Skip to main content

Duodenal tuberculosis with gastric outlet obstruction: a case report of successful diagnosis and treatment, with review of literature

Abstract

Background

Duodenal tuberculosis (TB) is extremely rare, and its diagnosis is challenging owing to the lack of specific symptoms and radiological or endoscopic findings. When it leads to gastric outlet obstruction (GOO), diagnosing it accurately and providing appropriate treatment is crucial. However, this is often overlooked.

Case presentation

A 35-year-old man presented with abdominal pain, fullness, vomiting, and weight loss. Upper gastrointestinal endoscopy and radiography revealed nearly pinpoint stenosis with edematous and reddish mucosa in the D1/D2 portion of the duodenum. Computed tomography (CT) showed the duodenal wall thickening, luminal narrowing, multiple enlarged abdominal lymph nodes, and portal vein stenosis. Conventional mucosal biopsy during endoscopy revealed ulcer scars. We initially suspected stenosis due to peptic ulcers; however, chest CT revealed cavitary lesions in both lung apices, suggesting tuberculosis. Due to the suspicion of duodenal TB and the need to obtain deeper tissue samples, endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) was performed. The tissue sample showed caseating granulomas with multinucleated giant cells, and acid-fast bacilli were positive by Ziehl–Neelsen staining. The patient was diagnosed with duodenal TB and subsequent GOO. Because the patient had difficulty eating, surgical intervention was prioritized over antitubercular drugs, and laparoscopic gastrojejunostomy was performed. The patient started an oral diet on the 3rd postoperative day and began antitubercular treatment immediately after discharge on the 11th day. During the 6th month of treatment, endoscopic examination revealed residual duodenal stenosis; however, the bypass route functioned well, and the patient remained asymptomatic.

Conclusions

An aggressive biopsy should be performed to diagnose duodenal TB. EUS-FNA has proven to be a useful tool in this regard. Both nutritional improvement and antitubercular treatment were achieved early and reliably by performing laparoscopic gastrojejunostomy for duodenal TB with GOO.

Background

According to a World Health Organization report [1], the estimated number of patients with tuberculosis (TB) worldwide in 2021 was 10.6 million, indicating that TB remains a significant infectious disease. Duodenal TB is an extremely rare form of this disease [2]; however, it is crucial to make an early and accurate diagnosis, leading to appropriate treatment. This is because it tends to cause obstructive symptoms as the disease progresses. Improvement in duodenal TB with obstruction can be expected with a combination of antitubercular therapy (ATT) and invasive interventions. However, owing to its rarity, nonspecific symptoms, uncharacteristic endoscopic findings, and low diagnostic rates in pathology and bacteriology, duodenal TB is often overlooked. Consequently, patients may experience periods without proper treatment or undergo unnecessary treatment.

We report a case of gastric outlet obstruction (GOO) caused by duodenal TB. In this case, a successful preoperative diagnosis was made using endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA). Laparoscopic bypass surgery was performed as a minimally invasive and effective treatment for duodenal TB with GOO. This procedure allowed the patient to resume eating and receive appropriate ATT as quickly as possible.

Case presentation

A 35-year-old man with a history of epigastric pain, fullness after eating, and vomiting during the previous month was admitted to our hospital. He had experienced weight loss of 12 (kg) in the past year. He came to Japan from Myanmar four years ago. He had no history of chronic cough, fever, or diseases requiring immunosuppressants, and his family had no history of TB. Blood test results were normal, and anti-human immunodeficiency virus antibodies were negative. Abdominal computed tomography (CT) revealed gastric dilatation, thickening of the duodenal wall with luminal narrowing, and multiple enlarged low-density abdominal lymph nodes. Furthermore, portal vein stenosis was observed due to a low-density area along the hepatoduodenal ligament (Fig. 1a, b).

