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CC BY 4.0 · Rev Bras Ortop (Sao Paulo) 2024; 59(S 01): e101-e103
DOI: 10.1055/s-0042-1757962
Relato de Caso

Uma causa atípica de claudicação infantil: Síndrome de Gorham-Stout com quadril fantasma

Article in several languages: português | English
Hanene Lassoued Ferjani 
1   Departamento de Reumatologia, Kassab Orthopedics Institute, Ksar Saïd, Tunisia
,
Yasmin Makhlouf 
1   Departamento de Reumatologia, Kassab Orthopedics Institute, Ksar Saïd, Tunisia
,
Dorra Ben Nessib 
1   Departamento de Reumatologia, Kassab Orthopedics Institute, Ksar Saïd, Tunisia
,
Kaouther Maatallah 
1   Departamento de Reumatologia, Kassab Orthopedics Institute, Ksar Saïd, Tunisia
,
Dhia Kaffel 
1   Departamento de Reumatologia, Kassab Orthopedics Institute, Ksar Saïd, Tunisia
,
Wafa Hamdi 
1   Departamento de Reumatologia, Kassab Orthopedics Institute, Ksar Saïd, Tunisia
› Author Affiliations Suporte Financeiro O presente estudo não recebeu suporte financeiro de fontes públicas, comerciais ou sem fins lucrativos.
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Resumo

A síndrome de Gorham-Stout (SGS) é uma doença óssea rara caracterizada pela proliferação anormal de vasos endoteliais e destruição do osso acometido. Por ser comum em crianças e adultos jovens, causa morbidade e mortalidade significativas. Até o momento, não há estratégia terapêutica estabelecida para a SGS.

Relatamos um caso raro de SGS no quadril e na crista ilíaca de uma criança.

Palavras-chave

criança - quadril - síndrome de Gorham-Stout

Estudo realizado no Instituto de Ortopedia de Kassab, Departamento de Reumatologia, Ksar Saïd, Tunísia; Universidade Tunis el Manar, Faculdade de Medicina, Tunísia, Tunísia.




Publication History

Received: 12 July 2022

Accepted: 15 September 2022

Article published online:
31 July 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)

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  • Referências

  • 1 Li MH, Zhang HQ, Lu YJ. et al. Successful Management of Gorham-Stout Disease in Scapula and Ribs: A Case Report and Literature Review. Orthop Surg 2018; 10 (03) 276-280
    CrossrefPubMedSearch in Google Scholar
  • 2 Saify FY, Gosavi SR. Gorham's disease: A diagnostic challenge. J Oral Maxillofac Pathol 2014; 18 (03) 411-414
    CrossrefPubMedSearch in Google Scholar
  • 3 Schneider KN, Masthoff M, Gosheger G. et al. Gorham-Stout disease: good results of bisphosphonate treatment in 6 of 7 patients. Acta Orthop 2020; 91 (02) 209-214
    CrossrefPubMedSearch in Google Scholar
  • 4 Takaya K, Sakamoto Y, Miwa T, Yoshida K, Kishi K. Gorham-Stout disease with parietal bone osteolysis: a case series and review of literature. Br J Neurosurg 2021; 35 (01) 27-31
    CrossrefPubMedSearch in Google Scholar
  • 5 Vaishya R, Vaish A, Singh LK, Baweja P. Management of a pathological fracture in a rare case of Gorham Stout disease of the hip with a mega prosthesis. J Orthop 2019; 18: 177-180
    CrossrefPubMedSearch in Google Scholar
  • 6 Dellinger MT, Garg N, Olsen BR. Viewpoints on vessels and vanishing bones in Gorham-Stout disease. Bone 2014; 63: 47-52
    CrossrefPubMedSearch in Google Scholar
  • 7 Albuquerque RJ, Hayashi T, Cho WG. et al. Alternatively spliced vascular endothelial growth factor receptor-2 is an essential endogenous inhibitor of lymphatic vessel growth. Nat Med 2009; 15 (09) 1023-1030
    CrossrefPubMedSearch in Google Scholar
  • 8 Fretz CJ, Jungi WF, Neuweiler J, Haertel M. [The malignant degeneration of Gorham-Stout disease?]. Röfo Fortschr Geb Röntgenstr Nuklearmed 1991; 155 (06) 579-581
    Thieme ConnectPubMedSearch in Google Scholar
  • 9 Jagtap R, Alansari R, Ruprecht A, Kashtwari D. Trichodentoosseous syndrome: a case report and review of literature. BJR Case Rep 2019; 5 (04) 20190039
    PubMedSearch in Google Scholar
  • 10 Ricci KW, Hammill AM, Mobberley-Schuman P. et al. Efficacy of systemic sirolimus in the treatment of generalized lymphatic anomaly and Gorham-Stout disease. Pediatr Blood Cancer 2019; 66 (05) e27614
    CrossrefPubMedSearch in Google Scholar