Takayasu Arteritis: Diagnosed and Treated as Labyrinthitis
The objective of this paper is to report a case of a patient with Takayasu arteritis (TA), diagnosed and treated as labyrinthitis for two years, with brief review of the literature. A 36-year-old woman, who presented vertigo, falling on the ground for losing consciousness for a few seconds, and.progressive loss of left vision, was admitted to the emergency with headache and impalpable carotid pulses. The erythrocyte sedimentation rate (ECR) and C-reactive protein (CRP) serological tests were increased; however, the ANF (Antinuclear factor), venereal disease research laboratory (VDRL) and fluorescent treponemal antibody absorption (FT-ABS) were negative. After aortography, she developed convulsive seizures, loss of consciousness, hemodynamic instability, and death. The cause of death was distributive shock.
de Souza AW, de Carvalho JF. Diagnostic and classification criteria of Takayasu arteritis. J Autoimmun 2014; 48-49: 79-83.
Terao C. Revisited HLA and non-HLA genetics of Takayasu arteritis-where are we? J Hum Genet 2016; 61(1): 27-32.
Matsuyama A, Sakai N, Ishigami M, Hiraoka H, Kashine S, Hirata A, et al. Matrix metalloproteinases as novel disease markers in Takayasu arteritis. Circulation 2003; 108(12): 1469-73.
Chatterjee S, Flamm SD, Tan CD, Rodriguez ER. Clinical diagnosis and management of large vessel vasculitis: Takayasu arteritis. Curr Cardiol Rep 2014; 16(7): 499.
Misra DP, Chowdhury AC, Lal H, Mohindra N, Agarwal V. Gangrene in Takayasu's arteritis: A report of two cases and review of literature. Rheumatol Int 2016; 36(3): 449-53.
Pons Dolset J, Lahoza Perez MD, Ilundain Gonzalez AI, Saenz Abad D, Jordan Domingo M, Marquina Barcos A. Takayasu arteritis presenting as acute pericarditis. Rev Esp Cardiol (Engl Ed) 2016; 69(10): 980-1.
Yamanaka T, Sawai Y, Hosoi H. Bilateral subclavian steal syndrome with vertigo. Auris Nasus Larynx 2014; 41(3): 307-9.
Pascual-Lopez M, Hernandez-Nunez A, Aragues-Montanes M, Dauden E, Fraga J, Garcia-Diez A. Takayasu's disease with cutaneous involvement. Dermatology 2004; 208(1): 10-5.
Frances C, Boisnic S, Bletry O, Dallot A, Thomas D, Kieffer E, et al. Cutaneous manifestations of Takayasu arteritis. A retrospective study of 80 cases. Dermatologica 1990; 181(4): 266-72.
Hidano A, Watanabe K. Pyoderma gangraenosum and cardio vasculopathies, particularly Takayasu arteritis. Review of the Japanese literature (author's transl). Ann Dermatol Venereol 1981; 108(1): 13 21.
Rocha LK, Romitti R, Shinjo S, Neto ML, Carvalho J, Criado PR. Cutaneous manifestations and comorbidities in 60 cases of Takayasu arteritis. J Rheumatol 2013; 40(5): 734-8.
Dey M, Kapur A, Goyal S, Wadhwa RD, Srivastava A, Agarwal R. Takayasu arteritis in pregnancy. Med J Armed Forces India 2015; 71(Suppl 1): S227-S229.
Ishikawa K. Diagnostic approach and proposed criteria for the clinical diagnosis of Takayasu's arteriopathy. J Am Coll Cardiol 1988; 12(4): 964-72.
Arend WP, Michel BA, Bloch DA, Hunder GG, Calabrese LH, Edworthy SM, et al. The American college of rheumatology 1990 criteria for the classification of takayasu arteritis. Arthritis Rheum 1990; 33(8): 1129-34.
Sharma BK, Jain S, Suri S, Numano F. Diagnostic criteria for Takayasu arteritis. Int J Cardiol 1996; 54(Suppl): S141-S147.
Burke AP, Tavora F. Practical cardiovascular pathology. Philadelphia, PA: Lippincott Williams & Wilkins; 2010.
Michel BA, Arend WP, Hunder GG. Clinical differentiation between giant cell (temporal) arteritis and Takayasu's arteritis. J Rheumatol 1996; 23(1): 106-11.