| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-104 |
Sentence |
denotes |
[An autopsy case of multiple system atrophy presenting with rapid progression of autonomic disturbance]. |
| TextSentencer_T2 |
105-223 |
Sentence |
denotes |
We report an autopsy case of multiple system atrophy (MSA) presenting with rapid progression of autonomic disturbance. |
| TextSentencer_T3 |
224-299 |
Sentence |
denotes |
He was admitted to our hospital because of gait disturbance and dysarthria. |
| TextSentencer_T4 |
300-428 |
Sentence |
denotes |
The patient was a Japanese man, who first noticed gait disturbance and dysarthria at age 58, followed by syncope 3 months later. |
| TextSentencer_T5 |
429-523 |
Sentence |
denotes |
He developed urinary incontinence and frequency of urination 8 months after the disease onset. |
| TextSentencer_T6 |
524-689 |
Sentence |
denotes |
His gait disturbance, dysarthria, syncope, and urinary symptoms progressed, and he was admitted to the department of neurology 1 year after the onset of the disease. |
| TextSentencer_T7 |
690-774 |
Sentence |
denotes |
He was clinically diagnosed as having MSA and was followed in the outpatient office. |
| TextSentencer_T8 |
775-890 |
Sentence |
denotes |
He deteriorated rapidly and was readmitted to the department of neurology 19 months after the onset of the disease. |
| TextSentencer_T9 |
891-943 |
Sentence |
denotes |
Physical examination showed orthostatic hypotension. |
| TextSentencer_T10 |
944-1201 |
Sentence |
denotes |
Neurological examination revealed nystagmus, dysarthria of cerebellar type, increased deep tendon reflexes, bilateral positive Babinski signs, ataxic and spastic gait, mild right hypesthesia and hypalgesia, impotence, constipation, and urinary incontinence. |
| TextSentencer_T11 |
1202-1285 |
Sentence |
denotes |
Routine blood examination showed slight anemia, elevated BUN, GOT, and blood sugar. |
| TextSentencer_T12 |
1286-1384 |
Sentence |
denotes |
Electrocardiography revealed sinus tachycardia and chest rentogenogram showed cardiac enlargement. |
| TextSentencer_T13 |
1385-1463 |
Sentence |
denotes |
Brain MRI showed atrophy of cerebellum and pons, and lacunae in basal ganglia. |
| TextSentencer_T14 |
1464-1564 |
Sentence |
denotes |
Autonomic function tests revealed abnormal in head-up tilt test, and CVR-R in May and November 1995. |
| TextSentencer_T15 |
1565-1686 |
Sentence |
denotes |
However 123I-MIBG myocardial scintigraphy showed normal uptake of MIBG in May 1995 and decreased uptake in November 1995. |
| TextSentencer_T16 |
1687-1732 |
Sentence |
denotes |
He deteriorated rapidly and died in May 1996. |
| TextSentencer_T17 |
1733-1916 |
Sentence |
denotes |
Autopsy findings revealed not only prominent olivopontocerebellar and slight striatonigral lesions, but also autonomic lesions with massive appearance of glial cytoplasmic inclusions. |
| TextSentencer_T18 |
1917-1962 |
Sentence |
denotes |
He was pathologically verified as having MSA. |
| TextSentencer_T19 |
1963-2125 |
Sentence |
denotes |
In the present patient, autonomic nervous system, especially cardiac sympathetic nerve, deteriorated rapidly, which might result in short duration of the illness. |
| T1 |
0-104 |
Sentence |
denotes |
[An autopsy case of multiple system atrophy presenting with rapid progression of autonomic disturbance]. |
| T2 |
105-223 |
Sentence |
denotes |
We report an autopsy case of multiple system atrophy (MSA) presenting with rapid progression of autonomic disturbance. |
| T3 |
224-299 |
Sentence |
denotes |
He was admitted to our hospital because of gait disturbance and dysarthria. |
| T4 |
300-428 |
Sentence |
denotes |
The patient was a Japanese man, who first noticed gait disturbance and dysarthria at age 58, followed by syncope 3 months later. |
| T5 |
429-523 |
Sentence |
denotes |
He developed urinary incontinence and frequency of urination 8 months after the disease onset. |
| T6 |
524-689 |
Sentence |
denotes |
His gait disturbance, dysarthria, syncope, and urinary symptoms progressed, and he was admitted to the department of neurology 1 year after the onset of the disease. |
| T7 |
690-774 |
Sentence |
denotes |
He was clinically diagnosed as having MSA and was followed in the outpatient office. |
| T8 |
775-890 |
Sentence |
denotes |
He deteriorated rapidly and was readmitted to the department of neurology 19 months after the onset of the disease. |
| T9 |
891-943 |
Sentence |
denotes |
Physical examination showed orthostatic hypotension. |
| T10 |
944-1201 |
Sentence |
denotes |
Neurological examination revealed nystagmus, dysarthria of cerebellar type, increased deep tendon reflexes, bilateral positive Babinski signs, ataxic and spastic gait, mild right hypesthesia and hypalgesia, impotence, constipation, and urinary incontinence. |
| T11 |
1202-1285 |
Sentence |
denotes |
Routine blood examination showed slight anemia, elevated BUN, GOT, and blood sugar. |
| T12 |
1286-1384 |
Sentence |
denotes |
Electrocardiography revealed sinus tachycardia and chest rentogenogram showed cardiac enlargement. |
| T13 |
1385-1463 |
Sentence |
denotes |
Brain MRI showed atrophy of cerebellum and pons, and lacunae in basal ganglia. |
| T14 |
1464-1564 |
Sentence |
denotes |
Autonomic function tests revealed abnormal in head-up tilt test, and CVR-R in May and November 1995. |
| T15 |
1565-1686 |
Sentence |
denotes |
However 123I-MIBG myocardial scintigraphy showed normal uptake of MIBG in May 1995 and decreased uptake in November 1995. |
| T16 |
1687-1732 |
Sentence |
denotes |
He deteriorated rapidly and died in May 1996. |
| T17 |
1733-1916 |
Sentence |
denotes |
Autopsy findings revealed not only prominent olivopontocerebellar and slight striatonigral lesions, but also autonomic lesions with massive appearance of glial cytoplasmic inclusions. |
| T18 |
1917-1962 |
Sentence |
denotes |
He was pathologically verified as having MSA. |
| T19 |
1963-2125 |
Sentence |
denotes |
In the present patient, autonomic nervous system, especially cardiac sympathetic nerve, deteriorated rapidly, which might result in short duration of the illness. |