339
Views
6
CrossRef citations to date
0
Altmetric
Original Articles

Gorham-Stout disease with parietal bone osteolysis: a case series and review of literature

, , , &
Pages 27-31 | Received 27 Jan 2019, Accepted 16 Mar 2020, Published online: 27 Mar 2020

References

  • Nir V, Guralnik L, Livnat G, et al. Propranolol as a treatment option in Gorham-Stout syndrome: a case report. Pediatr Pulmonol 2014;49:417–9.
  • Gorham LW, Wright AW, Shultz HH, et al. Disappearing bones: a rare form of massive osteolysis; report of two cases, one with autopsy findings. Am J Med 1954;17:674–82.
  • Amirjamshidi A, Karimi-Yarandi K, Hosseini M, et al. Painful sporadic osteolysis of the parietal bone ‘Gorham’s disease’. Br J Neurosurg 2016;30:687–8.
  • Choma ND, Biscotti CV, Bauer TW, et al. Gorham’s syndrome: a case report and review of the literature. Am J Med 1987;83:1151–6.
  • Mawk JR, Obukhov SK, Nichols WD, et al. Successful conservative management of Gorham disease of the skull base and cervical spine. Childs Nerv Syst 1997;13:622–5.
  • Ohla V, Bayoumi AB, Hefty M, et al. Complex single step skull reconstruction in Gorham’s disease – a technical report and review of the literature. BMC Surg 2015;15:24.
  • Nagashima H, Mizukawa K, Taniguchi M, et al. Cerebrospinal fluid leakage and Chiari I malformation with Gorham's disease of the skull base: a case report. Neurol Neurochir Pol 2017;51:427–31.
  • Nozawa A, Ozeki M, Kuze B, et al. Gorham-Stout disease of the skull base with hearing loss: dramatic recovery and antiangiogenic therapy. Pediatr Blood Cancer 2016;63:931–4.
  • Coulter IC, Khan SA, Flanagan AM, et al. Chiari I malformation associated with Gorham’s disease of the skull base. Clin Neurol Neurosurg 2014;116:83–6.
  • Morimoto N, Ogiwara H, Miyazaki O, et al. Gorham-Stout syndrome affecting the temporal bone with cerebrospinal fluid leakage. Int J Pediatr Otorhinolaryngol 2013;77:1596–600.
  • Hernández-Marqués C, Serrano González A, Cordobés Ortega F, et al. Gorham-Stout disease and cerebrospinal fluid otorrhea. Pediatr Neurosurg 2011;47:299–302.
  • Heyd R, Micke O, Surholt C, et al. Radiation therapy for Gorham-Stout syndrome: results of a national patterns-of-care study and literature review. Int J Radiat Oncol Biol Phys 2011;81:e179–85.
  • Cushing SL, Ishak G, Perkins JA, et al. Gorham-stout syndrome of the petrous apex causing chronic cerebrospinal fluid leak. Otol Neurotol 2010;31:789–92.
  • Frankel DG, Lewin JS, Cohen B. Massive osteolysis of the skull base. Pediatr Radiol 1997;27:265–7.
  • Parihar V, Yadav YR, Sharma D. Gorham’s disease involving the left parietal bone: a case report. Cases J 2008;1:258.
  • Lo CP, Chen CY, Chin SC, et al. Disappearing calvarium in Gorham disease: MR imaging characteristics with pathologic correlation. AJNR Am J Neuroradiol 2004;25:415–8.
  • Chai WX, Wu JP, Chen KF. Massive osteolysis of the skull: long-term followup observations after cranioplasty. Report of two cases. Acta Neurochir 1984;73:201–6.
  • McNeil KD, Fong KM, Walker QJ, et al. Gorham’s syndrome: a usually fatal cause of pleural effusion treated successfully with radiotherapy. Thorax 1996;51:1275–6.
  • Ricalde P, Ord RA, Sun CC. Vanishing bone disease in a five year old: report of a case and review of the literature. Int J Oral Maxillofac Surg 2003;32:222–6.
  • Ozeki M, Fukao T. Generalized lymphatic anomaly and Gorham-Stout disease: overview and recent insights. Adv Wound Care (New Rochelle) 2019;8:230–45.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.