Literature DB >> 164754

New kind of cytoplasmic inclusions of plasma cells in acid maltase deficiency.

H Pralle, R Schröder, H Löffler.   

Abstract

Extensive 'vacuolization' could be demonstrated in nearly all plasma cells and in some lymphocytes of an adult with glycogenosis type II (Pompe's disease). The biochemically defined diagnosis acid maltase deficiency (AMD) could be ascertained by examination of the maltase activity of the patient's leukocytes. Electron microscopical, microspectrographic, and cytochemical investigations revealed electron dense inclusions, which show an UV absorption at 276 nm and a positive reaction after PAS staining of plastic embedded material. Since no other abnormalities of the plasma cells could be found, our results are presumably indicative for a connection of AMD and a glycoprotein storage in the plasma cells of the patient.

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Year:  1975        PMID: 164754     DOI: 10.1159/000208164

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  3 in total

1.  Bone marrow findings of the newly described TEMPI syndrome: when erythrocytosis and plasma cell dyscrasia coexist.

Authors:  Flavia G Rosado; Jennifer L Oliveira; Aliya R Sohani; Wilfried Schroyens; David B Sykes; Saad S Kenderian; Martha Q Lacy; Robert A Kyle; James D Hoyer
Journal:  Mod Pathol       Date:  2014-09-12       Impact factor: 7.842

2.  [Plasma cell inclusions in Pompe's disease (glycogenosis type II). Second case of a new anomaly].

Authors:  H Pralle; H Löffler
Journal:  Blut       Date:  1976-11

3.  Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease - a new type of neuronal ceroid lipofuscinosis (CLN15)?

Authors:  Stefanie Beck-Wödl; Klaus Harzer; Marc Sturm; Rebecca Buchert; Olaf Rieß; Hans-Dieter Mennel; Elisabeth Latta; Axel Pagenstecher; Ursula Keber
Journal:  Acta Neuropathol Commun       Date:  2018-12-27       Impact factor: 7.801

  3 in total

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