Literature DB >> 22823281

Invasive lymphatic malformation (gorham-stout) of the pelvis with prominent skin involvement.

Inês Leite1, Angela Hernández-Martín, Isabel Colmenero, Juan C López-Gutiérrez, Antonio Torrelo.   

Abstract

Gorham-Stout syndrome is a rare disease characterized by progressive osteolysis leading to disappearance of the bone. Vascular proliferations have been implicated in the pathogenesis of this syndrome. The case of a 7-year-old girl with a prominent invasive lymphatic malformation on the lumbosacral area and massive osteolysis of the pelvic girdle is reported.
© 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22823281     DOI: 10.1111/j.1525-1470.2012.01814.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  4 in total

Review 1.  Vanishing bone disease (Gorham-Stout syndrome): A review of a rare entity.

Authors:  Vasileios S Nikolaou; Dimitrios Chytas; Demitrios Korres; Nicolas Efstathopoulos
Journal:  World J Orthop       Date:  2014-11-18

2.  VEGF-C promotes the development of lymphatics in bone and bone loss.

Authors:  Devon Hominick; Asitha Silva; Noor Khurana; Ying Liu; Paul C Dechow; Jian Q Feng; Bronislaw Pytowski; Joseph M Rutkowski; Kari Alitalo; Michael T Dellinger
Journal:  Elife       Date:  2018-04-05       Impact factor: 8.140

3.  99mTc-SC lymphoscintigraphy and SPECT/CT findings in a case report of Gorham-Stout disease presenting with chylothorax and bone pain.

Authors:  Yuanyuan Jiang; Guozhu Hou; Wuying Cheng
Journal:  Medicine (Baltimore)       Date:  2019-04       Impact factor: 1.817

Review 4.  Current concepts from diagnosis to management in Gorham-Stout disease: a systematic narrative review of about 350 cases.

Authors:  Andrea Angelini; Nicolò Mosele; Elisa Pagliarini; Pietro Ruggieri
Journal:  EFORT Open Rev       Date:  2022-01-11
  4 in total

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