Gorham-Stout disease of skull base leading to cranial settling and rhinorrhea: a case-based review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00381-021-05394-3.pdf
Reference46 articles.
1. Gorham LW, Stout AP (1955) Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone); its relation to hemangiomatosis. Bone Jt Open 37-a(5):985–1004
2. Somoza Argibay I, Díaz González M, Martínez Martínez L, Ros Mar Z, López-Gutiérrez JC (2003) [Heterogenicity of Gorham-Stout syndrome: association with lymphatic and venous malformations]. Anales de pediatria (Barcelona, Spain : 2003) 58(6):599–603
3. Choma ND, Biscotti CV, Bauer TW, Mehta AC, Licata AA (1987) Gorham's syndrome: a case report and review of the literature. Am J Med 83(6):1151–1156
4. Takamoto RM, Armstrong RG, Stanford W, Fontenelle LJ, Troxler G (1971) Chylothorax with multiple lymphangiomata of the bone. Chest 59(6):687–689
5. Ozeki M, Fujino A, Matsuoka K, Nosaka S, Kuroda T, Fukao T (2016) Clinical features and prognosis of generalized lymphatic anomaly, kaposiform lymphangiomatosis, and Gorham-Stout Disease. Pediatr Blood Cancer 63(5):832–838
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2. Gorham-Stout disease affecting the spine with cerebrospinal fluid leakage and Chiari-like tonsillar herniation: a rare case report and review of literature;BMC Neurology;2023-02-03
3. Defining and measuring objective and subjective spinal stiffness: a scoping review;Disability and Rehabilitation;2022-12-14
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