Literature DB >> 230790

A specific ultrastructural marker for disseminated lipogranulomatosis (Faber).

C Schmoeckel, M Hohlfed.   

Abstract

An ultrastructural investigation of two cutaneous lesions in a two-year-old Turkish boy with disseminated lipogranulomatosis (Farber) revealed curvilinear bodies in fibroblasts, histiocytes, and endothelial cells; "elongated membranes" in fibroblasts and endothelial cells; "zebra bodies" in endothelial cells; and spindle-shaped bodies in Schwann cells. In peripheral lymphocytes only alterations of mitochondria (swelling and ruptured cristae) but no inclusion bodies were found. Curvilinear bodies were numerous and easily identifiable; they appear to be characteristic of Farber's disease, and naming them "Farber bodies" is proposed. The diagnosis of this ceramide storage disease, in which the histological examination is relatively unspecific, can therefore be confirmed ultrastructurally.

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Year:  1979        PMID: 230790     DOI: 10.1007/bf00694628

Source DB:  PubMed          Journal:  Arch Dermatol Res        ISSN: 0340-3696            Impact factor:   3.017


  18 in total

1.  FINE STRUCTURE OF THE LIPID BODIES IN JUVENILE AMAUROTIC IDIOCY.

Authors:  W ZEMAN; S DONAHUE
Journal:  Acta Neuropathol       Date:  1963-11-05       Impact factor: 17.088

2.  ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM.

Authors:  F P ALEU; R D TERRY; H ZELLWEGER
Journal:  J Neuropathol Exp Neurol       Date:  1965-04       Impact factor: 3.685

3.  [Disseminated lipogranulomatosis (Farber). Case report of the 16th case of a ceramidose (author's transl)].

Authors:  H Becker; L Auböck; M Haidvogl; H Bernheimer
Journal:  Verh Dtsch Ges Pathol       Date:  1976

4.  A lipid metabolic disorder: disseminated lipogranulomatosis; a syndrome with similarity to, and important difference from, Niemann-Pick and Hand-Schüller-Christian disease.

Authors:  S FARBER
Journal:  AMA Am J Dis Child       Date:  1952-10

5.  [Farber's disease. Anatomoclinical and ultrastructural study].

Authors:  P Dustin; M Tondeur; G Jonniaux; E Vamos-Hurwitz; S Pelc
Journal:  Bull Acad R Med Belg       Date:  1974-10

6.  Fine structure of phytohemagglutinin transformed lymphocytes. From patients with Niemann-Pick disease.

Authors:  S S Lazarus; V G Vethamany; B W Volk
Journal:  Arch Pathol       Date:  1968-08

7.  [A rare neurolipidosis with subcutaneous and articular node lesions: disseminated Farber's lipogranulomatosis].

Authors:  J Battin; C Vital; X Azanza
Journal:  Ann Dermatol Syphiligr (Paris)       Date:  1970

8.  Ceramidase deficiency in Farber's disease (lipogranulomatosis).

Authors:  M Sugita; J T Dulaney; H W Moser
Journal:  Science       Date:  1972-12-08       Impact factor: 47.728

9.  The cellular lesions of Farber's disease and their experimental reproduction in tissue culture.

Authors:  J Rutsaert; M Tondeur; E Vamos-Hurwitz; P Dustin
Journal:  Lab Invest       Date:  1977-05       Impact factor: 5.662

10.  Fine structural and ultracytochemical studies on the lymphocytes in three types of genetic mucopolysaccharidoses.

Authors:  F Murata; H Wohltman; S S Spicer; T Nagata
Journal:  Virchows Arch B Cell Pathol       Date:  1977-10-07
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  6 in total

Review 1.  Farber disease: an ultrastructural study. Report of a case and review of the literature.

Authors:  L Zappatini-Tommasi; C Dumontel; P Guibaud; C Girod
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1992

2.  Farber's disease in two siblings, sural nerve and subcutaneous biopsies by light and electron microscopy.

Authors:  J F Pellissier; M Berard-Badier; N Pinsard
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

3.  Rare Diseases in Glycosphingolipid Metabolism.

Authors:  Hongwen Zhou; Zhoulu Wu; Yiwen Wang; Qinyi Wu; Moran Hu; Shuai Ma; Min Zhou; Yan Sun; Baowen Yu; Jingya Ye; Wanzi Jiang; Zhenzhen Fu; Yingyun Gong
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 2.622

4.  A case of lipogranulomatosis Farber: some clinical and ultrastructural aspects.

Authors:  U Burck; H W Moser; H H Goebel; R Grüttner; K R Held
Journal:  Eur J Pediatr       Date:  1985-01       Impact factor: 3.183

5.  A case of combined Farber and Sandhoff disease.

Authors:  C Fusch; R Huenges; H W Moser; A C Sewell; W Roggendorf; B Kustermann-Kuhn; A Poulos; W F Carey; K Harzer
Journal:  Eur J Pediatr       Date:  1989-04       Impact factor: 3.183

Review 6.  Acid ceramidase deficiency: Farber disease and SMA-PME.

Authors:  Fabian P S Yu; Samuel Amintas; Thierry Levade; Jeffrey A Medin
Journal:  Orphanet J Rare Dis       Date:  2018-07-20       Impact factor: 4.123

  6 in total

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