Zobrazeno 1 - 10
of 12
pro vyhledávání: '"José G. Casas"'
Publikováno v:
Dermatología Argentina. 27:111-114
La foliculitis pseudolinfomatosa, descripta por McNutt en 1986, es una afección de etiología desconocida y poco frecuente, que simula un linfoma cutáneo tanto por su clínica como por su histología. Se presenta como una lesión nodular soli
Autor:
José G. Casas, Omar P. Sangueza
Publikováno v:
The American Journal of Dermatopathology. 42:397-398
Autor:
María Eugenia Abad, Margarita Larralde, Virginia M. González, José G. Casas, Felix Vigovich, Paula Carolina Luna
Publikováno v:
Pediatric Dermatology. 33:e65-e68
Erythrosis pigmentosa peribuccalis is an infrequent condition, with fewer than 35 cases reported in the literature, that affects mainly women. It presents as small papules that form a hyperpigmented plaque around the mouth and nose. Little is known a
Publikováno v:
Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Vol 93, Iss 2, Pp 289-290 (2018)
Anais Brasileiros de Dermatologia, Vol 93, Iss 2, Pp 289-290 (2018)
Inflammatory breast cancer is an aggressive and infiltrative malignancy that is often misdiagnosed as an infection because of its symptoms and signs of inflammation, delaying proper diagnosis and treatment. We report a case of inflammatory breast can
Autor:
Margarita Larralde, Felix Vigovich, Paula C. Luna, José G. Casas, Carolina I. Martin, Anabel A. Pannizardi
Publikováno v:
Pediatric dermatology. 33(3)
Background/Objective Papular epidermal nevus with skyline basal cell layer (PENS) is a recently described type of epidermal nevus with characteristic histopathologic findings, mainly regular, rectangular acanthosis and a well-demarcated basal cell la
Publikováno v:
APMIS. 120:397-404
Polyomavirus has been used extensively to study tumour induction in mice. Although most neoplasms are well characterized, those arising from hair follicles have been referred to by different names during the last four decades. The purpose of this res
Autor:
Julio E Bruetman, José G. Casas, Felix Vigovich, María Massa, German Stemmelin, Bárbara C Finn, Gonzalo Fleire, Amanda Ruades, Pablo Young, Daniel Sutovsky, Pablo Dezanzo
Publikováno v:
Revista médica de Chile v.143 n.8 2015
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Intravascular lymphoma is a rare subtype of extranodal diffuse large B-cell lymphoma characterized by clonal proliferation of lymphocytes inside of small and medium caliber vessels. Its incidence is estimated at one case per million. The clinical pic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e45c79ee9be495a9dcc3416acba0482
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872015000800017
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872015000800017
Autor:
Pablo, Young, María, Massa, Bárbara C, Finn, Gonzalo, Fleire, Germán R, Stemmelin, Amanda, Ruades, Daniel, Sutovsky, José G, Casas, Pablo, Dezanzo, Félix, Vigovich, Julio E, Bruetman
Publikováno v:
Revista medica de Chile. 143(8)
Intravascular lymphoma is a rare subtype of extranodal diffuse large B-cell lymphoma characterized by clonal proliferation of lymphocytes inside of small and medium caliber vessels. Its incidence is estimated at one case per million. The clinical pic
Publikováno v:
Sempau, Leticia; Larralde, Margarita; Luna, Paula Carolina; Casas, Jose; & Staiger, Hernan. (2012). Eosinophilic annular erythema. Dermatology Online Journal, 18(3). Retrieved from: http://www.escholarship.org/uc/item/3zs95220
Eosinophilic annular erythema is a rare benign recurrent disease, originally described in children, characterized by the recurrent appearance of persistent non-pruritic, urticarial annular lesions. Histologically a perivascular infiltrate composed of
Autor:
Elena Yeyati, Gabriel Magariños, Alejandro Malbrán, Luz Stella Parra, José G. Casas, Mario A. Marini, Eloisa Malbrán
Publikováno v:
Malbrán, Alejandro; Parra, Luz Stella; Casas, José G; Malbrán, Eloisa; Yeyati, Elena; Magariños, Gabriel; et al.(2009). Case Report: Diffuse plane xanthoma with low C4 and systemic inflammatory symptoms. Dermatology Online Journal, 15(4). Retrieved from: http://www.escholarship.org/uc/item/3p17h4jx
A normolipemic patient with diffuse plane xanthomas, IgG monoclonal gammopathy of unknown significance, low levels of C4, and systemic inflammatory symptoms is presented. Delay from disease onset to diagnosis is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::688484449a3d6de4dc40f2cf9d132f3b
http://www.escholarship.org/uc/item/3p17h4jx
http://www.escholarship.org/uc/item/3p17h4jx