A report of two children with Gorham-Stout disease
Abstract Background Gorham-Stout disease is a rare condition characterized by unifocal and massive type IV osteolysis (variant of idiopathic nonhereditary osteolytic disease) with a slow progression, which is self-limiting for some years. It is characterized by recurrent vascular tumors with disrupt...
Main Authors: | Mario Edgar Tena-Sanabria, Larisa Yarindy Jesús-Mejenes, Gabriela Fuentes-Herrera, Félix Alejandro Álvarez-Martínez, Nora Patricia Victorio-García, Juan Carlos Núñez-Enríquez |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2019-06-01
|
Series: | BMC Pediatrics |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12887-019-1561-0 |
Similar Items
-
Presentación atípica del síndrome de Gorham-Stout. Caso clínico
by: González Luna, Alejandro, et al.
Published: (2015) -
GORHAM-STOUT SYNDROME: DESCRIPTION OF A CASE
by: Elvira Nikolayevna Otteva, et al.
Published: (2010-08-01) -
Gorham-Stout disease of the malleolus: a rare case report
by: Chuanxi Zheng, et al.
Published: (2019-12-01) -
Gorham-Stout Disease with Multiple Bone Involvement—Challenging Diagnosis of a Rare Disease and Literature Review
by: Alina Momanu, et al.
Published: (2021-07-01) -
A case report of Gorham-Stout disease diagnosed during the course of recurrent meningitis and cholesteatoma
by: Makoto Hosoya, et al.
Published: (2020-04-01)