Fig. 1
figure 1

Abdominal computed tomography (CT) images on admission. a Duodenal stricture and wall thickening (black arrow). b Numerous enlarged abdominal lymph nodes (white arrows). Some of them have low CT values, suggesting necrosis. The portal vein is constricted by a low-density area along the hepatoduodenal ligament (head arrow)

The patient underwent an upper gastrointestinal (GI) endoscopy several days after the nasogastric tube placement. Endoscopic examination revealed a near-pinhole stricture in the D1/D2 portions of the duodenum (Fig. 2a). The narrowed area showed an edematous and reddish mucosa and a 5.8-mm-diameter scope could pass through, but a 9.7-mm-diameter scope could not. No distinct ulcers are observed. A biopsy of the mucosa revealed histopathological features consistent with ulcer scars. Upper GI radiography revealed a short stenotic segment in D1/D2 (Fig. 2b).

Fig. 2
figure 2

Images of Gastrointestinal (GI) Endoscopy and Upper GI Radiography. a Endoscopy showing a duodenal pinhole stricture. The mucosa exhibited edema and redness; however, no clear ulcerations were observed. b Upper GI contrast showing a short stricture at D1/D2 of the duodenum (arrow)

Our initial impression was duodenal stenosis caused by peptic ulcers. Therefore, intravenous omeprazole therapy was initiated immediately after admission. However, chest CT revealed cavitary lesions in both the lung apices (Fig. 3). We suspected tuberculosis and believe that there is a need for further detailed investigation of the abdominal lesions. A QuantiFERON-TB Gold (QFT) blood test revealed a positive result. However, sputum and gastric juice samples were negative on smear microscopy, acid-fast bacilli cultures, and Mycobacterium tuberculosis polymerase chain reaction (PCR) tests. A second-look endoscopy showed no improvement in duodenal narrowing despite the continuous administration of omeprazole. We identified a new ulcerative lesion in the lesser curvature of the upper gastric body (Fig. 4a) and performed multiple mucosal biopsies. Concurrently, we planned EUS-FNA to obtain biopsies from deeper layers. EUS revealed that the lymph nodes adjacent to the gastric wall had penetrated and formed a gastric ulcer. Therefore, EUS-FNA was performed (Fig. 4b). Unfortunately, the duodenum could not be observed using EUS because it was too narrow to allow scope insertion. Histopathological examination revealed granulomatous inflammation in the biopsied tissues of the duodenal mucosa and gastric ulcers (Fig. 5a). Furthermore, granulomatous inflammation with caseating necrosis and multinucleated giant cells were identified in the lymph node tissue obtained from EUS-FNA (Fig. 5b, c). Ziehl–Neelsen staining confirmed the presence of acid-fast bacilli (Fig. 5d); however, the bacterial culture did not confirm the presence of tuberculous bacilli.

Fig. 3
figure 3

Image of lung computed tomography (CT). Cavitary lesions noted in the apices of both lungs (arrows)

Fig. 4
figure 4

Images of the second gastrointestinal endoscopy and ultrasound endoscopy. a An ulcerative lesion is found on the lesser curvature of the upper body of the stomach. b Endoscopic ultrasound-guided fine-needle aspiration was performed on lymph nodes contiguous with a gastric ulcer

Fig. 5
figure 5

Pathological findings in biopsied tissue. a Epithelioid granuloma in duodenal mucosal tissue. b Granuloma with caseous necrosis in the lymph node obtained by EUS-FNA. c Enlarged image of b. Epithelioid granuloma with multinucleated giant cells. d Ziehl–Neelsen staining of lymphoid tissue was positive for mycobacteria

The repeat sputum PCR test was positive for Mycobacterium tuberculosis. The patient was diagnosed with duodenal TB with duodenal stenosis, tuberculous abdominal lymphadenitis, and pulmonary TB. Due to the difficulty in eating caused by GOO, surgical intervention was prioritized over ATT. The patient underwent laparoscopic bypass surgery. To prevent the airborne transmission of TB bacteria, we employed a closed-circuit insufflation management system (AirSeal® System; CONMED Corporation, Florida, USA). The laparoscopic observation revealed that the area around the hepatoduodenal ligament, antrum, and duodenum D1/D2 was shrunk with redness and the stomach deformed into a horseshoe shape (Fig. 6b). We performed laparoscopic gastrojejunostomy and Braun anastomosis using an automatic stapler (Fig. 6c). The operation time was 211 min, with minimal bleeding.

