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Michael C. Iannuzzi, M.D., Benjamin A. Rybicki, Ph.D., and Alvin S. Teirstein, M.D. “Sarcoidosis”, N Engl J Med 2007; 357: 2153-2165.

has been cited by the following article:

Article

Golimumab Induced CNS, Pulmonary, and Cardiac Sarcoidosis - A Case Report and Literature Review

1Internal Medicine Department, Rutgers-New Jersey Medical School, Newark, New Jersey, United States


American Journal of Medical Case Reports. 2016, Vol. 4 No. 9, 298-300
DOI: 10.12691/ajmcr-4-9-1
Copyright © 2016 Science and Education Publishing

Cite this paper:
Zhen Wang MD, Eugenio Capitle MD, Michael Jaker MD, Smita Mahendrakar MD, Riju Banerjee MD. Golimumab Induced CNS, Pulmonary, and Cardiac Sarcoidosis - A Case Report and Literature Review. American Journal of Medical Case Reports. 2016; 4(9):298-300. doi: 10.12691/ajmcr-4-9-1.

Correspondence to: Zhen  Wang MD, Internal Medicine Department, Rutgers-New Jersey Medical School, Newark, New Jersey, United States. Email: jameszwang@gmail.com

Abstract

Tumor necrosis factor alpha (TNF-α) antagonist has been widely used in the treatment of inflammatory conditions such as rheumatoid arthritis (RA). Recently there have been case reports of the development of sarcoidosis in patients receiving TNF-α antagonists. Agents such as Infliximab, Adalimumab, and Etanercept have all been linked. However, incidents related to Golimumab, another member of the class, has not yet been described. We present the first case of Golimumab induced CNS, Pulmonary, and Cardiac sarcoidosis in a patient who presented with weakness and weight loss and was later found to have multi-organ (lung, brain, heart) sarcoid like involvement. Patient was diagnosed with seropositive (RF and CCP) RA maintained on Golimumab and Methotrexate for 2 years prior to diagnosis. Resolution of symptoms was achieved through the cessation of Golimumab and the use of systemic steroids.

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