Literature DB >> 19322127

Splenic lymphangiomatosis associated with skeletal involvement (Gorham's disease): a new case and review of literature.

M Barbagallo1, G Incorpora, G Magro, S D'Amico, V Pavone.   

Abstract

Lymphangiomatosis is a well-recognized congenital benign tumour, frequently seen in infancy and childhood, characterized by the presence of multiple lymphangiomas. Diffuse lymphangiomatosis also involving bony tissue is called Gorham's disease. This condition generally affects somatic soft tissue, where lymphatics are normally found. A predilection of this affection for bone, thoracic and neck involvement is well known, while involvement of abdominal viscera is very unusual. In bone this non malignant proliferation of lymphatic channels results in destruction and resorption of the osseous matrix. We report on a child in whom lymphangiomatosis involved both the bone and the spleen. A review of 166 cases is also reported.

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Year:  2009        PMID: 19322127

Source DB:  PubMed          Journal:  Minerva Pediatr        ISSN: 0026-4946            Impact factor:   1.312


  3 in total

1.  Diffuse lymphangiomatous hyperplasia of the spleen with hyaline bodies. A pseudotumoral proliferation arising from the lymphatic vessels of the periarteriolar lymphatic sheath.

Authors:  Dimas Suárez-Vilela; Francisco Miguel Izquierdo; Jose Ramón Méndez; Juliana Escobar; Gerardo Urdiales; Pilar Junco
Journal:  Virchows Arch       Date:  2011-02-20       Impact factor: 4.064

2.  The First Clinical Case of Gorham-Stout Syndrome of Humerus in an 18-year-old Female Reported in Pakistan.

Authors:  Maratib Ali; Maryam Khan; Syeda Rida Abdi; Laila Tul Qadar; Mohammad Tahir Lakho
Journal:  Cureus       Date:  2019-06-04

3.  Intra-Abdominal Lymphangiomatosis with Bone Marrow Involvement in a 7-Year Old Girl: A Case Report.

Authors:  Kourosh Goudarzi Pour; Borhan Moradvaesi; Maryam Nouri; Maliheh Khoddami; Farzenaeh Jadali
Journal:  Oman Med J       Date:  2013-03
  3 in total

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