Bacillarity at autopsy in pulmonary tuberculosis: Mycobacterium tuberculosis is often disseminated

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Standard

Bacillarity at autopsy in pulmonary tuberculosis : Mycobacterium tuberculosis is often disseminated. / Lillebaek, Troels; Kok-Jensen, Axel; Viskum, Kaj.

I: APMIS, Bind 110, Nr. 9, 01.09.2002, s. 625-629.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Lillebaek, T, Kok-Jensen, A & Viskum, K 2002, 'Bacillarity at autopsy in pulmonary tuberculosis: Mycobacterium tuberculosis is often disseminated', APMIS, bind 110, nr. 9, s. 625-629. https://doi.org/10.1034/j.1600-0463.2002.1100905.x

APA

Lillebaek, T., Kok-Jensen, A., & Viskum, K. (2002). Bacillarity at autopsy in pulmonary tuberculosis: Mycobacterium tuberculosis is often disseminated. APMIS, 110(9), 625-629. https://doi.org/10.1034/j.1600-0463.2002.1100905.x

Vancouver

Lillebaek T, Kok-Jensen A, Viskum K. Bacillarity at autopsy in pulmonary tuberculosis: Mycobacterium tuberculosis is often disseminated. APMIS. 2002 sep. 1;110(9):625-629. https://doi.org/10.1034/j.1600-0463.2002.1100905.x

Author

Lillebaek, Troels ; Kok-Jensen, Axel ; Viskum, Kaj. / Bacillarity at autopsy in pulmonary tuberculosis : Mycobacterium tuberculosis is often disseminated. I: APMIS. 2002 ; Bind 110, Nr. 9. s. 625-629.

Bibtex

@article{522e475bdd944f7b8fd2679d7f9f4469,
title = "Bacillarity at autopsy in pulmonary tuberculosis: Mycobacterium tuberculosis is often disseminated",
abstract = "The aim of this investigation was to quantify dissemination of Mycobacterium tuberculosis infection in patients with pulmonary tuberculosis and to show the pattern of eradication during treatment. The study is based on 98 out of the 113 patients with pulmonary tuberculosis who died during their admission to hospital in the Municipality of Copenhagen from 1963 to 1971. These patients had cultures for M. tuberculosis performed from different organs at autopsy: 78% treated <=100 days had dissemination of bacteria, cultured with decreasing frequency in the lungs, spleen, liver, and kidneys, respectively. In comparison, 23% treated >100 days had dissemination of bacteria, among which 50% occurred in patients with records of poor treatment compliance, 14% in patients with good treatment compliance. 81% of all patients had at least one chest x-ray judged to be without a miliary pattern. This study emphasizes that M. tuberculosis is often disseminated to organs other than the lungs in severe pulmonary tuberculosis. Eradication of bacteria in these organs can take several months. This observation adds to our understanding of the natural history of tuberculosis: M. tuberculosis is a resilient organism that can adapt to a wide variety of environmental conditions.",
keywords = "Autopsy, Culture, Pulmonary, Treatment, Tuberculosis",
author = "Troels Lillebaek and Axel Kok-Jensen and Kaj Viskum",
year = "2002",
month = sep,
day = "1",
doi = "10.1034/j.1600-0463.2002.1100905.x",
language = "English",
volume = "110",
pages = "625--629",
journal = "Acta Pathologica et Microbiologica Scandinavica - Section A Pathology",
issn = "0365-4184",
publisher = "Munksgaard International Publishers",
number = "9",

}

RIS

TY - JOUR

T1 - Bacillarity at autopsy in pulmonary tuberculosis

T2 - Mycobacterium tuberculosis is often disseminated

AU - Lillebaek, Troels

AU - Kok-Jensen, Axel

AU - Viskum, Kaj

PY - 2002/9/1

Y1 - 2002/9/1

N2 - The aim of this investigation was to quantify dissemination of Mycobacterium tuberculosis infection in patients with pulmonary tuberculosis and to show the pattern of eradication during treatment. The study is based on 98 out of the 113 patients with pulmonary tuberculosis who died during their admission to hospital in the Municipality of Copenhagen from 1963 to 1971. These patients had cultures for M. tuberculosis performed from different organs at autopsy: 78% treated <=100 days had dissemination of bacteria, cultured with decreasing frequency in the lungs, spleen, liver, and kidneys, respectively. In comparison, 23% treated >100 days had dissemination of bacteria, among which 50% occurred in patients with records of poor treatment compliance, 14% in patients with good treatment compliance. 81% of all patients had at least one chest x-ray judged to be without a miliary pattern. This study emphasizes that M. tuberculosis is often disseminated to organs other than the lungs in severe pulmonary tuberculosis. Eradication of bacteria in these organs can take several months. This observation adds to our understanding of the natural history of tuberculosis: M. tuberculosis is a resilient organism that can adapt to a wide variety of environmental conditions.

AB - The aim of this investigation was to quantify dissemination of Mycobacterium tuberculosis infection in patients with pulmonary tuberculosis and to show the pattern of eradication during treatment. The study is based on 98 out of the 113 patients with pulmonary tuberculosis who died during their admission to hospital in the Municipality of Copenhagen from 1963 to 1971. These patients had cultures for M. tuberculosis performed from different organs at autopsy: 78% treated <=100 days had dissemination of bacteria, cultured with decreasing frequency in the lungs, spleen, liver, and kidneys, respectively. In comparison, 23% treated >100 days had dissemination of bacteria, among which 50% occurred in patients with records of poor treatment compliance, 14% in patients with good treatment compliance. 81% of all patients had at least one chest x-ray judged to be without a miliary pattern. This study emphasizes that M. tuberculosis is often disseminated to organs other than the lungs in severe pulmonary tuberculosis. Eradication of bacteria in these organs can take several months. This observation adds to our understanding of the natural history of tuberculosis: M. tuberculosis is a resilient organism that can adapt to a wide variety of environmental conditions.

KW - Autopsy

KW - Culture

KW - Pulmonary

KW - Treatment

KW - Tuberculosis

UR - http://www.scopus.com/inward/record.url?scp=0036757249&partnerID=8YFLogxK

U2 - 10.1034/j.1600-0463.2002.1100905.x

DO - 10.1034/j.1600-0463.2002.1100905.x

M3 - Journal article

C2 - 12529015

AN - SCOPUS:0036757249

VL - 110

SP - 625

EP - 629

JO - Acta Pathologica et Microbiologica Scandinavica - Section A Pathology

JF - Acta Pathologica et Microbiologica Scandinavica - Section A Pathology

SN - 0365-4184

IS - 9

ER -

ID: 247166460