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  • 1
    ISSN: 1432-0533
    Keywords: Cytomegalovirus (CMV) ; Acquired immunodeficiency syndrome (AIDS) ; Encephalitis ; DNA hybridization ; Immunocytochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Brain tissues from 45 patients with AIDS and two brains with connatal cytomegalic inclusion body disease were investigated for a cytomegalovirus (CMV) etiology of encephalitic lesions. Nineteen brains showed evidence of CMV infection by histology, immunocytochemistry (ICC) using two different antibodies (mono- and polyclonal), and in situ hybridization (ISH). Fourteen cases with typical cytomegalic cells in conventional histology [eight with focally necrotizing encephalitis/ventriculitis including the two connatal infections and six with nodular encephalitis (NE)] revealed CMV with any method. In 5 of 15 AIDS cases of NE without cytomegalic cells, CMV infection was established by ISH, whereas ICC remained negative in these cases. Typical lesions of human immunodeficiency virus (HIV)-induced multifocal giant cell encephalitis (HIV encephalitis) in 13 brains were never labeled for CMV. In necrotizing encephalitis/ventriculitis, cell types which labeled for CMV, with and without cytomegalic change, comprised neurons, astrocytes, oligodendrocytes, ependyma, choroid plexus, endothelia, and cells in periand endoneurium, and in leptomeninges. Both ISH and ICC were able to detect widespread non-cytomegalic CMV-infected cells in normal parenchyma, well beyound the necrotizing lesions, in two AIDS cases. Labeling patterns of nuclei versus cytoplasms varied between the three methods for CMV detection. We conclude that in CNS tissues with cytomegalic cells, ICC and ISH are of comparable sensitivity; however, a diagnosis of CMV disease is possible in such cases by conventional histology. For an in situ diagnosis of CMV infection in NE without cytomegalic cells in AIDS, ISH is the method of choice. A selective vulnerability to CMV infection of any specific cell type of the human CNS is absent. With our detection methods, typical lesions of HIV encephalitis do not show local co-infection by CMV.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1433-0474
    Keywords: Schlüsselwörter Dyspnoe ; Chronischer Husten ; Kindesalter ; Pleuropulmonales Blastom ; Kombinierte Therapie ; Key words Dyspnea ; Chronic cough ; Childhood ; Pleuropulmonary blastoma ; Combined therapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Background: Chronic cough and thoracic pain, commonly caused by upper airway infections, are frequently seen symptoms in pediatrics. These “benign” symptoms are very seldom caused by malignant disorders. Methods: In two patients (male, age 41/12 and 43/12 years) chronic cough and thoracic pain were due to a malignant pulmonary neoplasm (Pleuropulmonary blastoma). Results: Pleuropulmonary blastoma is a rare malignant primary pulmonary neoplasm in childhood with a poor prognosis. An incomplete resection was performed in both cases. Both patients received postoperative radiotherapy and combination chemotherapy. One boy died, the other one is alive and well more than 6 years after diagnosis without evidence of disease. Conclusion: Our findings indicate that even after incomplete resection subsequent multimodal therapy (adjuvant chemotherapy and radiotherapy) can provide a long term remission.
    Notes: Zusammenfassung Fragestellung: Dyspnoe, chronischer Husten und Brustschmerzen sind häufige Symptome in der pädiatrischen Praxis und werden meist durch banale Infekte der Atemwege verursacht. Nur sehr selten verbirgt sich hinter diesen „gutartigen“ Symptomen eine bösartige Erkrankung. Methode: Wir berichten über 2 Knaben (Alter 4 1/12 und 4 3/12 Jahre) bei denen chronischer Husten und Thoraxschmerzen durch einen bösartigen Lungentumor (pleuropulmonales Blastom) verursacht worden waren. Ergebnisse: Das pleuropulmonale Blastom (PPB) ist ein ausgesprochen seltener, primär intrathorakaler Tumor des Kindesalters mit schlechter Prognose. Bei keinem der beiden Patienten gelang chirurgisch eine vollständige Tumorentfernung. Beide Kinder erhielten postoperativ eine kombinierte Chemo- und Radiotherapie. Ein Knabe verstarb, der 2. Patient ist mehr als 6 Jahre nach der Diagnose ohne Krankheitszeichen. Schlußfolgerungen: Diese Erfahrung zeigt, daß auch nach unvollständiger chirurgischer Tumorentfernung bei konsequenter Anwendung eines multimodalen Therapiekonzepts eine länger anhaltende Remission möglich ist.
    Type of Medium: Electronic Resource
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