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  • Nodular paragranuloma  (2)
  • Amyloidosis  (1)
  • Blind-Loop Syndrome  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Virchows Archiv 399 (1983), S. 233-236 
    ISSN: 1432-2307
    Schlagwort(e): Amyloid ; Amyloidosis ; Lymph nodes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary A case of a patient presenting with supraclavicular and cervical lymph node enlargement with demonstration of amyloid is presented. Histologic features are described. Amyloid deposition was not found in any other organ. Immunohistochemical typing with antisera raised against protein AA, Aλ, and Aκ showed a reaction only against Aλ. Thus, this case belongs to the immunoglobulin λ light chain-derived types that occur in many other parts of the body, particularly the respiratory tract.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Journal of cancer research and clinical oncology 95 (1979), S. 57-63 
    ISSN: 1432-1335
    Schlagwort(e): Hodgkin's disease ; Nodular paragranuloma ; Epidemiology
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The age and sex distribution and the localization of excised lymph nodes from 206 patients with a nodular variant of Hodgkin's disease with lymphocytic predominance, called “nodular paragranuloma”, are presented and compared with data on other types of Hodgkin's disease. The age curve of nodular paragranuloma showed a peak in the fourth decade, which was clearly separated from the peak in the third decade exhibited by the nodular sclerosis type of Hodgkin's disease and from the peak in the sixth and seventh decades of the mixed cellularity type. The peak in the age curve of nodular paragranuloma resulted from the high frequency in men in the fourth decade; the female age curve had no peaks. The overall male-to-female ratio was 2.4:1. The age and sex distribution of diffuse paragranuloma was nearly identical to that of nodular paragranuloma, whereas the age and sex distribution of cases of the lymphocytic predominance type other than paragranuloma resembled that of the mixed cellularity type. These data indicate that the lymphocytic predominance type of Hodgkin's disease is not a uniform group and support the view that paragranuloma is a separate entity.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of cancer research and clinical oncology 108 (1984), S. 321-330 
    ISSN: 1432-1335
    Schlagwort(e): Nodular paragranuloma ; Hodgkin's disease, lymphocyte predominance type, nodular ; Clinical investigation ; Symptoms ; Prognosis ; Therapy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Clinical aspects of 145 cases of nodular paragranuloma (nodular subtype of lymphocyte predominance type of Hodgkin's disease) were investigated. There was a marked male predominance, and the age curve showed a peak in the 4th decade. In a majority of cases lymphadenopathy developed within 1 year. General (B) symptoms were observed in only 15 patients. The most frequent sites of primary involvement were cervical, axillary, and inguinal lymph nodes. Other organs were rarely involved. At the time of diagnosis 50% of patients were in stage I, 21% in stage II, 22% in stage III, and 7% in stage IV. The prognosis was usually favorable or very favorable and depended on the stage of disease at diagnosis and on the age of the patient. Patients with stage I or III disease without splenic involvement had about the same probability of survival as the normal population. Stage III patients with splenic involvement had a lower probability of survival. The prognosis for stage II was also less favorable. Patients in stage IV had the lowest probability of survival. Closer analysis of the ten stage IV cases revealed two groups with different outcomes. Four cases showed progressive disease that did not respond to treatment and led to death within 12 months. The second, more favorable form (6 patients) responded well to chemotherapy. Nine patients in stage I who were not treated after lymph node biopsy were free of disease even after periods of up to 14 years. A total of 52 patients had one or more relapses. The recurrent tumors developed locally in a majority of cases. There was transformation of nodular paragranuloma into another subtype of Hodgkin's disease in only four cases. Five cases showed transformation into large-cell tumors that resembled immunoblastic lymphoma and require further immunological study.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Langenbeck's archives of surgery 333 (1973), S. 81-90 
    ISSN: 1435-2451
    Schlagwort(e): Blind-Loop Syndrome ; Small Intestine
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Beschreibung / Inhaltsverzeichnis: Zusammenfassung Das Dünndarmstase-Syndrom ist gekennzeichnet durch das Auftreten von gastrointestinalen Beschwerden und makrocytären Anämien. Es wurde im Erwachsenenalter nach Magenoperationen, Strikturen und Divertikelbildungen des Dünndarms und nach Seit-zu-Seit-Anastomosen beobachtet. Im Kindesalter entwickeln sich Blindsäcke vorwiegend durch das physiologische Wachstum der blindverschlossenen Darmenden. Im Mittelpunkt der Pathogenese steht die pathologische Keimvermehrung im befallenen Darmabschnitt. Die histologischen Befunde der untersuchten Blindsäcke lassen jedoch vermuten, daß die stark hyperplastischen Zotten bei unauffälligen oder verschmälerten Krypten in ihrer Funktion eingeschränkt sind. Von 15 nachuntersuchten Patienten mit Seit-zu-Seit-Anastomosen waren nur 7 beschwerdefrei. 6 Patienten klagten über Obstipation oder Durchfälle, 2 davon hatten gleichzeitig eine hypochrome Anämie. Bei 2 Patienten handelte es sich um einen Zufallsbefund. Bei 6 von 8 nachgewiesenen Blindsackbildungen nach Seit-zu-Seit-Anastomose wurde die Operation im Wachstumsalter durchgeführt.
    Notizen: Summary The small bowel stasis syndrome is characterized by gastrointestinal disorders and macrocytic anemia. It was observed in adults after gastric operations, strictures and diverticulosis of the small intestine. In childhood the pouch develops mainly by physiological growth of the closed cut-ends of the intestine. The principle pathological feature is the abnormal contamination in involved loops. Histological studies of blind-loops show, that the function of the markedly hyperplastic villi in presence of normal and narrow crypt is limited. Out of 15 follow-up patients only 7 were free of complaints following side-to-side anastomoses. 6 had constipation or diarrhoea 2 from them had hypochromic anemia. In 2 of our cases the blind-loop was encountered accidently. In 6 cases an operation was performed.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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