Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Juana Irma Garza-Chapa"'
Autor:
Zachary Ingersoll, Juana Irma Garza-Chapa, Ryan Pham, Peter Malouf, Joseph Susa, Stephen Weis
Publikováno v:
Case Reports in Dermatology, Vol 10, Iss 2, Pp 203-207 (2018)
Granuloma gluteale infantum is a rare pediatric dermatological disorder of uncertain etiology. Suggested causes include fluorinated corticosteroids, Candida albicans, and irritant contact dermatitis. We present the case of a 3-year-old boy with recur
Externí odkaz:
https://doaj.org/article/a28bf781308747dabac69a10d0fe8ef9
Autor:
Jorge Ocampo-Garza, Maira Elizabeth Herz-Ruelas, Elias Eugenio González-Lopez, Eric Eduardo Mendoza-Oviedo, Juana Irma Garza-Chapa, Sonia Sofía Ocampo-Garza, Norma Elizabeth Vázquez-Herrera, Ivett Miranda-Maldonado, Jorge Ocampo-Candiani
Publikováno v:
Case Reports in Dermatology, Vol 6, Iss 3, Pp 291-295 (2014)
Angioimmunoblastic T-cell lymphoma (AITL) accounts for 15-20% of all peripheral T-cell lymphomas. It is a rare subtype of CD4 T-cell peripheral lymphoma that affects aged individuals, causing B symptoms, generalized lymphadenopathy and hepatosplenome
Externí odkaz:
https://doaj.org/article/d1835d15741b423ea6fd70523de5ca9d
Publikováno v:
Case Reports in Dermatological Medicine, Vol 2017 (2017)
Comedones occur when an overproliferation of keratinocytes blocks sebum secretion in a pilosebaceous duct. Comedones have multiple possible etiologies and contributing factors. While comedones are common to acne, they are also seen in occupational ex
Externí odkaz:
https://doaj.org/article/b4d5478da8414a96a9c27ca752428fe5
Autor:
Jorge Ocampo-Candiani, Victor Andres Cab-Morales, David Emmanuel Kubelis-López, Maira Elizabeth Herz-Ruelas, Sonia Chavez-Alvarez, Juana Irma Garza-Chapa
Publikováno v:
Skin Appendage Disord
Netherton syndrome (NS) is a rare genodermatosis with an autosomal recessive pattern of inheritance caused by pathogenic variants in the SPINK5 gene. It is characterized by a triad consisting of atopic diathesis, ichthyosis linearis circumflexa, and
Autor:
Stephen E. Weis, Zachary Ingersoll, Peter Malouf, Juana Irma Garza-Chapa, Joseph S. Susa, Ryan Pham
Publikováno v:
Case Reports in Dermatology, Vol 10, Iss 2, Pp 203-207 (2018)
Case Reports in Dermatology
Case Reports in Dermatology
Granuloma gluteale infantum is a rare pediatric dermatological disorder of uncertain etiology. Suggested causes include fluorinated corticosteroids, Candida albicans, and irritant contact dermatitis. We present the case of a 3-year-old boy with recur
Publikováno v:
The American Journal of Dermatopathology. 41:615-616
Publikováno v:
The American Journal of Dermatopathology. 41:e82-e83
Publikováno v:
Case Reports in Dermatological Medicine
Case Reports in Dermatological Medicine, Vol 2017 (2017)
Case Reports in Dermatological Medicine, Vol 2017 (2017)
Comedones occur when an overproliferation of keratinocytes blocks sebum secretion in a pilosebaceous duct. Comedones have multiple possible etiologies and contributing factors. While comedones are common to acne, they are also seen in occupational ex
Autor:
Jorge Ocampo-Candiani, Oliverio Welsh, Juana Irma Garza-Chapa, Sylvia Aide Martínez-Cabriales, Minerva Gómez-Flores, Jorge Ocampo-Garza
Publikováno v:
Australasian Journal of Dermatology. 57:e49-e52
Coccidioidomycosis is an endemic fungal infection in the southwestern USA and northern Mexico. It is caused by Coccidioides immitis and C. posadasii. This infection occurs due to the inhalation of airborne arthroconidia, causing a mild pulmonary infe
Autor:
Elias Eugenio Gonzalez-Lopez, Maira Elizabeth Herz-Ruelas, Jorge Ocampo-Garza, Sonia Sofia Ocampo-Garza, Juana Irma Garza-Chapa, Norma Elizabeth Vázquez-Herrera, Jorge Ocampo-Candiani, Eric Eduardo Mendoza-Oviedo, Ivett Miranda-Maldonado
Publikováno v:
Case Reports in Dermatology, Vol 6, Iss 3, Pp 291-295 (2014)
Case Reports in Dermatology
Case Reports in Dermatology
Angioimmunoblastic T-cell lymphoma (AITL) accounts for 15-20% of all peripheral T-cell lymphomas. It is a rare subtype of CD4 T-cell peripheral lymphoma that affects aged individuals, causing B symptoms, generalized lymphadenopathy and hepatosplenome