Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Ramon Ruiz-Maldonado"'
Autor:
Ramon Ruiz-Maldonado, Carola Duran-Mckinster, Raquel Lara-Carpio, Carolina Palacios-Lopez, Marimar Sáez-de-Ocariz, Luz Orozco-Covarrubias
Publikováno v:
Pediatric Dermatology. 30:706-711
Dermoid cysts (DCs) are benign cutaneous tumors that tend to persist and grow. The aim of this study was to examine the clinicopathologic features of congenital DCs. We present a case series of 75 children with a clinicopathologic diagnosis of DC. Se
Autor:
Ramon Ruiz-Maldonado, Carola Duran-Mckinster, Marimar Sáez-de-Ocariz, Rolando Elias Julián-Gónzalez, Carolina Palacios-Lopez, Luz Orozco-Covarrubias
Publikováno v:
Pediatric Dermatology. 29:580-583
The common manifestations of atopic dermatitis (AD) appear sequentially with involvement of the cheeks in infancy, flexural extremities in childhood, and hands in adulthood. Although less common clinical manifestations are well described, they have n
Autor:
Ramon Ruiz-Maldonado, Carola Duran-Mckinster, Helena Vidaurri-de la Cruz, Lourdes Tamayo-Sanchez, María De La Luz Orozco-Covarrubias
Publikováno v:
Pediatric Dermatology. 21:432-439
Of the patients with epidermal nevi, 10-18% may have disorders of the eye, nervous, and musculoskeletal systems. A predisposition to malignant neoplasms in ectodermal and mesodermal structures may also be found. There are six different epidermal nevu
Autor:
Leticia Lara-Mendoza, Daniel Carrasco-Daza, Ana Diaz-Noriega, Ramon Ruiz-Maldonado, Luz Orozco-Covarrubias
Publikováno v:
Pediatric Dermatology. 33:e36-e37
Cutaneous rhabdomyomatous mesenchymal hamartoma (RMH) is a rare benign tumor composed of two or more types of mesenchymal-derived cells. RMHs are generally sporadic and independent, but they can be associated with congenital abnormalities. We report
Autor:
Ramon Ruiz-Maldonado, Daniel Carrasco-Daza, Marimar Saez-De-Ocaris, Carola Duran-Mckinster, Luz Orozco-Covarrubias, Carolina Palacios-Lopez, Rolando Elias Julián-Gónzalez
Publikováno v:
Pediatric Dermatology. 28:460-462
Congenital cutaneous angioleiomyoma is an extremely rare benign smooth muscle tumor. We present a case of a firm, painful subcutaneous mass noticed at birth on the left leg that on surgical excision proved to be an angioleiomyoma. Prognosis is good,
Publikováno v:
Pediatric Dermatology. 17:91-96
Primary immunodeficiency diseases (PIDs) are rare but important conditions found predominantly in children. We studied PIDs in a large pediatric hospital, their association with cutaneous alterations, and the importance of cutaneous alterations as di
Publikováno v:
New England Journal of Medicine. 332:656-662
To give a child the ominous diagnosis of malignant melanoma is a very difficult decision for both clinician and pathologist. Difficulties in histologic diagnosis combined with a reluctance on the part of the clinician may lead to delays in diagnosis
Autor:
Rolando Elias, Julián-Gónzalez, Luz, Orozco-Covarrubias, Carola, Durán-McKinster, Carolina, Palacios-Lopez, Ramon, Ruiz-Maldonado, Marimar, Sáez-de-Ocariz
Publikováno v:
Pediatric dermatology. 29(5)
The common manifestations of atopic dermatitis (AD) appear sequentially with involvement of the cheeks in infancy, flexural extremities in childhood, and hands in adulthood. Although less common clinical manifestations are well described, they have n
Autor:
Luz, Orozco-Covarrubias, Daniel, Carrasco-Daza, Rolando, Julian-Gonzalez, Marimar, Saez-de-Ocaris, Carola, Duran-McKinster, Carolina, Palacios-Lopez, Ramon, Ruiz-Maldonado
Publikováno v:
Pediatric dermatology. 28(4)
Congenital cutaneous angioleiomyoma is an extremely rare benign smooth muscle tumor. We present a case of a firm, painful subcutaneous mass noticed at birth on the left leg that on surgical excision proved to be an angioleiomyoma. Prognosis is good,
Publikováno v:
Basic and Clinical Dermatology ISBN: 1420021184
Retinoids and Carotenoids in Dermatology
Retinoids and Carotenoids in Dermatology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dc4aff034898ae0e2dbbc0e786c3e3c
https://doi.org/10.3109/9781420021189.009
https://doi.org/10.3109/9781420021189.009