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BMJ Case Reports 2017; doi:10.1136/bcr-2016-218741
  • Reminder of important clinical lesson
  • CASE REPORT

The clinical conundrum of diagnosing and treating systemic sarcoidosis in a high TB burden area

  1. Pravinkumar Rejliwal1
  1. 1Internal Medicine, MIOT International, Chennai, India
  2. 2Nuclear Medicine, MIOT International, Chennai, India
  1. Correspondence to Dr Krishnadas Thulasidoss, tkrisnadas{at}gmail.com
  • Accepted 23 March 2017
  • Published 12 May 2017

Summary

A 53-year-old woman from Southern India presented with weight loss, anorexia, fever and asthenia. Whole body positron emission tomography/computed tomography (PET-CT) showed fluorodeoxyglucose-avid mediastinal and abdominal lymphadenopathy with hepatic, splenic, parotid and lacrimal glandular inflammations. Endoscopic ultrasound-guided fine needle aspiration of subcarinal lymph node showed non-caseating granulomas. Initial serum ACE level was elevated but with normal calcium. Despite the suspicion of sarcoidosis, a trial of antituberculosis therapy was started empirically due to similar presentations of disseminated tuberculosis (TB) in this high endemic area. The patient subsequently deteriorated and was admitted with symptomatic hypercalcaemia. Her subsequent ACE levels were very high, supportive of a diagnosis of systemic sarcoidosis. She was given steroid pulse therapy, and 5 months later had fully recovered. This case highlights the challenges faced by physicians in high TB-endemic areas when managing granulomatous diseases as they are concerned about missing TB, the difficulties in diagnosing sarcoidosis and the role of pulse steroid therapy.

Footnotes

  • Contributors KT, LA and PR contributed to writing the clinical and pathological aspects of the report; PC contributed to the radiological aspect of the report.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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