Literature DB >> 315965

Sea blue histiocytosis in a patient with chronic non-neuropathic Niemann-Pick disease.

N Dewhurst, G T Besley, N D Finlayson, A C Parker.   

Abstract

A patient with Niemann-Pick disease is reported together with family studies. Her liver and bone marrow were shown to be infiltrated with sea blue histiocytes. Other organs, spleen and lung, were presumably also involved but histological proof was not obtained. Enzyme assay of leucocytes, lymphocytes, and cultured skin fibroblasts showed the patient to be deficient in sphingomyelinase activity. In fibroblasts, activity was 5% of normal while for the parents activity was about 50% of normal. The expected partial deficiency was not found using leucocytes or lymphocytes from the parents. Heat stability studies on fresh fibroblast extracts from the propositus indicated that residual sphingomyelinase activity was slightly more labile than that of the controls. It seems clear that chronic Niemann-Pick disease without neurological involvement is associated with sea blue histiocytosis.

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Year:  1979        PMID: 315965      PMCID: PMC1145910          DOI: 10.1136/jcp.32.11.1121

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  18 in total

1.  Sphingomyelinase defect in Niemann-Pick disease, type C, fibroblasts.

Authors:  G T Besley
Journal:  FEBS Lett       Date:  1977-08-01       Impact factor: 4.124

2.  LIPID HISTOCHEMISTRY AND ELECTRON MICROSCOPY IN ADULT NIEMANN-PICK DISEASE.

Authors:  R LYNN; R D TERRY
Journal:  Am J Med       Date:  1964-12       Impact factor: 4.965

3.  The cerebral defect in Tay-Sachs disease and Niemann-Pick disease.

Authors:  A C CROCKER
Journal:  J Neurochem       Date:  1961-04       Impact factor: 5.372

4.  A new form of Niemann-Pick disease characterised by temperature-labile sphingomyelinase.

Authors:  E L Schneider; P G Pentchev; S R Hibbert; A Sawitsky; R O Brady
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

5.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

6.  Nine cases of sphingomyelin lipidosis, a new variant in Spanish-American Children. Juvenile variant of Niemann-Pick Disease with foamy and sea-blue histiocytes.

Authors:  D A Wenger; G Barth; J H Githens
Journal:  Am J Dis Child       Date:  1977-09

7.  Sea-blue histiocytosis associated with hyperlipidaemia.

Authors:  A C Parker; A D Bain; W G Brydon; R A Harkness; A F Smith; I I Smith; D H Boyd
Journal:  J Clin Pathol       Date:  1976-07       Impact factor: 3.411

8.  The syndrome of the sea-blue histiocyte.

Authors:  M N Silverstein; R D Ellefson
Journal:  Semin Hematol       Date:  1972-07       Impact factor: 3.851

9.  Biochemical, genetic and ultrastructural study of a family with the sea-blue histiocyte syndrome/chronic non-neuronopathic Niemann-Pick disease.

Authors:  K Fried; S Beer; H I Krespin; H Leiba; M Djaldetti; D Zitman; C Klibansky
Journal:  Eur J Clin Invest       Date:  1978-08       Impact factor: 4.686

10.  Adult Niemann-Pick disease: its relationship to the syndrome of the sea-blue histiocyte.

Authors:  R G Long; B D Lake; J E Pettit; P J Scheuer; S Sherlock
Journal:  Am J Med       Date:  1977-04       Impact factor: 4.965

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  7 in total

1.  Evidence of polyglandular involvement in Niemann-Pick disease type B.

Authors:  P Strisciuglio; S Di Maio; G Parenti; A Franzese; P Lubrano; A Mariano; G Andria
Journal:  Eur J Pediatr       Date:  1987-07       Impact factor: 3.183

2.  Niemann-Pick disease type B: clinical signs and follow-up of a new case.

Authors:  L Pavone; A Fiumara; M LaRosa
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  Late Niemann-Pick disease with neurovisceral storage: a classification problem.

Authors:  J McFarlane; L Murray; K Bradbury; P N Cowen
Journal:  J Clin Pathol       Date:  1988-06       Impact factor: 3.411

4.  Cirrhosis and liver failure: expanding phenotype of Acid sphingomyelinase-deficient niemann-pick disease in adulthood.

Authors:  Olivier Lidove; Frédéric Sedel; Frédéric Charlotte; Roseline Froissart; Marie T Vanier
Journal:  JIMD Rep       Date:  2014-04-10

5.  Very low levels of high density lipoprotein cholesterol in four sibs of a family with non-neuropathic Niemann-Pick disease and sea-blue histiocytosis.

Authors:  M B Viana; R Giugliani; V H Leite; M L Barth; C Lekhwani; C M Slade; A Fensom
Journal:  J Med Genet       Date:  1990-08       Impact factor: 6.318

6.  A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rate.

Authors:  W Sperl; G Bart; M T Vanier; H Christomanou; I Baldissera; E Steichen-Gersdorf; E Paschke
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

7.  Somatic cell hybridisation studies showing different gene mutations in Niemann-Pick variants.

Authors:  G T Besley; A J Hoogeboom; A Hoogeveen; W J Kleijer; H Galjaard
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  7 in total

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