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Clinical and Laboratory Diagnosis of Intestinal Tuberculosis

BACKGROUND: Tuberculosis (TB) remains a worldwide problem. Intestinal TB (ITB) constitutes a major public health problem in developing countries and has been associated with significant morbidity and mortality. The aim of this study was to characterize the clinical, radiological, endoscopic, and pat...

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Autores principales: Shi, Xiao-Chun, Zhang, Li-Fan, Zhang, Yue-Qiu, Liu, Xiao-Qing, Fei, Gui-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894044/
https://www.ncbi.nlm.nih.gov/pubmed/27231171
http://dx.doi.org/10.4103/0366-6999.182840
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author Shi, Xiao-Chun
Zhang, Li-Fan
Zhang, Yue-Qiu
Liu, Xiao-Qing
Fei, Gui-Jun
author_facet Shi, Xiao-Chun
Zhang, Li-Fan
Zhang, Yue-Qiu
Liu, Xiao-Qing
Fei, Gui-Jun
author_sort Shi, Xiao-Chun
collection PubMed
description BACKGROUND: Tuberculosis (TB) remains a worldwide problem. Intestinal TB (ITB) constitutes a major public health problem in developing countries and has been associated with significant morbidity and mortality. The aim of this study was to characterize the clinical, radiological, endoscopic, and pathological features of ITB and to define the strategy for establishing the diagnosis. METHODS: A retrospective study (from January 2000 to June 2015) was carried out in Peking Union Medical College Hospital and all hospitalized cases were diagnosed as ITB during the study period were included. The relevant clinical information, laboratory results, microbiological, and radiological investigations were recorded. RESULTS: Of the 85 cases, 61 cases (71.8%) were ranged from 20 to 50 years. The ileocecal region was involved in about 83.5% (71/85) of patients. About 41.2% (35/85) of patients had co-existing extra ITB, especially active pulmonary TB. Abdominal pain (82.4%) was the most common presenting symptom followed by weight loss (72.9%) and fever (64.7%). Both T-cell spot of TB test (T-SPOT.TB) and purified protein derivatives (PPD) tests were performed in 26 patients: 20 (76.9%) positive T-SPOT.TB and 13 (50.0%) positive PPD were detected, with a statistical significant difference (P = 0.046). Twenty cases (23.5%) were histopathology and/or pathogen confirmed TB; 27 cases (31.8%) were diagnosed by clinical manifestation consistent with ITB and evidence of active extra ITB; 38 cases (44.7%) were diagnosed by good response to diagnostic anti-TB therapy. CONCLUSIONS: ITB is difficult to diagnose even with modern medical techniques due to its nonspecific clinical and laboratory features. At present, combination of clinical, endoscopic, radiological, and pathological features continues to be the key to the diagnosis of ITB.
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spelling pubmed-48940442016-06-13 Clinical and Laboratory Diagnosis of Intestinal Tuberculosis Shi, Xiao-Chun Zhang, Li-Fan Zhang, Yue-Qiu Liu, Xiao-Qing Fei, Gui-Jun Chin Med J (Engl) Original Article BACKGROUND: Tuberculosis (TB) remains a worldwide problem. Intestinal TB (ITB) constitutes a major public health problem in developing countries and has been associated with significant morbidity and mortality. The aim of this study was to characterize the clinical, radiological, endoscopic, and pathological features of ITB and to define the strategy for establishing the diagnosis. METHODS: A retrospective study (from January 2000 to June 2015) was carried out in Peking Union Medical College Hospital and all hospitalized cases were diagnosed as ITB during the study period were included. The relevant clinical information, laboratory results, microbiological, and radiological investigations were recorded. RESULTS: Of the 85 cases, 61 cases (71.8%) were ranged from 20 to 50 years. The ileocecal region was involved in about 83.5% (71/85) of patients. About 41.2% (35/85) of patients had co-existing extra ITB, especially active pulmonary TB. Abdominal pain (82.4%) was the most common presenting symptom followed by weight loss (72.9%) and fever (64.7%). Both T-cell spot of TB test (T-SPOT.TB) and purified protein derivatives (PPD) tests were performed in 26 patients: 20 (76.9%) positive T-SPOT.TB and 13 (50.0%) positive PPD were detected, with a statistical significant difference (P = 0.046). Twenty cases (23.5%) were histopathology and/or pathogen confirmed TB; 27 cases (31.8%) were diagnosed by clinical manifestation consistent with ITB and evidence of active extra ITB; 38 cases (44.7%) were diagnosed by good response to diagnostic anti-TB therapy. CONCLUSIONS: ITB is difficult to diagnose even with modern medical techniques due to its nonspecific clinical and laboratory features. At present, combination of clinical, endoscopic, radiological, and pathological features continues to be the key to the diagnosis of ITB. Medknow Publications & Media Pvt Ltd 2016-06-05 /pmc/articles/PMC4894044/ /pubmed/27231171 http://dx.doi.org/10.4103/0366-6999.182840 Text en Copyright: © 2016 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Shi, Xiao-Chun
Zhang, Li-Fan
Zhang, Yue-Qiu
Liu, Xiao-Qing
Fei, Gui-Jun
Clinical and Laboratory Diagnosis of Intestinal Tuberculosis
title Clinical and Laboratory Diagnosis of Intestinal Tuberculosis
title_full Clinical and Laboratory Diagnosis of Intestinal Tuberculosis
title_fullStr Clinical and Laboratory Diagnosis of Intestinal Tuberculosis
title_full_unstemmed Clinical and Laboratory Diagnosis of Intestinal Tuberculosis
title_short Clinical and Laboratory Diagnosis of Intestinal Tuberculosis
title_sort clinical and laboratory diagnosis of intestinal tuberculosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894044/
https://www.ncbi.nlm.nih.gov/pubmed/27231171
http://dx.doi.org/10.4103/0366-6999.182840
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