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. 2017 Feb 28;8:62. doi: 10.3389/fneur.2017.00062

Table 1.

Final diagnosis and distribution of patients in three subgroups.

Groups N (%) of patients Age at onset (median) Female/male No. (%) of immunosuppressive therapya
(NMOSD)-ONTM 70 (100) 30 60/10 7 (10)
NMO* 38 (54.3) 30 35/3 3 (7.9)
RLETM 8 (11.4) 39 7/1 1 (12.5)
APTM 3 (4.3) 28 2/1 0
MON 3 (4.3) 30 3/0 0
RON 2 (2.9) 28.43 1/1 0
Othersb 16 (22.9) 26 12/4 3 (18.8%)
NMOSD-ON+ 95 (100) 37 83/12 22 (23.2%)
NMO* 78 (82.1) 38 69/9 20 (25.6%)
RON 12 (12.6) 37 9/3 2 (16.7%)
MON 5 (5.3) 25 5/0 0
NMOSD-TM+ 116 (100) 40 98/18 10 (8.6)
NMO* 51 (44.00) 42 44/7 5 (9.8)
RLETM 40 (34.5) 40 34/6 5 (12.5)
MLETM 22 (19.0) 43 17/5 0
APTM 3 (2.6) 36 3/0 0 (0)
NMO 11 (100) 49 11/0 2 (6.8)

NMOSD, neuromyelitis optica spectrum disorder; NMO, neuromyelitis optica; RLETM, recurrent longitudinal extensive transverse myelitis; MLETM, monophasic LETM; APTM, acute partial transverse myelitis; RON, recurrent optic neuritis; MON, monophasic ON.

aLong therapy with azathioprine, cyclophosphamide, methotrexate, and mycophenolate mofetil.

bPatients without optic neuritis (ON) and transverse myelitis (TM).

*Significantly different among the three groups (p < 0.0001).