Literature DB >> 2353208

The radiographic features of familial expansile osteolysis.

M D Crone1, R G Wallace.   

Abstract

The radiographic features of a unique autosomal dominant bone dysplasia are presented. The features are classified as generalised and/or focal. Generalised features are either altered trabecular pattern or modelling abnormalities. Focal features comprise lytic areas which progressively enlarge, producing expansion of the bone and eventual disintegration due to fibrous and finally fatty replacement of the normal medulla. Almost 90% of these lesions occur in the appendicular skeleton. Clinically, hearing loss is the earliest manifestation of the disease, presenting sometimes as early as 4 years of age. Apical and cervical resorption of teeth is extremely common, resulting in premature loss of teeth. Radiologically, the differential diagnosis refers to Paget's disease, polyostotic fibrous dysplasia, and osteofibrous dysplasia. The progressive destruction of the bone is similar to massive osteolysis (Gorham's disease). The radiographic features in combination with the histopathology render the condition unique.

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Mesh:

Year:  1990        PMID: 2353208     DOI: 10.1007/bf00191665

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN: 0364-2348            Impact factor:   2.199


  7 in total

1.  The natural history of fibrous dysplasia. An orthopaedic, pathological, and roentgenographic study.

Authors:  W H HARRIS; H R DUDLEY; R J BARRY
Journal:  J Bone Joint Surg Am       Date:  1962-03       Impact factor: 5.284

2.  Paget's disease (osteitis deformans); review of one hundred eleven cases.

Authors:  J A ROSENKRANTZ; J WOLF; J J KAICHER
Journal:  AMA Arch Intern Med       Date:  1952-11

3.  Familial expansile osteolysis. A new dysplasia.

Authors:  P H Osterberg; R G Wallace; D A Adams; R S Crone; G R Dickson; J A Kanis; R A Mollan; N C Nevin; J Sloan; P G Toner
Journal:  J Bone Joint Surg Br       Date:  1988-03

4.  Fibrous dysplasia: a review of the disease and its manifestations in the temporal bone.

Authors:  G T Nager; D W Kennedy; E Kopstein
Journal:  Ann Otol Rhinol Laryngol Suppl       Date:  1982 May-Jun

5.  Bone tissue in Paget's disease of bone. Ultrastructure and Immunocytology.

Authors:  A Rebel; M Basle; A Pouplard; K Malkani; R Filmon; A Lepatezour
Journal:  Arthritis Rheum       Date:  1980-10

6.  Hearing loss and Paget's disease.

Authors:  N L Sparrow; A J Duvall
Journal:  J Laryngol Otol       Date:  1967-06       Impact factor: 1.469

7.  Osteofibrous dysplasia of the tibia and fibula.

Authors:  M Campanacci; M Laus
Journal:  J Bone Joint Surg Am       Date:  1981-03       Impact factor: 5.284

  7 in total
  3 in total

1.  Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutation.

Authors:  Elahe Elahi; Yousef Shafaghati; Sareh Asadi; Farnaz Absalan; Hani Goodarzi; Nava Gharaii; Mohammad Hassan Karimi-Nejad; Farhad Shahram; Anne E Hughes
Journal:  J Bone Miner Metab       Date:  2007-04-20       Impact factor: 2.626

2.  Familial expansile osteolysis--not exclusively an adult disorder.

Authors:  Ivo Marik; A Marikova; E Hyankova; K Kozlowski
Journal:  Skeletal Radiol       Date:  2006-02-10       Impact factor: 2.199

3.  Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANK.

Authors:  Sean J Iwamoto; Micol S Rothman; Shenghui Duan; Jonathan C Baker; Steven Mumm; Michael P Whyte
Journal:  Bone       Date:  2020-01-08       Impact factor: 4.398

  3 in total

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