Fig. 6
figure 6

Images of surgical procedure. a Port placement. The 12-mm port highlighted in red is an access port for the AirSeal System. b Surgical findings. The hepatoduodenal ligament was shortened and the stomach deformed into a horseshoe shape. c Scheme of bypass surgery

The postoperative course progressed smoothly. The patient resumed eating on the 3rd day after surgery and no longer required intravenous fluids on the 4th day. The patient was transferred to a specialized hospital on the 11th postoperative day. Because drug-resistant TB was not detected, ATT was initiated with isoniazid, rifampicin, pyrazinamide, and ethambutol. After receiving ATT for 6 months, follow-up endoscopy and CT were performed. In the follow-up endoscopy, the duodenal stricture showed slight improvement, but the 9.7-mm-diameter scope still could not pass through (Fig. 7a), and upper GI radiography also indicated the presence of residual stenosis (Fig. 7b). CT showed an improvement in the duodenal edema; however, the reduction in the size of the enlarged lymph nodes and improvement in portal vein stenosis were only marginal (Fig. 7c, d). The pulmonary cavitary lesions decreased in size and were mostly scars. To achieve further improvement, isoniazid and rifampicin continued for an additional 3 months. Despite persistent duodenal stricture, the bypass procedure functioned effectively, enabling the patient to eat easily. The patient's body weight showed steady and consistent recovery.

Fig. 7
figure 7

Follow-up images at 6 months after starting antituberculosis treatment. a The mucosal edema and stricture of the duodenum have improved slightly. b Upper GI also shows residual duodenal stricture (arrow). c Edema of the duodenal wall has improved (arrow). d There was a slight reduction in lymph nodes (white arrows) and some improvement in portal vein stenosis (head arrow)

Discussion

Duodenal TB is a rare form of gastrointestinal tuberculosis (GI TB), accounting for 1–6% of GI TB cases [2]; but it is often reported in the literature. We searched for case reports of duodenal TB with GOO in PubMed using the keywords “duodenal tuberculosis” and “obstruction.” We reviewed 21 cases, including 17 full-text articles [3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19] and our own (Table 1). In this case, it is particularly noteworthy that we report the utility of EUS-FNA in diagnosing duodenal TB. In addition, we demonstrated that laparoscopic bypass surgery is a minimally invasive and safe approach for patients with nutritional deficiencies associated with GOO caused by duodenal TB.

Table 1 Details of previous reports and our case

Diagnosing duodenal TB is difficult due to the lack of specific clinical, endoscopic, and radiological features [20]. As shown in Table 1, among the 13 patients who underwent surgery, only one [15] had a confirmed diagnosis of TB before surgery in addition to ours. Therefore, most patients lack an accurate preoperative clinical diagnosis. Several case series from India, a country with a high TB burden, have shown similar patterns. In a case series of 23 patients, all underwent multiple biopsies during endoscopy but only two were diagnosed preoperatively [21]. In other reports of 30 cases of duodenal TB [22] and in five pediatric cases [23], the diagnosis of TB was made only after surgery in all patients. These facts indicate that despite the importance of making an accurate diagnosis for early and appropriate treatment, the diagnosis of duodenal TB is often delayed.

