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pro vyhledávání: '"Marta Almeida Pereira"'
Autor:
Sara Pires da Silva, Catarina Viveiros, Rui Almeida, Marta Almeida Pereira, Rute Vaz, Alexandrina Portela
Publikováno v:
Revista Paulista de Pediatria, Iss 0 (2019)
ABSTRACT Objective: To report a rate case of Juvenile xanthogranuloma in a newborn infant. Case description: We present the case of a 31-week preterm newborn with multiple skin lesions whose clinical, histological and immunohistochemical findings all
Externí odkaz:
https://doaj.org/article/8a9583d0d6134aed8aae76e7c517b01c
Autor:
Marta Almeida Pereira, Rui M. Almeida, Catarina Viveiros, Sara Pires da Silva, Rute Vaz, Alexandrina Portela
Publikováno v:
Revista Paulista de Pediatria, Iss 0 (2019)
Revista Paulista de Pediatria, Volume: 37, Issue: 2, Pages: 257-260, Published: 25 FEB 2019
Revista Paulista de Pediatria, Issue: ahead, Published: 25 FEB 2019
Revista Paulista de Pediatria
Revista Paulista de Pediatria v.37 n.2 2019
Revista Paulista de Pediatria (Ed. Português. Online)
Sociedade de Pediatria de São Paulo (SPSP)
instacron:SPSP
Revista Paulista de Pediatria, Volume: 37, Issue: 2, Pages: 257-260, Published: 25 FEB 2019
Revista Paulista de Pediatria, Issue: ahead, Published: 25 FEB 2019
Revista Paulista de Pediatria
Revista Paulista de Pediatria v.37 n.2 2019
Revista Paulista de Pediatria (Ed. Português. Online)
Sociedade de Pediatria de São Paulo (SPSP)
instacron:SPSP
Objective: To report a rate case of Juvenile xanthogranuloma in a newborn infant. Case description: We present the case of a 31-week preterm newborn with multiple skin lesions whose clinical, histological and immunohistochemical findings allowed the
Publikováno v:
Pereira, Marta Almeida; Baudrier, Teresa; Costa, Alice; Magalhães, João; & Azevedo, Filomena. (2008). Cutaneous metastatic plasmacytomas with tropism for a previously injured limb. Dermatology Online Journal, 14(9). Retrieved from: http://www.escholarship.org/uc/item/37n527v0
Cutaneous plasmacytoma is an uncommon observation in clinical practice. It is usually a consequence of direct extension from an underlying bony lesion, in the setting of multiple myeloma. In our case, a 77-year-old woman, with stage IIIA IgG lambda m