Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Paola C, Stefano"'
Publikováno v:
Harper's Textbook of Pediatric Dermatology
Autor:
María Celeste Di Matteo, Marcela Bocian, Ana Cirio, Paola C Stefano, Andrea B Cervini, María del Valle Centeno, Beatriz López
Publikováno v:
Archivos Argentinos de Pediatria. 117
Rosacea is a chronic skin disease characterized by erythema, telangiectasia, papules and pustules in the central facial region. It most often affects adults and is rare in children. Rosacea can also present ocular involvement. Symptoms can precede cu
Autor:
María N Castro, Sebastián N Apa, Susana A Grees, María del Valle Centeno, Daniel Navacchia, Andrea B Cervini, Adriana Natalia Torres Huamani, Paola C Stefano, Jésica L Vivoda, Jorge A Laffargue, Ana G Bellelli, Mónica Liliana Yarza
Publikováno v:
Archivos argentinos de pediatria. 117(5)
A pilomatrixoma is a benign skin tumor common in children, which develops from the matrix cells of hair follicles. It presents as a nodule or tumor of approximately 0.5-3 cm in size, with calcium-like consistency, faceted edges, and blue erythematous
Autor:
María C, Di Matteo, Paola C, Stefano, Ana, Cirio, Beatriz, López, María, Centeno, Marcela, Bocian, Andrea B, Cervini
Publikováno v:
Archivos argentinos de pediatria. 117(2)
Rosacea is a chronic skin disease characterized by erythema, telangiectasia, papules and pustules in the central facial region. It most often affects adults and is rare in children. Rosacea can also present ocular involvement. Symptoms can precede cu
Publikováno v:
Archivos Argentinos de Pediatria. 116
Phakomatosis pigmentovascularis (PPV) is a syndrome characterized by the association of a vascular nevus with a congenital pigmented lesion (epidermal nevus, nevus spilus, and dermal melanocytosis). There are different types of PPV according to the p
Publikováno v:
Archivos argentinos de pediatria. 116(1)
Phakomatosis pigmentovascularis (PPV) is a syndrome characterized by the association of a vascular nevus with a congenital pigmented lesion (epidermal nevus, nevus spilus, and dermal melanocytosis). There are different types of PPV according to the p
Autor:
Andrea Bettina Cervini, Paola C Stefano, Marcela Bocian, Adrián M. Pierini, G. Leticia Lazarte, Verónica Solernou
Publikováno v:
Archivos Argentinos de Pediatria. 115
Juvenile xanthogranuloma is a bening pathology and it represents the most common form of non-Langerhans cell histiocytosis. It is characterized by the presence of papules or firm nodules of a pinkish or yellow-brownish nature, which mainly compromise
Autor:
Paola C Stefano, Patricia Lamy, Norberto Giglio, María Florencia Nolte, Mónica Garello, Angela Gentile, Vanesa Castellano
Publikováno v:
Archivos Argentinos de Pediatria. 115
Nicolau syndrome, also known as embolia cutis medicamentosa or livedo-like dermatitis, is a sudden tissue necrosis, a rare complication of intramuscular injection of some drugs. We report a case of a 6-month-old girl who received intramuscularly the
Autor:
Paola C, Stefano, Mónica, Garello, María F, Nolte, Patricia, Lamy, Norberto, Giglio, Vanesa, Castellano, Ángela, Gentile
Publikováno v:
Archivos argentinos de pediatria. 115(1)
Nicolau syndrome, also known as embolia cutis medicamentosa or livedo-like dermatitis, is a sudden tissue necrosis, a rare complication of intramuscular injection of some drugs. We report a case of a 6-month-old girl who received intramuscularly the
Autor:
Leticia, Lazarte, Paola C, Stefano, Marcela, Bocian, Verónica, Solernou, Adrián Martín, Pierini, Andrea Bettina, Cervini
Publikováno v:
Archivos argentinos de pediatria. 115(1)
Juvenile xanthogranuloma is a bening pathology and it represents the most common form of non-Langerhans cell histiocytosis. It is characterized by the presence of papules or firm nodules of a pinkish or yellow-brownish nature, which mainly compromise