complications
7.
Skinmed ; 13(4): 325-8, 2015.
Article in English | MEDLINE | ID: mdl-26861436

ABSTRACT

A 46-year-old woman was diagnosed with Brooke-Spiegler syndrome (BSS) with lesions on her head, predominantly on the center of her face, auricles, and scalp. The facial lesions were polymorphic, pale, confluent, skin-colored, and papular, whereas the scalpel lesions appeared as erythematous and violet lumps that varied in size (Figure 1A, B).


Subject(s)
Carcinoma, Basal Cell/pathology , Neoplastic Syndromes, Hereditary/pathology , Skin Neoplasms/pathology , Carcinoma, Basal Cell/diagnosis , Carcinoma, Basal Cell/etiology , Facial Neoplasms/diagnosis , Facial Neoplasms/etiology , Facial Neoplasms/pathology , Female , Humans , Middle Aged , Neoplastic Syndromes, Hereditary/diagnosis , Scalp/pathology , Skin Neoplasms/diagnosis
8.
Dermatol. rev. mex ; 38(6): 411-3, nov.-dic. 1994. ilus
Article in Spanish | LILACS | ID: lil-147761

ABSTRACT

El quiste broncogénico es una entidad rara que habitualmente se presenta en cuello y tronco. Se reporta un caso con localización en pecho y otro con topografía poco habitual en mentón. Se hace una revisión de las características clínicas, histológicas y posibles diagnósticos diferenciales, embriología y tratamiento


Subject(s)
Child , Adolescent , Humans , Male , Female , Chin/physiopathology , Bronchogenic Cyst/diagnosis , Bronchogenic Cyst/physiopathology
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