Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ximena Calderón-Castrat"'
Autor:
Ximena Calderón-Castrat, MD, Concepción Román-Curto, MD, PhD, Angel Santos-Briz, MD, PhD, Emilia Fernández-López, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 3, Iss 6, Pp 492-494 (2017)
Externí odkaz:
https://doaj.org/article/eced5ffe882846f0a106b897e5a5ae58
Autor:
Angel Santos-Briz, Monica Roncero-Riesco, Ximena Calderón-Castrat, Emilia Fernández-López, María Teresa Alonso-San Pablo
Publikováno v:
Dermatologic Surgery. 43:757-761
Autor:
Cesar Chian, Marjorie Villate Caballero, Ximena Calderón-Castrat, Rosa Castro, Johanna Peceros-Escalante, Rosalía Ballona
Publikováno v:
Pediatric Dermatology. 34:e109-e115
Pediatric Degos disease is rare, with only 36 cases reported in the medical literature. Classically the diagnosis has been established according to pathognomonic histopathologic findings, but when these features are not present, there may be a delay
Publikováno v:
International Journal of Dermatology. 59
Autor:
Roxana Maybor Lipa‐Chancolla, Rosalía Ballona, Ximena Calderón-Castrat, Reynaldo Pomar, Rosa Castro, Consuelo Apagüeño
Publikováno v:
Pediatric dermatologyREFERENCES. 36(6)
Leukemia cutis is the direct infiltration of cutaneous tissues by leukemic cells and can present as a blueberry muffin baby. We present a case of neonatal leukemia cutis highlighting its dermoscopic features, the presence of fine telangiectatic arbor
Publikováno v:
Dermatologic Surgery. 42:264-267
Autor:
Beatriz Ingar Carbone, Angel Santos-Briz, Luis Jesús Allemant Ortiz, Alex Orellana Cortez, Ximena Calderón-Castrat
Publikováno v:
Pediatric Dermatology. 34:e216-e218
Fibroblastic connective tissue nevus (FCTN) is a rare, benign, dermal mesenchymal hamartoma that affects children. We report a 15-year-old boy with a congenital FCTN and describe the clinical, dermatoscopic, and histopathologic features.
Autor:
Carlos Santos-Duran, Ximena Calderón-Castrat, Mónica Roncero-Riesco, Nuria María Villamarín-Bello
Publikováno v:
Journal of the American Academy of Dermatology. 76:e127-e129
Autor:
Johanna Peceros-Escalante, Jorge Luis Idrogo-Bustamante, Ximena Calderón-Castrat, Rosalía Ballona
Publikováno v:
International Journal of Dermatology. 56:330-332
Publikováno v:
Pediatric dermatology. 34(2)
Keratitis ichthyosis deafness (KID) syndrome is a rare genodermatosis with a high risk of cutaneous malignancy and infections. Infections can induce pseudocarcinomatous epidermal hyperplasia, leading to erroneous diagnosis of squamous cell carcinoma.