Extremely Rare Concomitance Of Tubercular Lymphadenitis With T Cell Non Hodgkin’s Lymphoma – A Diagnostic Challenge For Clinician
Extremely rare concomitance of Tubercular lymphadenitis with T cell non Hodgkin’s lymphoma
DOI:
https://doi.org/10.70284/njirm.v7i5.1151Keywords:
Tuberculosis, Non Hodgkin’s lymphoma, lymphadenitisAbstract
Tuberculosis (TB) presenting with Non Hodgkin's Lymphoma is an extremely rare clinical presentation and is quite difficult to diagnose because of similar signs & symptoms including lymphadenopathy, weight loss, anorexia and generalised weakness. Herein we report a case of 40 year old male who presented with enlarged cervical and axillary lymph nodes, diagnosed and initiated on therapy for TB based on the axillary node FNAC that showed granulomatous lymphadenitis suggestive of TB but was later confirmed to be a case of non Hodgkin’s lymphoma by excisional biopsy followed by histopathology and immunohistochemistry . [Anand A NJIRM 2016; 7(5):95-97]
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2. Rizvi MA, Evens AM, Tallman MS, Nelson BP, and Rosen ST. T- cell non-Hodgkin lymphoma. Blood.2006;1255:1255-64.
3. Reddy RC, Mathew M, Parameswaran A, Narasimhan R. A case of concomitant Hodgkin’s lymphoma with tuberculosis. Lung India: 2014;31(1):59-62.
4. Askling J and Ekbom A. Risk of non-Hodgkin’s lymphoma following tuberculosis. British Journal of Cancer .2001; 84: 113–115.
5. Dres M, Demoule A, Schmidt M, Similowski T. Tuberculosis hiding a non-Hodgkin lymphoma “there may be more to this than meets the eyeâ€. Respiratory Medicine Case Reports 2012 ;7 :15-16.
6. Nyunt WW, Wong YP, Wan Jamaludin WF, Abdul Wahid SF. Diffuse large B cell lymphoma with chronic granulomatous inflammation.Malays J Pathol 2016 ;38 :55-9.
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Published
2018-01-24
How to Cite
Agrawal, A., Vyas, A., Duhan, A., Yadav, S., & Madan, C. (2018). Extremely Rare Concomitance Of Tubercular Lymphadenitis With T Cell Non Hodgkin’s Lymphoma – A Diagnostic Challenge For Clinician: Extremely rare concomitance of Tubercular lymphadenitis with T cell non Hodgkin’s lymphoma. National Journal of Integrated Research in Medicine, 7(5), 95–97. https://doi.org/10.70284/njirm.v7i5.1151
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Case Report
