Abstract

Intestinal tuberculosis (ITB) and Crohn's disease (CD) are granulomatous disorders with similar clinical manifestations and pathological features that are often difficult to differentiate. This study evaluated the value of fluorescent quantitative polymerase chain reaction (FQ-PCR) for Mycobacterium tuberculosis (MTB) in fecal samples and biopsy specimens to differentiate ITB from CD. From June 2010 to March 2013, 86 consecutive patients (38 females and 48 males, median age 31.3 years) with provisional diagnoses of ITB and CD were recruited for the study. The patients' clinical, endoscopic, and histological features were monitored until the final definite diagnoses were made. DNA was extracted from 250 mg fecal samples and biopsy tissues from each patient. The extracted DNA was amplified using FQ-PCR for the specific MTB sequence. A total of 29 ITB cases and 36 CD cases were included in the analysis. Perianal disease and longitudinal ulcers were significantly more common in the CD patients (P<0.05), whereas night sweats, ascites, and circumferential ulcers were significantly more common in the ITB patients (P<0.05). Fecal FQ-PCR for MTB was positive in 24 (82.8%) ITB patients and 3 (8.3%) CD patients. Tissue PCR was positive for MTB in 16 (55.2%) ITB patients and 2 (5.6%) CD patients. Compared with tissue FQ-PCR, fecal FQ-PCR was more sensitive (X2=5.16, P=0.02). We conclude that FQ-PCR for MTB on fecal and tissue samples is a valuable assay for differentiating ITB from CD, and fecal FQ-PCR has greater sensitivity for ITB than tissue FQ-PCR.

Highlights

  • Intestinal tuberculosis (ITB) and Crohn’s disease (CD) are chronic granulomatous disorders [1] with similar clinical presentations and pathologies

  • This study evaluated the value of fluorescent quantitative polymerase chain reaction (FQ-PCR) for Mycobacterium tuberculosis (MTB) in fecal samples and biopsy specimens to differentiate ITB from CD

  • A total of 29 ITB cases and 36 CD cases were included in the analysis

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Summary

Introduction

Intestinal tuberculosis (ITB) and Crohn’s disease (CD) are chronic granulomatous disorders [1] with similar clinical presentations and pathologies. The annual incidence of tuberculosis (TB) in China is approximately 1.3 million cases (second only to India) [2] and accounts for 14.3% of worldwide TB cases. The incidence of ITB, a common form of extrapulmonary TB, has increased in parallel with the overall resurgence of TB. In China, the prevalence of inflammatory bowel disease (IBD) has increased rapidly in recent years, mimicking its rapid growth in the developed world. Misdiagnosis of CD and ITB is common in developing countries [4], China [5]. In the case of ITB misdiagnosis, unnecessary anti-TB therapy poses a risk of toxicity and delays the treatment of CD. Treating ITB with steroids alone can lead to severe deterioration, or even death

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