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  • 1
    ISSN: 1600-0846
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background/aims :The fasciitis-panniculitis syndromes include several disorders characterized by skin induration due to fibrotic thickening of the septa of the subcutis and muscular fascia associated with chronic inflammation. Representative of the idiopathic form, eosinophilic fasciitis, is the prototype of the fasciitis-panniculitis syndromes. Secondary forms of the syndromes are causally related to a variety of diseases, such as infections, circulatory disorders, physical injuries and neoplasms.Methods: Histological sections of 10 idiopathic and 20 secondary cases of the fasciitis-panniculitis syndromes were assessed by means of computer-assisted image analysis. The percent of fibrous tissue, referred to as “extent of fibrosis”, and the number of lymphocytes, macrophages, eosinophils, plasma cells, and mast cells within the subcutaneous-fascial complex were assessed.Results: The “extent of fibrosis” varied from 1% to 2% in the control cases and from 4% to 98% in the index cases. The number of inflammatory cells per high power field varied from 0 to 33 in the control cases and from 9 to 323 in the index cases.Conclusions: There is a direct and positive correlation between the “extent of fibrosis” and the number of inflammatory cells. The “extent of fibrosis” and intensity of the inflammatory infiltration do not correlate with the nature of the underlying diseases, the patients’demographic data, the anatomic location of the subcutaneous induration or the duration of the lesion. It is suggested that the fasciitis-panniculitis syndromes are the morphological expression of a chronic, relapsing, inflammatory-sclerosing reaction pattern that is essentially identical in the idiopathic and the secondary forms of the disorder.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The international journal of angiology 5 (1996), S. 149-156 
    ISSN: 1615-5939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Sporadic reports allude to the similarities between the subcutaneous and fascial sclerosis of venous disease and lymphedema with that of eosinophilic fasciitis and the related fasciitis-panniculitis syndrome. The objective of the present study was to compare the clinical and histological features of the subcutaneous induration in patients with impairment of the venous, arterial, and lymphatic circulation (6 patients) with those of patients with the fasciitispanniculitis syndrome of diverse etiologies (12 patients). The semiquantitative analysis of the microscopic changes evinces the equivalent intensity of subcutaneous septal fibrosis, inflammation and mucinosis, lobular panniculitis, fascial fibrosis and inflammation, as well as microscopic phlebitis and phlebosclerosis in both groups of patients. The similarities of the pathological alterations of the subcutaneous layers are indicative of a shared reaction pattern to a variety of insults. In the patients with circulatory disorders, analysis of the clinical circumstances establishes the convergence of synergistically acting factors in the causation of the fasciitis-panniculitis syndrome. The circulatory impediment is insufficient to induce the syndrome, but it apparently acts as a predisposing factor such that it amplifies the inflammatory-cicatrizing response to one ordinary damage or another. Awareness of the multifactorial etiopathogenesis of the fasciitis-panniculitis syndrome in patients with circulatory disturbances ushers in a novel perspective of therapeutic intervention at multiple levels.
    Type of Medium: Electronic Resource
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