Primary adrenal insufficiency secondary to ileocecal tuberculosis

Authors

  • Adesh Kumar Department of General Medicine, K. S. Hegde Medical Academy, Nitte Deemed to be University, Mangalore, Karnataka, India
  • Debasmita Pal Department of General Medicine, K. S. Hegde Medical Academy, Nitte Deemed to be University, Mangalore, Karnataka, India
  • Aditya Ojha Department of General Medicine, K. S. Hegde Medical Academy, Nitte Deemed to be University, Mangalore, Karnataka, India

DOI:

https://doi.org/10.18203/2320-6012.ijrms20262658

Keywords:

Disseminated tuberculosis, Adrenal tuberculosis, Addison's disease, Ileocecal tuberculosis, Mycobacterium tuberculosis

Abstract

Ileocecal tuberculosis, the most common form of gastrointestinal tuberculosis, is usually caused by Mycobacterium tuberculosis, which is also the leading infectious cause of adrenalitis. Adrenal involvement can result in primary adrenal insufficiency, presenting with weakness, fatigue, hypotension, electrolyte imbalance, and hyperpigmentation. We present the case of a 43-year-old male with recurrent vomiting, fatigue, orthostatic dizziness, and generalized hyperpigmentation. His blood pressure was 100/80 mmHg, and laboratory tests showed low serum cortisol, elevated ACTH, hyponatremia, and hyperkalemia—findings consistent with primary adrenal insufficiency. Imaging revealed bilateral adrenal enlargement, a thickened ileocecal junction, and enlarged mesenteric lymph nodes. Colonoscopy demonstrated a terminal ileal stricture with granulomatous inflammation, and adrenal biopsy showed caseous necrosis. GeneXpert confirmed rifampicin-sensitive M. tuberculosis, indicating disseminated tuberculosis originating from the ileocecal region. The patient was started on standard anti-tubercular therapy with corticosteroid replacement for Addison’s disease. This case report highlights disseminated tuberculosis presenting as primary adrenal insufficiency secondary to ileocecal tuberculosis, an uncommon yet clinically significant association. Adrenal tuberculosis should be suspected with hyperpigmentation, electrolyte imbalance, and bilateral adrenal lesions; early diagnosis enables therapy, preventing adrenal crisis.

References

Sachdeva KS, Kumar A, Dewan P, Kumar A, Satyanarayana S. New vision for Revised National Tuberculosis Control Programme (RNTCP): Universal access – “reaching the un-reached”. Indian J Med Res. 2012;135(5):690–4.

Ridolfo S, Cammarata F, Bonomi AM, Troci A, Crespi M, Molteni P, et al. Gastrointestinal tuberculosis presenting as acute abdomen: a case report. J Surg Case Rep. 2022;2022(6):rjac305.

Udgirkar S, Jain S, Pawar S, Chandnani S, Contractor Q, Rathi P. Clinical profile, drug resistance pattern and treatment outcomes of abdominal tuberculosis patients in western India. Arq Gastroenterol. 2019;56(2):178–83.

Kwon CI, Park PW, Kang H, Kim GI, Cha ST, Kim KS, et al. Usefulness of angiotensin converting enzyme in the differential diagnosis of Crohn’s disease and intestinal tuberculosis. Korean J Intern Med. 2007;22(1):1–5.

Puar THK, Stikkelbroeck NMML, Smans LCCJ, Zelissen PMJ, Hermus AdRMM. Adrenal crisis: still a deadly event in the 21st century. Am J Med. 2016r;129(3):339.e1–9.

Neary N, Nieman L. Adrenal insufficiency: aetiology, diagnosis and treatment. Curr Opin Endocrinol Diabetes Obes. 2010;17(3):217–23.

Charmandari E, Nicolaides NC, Chrousos GP. Adrenal insufficiency. Lancet. 2014;383(9935):2152–67.

Gupta S, Ansari MAM, Gupta AK, Chaudhary P, Bansal LK. Current approach for diagnosis and treatment of adrenal tuberculosis—our experience and review of literature. Surg J (N Y). 2022;8(1):e92–7.

Suri S, Gupta S, Suri R. Computed tomography in abdominal tuberculosis. Br J Radiol. 1999;72(853):92–8.

Mehta V, Desai D, Abraham P, Gupta T, Rodrigues C, Joshi A, et al. Do additional colonoscopic biopsies increase the yield of Mycobacterium tuberculosis culture in suspected ileocolonic tuberculosis? Indian J Gastroenterol. 2018;37(3):226–30.

Wang YX, Chen CR, He GX, Tang AR. CT findings of adrenal glands in patients with tuberculous Addison’s disease. J Belge Radiol. 1998;81(5):226–8.

Yokoyama T, Toda R, Kimura Y, Mikagi M, Aizawa H. Addison’s disease induced by miliary tuberculosis and rifampicin administration. Intern Med. 2009;48(15):1297–300.

Gaballa S, Memon A, Roberts M. Atypical adrenocortical incidentaloma causing autonomous cortisol secretion and cardiovascular complications. J Endocr Soc. 2021;5(Suppl_1): A118–8.

Moule MG, Cirillo JD. Mycobacterium tuberculosis dissemination plays a critical role in pathogenesis. Front Cell Infect Microbiol. 2020;10:65.

Wafa S, Kefi A, Ach M, Jaziri F, Abdelghani KB, Turki S, et al. Primary Sjögren’s syndrome in men. Ann Rheum Dis. 2020;79(Suppl 1):1524.

Boddu R, Sharma A, Mishra K, Kumar S. Rifampicin-induced thrombocytopenia in a patient with abdominal tuberculosis. Ann Natl Acad Med Sci (India). 2024;60:26–9.

Krain RL, Gaffney RG, Keyes ER, Feng R, Werth VP. Comparing the performance of two interferon-gamma release assays in autoimmune skin disease patients: a prospective study. Ann Transl Med. 2021;9(5):AB021.

Park DW, Chung SJ, Yeo Y, Park TS, Lee H, Moon JY, et al. Therapeutic issues and long-term outcomes of pulmonary mycobacterial tuberculosis treatment in autoimmune rheumatic disease. J Thorac Dis. 2019;11(11):4573–82.

Cooper AM, Mayer-Barber KD, Sher A. Role of innate cytokines in mycobacterial infection. Mucosal Immunol. 2011 Mar;4(3):252–60.

Weledji EP, Pokam BT. Abdominal tuberculosis: is there a role for surgery? World J Gastrointest Surg. 2017;9(8):174–81

Downloads

Published

2026-07-30

How to Cite

Kumar, A., Pal, D., & Ojha, A. (2026). Primary adrenal insufficiency secondary to ileocecal tuberculosis. International Journal of Research in Medical Sciences, 14(8), 3615–3620. https://doi.org/10.18203/2320-6012.ijrms20262658

Issue

Section

Case Reports