In addition, diagnostic delay may be due to the low accuracy in obtaining adequate tissue samples from the lesion. According to the guidelines [20], a definitive diagnosis of GI TB can be established if any of the following four criteria are present: demonstrating acid-fast bacilli, a positive TB PCR, caseating granulomas, or a positive TB culture on a biopsy specimen. However, diagnosis of duodenal TB from routine biopsy material is rare because tuberculous granulomas are mainly located in the submucosa [2, 20]. Routine biopsies may not collect sufficient tissue from the deeper layers, including the submucosal region. Therefore, EUS-FNA may provide a higher diagnostic sample yield. In our case, the initial endoscopic biopsy only revealed nonspecific inflammation, and the second biopsy showed granulomas with epithelioid cells but was inconclusive. Characteristic necrotic granulomas and acid-fast bacilli were successfully observed in the lymphoid tissue obtained using EUS-FNA, confirming the diagnosis of tuberculosis. Al-Hilou et al. [3] have also demonstrated the advantages of obtaining tissue microbiopsies using EUS-FNA. Additionally, Puri et al. [24] reported a histological diagnostic rate of 92% in patients with gastroduodenal TB by combining endoscopic biopsies with endoscopic mucosal resection. Both reports emphasize the importance of proactive biopsies when TB is highly suspected. In cases with a high index of clinical suspicion and where there is no target for EUS-FNA, a combination of multiple diagnostic methods following the guidelines [20] is necessary. There is no established gold standard for early detection of abdominal TB and no single test is deemed appropriate. Most importantly, to avoid delays in diagnosis, TB should always be considered in the differential diagnosis of unusual gastrointestinal presentations.

GOO is the most common symptom and clinically significant issue in the management of duodenal TB, affecting 60.8% to 84.3% of patients [21, 22, 25]. The mainstay of TB treatment is long-term combination therapy with multiple anti-TB drugs. However, for duodenal TB with GOO, rapid intervention is necessary, considering aspects such as early improvement in the patient’s nutritional status, the route of anti-TB drugs, and the potential for delayed improvement of stenosis due to drug-resistant TB.

GOO treatment includes two main approaches: endoscopic balloon dilation and surgical intervention. Puri et al. [24] reported a high success rate of 92% with endoscopic balloon dilatation of stenotic segments in 13 patients with gastroduodenal TB. However, endoscopic treatment for GOO requires repetitive procedures [26, 27]. Laparoscopic gastrojejunostomy is considered a better approach due to its shorter treatment period and earlier initiation of a regular diet compared to endoscopic therapy.

Relieving GOO before initiating ATT may be appropriate as a treatment strategy for duodenal TB with GOO. Endoscopic mucosal healing has been reported to occur in 81% of cases as early as 2 months after starting ATT and in 100% of cases by 6 months [28, 29]. However, treatment response to ATT varies among patients and is unpredictable. In our case, despite the absence of drug-resistant TB, endoscopy performed in the sixth month after starting ATT revealed a residual duodenal stricture. Lee et al. [15] reported cases where ATT alone was initiated but showed no improvement, necessitating bypass surgery. As demonstrated in these cases, a bypass route allows for unimpeded food intake, even in patients with a poor response to ATT.

Conclusions

Although duodenal TB is rare, it is important to accurately diagnose it and provide appropriate treatment, especially in patients presenting with GOO. Aggressive biopsies with high suspicion are necessary for diagnosis, and EUS-FNA has proven to be a useful tool in this regard. In patients with strictures, where estimating the therapeutic response to ATT is challenging, and early improvement in nutritional status is desired, laparoscopic bypass surgery is an appropriate choice because of its minimally invasive nature and rapid recovery.

Availability of data and materials

The datasets used and/or analyzed in the current study are available from the corresponding author upon reasonable request.

Abbreviations

ATT:

Antitubercular therapy

CT:

Computed tomography

EUS-FNA:

Endoscopic ultrasound-guided fine-needle aspiration

GI TB:

Gastrointestinal tuberculosis

GOO:

Gastric outlet obstruction

PCR:

Polymerase chain reaction

TB:

Tuberculosis

References

  1. Global tuberculosis report 2022. Geneva: World Health organization 2022. license: cc bY-Nc-sa 3.0 iGo. https://www.who.int/publications/i/item/9789240061729. Accessed 21 July 2023.

