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Current Medical Imaging

Editor-in-Chief

ISSN (Print): 1573-4056
ISSN (Online): 1875-6603

Case Report

A Case of Neurosarcoidosis Mimicking Brain Tumor

Author(s): Lutfullah Sari*, Abdusselim A. Peker, Dilek H. Cesme and Alpay Alkan

Volume 17, Issue 5, 2021

Published on: 18 November, 2020

Page: [657 - 659] Pages: 3

DOI: 10.2174/1573405616666201118114152

Price: $65

Abstract

Background: Neurosarcoidosis manifests symptomatically in 5% of patients with sarcoidosis and diagnosis can be challenging if not clinically suspected. Cerebral mass-like presentation of neurosarcoidosis rarely reported in the literature. We presented a woman with neurosarcoidosis who had a cerebral mass-like lesion which completely disappeared after medical treatment.

Discussion: A 37-year-old woman with history of pulmonary sarcoidosis referred to the emergency service of our hospital with a one-month history of progressive dizziness, nausea and seeing flashing lights. At neurologic examination, numbness and weakness on the left side of the body, deviation of uvula toward the right side was seen. Cranial MRI demonstrated a 2.5x2 cm in size mass lesion which hypointense on T1 WI, heterogeneous hyperintense on T2 and FLAIR sequence with peripheral vasogenic edema and heterogeneous, irregular contrast enhancement simulating brain tumor. Also, leptomeningeal and nodular contrast enhancement was seen on brainstem, cerebellar vermis, perimesencephalic cistern and left frontal, bilateral parietooccipital sulcus. In laboratory tests; The level of serum angiotensin-converting enzyme (ACE) was 53 IU/mL (N:8-52 IU/mL) and cerebrospinal fluid (CSF) ACE was 23 IU/mL (N:0-2.6 IU/mL). CSF cytology analysis was normal. Pattern 2 oligoclonal bands were present. With these clinical, laboratory and radiological findings, cerebral involvement of sarcoidosis was suspected. Biopsy was not performed due to the high risk of morbidity caused by the deep location of the lesion.Patient was treated with methylprednisolone and Azathioprine for a month.On post-treatment control imaging; lesion disappeared completely without residual leptomeningeal and nodular contrast enhancement.Also, neurologic symptoms were decreased remarkably.

Conclusion: Multi-system inflammatory disorders like sarcoidosis, can present with mass-like lesion in the brain parenchyma. While early diagnosis is important to prevent unnecessary interventions like biopsy and surgery, it is crucial to initiate the necessary treatment with the aim of recovery without sequelae. Radiological and clinical follow-up are fundamental in differential diagnosis.

Keywords: Mimicking tumor, brain tumor, neurosarcoidosis, elderly patients, MRI, neurologic examination, heterogeneous hyperintense.

Graphical Abstract

[1]
Wessendorf TE, Bonella F, Costabel U. Diagnosis of sarcoidosis. Clin Rev Allergy Immunol 2015; 49(1): 54-62.
[http://dx.doi.org/10.1007/s12016-015-8475-x] [PMID: 25779004]
[2]
Neurosarcoidosis. Curr Neuropharmacol 2011; 9: 429-36.
[http://dx.doi.org/10.2174/157015911796557975] [PMID: 22379457]
[3]
Ibitoye RT, Wilkins A, Scolding NJ. Neurosarcoidosis: a clinical approach to diagnosis and management. J Neurol 2017; 264(5): 1023-8.
[http://dx.doi.org/10.1007/s00415-016-8336-4] [PMID: 27878437]
[4]
Zajicek JP, Scolding NJ, Foster O, et al. Central nervous system sarcoidosis-diagnosis and management. QJM 1999; 92(2): 103-17.
[http://dx.doi.org/10.1093/qjmed/92.2.103] [PMID: 10209662]
[5]
Joseph FG, Scolding NJ. Neurosarcoidosis: a study of 30 new cases. J Neurol Neurosurg Psychiatry 2009; 80(3): 297-304.
[http://dx.doi.org/10.1136/jnnp.2008.151977] [PMID: 18977817]
[6]
Kumar G, Kang CA, Giannini C. Neurosarcoidosis presenting as a cerebellar mass. J Gen Intern Med 2007; 22(9): 1373-6.
[http://dx.doi.org/10.1007/s11606-007-0272-7] [PMID: 17619108]
[7]
Shimizu K, Yuki K, Sadatomo T, Kurisu K. Isolated neurosarcoidosis presenting with multiple cranial nerve palsies. Surg Neurol Int 2016; 7: 44.
[http://dx.doi.org/10.4103/2152-7806.180765] [PMID: 27168947]
[8]
Bajantri B, Venkatram S, Niazi M, Singh T, Diaz-Fuentes G. Case report: middle-aged woman from Ghana with unsteady gait and enlarging cerebellar mass. Medicine (Baltimore) 2017; 96(45): e8516.
[http://dx.doi.org/10.1097/MD.0000000000008516] [PMID: 29137054]
[9]
Kimball MM, Wind JJ, Codispoti KE, Jones RV, Leiphart JW. Neurosarcoidosis presenting as an isolated intrasellar mass: case report and review of the literature. Clin Neuropathol 2010; 29(3): 156-62.
[http://dx.doi.org/10.5414/NPP29156] [PMID: 20423690]
[10]
Krenzlin H, Jussen D, Musahl C, Scheil-Bertram S, Wernecke K, Horn P. A rare case of isolated cerebral sarcoidosis presenting as suprasellar mass lesion with salt-wasting hypopituitarism. J Neurol Surg Rep 2015; 76(1): e140-5.
[http://dx.doi.org/10.1055/s-0035-1549310] [PMID: 26251792]
[11]
Elia M, Kombo N, Huang J. Neurosarcoidosis Masquerading As A Central Nervous System Tumor. Retin Cases Brief Rep 2017; 11(Suppl. 1): S166-9.
[http://dx.doi.org/10.1097/ICB.0000000000000402] [PMID: 27571425]
[12]
Gizzi MS, Lidov M, Rosenbaum D. Neurosarcoidosis presenting as a tumour of the basal ganglia and brainstem: sequential MRI. Neurol Res 1993; 15(2): 93-6.
[http://dx.doi.org/10.1080/01616412.1993.11740116] [PMID: 8099215]
[13]
Dash D, Puri I, Tripathi M, Padma MV. Neurosarcoidosis presenting as a large dural mass lesion. BMJ Case Rep 2016; 2016: bcr2016216793.
[http://dx.doi.org/10.1136/bcr-2016-216793] [PMID: 27873749]

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