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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    British journal of dermatology 134 (1996), S. 0 
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Summary We describe two boys affected by Down syndrome (DS), who showed milia-like idiopathic calcinosis cutis (MICC). The clinical diagnosis was confirmed by histological examination. All reported cases are reviewed and compared. Syringeal structures play a significant part in the pathogenesis of this dermatosis. MICC appears to be a poorly recognized condition which, rarely, is associated with DS.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    International journal of dermatology 35 (1996), S. 0 
    ISSN: 1365-4632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden , USA : Munksgaard International Publishers
    Journal of cutaneous pathology 31 (2004), S. 0 
    ISSN: 1600-0560
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background:  Melanocytic nevi in the genital, acral, and flexural sites often display clinical and histologic features that may simulate melanoma. We verified whether this is the case also for nevi of the breast.Methods:  Eleven dermatopathologists, from nine Italian Institutions, collected the specimens of melanocytic lesions from the breast and other body sites, excluding the acral, genital, and flexural areas, as controls. Cases and controls were matched for sex and age. All nevi were observed ‘blindly’ and simultaneously by all participants. For each lesion, 10 histological parameters were analyzed: asymmetry, absence of lateral demarcation of melanocytes, lentiginous proliferation, nested and dyshesive pattern, intraepidermal melanocytes above the basal layer, involvement of the hair follicle, absence of maturation of dermal melanocytes, melanocytic atypia, fibroplasia of the papillary dermis, and lymphocytic dermal infiltrate. Each parameter was scored 2 when present and 1 when absent or not valuable. A total score was calculated for each lesion. Results were statistically analyzed by the chi-square test and the Mann–Whitney U-test.Results:  One hundred and one nevi came from the breast area and 97 from elsewhere. Breast nevi exhibited significantly more atypical features than nevi from other sites. In particular, breast nevi with intraepidermal melanocytes, melanocytic atypia, and dermal fibroplasia were significantly more numerous. We did not find any sexual difference.Conclusions:  To avoid undue concerns, dermatopathologists should be aware that melanocytic nevi of the breast may show a high degree of atypical features.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 70 (1967), S. 31-38 
    ISSN: 1432-1335
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary In tumor cells (plasmacytoma, chorioepithelioma), in oogonia of the rabbit, and in hepatic cells of the human fetus “clear zones” of granular-fibrillar character were observed in sharply demarcated, condensed nucleoli. These zones could be distinguished clearly from the remaining nucleolus by their reduced osmiophilia. Histochemical studies indicated the presence of RNA in these «clear zones», an accumulation probably related to a disturbance of protein metabolism.
    Notes: Zusammenfassung In Tumorzellen (Plasmocytom und Chorionepitheliom) ebenso wie in den Oogonien des Kaninchens und in Leberzellen des menschlichen Fetus wurden in scharf begrenzten Nucleolen von kompaktem Aussehen „helle Zonen” von körnigfädiger Beschaffenheit beobachtet, welche sich durch ihre geringere Osmiophilie deutlich vom übrigen Nucleolus unterscheiden. Histochemische Untersuchungen deuten auf die Anwesenheit von RNS in diesen „hellen Zonen” hin, die wahrscheinlich mit einer Störung des Proteinstoffwechsels zusammenhängen dürften.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Neurological sciences 14 (1993), S. 49-54 
    ISSN: 1590-3478
    Keywords: Amyotrophic choreo-acanthocytosis ; degenerative disease ; neuropathology ; immunohistochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Un paziente di 47 anni, membro di una fratria affetta da Coreo-Acantocitosi Amiotrofica, è stato oggetto di studio neuropatologico, dopo alcuni anni di osservazione clinica. Oltre ai già noti reperti di microscopia ottica (perdita neuronale, gliosi astrocitaria e “status spongiosus” a livello dei nuclei della base, soprattutto del nucleo caudato), immunocitochimicamente furono evidenziati alcuni neuroni striatali MEnk+ e NPY+. A livello del midollo spinale non era riconoscibile perdita neuronale, invece si osservavano modesta demielinizzazione e iperplasia astrocitaria interfascicolare a carico dei tratti lunghi. I reperti presenti a livello del muscolo striato e del tronco nervoso periferico corrispondevano a quelli già descritti su materiale bioptico dello stesso paziente, prelevato alcuni anni prima. I diversi dati neuropatologici e immunocitochimici del caso osservato sono discussi particolarmente in riferimento alla diagnosi differenziale tra Coreo-Acantocitosi Amiotrofica e Corea di Huntington.
    Notes: Abstract A 47 year old man, one of a sibship affected by amyotrophic choreo-acanthocytosis was studied neuropathologically after some years of clinical observation. Besides the classic optical findings (neuronal loss, astrocytic gliosis and “status spongiosus” in the basal ganglia, namely in the caudate nucleus) a few MEnk+ and NPY+ neurons were observed immunocytochemically in the striatum. In the spinal cord also, while no neuronal loss was perceivable, both mild demyelination and interfibrillary astrocytic hyperplasia of the long tracts were present. On the other hand, microscopic findings of muscle and peripheral nerve showed no differences from what was previously intra-vitam appreciated in the same patient. The neuropathological and immunocytochemical findings of this case are discussed in relation to the differential diagnosis between amyotrophic choreoacanthocytosis and Huntington's disease.
    Type of Medium: Electronic Resource
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