Fratura por fragilidade na infância em recêm nascido com a síndrome de Prune-Belly
Palavras-chave:
Síndrome Prune-Belly, insuficiência renal, fragilidade óssea na infânciaResumo
A Síndrome de Prune Belly não tem etiologia e fisiopatologia bem esclarecidas. O osso fica suscetível a fraturas, dor óssea, necrose vascular, retardo de crescimento e deformidades ósseas. O objetivo desse caso é relatar a presença de fraturas recém-nascidas com a Síndrome Prune-Belly e discutir sua relação com a fragilidade óssea na infância.
Referências
Behrman RE, Kliegman R, Jenson HB. Nelson: Tratado de Pediatria. 19ª ed. Rio de Janeiro: Elsevier; 2014.
Bomfim KB, Silva-Hamu TCD. Aspectos clínicos da Síndrome de Prune Belly: revisão de literatura. Movimenta. 2013;6(4):596-605
Lopes RI, Baker LA, Dénes FT. Modern management of and update on prune belly syndrome. J Pediatr Urol. 2021 Aug;17(4):548-554. doi: 10.1016/j.jpurol.2021.04.010. Epub 2021 Apr 24. PMID: 34016542; PMCID: PMC8502198.
Herman TE, Siegel MJ. Prune belly syndrome. J Perinatol. 2009; 29:69-71
Arlen AM, Nawaf C, Kirsch AJ. Prune belly syndrome: current perspectives. Pediatric Health, Medicine and Therapeutics. 2019; 10:75-81.
Thomas ZPA-C. "Prune belly syndrome: A Case report". Lynchburg Journal of Medical Science. 2019; 1(3).
Tibor-Denes F, Tavares A, Cocuzza M, Tiseu B, Machado MG, Giron AM, Srougi M. Gonadal function and reproductive system anatomy in post puberal prune belly syndrome patients. The Journal of Urology. 2017; 197(4):e863
Woods AG, Brandon DH. Prune Belly Syndrome: A Focused Physical Assessment. Adv Neonatal Care. 2007;7(3):132-43.
Bogart MM, Arnald HE, Greer K. Prune-Belly Syndrome in Two Children and Review of the Literature. Pediatr Dermatol. 2006;23(4):342–5.
Haeri S, Devers P, Kaiser-Rogers KA, Moylan VJ, Torchia BS, Horton AL, et al. Deletion of Hepatocyte Nuclear Factor-1-Beta in an infant with Prune Belly Syndrome. Am J Perinatol. 2010; 27(7)559-63.
Brinker MR, Palutsis RS, Sawark JF. The Orthopaedic Manifestations of Prune-Belly (Eagle-Barrett) Syndrome. J Bone Jt Surg. 1995; 77(2): 251-7.
Xu WZ, Yang CX. Prune Belly syndrome complicated by pectus excavatum, spleen and left kidney congenital absence and situs inversus viscerum: a case report. Zhon Dai Er Ke Za Zhi. 2010; 12(11):924.
Lam KS, Mehdian H. The importance of an intact abdominal musculature mechanism in maintaining spinal sagittal balance: Case illustration in Prune- -Belly Syndrome. Spine. 1999;24(7):719-2.
Loder RT, Guiboux JP, Bloom DA, Hensinger RN. Musculoskeletal aspects of prune-belly syndrome. Description and pathogenesis. Am J Dis Child. 1992 Oct;146(10):1224-9. doi: 10.1001/archpedi.1992.02160220110034. PMID: 1415053.
Kemper MJ, van Husen M. Renal osteodystrophy in children: pathogenesis, diagnosis and treatment. Curr Opin Pediatr. 2014 Apr;26(2):180-6. doi: 10.1097/MOP.0000000000000061. PMID: 24553631.
Salusky IB, Kuizon BG, Jüppner H. Special aspects of renal osteodystrophy in children. Semin Nephrol. 2004 Jan;24(1):69-77. doi: 10.1053/j.semnephrol.2003.08.009. PMID: 14730512.
Lima, Eleonora Moreira, Gesteira, Maria de Fátima Câmera e Bandeira, Maria de Fátima Santos. Diretrizes do distúrbio do metabolismo mineral e ósseo na doença renal crônica da criança. Brazilian Journal of Nephrology [online]. 2011, v. 33, n. 2 [Acessado 11 Agosto 2023], pp. 189-247. Disponível em: <https://doi.org/10.1590/S0101-28002011000200021>. Epub 30 Ago 2011. ISSN 2175-8239. https://doi. org/10.1590/S0101-28002011000200021.
