Memphis Eye, Ear, Nose, and Throat Society

Memphis Eye, Ear, Nose, and Throat Society

SOCIETY 902 PROCEEDINGS cases o f complete optic atrophy in which the amaurosis is complete. In the cases o f more or less marked amblyopia, the op...

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SOCIETY

902

PROCEEDINGS

cases o f complete optic atrophy in which the amaurosis is complete. In the cases o f more or less marked amblyopia, the ophthalmoscopic appearance o f the papilla is misleading. W e often see papillas rather pale and almost atrophic looking associated with relatively g o o d vision; on the other hand, there are cases with marked loss o f vision in which the optic papillas appear almost normal. Joseph I. Pascal, Translator.

MEMPHIS EYE, EAR, NOSE, AND THROAT SOCIETY PSEUDOGLAUCOMA DR. H . C O N D R O N presented a 23-year-old white man, w h o was admitted to the K e n nedy Veterans Hospital as a transfer from Birmingham, Alabama, on March 29, 1954. T h e patient's chief complaint was chronic drainage from the left ear; his transfer diagnosis was suspected chronic otitis media, left ear. His ear difficulty dated back to childhood when he had recurrent drainage from the left ear; on several occasions it had to be "lanced." One month following entry into the service in 1951, he again had left-ear drainage because o f which he was given a medical discharge in late 1951. Since then he has had recurrent bouts o f drainage from the left ear.

T h e past history revealed nothing abnormal except for vague gastrointestinal complaints, not associated with any acute pain, hemoptysis, or melena. T h e patient had no ocular complaint or history. Physical examination: showed a well-developed, 23-year-old white man, in no acute distress. The blood pressure was 1 1 0 / 6 0 mm. H g . The only positive finding was a slurring of the apical systolic sound. T h e liver was palpable two finger breaths below the costal margin; it was nontender, smooth in outline, and sharply edged. Special eye examination revealed: V i s i o n : R.E., 2 0 / 2 0 ; L.E., 2 0 / 2 0 . Extraocular

muscles were normal. Corneas, lids, and conjunctivas were normal. T h e pupils were round, equal, and reacted to light and accommodation. Tension by Schiøtz: R . E . , 20 mm. H g ; L.E., 20 mm. H g . T h e corneas and media were clear. T h e nerveheads showed a deep, glaucomatous-type excavation. T h e retinal vessels appeared normal. There were no retinal lesions. Visual fields showed no contraction; however, the blindspots could not be charted. T h e patient would not admit to blindspots with any size target. Laboratory findings: Chest X - r a y films, negative; C B C , within normal limits; urinalysis, negative; S T S , negative. Tension readings were taken a number o f times and the highest recording was 20 mm. H g , O . U . T h e patient's eyes were dilated with 10-percent neosynephrine and the tension was again taken and recorded at oneand two-hour intervals. A t the end o f one hour the tension was 17 mm. H g , O . U . ; at the end o f the second hour the tension was unchanged. T h e patient has never had any ocular complaints, has never worn glasses, and states that he has never known anything to be w r o n g with his eyes. H e denies any noticeable field loss and seems confused by all the interest shown in his eyes. T h e problem in this case is whether a l o w tension glaucoma or a pseudocoloboma of both optic nerves may be present. T h e absence o f any field loss is against low-tension glaucoma. There appears to be normal nerve tissue about the entire circumference o f the disc. If a coloboma is present, it probably is limited to the lamina cribrosa. T h e clinical picture is certainly that o f glaucomatous cupp i n g ; however, with such a picture there should be some sort o f field defect. Still there is none. Diagnosis is deferred. ANGIOSPASTIC RETINOPATHY DR. H . G . P A R I S H reported A . F., a 49year-old Negress, w h o was presented to the society last year. A t that time she showed a macular lesion in the right eye, which was thought to be a disciform degeneration. The other possibilities considered at that time

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SOCIETY PROCEEDINGS

were melanoma because o f questionable ele­

hospital f o r a course o f typhoid-vaccine ther­

vation in the region o f the macula, chorio­

apy. Three injections were given

retinitis, and a metastatic tumor. Because o f

nously, with fever reactions up to 101.5°F.

a nodular mass at the sternoclavicular j u n c ­

each time. T h e last dose was 30,000,000 or­

tion, she was seen by the orthopedic service

ganisms. Objectively, it was doubtful if the

intrave­

which reported that the lesion was not malig­

status o f the left eye had changed. It seemed

nant. Since that time she has been seen at

to be the logical conclusion that the vitreous

regular intervals with gradual apparent flat­

haze was due to hemorrhage.

tening and recession o f the macular lesion.

