APA 6th Edition Beroš, V., Houra, K., Rotim, K., Kovač, D. i Čupić, H. (2008). Thoracic Intramedullary Sarcoidosis Mimicking an Intramedullary Tumor. Collegium antropologicum, 32 (2), 645-647. Preuzeto s https://hrcak.srce.hr/27213
MLA 8th Edition Beroš, Vili, et al. "Thoracic Intramedullary Sarcoidosis Mimicking an Intramedullary Tumor." Collegium antropologicum, vol. 32, br. 2, 2008, str. 645-647. https://hrcak.srce.hr/27213. Citirano 15.07.2019.
Chicago 17th Edition Beroš, Vili, Karlo Houra, Krešimir Rotim, Damir Kovač i Hrvoje Čupić. "Thoracic Intramedullary Sarcoidosis Mimicking an Intramedullary Tumor." Collegium antropologicum 32, br. 2 (2008): 645-647. https://hrcak.srce.hr/27213
Harvard Beroš, V., et al. (2008). 'Thoracic Intramedullary Sarcoidosis Mimicking an Intramedullary Tumor', Collegium antropologicum, 32(2), str. 645-647. Preuzeto s: https://hrcak.srce.hr/27213 (Datum pristupa: 15.07.2019.)
Vancouver Beroš V, Houra K, Rotim K, Kovač D, Čupić H. Thoracic Intramedullary Sarcoidosis Mimicking an Intramedullary Tumor. Collegium antropologicum [Internet]. 2008 [pristupljeno 15.07.2019.];32(2):645-647. Dostupno na: https://hrcak.srce.hr/27213
IEEE V. Beroš, K. Houra, K. Rotim, D. Kovač i H. Čupić, "Thoracic Intramedullary Sarcoidosis Mimicking an Intramedullary Tumor", Collegium antropologicum, vol.32, br. 2, str. 645-647, 2008. [Online]. Dostupno na: https://hrcak.srce.hr/27213. [Citirano: 15.07.2019.]
Sažetak Sarcoidosis is a chronic, systemic granulomatous reticulosis of unknown origin, characterized by formation of hard
tubercles and noncaseating granulomas1. Since other infectious diseases such as berylliosis, mycobacterium and fungal
infections may present with a noncaseating granulomas, histological diagnosis of sarcoidosis is made using the elimination
method. Central nervous system manifestations of sarcoidosis may be present in 5–10% of the cases2–5 involving cranial
nerves, leptomeninges and third ventricle respectively. Any part of the central nervous system can be affected. Involvement
of spinal cord in sarcoidosis is extremely rare and presents with only 0.3–0.4% in patients with systemic sarcoidosis2.
Intramedullary sarcoidosis is a rare first manifestation of the disease and it can mimic an intramedullary tumor,
which is often manifested with symptoms that initiate from spinal cord compression, resulting in paraparesis, sensory
disorders and sphincter dysfunction6–11. We present a case of intramedullary sarcoidosis that mimics a tumor of the thoracic
spinal cord. Clinical features, neuroradiological, pathohistological findings, laboratory analysis and surgical
treatment of such a rare entity are being discussed.