Literature DB >> 1664226

Familial expansile osteolysis: a morphological, histomorphometric and serological study.

G R Dickson1, P V Shirodria, J A Kanis, M N Beneton, K E Carr, R A Mollan.   

Abstract

Biopsies from the diseased bones of patients with familial expansile osteolysis (FEO) were examined by light and electron microscopy. Focal concentrations of multinuclear osteoclasts were present, and these contained viral-like microcylindrical inclusions which appeared exclusive to their nuclei. No consistent relationship was found between osteoclast size and the number of osteoclast nuclei containing microcylindrical inclusions. Quantitative histomorphometry showed evidence of increased bone remodelling with high bone cell densities and a decrease of the reversal period in bone remodelling. The lesions contained prominent woven bone and fibrovascular tissue, together with mononuclear cells and adipocytes. Little bone was found in the most radiolucent lesions, which were almost totally occupied by adipocytes and fibrovascular tissue. Serology did not reveal any significant differences between the viral antibody titres of patients and their age- and sex-matched controls. The present study suggests that intranuclear viral-like microcylindrical inclusions of osteoclasts are not a specific feature of Paget's disease, and are found in other disorders of osteoclast function, including pycnodysostosis, osteopetrosis, giant cell tumours, and familial expansile osteolysis.

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Year:  1991        PMID: 1664226     DOI: 10.1016/8756-3282(91)90019-f

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  5 in total

1.  Genetic linkage of Paget disease of the bone to chromosome 18q.

Authors:  J D Cody; F R Singer; G D Roodman; B Otterund; T B Lewis; M Leppert; R J Leach
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

Review 2.  Paget's disease of bone-genetic and environmental factors.

Authors:  Frederick R Singer
Journal:  Nat Rev Endocrinol       Date:  2015-08-18       Impact factor: 43.330

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

4.  The Use of Patient-Specific Induced Pluripotent Stem Cells (iPSCs) to Identify Osteoclast Defects in Rare Genetic Bone Disorders.

Authors:  I-Ping Chen
Journal:  J Clin Med       Date:  2014-12-17       Impact factor: 4.241

5.  Multiple Idiopathic Cervical Root Resorption: A Challenge for a Transdisciplinary Medical-Dental Team.

Authors:  Emily Y Chu; Janina Golob Deeb; Brian L Foster; Evlambia Hajishengallis; Martha J Somerman; Vivek Thumbigere-Math
Journal:  Front Dent Med       Date:  2021-03-26
  5 in total

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