Since this discharge she has had no ther­

In July, vision was 2 0 / 4 0 , O . D . , and the

apy, more because she became intolerant to

staff was o f the opinion that this was defi­

nicotinic acid than an independent decision

nitely a case o f angiospastic retinopathy. She

to cease treatment o n our part. T h e fundus

was placed on nicotinic acid, 50 mg., three

in the left eye can n o w be well visualized

times daily. N o local medication was given.

temporal to the disc. T h e nasal portion is still

O n August 30th, she returned f o r a rou­

obscured by vitreous opacities and

floaters,

tine check up, complaining o f a "skim over

evidently posterior to the equator. T h e mac­

the left e y e . " Despite the complaint, vision

ula o f the right eye is n o w quiescent but

w a s : O . D . , 2 0 / 2 5 4 - ; O . S . , 2 0 / 2 5 - f . In the

shows definite residual degeneration. T o d a y

left eye, there was a generalized

her vision with correction is 2 0 / 1 5 , O . U .

vitreous

haze, much more dense on the nasal side. T h e details o f the fundus could not be seen. T h e macular lesion in the right eye appeared somewhat flatter, with increased

pigmenta­

tion.

RETROLENTAL FIBROPLASIA DR.

JAMES

E . W I L S O N reported cases o f

retroiental fibroplasia in identical twin boys, Stanley and Stephen P., aged six months,

O n this date, she was admitted to the hos­

w h o were first seen January 26, 1954.

pital f o r observation and diagnosis. She was

T h e mother has one normal boy, aged five

observed for some time without change in the

years, and she has never had a miscarriage.

cloudiness in the left eye. A s there was n o

During pregnancy with the twins she had

improvement by bedrest foreign-protein in­

never been ill in any way.

jections, and atropinization,

she was dis­

charged on nicotinic acid.

A t seven and three-quarters months she went into labor spontaneously. Urine, blood

She was not seen again until September

work, and Kahn test did not indicate any dis­

29th when she reported to the clinic with

ease. L a b o r was normal. She had scopola­

vision o f 2 0 / 3 0 + 4, O . D . ; 2 0 / 2 0 , O . S . T h e

mine and Demarol followed b y 10 minutes

vitreous haze had cleared to the extent that

o f CaHs anesthesia during actual birth o f the

temporally.

twins. A l l three stages o f labor lasted a total

T h e nasal retina was still obscured by a deep

o f five hours. O n e child was born vertex and

vitreous haze. In the macula o f the right eye,

the other breech. Stanley, weighing four lb.

there was n o w a circumscribed area which

and eight oz., was born at 10:25 P . M . on

appeared to be a serous infiltration under the

July 28, 1953, and Stephen, weighing three

retina. She was continued on nicotinic acid.

lb. and 15 oz., was born two minutes later.

fundus

details

could be seen

T h e next visit, one week later, revealed

Physical examination o f each shortly after

two such circumscribed areas lateral and in­

birth showed the heart to be normal, no

ferior to the macula. T h e y had a pinkish

anomalies were noted, but both had grunting

color. O n this date, October 8th, the disc in

respiration, poor aeration, and possibly atel­

the left eye could be seen f o r the first time.

ectasis at the base o f the lungs.

There was little loss o f vision throughout these episodes. O n November 5th she was admitted

Orders f o r the t w o infants were identical: ( 1 ) Both were put into the same isolette and

to

o x y g e n was used at a rate o f four liters per

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SOCIETY PROCEEDINGS

minute; ( 2 ) nothing by mouth for 24 hours

A t the papilla it was twice the size o f the

then glucose water; ( 3 ) Synkamin (I.O cc.

disc and completely obscured it. This band

hypodermically, d a i l y ) ; ( 4 ) caffeine sodium

stopped at the disc and joined a similar band

benzoate ( f o u r drops hypodermically when

which came from the periphery originating

necessary for stimulation).

from just above the horizontal on the tem­

After one week Stephen was doing well and was removed from the isolette and put

poral side. This band came across the posi­ tion o f the macula involving it.

in an older type o f incubator in which the

Stephen's external eye examination was

oxygen concentration was not so high. A f t e r

similar except that there was a very poor re­

21 days, they were both removed from o x y ­

action o f the left pupil.

gen without any tapering off in concentra­ tion.

