Literature DB >> 7004304

The histiocytic disorders: a pathophysiologic analysis.

J E Groopman, D W Golde.   

Abstract

The histiocytoses are a diverse group of disorders involving cells of the mononuclear phagocyte series. These diseases are usually characterized by proliferation and activation of macrophages caused either by external stimuli or by an intrinsic cellular abnormality. We propose that these conditions be classified as reactive histiocytosis (inciting agent known or unknown), lipid storage disorder, and mononuclear phagocyte neoplasia based on apparent cause and natural history. Recent knowledge of monocyte-macrophage development and function allows for construction of pathophysiologic models of diseases formerly approached in a descriptive fashion. Macrophage activation appears to mediate many clinical features of th histiocytic disorders, such as hemophagocytosis, fever, and osteolysis. Further understanding of the pathogenesis of the histiocytic disorders should lead to improved therapy.

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Year:  1981        PMID: 7004304     DOI: 10.7326/0003-4819-94-1-95

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  17 in total

1.  Eosinophilic granuloma of the skull associated with epidural haematoma: a case report and review of the literature.

Authors:  Melike Mut; Oğuz Cataltepe; Bülent Bakar; Ayşenur Cila; Nejat Akalan
Journal:  Childs Nerv Syst       Date:  2004-10       Impact factor: 1.475

2.  Haemophagocytosis in hereditary fructose intolerance: a diagnostic dilemma.

Authors:  H Mandel; D Gozal; A Aizin; S Tavori; M Jaffe
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Gastric polyposis caused by multifocal histiocytosis X.

Authors:  R Wada; S Yagihashi; R Konta; T Ueda; T Izumiyama
Journal:  Gut       Date:  1992-07       Impact factor: 23.059

4.  Indeterminate cell histiocytosis in a pediatric patient: successful treatment with thalidomide.

Authors:  Béla Tóth; Mária Katona; Judit Hársing; Agota Szepesi; Sarolta Kárpáti
Journal:  Pathol Oncol Res       Date:  2011-06-19       Impact factor: 3.201

5.  Favourable prognostic features in histiocytosis X: bone involvement and absence of skin disease.

Authors:  V Broadbent
Journal:  Arch Dis Child       Date:  1986-12       Impact factor: 3.791

6.  Pulmonary histiocytosis X.

Authors:  T W Marcy; H Y Reynolds
Journal:  Lung       Date:  1985       Impact factor: 2.584

7.  Histiocytosis X--current controversies.

Authors:  V Broadbent; J Pritchard
Journal:  Arch Dis Child       Date:  1985-07       Impact factor: 3.791

8.  Malignant histiocytosis associated with SIADH and retinal hemorrhages.

Authors:  C D Simpson; S E Aitken
Journal:  Can Med Assoc J       Date:  1982-08-15       Impact factor: 8.262

9.  Angiotensin converting enzyme: a tumour marker in malignant histiocytosis.

Authors:  F Boomsma; J J Michiels; E Prins; J Abels; M A Schalekamp
Journal:  Br Med J (Clin Res Ed)       Date:  1983-04-02

10.  Malignant fibrous histiocytoma of the gingiva.

Authors:  D Vijayalakshmi; Shabana Fathima; K Ramakrishnan; M Devi
Journal:  BMJ Case Rep       Date:  2012-12-19
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