  2. Al-Zanbagi AB, Shariff MK. Gastrointestinal tuberculosis: a systematic review of epidemiology, presentation, diagnosis and treatment. Saudi J Gastroenterol. 2021;27:261–74.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Al-Hilou H, Carroll N, Jah A, Davies S, Parkes M. A rare cause of duodenal stricture. BMJ Case Rep. 2011;2011:bcr1020103379.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Ahmad M, Ahmed M. Duodenal tuberculosis. J Pak Med Assoc. 1985;35:53–4.

    CAS  PubMed  Google Scholar 

  5. Kriplani AK, Kumar S, Sharma LK. Obstruction of the third part of the duodenum in tuberculosis. Postgrad Med J. 1986;62:879–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Mani S, Rananavare R. Duodenal tuberculosis. Eur J Radiol. 1996;23:102–3.

    Article  CAS  PubMed  Google Scholar 

  7. Rautou PE, Corcos O, Hammel P, Cazals-Hatem D, Slama JL, Morin AS, et al. Pseudo Zollinger-Ellison syndrome in a patient with duodenal stenosis caused by tuberculosis. Gastroenterol Clin Biol. 2005;29:1164–8.

    Article  PubMed  Google Scholar 

  8. Benzekri O, Mouhadi SE, Chourak M, Boussetta S, Absi ME, Echarab M, et al. Tuberculous duodenal stenosis: report of two cases. Case Rep Gastroenterol. 2008;2:444–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Flores HB, Zano F, Ang EL, Estanislao N. Duodenal tuberculosis presenting as gastric outlet obstruction: a case report. World J Gastrointest Endosc. 2011;3:16–9.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Chawla I, Aery V, Singh K, Singla B, Singh V. Duodenal tuberculosis presenting as gastric outlet obstruction. J Surg Case Rep. 2012;2012:13.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Padmanabhan H, Rothnie A, Singh P. An unusual case of gastric outlet obstruction caused by tuberculosis: challenges in diagnosis and treatment. BMJ Case Rep. 2013;2013:bcr2012008277.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Sisodiya R, Ramachandra L. Tubercular duodenal, jejunal and ileocecal stricture in a patient. BMJ Case Rep. 2013;2013:bcr2013200347.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Fatemi SR, Ghobakhlou M, Alizadeh L. Obstructive pseudotumor of tuberculosis in a young woman: a rare presentation. Case Rep Gastrointest Med. 2014;2014: 914253.

    PubMed  PubMed Central  Google Scholar 

  14. Kalpande S, Pandya JS, Tiwari A, Adhikari D. Gastric outlet obstruction: an unusual case of primary duodenal tuberculosis. BMJ Case Rep. 2017;2017:bcr2016217966.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Lee JM, Kim ES, Chun HJ. Gastrointestinal: unexpected cause of refractory vomiting. J Gastroenterol Hepatol. 2017;32(3):543.

    Article  CAS  PubMed  Google Scholar 

  16. Udgirkar S, Surude R, Zanwar V, Chandnani S, Contractor Q, Rathi P. Gastroduodenal tuberculosis: a case series and review of literature. Clin Med Insights Gastroenterol. 2018;11:1179552218790566.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Meregildo-Rodríguez E, Méndez-Florián K, Espino-Saavedra W. Duodenal obstruction and upper gastrointestinal bleeding as the initial presentation of an isolated duodenal tuberculosis. Rev Chilena Infectol. 2019;36(3):387–91.

    Article  PubMed  Google Scholar 

  18. Chang A, Chantarojanasiri T, Pausawasdi N. Duodenal tuberculosis; uncommon cause of gastric outlet obstruction. Clin J Gastroenterol. 2020;13:198–202.

