dc.creatorBonilha L.R.D.C.M.
dc.creatorCogo G.R.
dc.creatorNeto A.C.
dc.creatorDe Oliveira Jr. E.B.
dc.creatorDe Pieri J.V.B.
dc.creatorTonello C.C.
dc.creatorCogo L.J.R.
dc.creatorMartins J.L.D.
dc.creatorVerri L.A.
dc.date2010
dc.date2015-06-26T12:35:28Z
dc.date2015-11-26T15:25:33Z
dc.date2015-06-26T12:35:28Z
dc.date2015-11-26T15:25:33Z
dc.date.accessioned2018-03-28T22:34:20Z
dc.date.available2018-03-28T22:34:20Z
dc.identifier
dc.identifierRevista Paulista De Pediatria. , v. 28, n. 3, p. 362 - 366, 2010.
dc.identifier1030582
dc.identifier10.1590/S0103-05822010000300016
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-78149477336&partnerID=40&md5=bf860b369ad31bcd31485fb5a6020c16
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/90941
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/90941
dc.identifier2-s2.0-78149477336
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1260933
dc.descriptionObjective: To report a case of chronic granulomatous disease diagnosed during the first infectious episode in order to collaborate with the Brazilian Group for Immunodeficiency, in sensitizing the general pediatrician that the early diagnosis of primary immunodeficiency results in better quality of life and longer life expectancy for the patients. Case Description: Male patient, 39 days, admitted to the pediatric emergency ward with fever for the last five days and irritability. On the following day, a cervical abscess was noted and a community Staphylococcus aureus was isolated. During hospital stay, other abscesses were observed in the skin and in the deep ganglia chains, with a slow response to antibiotics. Investigation of immunodeficiency was requested and chronic granulomatous disease was confirmed by quantification of superoxide anions and nitrobluetetrazolium tests. The patient was transferred to a specialized clinic for bone marrow transplantation, performed six months after diagnosis. Four months afterwards, the normalization of oxidative burst was noted, indecating the success of the transplantation. Comments: The patient showed a typical presentation of the disease, which allowed its diagnosis by general pediatricians on the first infection, allowing the follow-up by experts in primary immunodeficiencies, the introduction of antimicrobial chemoprophylaxis, and the successful search for an HLA-compatible bone marrow donor.
dc.description28
dc.description3
dc.description362
dc.description366
dc.descriptionSoler-Palacin, P., Margareto, C., Llobet, P., Asensio, O., Hernandez, M., Caragol, I., Espanol-Boren, T., Chronic granulomatous disease in pediatric patients: 25 Years of experience (2007) Allergologia et Immunopathologia, 35 (3), pp. 83-89. , http://external.doyma.es/prepdf/water.asp?pident_articulo= 13106774&pident_usuario=797308&pident_revista=105&fichero= 105v35n03a13106774pdf001.pdf&ty=137&accion=L&origen=doyma&web= www.doyma.es&lan=es, DOI 10.1157/13106774
dc.descriptionPrando-Andrade, C., Agudelo-Florez, P., Lopez, J.A., Paiva, M.A., Costa-Carvalho, B.T., Condino-Neto, A., Autosomal chronic granulomatous disease: Case report and mutation analysis of two Brazilian siblings (2004) J Pediatr, 80, pp. 425-428. , Rio J
dc.descriptionGrumach, A.S., Bellinai-Pires, R., Araujo, I.S., Gonzalez, C.H., Carneiro-Sampaio, M.M., Chronic granulomatous disease of childhood: Differential diagnosis and prognosis (1993) Rev Paul Med, 111, pp. 472-476
dc.descriptionWinkelstein, J.A., Marino, M.C., Johnston Jr., R.B., Boyle, J., Curnutte, J., Gallin, J.I., Chronic granulomatous disease. Report on a national registry of 368 patients (2000) Medicine, 79, pp. 155-169. , Baltimore
dc.descriptionKhanna, G., Kao, S.C., Kirby, P., Satoe, Y., Imaging of chronic granulomatous disease in children (2005) Radiographics, 25 (5), pp. 1183-1195. , http://radiographics.rsnajnls.org/cgi/reprint/25/5/1183, DOI 10.1148/rg.255055011
dc.descriptionLiese, J., Kloos, S., Jendrossek, V., Petropoulou, T., Wintergerst, U., Notheis, G., Long-term follow-up and outcome of 39 patients with chronic granulomatous disease (2000) J Pediatr, 137, pp. 687-693
