Literature DB >> 469631

The pathology of cartilage in chondrodysplasias.

W S Hwang, E P Tock, K L Tan, L K Tan.   

Abstract

The pathology of four types of chondrodysplasias, viz., type II achondrogenesis, thanatophoric dwarfism, Saldino-Noonan syndrome, and chondrodysplasia punctata were studied. In each of these disorders, cells with features similar to the chief and dark chondrocytes of normal hyaline cartilage were seen to be altered in different ways. There was a total absence of chief cells in type II achondrogenesis. All the chondrocytes present were of one variety at different states of maturation, with the fully matured cell having features of dark chondrocytes. The absence of chief cells was associated with marked diminution of interlacunar matrix and failure of growth plate development. The chief chondrocytes in thanatophoric dwarfism appeared diminished in number. They were probably abnormal functionally as evident by their lack of cytoplasmic vacuolation and the formation of thick, occasionally branched collagen in the matrix. The growth plate was stunted and poorly developed. Striking changes involving the dark cells were noted in Saldino-Noonan syndrome, where unusually elongated dark cells were found in groups within abnormal cystic spaces. The chief cells were large and contained abnormal cytoplasmic filaments. There was no formation of a growth plate. In chondrodysplasia punctata, the chief cells were enlarged and abnormally vacuolated. The matrix showed excessive aggregates of coarse granular material. In addition, there were focal accumulations of highly abnormal chief and dark cells with abnormal matrix which contained increased amount of keratan sulphate and culminated in spotty calcification.

Entities:  

Mesh:

Year:  1979        PMID: 469631     DOI: 10.1002/path.1711270103

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  7 in total

1.  Thanatophoric dysplasia. Correlation among bone X-ray morphometry, histopathology, and gene analysis.

Authors:  Ugo E Pazzaglia; Carla M Donzelli; Claudia Izzi; Maurizia Baldi; Giuseppe Di Gaetano; MariaPia Bondioni
Journal:  Skeletal Radiol       Date:  2014-05-25       Impact factor: 2.199

2.  Differentiation and mineralization of murine mesenchymal C3H10T1/2 cells in micromass culture.

Authors:  Rani Roy; Valery Kudryashov; Stephen B Doty; Itzhak Binderman; Adele L Boskey
Journal:  Differentiation       Date:  2010-03-30       Impact factor: 3.880

Review 3.  Examination of products of conception terminated after prenatal investigation.

Authors:  S Knowles
Journal:  J Clin Pathol       Date:  1986-10       Impact factor: 3.411

4.  Case report 122: lethal short-limbed dwarfism: achondrogenesis type 2 (Fraccaro-Langer-Saldino).

Authors:  H D Dorfman; J Lorenzo
Journal:  Skeletal Radiol       Date:  1980       Impact factor: 2.199

5.  Dwarfism in the Alaskan Malamute: ultrastructural features of dwarf growth plate chondrocytes.

Authors:  S A Bingel; R D Sande; J Newbrey
Journal:  Calcif Tissue Int       Date:  1983       Impact factor: 4.333

6.  Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findings.

Authors:  H Hebestreit; R J Wanders; R B Schutgens; M Espeel; I Kerckaert; F Roels; B Schmausser; L Schrod; A Marx
Journal:  Eur J Pediatr       Date:  1996-12       Impact factor: 3.183

7.  An unusual case of metaphyseal chondrodysplasia with an abnormal perilacunar matrix associated with agranulocytosis and hypoplasia of the thymus.

Authors:  K Ichijima; H Yamabe; Y Kobashi; H Ogawa; K Akaishi
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1981
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.