    Article  PubMed  Google Scholar 

  19. Molla YD, Kassa SA, Tadesse AK. Rare case of duodenal tuberculosis causing gastric outlet obstruction, a case report. Int J Surg Case Rep. 2023;105: 108080.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Tahiri M, Goh KL, Abbas Z, Epstein D, Min-Hu C, Mulder CJJ, et al. Digestive tract tuberculosis guideline. J Clin Gastroenterol. 2023;57:643–50.

    Article  PubMed  Google Scholar 

  21. Rao YG, Pande GK, Sahni P, Chattopadhyay TK. Gastroduodenal tuberculosis management guidelines, based on a large experience and a review of the literature. Can J Surg. 2004;47:364–8.

    PubMed  PubMed Central  Google Scholar 

  22. Gupta SK, Jain AK, Gupta JP, Agrawal AK, Berry K. Duodenal tuberculosis. Clin Radiol. 1988;39:159–61.

    Article  CAS  PubMed  Google Scholar 

  23. Upadhyaya VD, Kumar B, Lal R, Sharma MS, Singh M, Rudramani. Primary duodenal tuberculosis presenting as gastric-outlet obstruction: Its diagnosis. Afr J Paediatr Surg. 2013;10:83–6.

    Article  PubMed  Google Scholar 

  24. Puri AS, Sachdeva S, Mittal VV, Gupta N, Banka A, Sakhuja P, et al. Endoscopic diagnosis, management and outcome of gastroduodenal tuberculosis. Indian J Gastroenterol. 2012;31:125–9.

    Article  PubMed  Google Scholar 

  25. Nagi B, Lal A, Gupta P, Kochhar R, Sinha SK. Radiological findings in duodenal tuberculosis: a 15-year experience. Abdom Imaging. 2015;40:1104–9.

    Article  PubMed  Google Scholar 

  26. Vij JC, Ramesh GN, Choudhary V, Malhotra V. Endoscopic balloon dilation of tuberculous duodenal strictures. Gastrointest Endosc. 1992;38:510–1.

    Article  CAS  PubMed  Google Scholar 

  27. Kochhar R, Kochhar S. Endoscopic balloon dilation for benign gastric outlet obstruction in adults. World J Gastrointest Endosc. 2010;2:29–35.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Pratap Mouli V, Munot K, Ananthakrishnan A, Kedia S, Addagalla S, Garg SK, et al. Endoscopic and clinical responses to anti-tubercular therapy can differentiate intestinal tuberculosis from Crohn’s disease. Aliment Pharmacol Ther. 2017;45:27–36.

    Article  CAS  PubMed  Google Scholar 

  29. Sharma V, Mandavdhare HS, Dutta U. Letter: mucosal response in discriminating intestinal tuberculosis from Crohn’s disease—when to look for it? Aliment Pharmacol Ther. 2018;47:859–60.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

None.

Funding

The authors received no financial support for preparing this case report.

Author information

Authors and Affiliations

Authors

Contributions

NS gathered patient data and wrote the manuscript. NS and KW performed surgeries. KT and YM performed EUS-FNA. YW was administered, and the patient was followed up. YH made the pathological diagnosis in this case. MS, KS, KM, TA, and SY discussed and analyzed the data and assisted in writing the manuscript. All the authors have approved the final manuscript.

Corresponding author

Correspondence to Nami Sato.

Ethics declarations

Ethics approval and consent to participate

All procedures performed in this study involving human participants were in accordance with the 1964 Helsinki Declaration and subsequent relevant ethics. Written informed consent was obtained from all the patients.

Consent for publication

Written informed consent was obtained from the patient for the publication of this case report and any accompanying images.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sato, N., Shiobara, M., Wakatsuki, K. et al. Duodenal tuberculosis with gastric outlet obstruction: a case report of successful diagnosis and treatment, with review of literature. surg case rep 10, 42 (2024). https://doi.org/10.1186/s40792-024-01840-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s40792-024-01840-x

Keywords