dc.descriptionHolland, S.M., Chronic granulomatous disease (2010) Clin Rev Allergy Immunol, 38, pp. 3-10
dc.descriptionMoreira, R.J., Barreto, I.C.P., Daguer, M.G.F., Brito, N.M.B., Barreto, B.A.P., Doença granulomatosa crônica: Relato de caso (2005) Rev Bras Alergia Imunopatol, 28, pp. 315-321
dc.descriptionPasic, S., Minic, A., Minic, P., Veljkovic, D., Lilic, D., Slavkovic, B., Long-term follow-up and prognosis of chronic granulomatous disease in Yugoslavia: Is there a role for early bone marrow transplantation? (2003) J Clin Immunol, 23, pp. 55-61
dc.descriptionSeger, R.A., Modern management of chronic granulomatous disease (2008) Br J Haematol, 140, pp. 255-266
dc.descriptionParikh, S.H., Szabolcs, P., Prasad, V.K., Lakshminarayanan, S., Martin, P.L., Driscoll, T.A., Correction of chronic granulomatous disease after second unrelated-donor umbilical cord blood transplantation (2007) Pediatr Blood Cancer, 49, pp. 982-984
dc.descriptionMochizuki, K., Kikuta, A., Ito, M., Akaihata, M., Sano, H., Ohto, H., Successful unrelated cord blood transplantation for chronic granulomatous disease: A case report and review of the literature (2009) Pediatr Transplant, 13, pp. 384-389
dc.descriptionCale, C.M., Jones, A.M., Goldblatt, D., Follow up of patients with chronic granulomatous disease diagnosed since 1990 (2000) Clin Exp Immunol, 120, pp. 351-355
dc.descriptionMartire, B., Rondelli, R., Soresina, A., Pignata, C., Broccoletti, T., Finocchi, A., Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: An Italian multicenter study (2008) Clin Immunol, 126, pp. 155-164
dc.descriptionRoesler, J., Koch, A., Pörksen, G., Von Bernuth, H., Brenner, S., Hahn, G., Benefit assessment of preventive medical check-ups in patients suffering from chronic granulomatous disease (CGD) (2005) J Eval Clin Pract, 11, pp. 513-521
dc.descriptionCarnide, E.G., Jacob, C.A., Castro, A.M., Pastorino, A.C., Clinical and laboratory aspects of chronic granulomatous disease in description of eighteen patients (2005) Pediatr Allergy Immunol, 16, pp. 5-9
dc.descriptionJones, L.B.K.R., McGrogan, P., Flood, T.J., Gennery, A.R., Morton, L., Thrasher, A., Goldblatt, D., Cant, A.J., Special Article: Chronic granulomatous disease in the United Kingdom and Ireland: A comprehensive national patient-based registry (2008) Clinical and Experimental Immunology, 152 (2), pp. 211-218. , DOI 10.1111/j.1365-2249.2008.03644.x
dc.descriptionA controlled trial of interferon gamma to prevent infection in chronic granulomatous disease (1991) N Engl J Med, 324, pp. 509-516. , [No authors listed]. The International Chronic Granulomatous Disease Cooperative Study Group
dc.descriptionGoldblatt, D., Butcher, J., Thrasher, A.J., Russell-Eggitt, I., Chorioretinal lesions in patients and carriers of chronic granulomatous disease (1999) J Pediatr, 134, pp. 780-783
dc.descriptionKim, S.J., Kim, J.G., Yu, Y.S., Chorioretinal lesions in patients with chronic granulomatous disease (2003) Retina, 23, pp. 360-365
dc.descriptionCardieri, J.M.A., Nakaie, C.M.A., Rozov, T., Doença granulomatosa crônica da infância: Relato de um caso (1985) Pediatria, 7, pp. 217-221. , São Paulo
dc.descriptionAgudelo-Flórez, P., Prando-Andrade, C.C., López, J.A., Costa-Carvalho, B.T., Quezada, A., Espinosa, F.J., Chronic granulomatous disease in Latin American patients: Clinical spectrum and molecular genetics (2006) Pediatr Blood Cancer, 46, pp. 243-252
dc.descriptionImunodeficiência Primária: Os 10 Sinais de Alerta, , www.imunopediatria.org.br, BRAGID. Brazilian Group for Immunodeficiency [homepage on the Internet]. [cited 2008 Jun 6]. Available from
dc.languagept
dc.publisher
dc.relationRevista Paulista de Pediatria
dc.rightsaberto
dc.sourceScopus
dc.titleChronic Granulomatous Disease: Diagnosis On The First Infection Episode [doença Granulomatosa Crônica: Diagnóstico No Primeiro Episódio Infeccioso]
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución