Literature DB >> 420557

[Dyschondroplasia with glioma of the brain. Third histologically verified case (author's transl)].

W Becker, A Thron.   

Abstract

Dyschondroplasia is a mesodermal dysplasia with typical skeletal malformations of varying extent and severity. The combination with other malformations has led to numerous disease entities (Maffucci's syndrome, M. Kast, M. Ollier) that should be regarded as different forms of the same syndrome. The importance of the rare disease lies in the high risk of sacomatous transformation of the skeletal lesions and furthermore in an increased risk of development of other tumours. Involvement of the central nervous system is possible through lesions of the bones of the skull or through primary intracranial tumours. The present report concerns a patient with dyschondroplasia complicated by the occurrence of a cerebral glioma and is the third reported case verifed by biopsy.

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Mesh:

Year:  1979        PMID: 420557     DOI: 10.1007/bf00389685

Source DB:  PubMed          Journal:  Arch Orthop Trauma Surg        ISSN: 0344-8444


  19 in total

1.  MAFFUCCI'S SYNDROME.

Authors:  G B TAIT
Journal:  J Int Coll Surg       Date:  1965-02

2.  Dyschondroplasia with hemangiomatosis, Maffucci's syndrome, and teratoid tumor of the ovary.

Authors:  J F KUZMA; J M KING
Journal:  Arch Pathol (Chic)       Date:  1948-07

3.  Dyschondroplasia with haemangiomata (Maffucci's syndrome); report of a case complicated by intracranial chondrosarcoma.

Authors:  C STRANG; I RANNIE
Journal:  J Bone Joint Surg Br       Date:  1950-08

4.  Ollier's disease: dyschondroplasia.

Authors:  S G NARDELL
Journal:  Br Med J       Date:  1950-09-02

Review 5.  Maffucci's syndrome: functional and neoplastic significance. Case report and review of the literature.

Authors:  R J Lewis; A S Ketcham
Journal:  J Bone Joint Surg Am       Date:  1973-10       Impact factor: 5.284

6.  [Nomenclature of dyschondroplasia].

Authors:  H Zwerina
Journal:  Z Orthop Ihre Grenzgeb       Date:  1972-10

7.  Intestinal hemangiomas and Maffucci's syndrome.

Authors:  B D Hall
Journal:  Arch Dermatol       Date:  1972-04

8.  Dyschondroplasia.

Authors:  M Miller
Journal:  Arch Dermatol       Date:  1972-10

9.  Cutaneous lymphangiomas with dyschondroplasia (Maffucci's syndrome). A unique variant of an unusual syndrome.

Authors:  D W Suringa; A B Ackerman
Journal:  Arch Dermatol       Date:  1970-04

10.  [Dyschondroplasia (Ollier) (author's transl)].

Authors:  E Gherman
Journal:  Z Orthop Ihre Grenzgeb       Date:  1975-10
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  5 in total

1.  Familial glioma: occurrence within the "familial cancer syndrome" and systemic malformations.

Authors:  P Vieregge; L Gerhard; H C Nahser
Journal:  J Neurol       Date:  1987-05       Impact factor: 4.849

2.  Ollier's disease and Maffucci's syndrome: distinct entities or a continuum. Case report: enchondromatosis complicated by an intracranial glioma.

Authors:  C D Mellon; J E Carter; D B Owen
Journal:  J Neurol       Date:  1988-07       Impact factor: 4.849

3.  Multifocal intracranial astrocytoma in a pediatric patient with Ollier disease.

Authors:  Girish Bathla; Sarika Gupta; Cheng Kang Ong
Journal:  Indian J Radiol Imaging       Date:  2012-01

Review 4.  Brain Gliomas and Ollier Disease: Molecular Findings as Predictive Risk Factors?

Authors:  Sergio Corvino; Giuseppe Mariniello; Giuseppe Corazzelli; Raduan Ahmed Franca; Marialaura Del Basso De Caro; Rosa Della Monica; Lorenzo Chiariotti; Francesco Maiuri
Journal:  Cancers (Basel)       Date:  2022-07-16       Impact factor: 6.575

5.  Characteristics of gliomas in patients with somatic IDH mosaicism.

Authors:  Charlotte Bonnet; Laure Thomas; Dimitri Psimaras; Franck Bielle; Elodie Vauléon; Hugues Loiseau; Stéphanie Cartalat-Carel; David Meyronet; Caroline Dehais; Jérôme Honnorat; Marc Sanson; François Ducray
Journal:  Acta Neuropathol Commun       Date:  2016-03-31       Impact factor: 7.578

  5 in total

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