2017, Number 3
Presentation of one patient of four month of age with a suprarrenal neuroblastoma
Language: Spanish
References: 10
Page: 939-945
PDF size: 413.38 Kb.
ABSTRACT
The neuroblastoma is a kind of cancer in infants that is commonly diagnosed in the first year of age. These tumors, caused by the neural crest are located in the adrenal glands or at extrarrenal area, having clinical and biological characteristics snoopers existing from cases with spontaneous remission to other ones with tumoral progression, scarce therapeutic response and the patient's death. A four -months–old female patient admitted at the Pediatric Hospital of Holguin referred from the patients´ health area. A solid mass of 38 x 36 mm with very well delimitated borders in the superior side of the left kidney was observed in the ultrasonography; the lab tests were negative. Resection of the tumor with adequate post-surgical evolution was performed. The biopsy informed suprarenal left-hand neuroblastoma, undiferenced, of poor estroma and unfavorable histology of 5 x 4 cm of diameter measures and infiltrates some places of the capsule.REFERENCES
Medina Domínguez R, Moreno Kim S, Robainas Fiall I, Medina Robainas RE, Fariñas González M, Dorta Robaina M. Neuroblastoma congénito cervical en recién nacido: presentación de un caso. Rev Méd Electrón. 2013[citado 24 feb 2016]; 35(6). Disponible en:http://www.revmatanzas.sld.cu/revista%20medica/ano%202013/vol6%202013/tema07.htm
Carrillo D, Ibarra X, Cuevas M, De Barbieri F, Oyanedel R, Zabala A, et al. Causa infrecuente de hipertensión arterial en lactantes: neuroblastoma congénito quístico suprarrenal. Caso clínico. Rev Chilena Pediatr. 2012 [citado 24 feb 2016]; 83(3):262-268. Disponible en: http://www.scielo.cl/pdf/rcp/v83n3/art08.pdf
Llombart Bosch A, Navarro S. Immunohistochemical detection of EWS and FLI-1 proteins in Ewing sarcoma and primitive neuroectodermal tumors: comparative analysis with CD99 (MIC-2) expresión. Appl Immunol Mol Morphol. 2001[citado 24 feb 2016]; 9(3):255-260. Disponible en: http://ovidsp.tx.ovid.com/sp-3.25.0a/ovidweb.cgi
Navarro S, Noguera R, Pellín A, López-Guerrero JA, Roselló-Sastre E, Cremades A. Atypical pleomorphic exotraosseous Ewing tumor/peripheral primitive neuroectodermal tumor with unusual phenotypic/genotypic profile. Diagn Mol Pathol. 2002[citado 24 feb 2016]; 11(1):9-15. Disponible en: http://journals.lww.com/molecularpathology/Abstract/2002/03000/Atypical