The left fundus showed a completely gray­ ish detached and elevated retina. T h e right

Both babies were fed the same, receiving all the mother could supply augmented by

fundus

showed a band originating in the

middle o f the lower temporal quadrant. It broadened out to obscure the disc and partly

evaporated milk and sugar. O n the 12th day Stephen developed an ab­

involve the macula. It continued upward to

scess o f the buttocks at an injection site and

the middle o f the upper temporal periphery.

was given penicillin (300,000 units daily for three d a y s ) .

Re-examination on March 5, 1954, did not show any change from the original examina­

O n the 2Sth hospital day Stanley devel­

tion on January 26, 1954.

oped diarrhea and was given paregoric (five drops twice daily for three d a y s ) . T h e y re­ ceived no other medications.

RACEMOSE DR.

A t the time of their discharge on Septem­

H E M A N G I O M A OF RETINA

PHILIP

M E R I W E T H E R L E W I S and

DOUGLAS H A W K E S

DR.

( b y invitation) presented

ber 1, 1953, Stanley weighed five lb., two o z . ;

a patient having both ocular and intracranial

Stephen weighed four lb., 13 o z .

angiomatosis.

W h e n the parents brought the twins to the

D . W . F . , a white boy, aged 10 years, was

office on January 26, 1954, they complained

first seen in 1947 at the age o f three years.

that neither of them appeared to see nor­

His mother stated he ran into things as if he

mally. The parents said that, when they tried

did not see well and he tilted his head to­

to look at something the eyes moved slowly

ward his right shoulder. Vision could not be

in searching movements. A grayish reflex

determined but it was felt that he could see

had been noticed in one pupil o f each child.

with both eyes. N o limitation

o f motion

had

could be detected. There was congestion o f

searching and rolling movements but no nys­

the conjuncti\fal vessels and a slight fullness

tagmus.

of the retinal vessels o f the left eye. Retinos­

Examination

showed that

Stanley

Both pupils reacted but

the

left

quicker. H e followed a light with the right

copy showed two diopters o f hyperopia o f

but did so only poorly with the left eye.

both eyes.

The right fundus showed the entire tem­

H e was not seen again until October 30,

poral retina to be detached and grayish and

1948, when he was convalescing from me-

a band came over and slightly beyond the

ningococcic meningitis. A t that time the blood

d i s c ; however, the nasal retina looked quite

vessels on the disc o f the left eye were

normal.

greatly dilated and angiomatosis was sus­

The left fundus showed a bluish white

pected. H e was not seen again until three

band, similar to that seen in retinitis prolif­

years later. Vision could then be determined.

erans, coming from the periphery where it

It w a s : 2 0 / 3 0 , R . E . , no light perception, L . E .

was narrow at the lower temporal position,

T h e vessels of the left temporal region and

spreading out as it went straight to the disc.

upper hd were engorged. There was an enor-

SOCIETY PROCEEDINGS

90S

mous dilatation o f the vessels o f the left disc

on July 28, 1953, revealed emmetropia, O . U .

and immediate surrounding retina. N o angi­

T h e fundus examination was normal.

oma w^as seen.

A diagnosis o f convergent squint, due to

In September, 1952, the left eye was con­

paralysis o f left external rectus and overac-

gested externally and highly divergent. There

tion o f left internal rectus with contracture,

was paralysis o f both elevators and o f the

was made. Consultation was obtained and a

medial rectus. The retinal vessels were enor­

Hummelsheim procedure was decided upon.

mously dilated and tortuous and seemed to

O n August 22, 1953, a five-mm. recession

be much more numerous than normal. T h e

o f the internal rectus and a seven mm. re­

engorgement was confined to the disc and

section o f external rectus plus a Hummel­

the surrounding retina. This was the

sheim tendon transplant was performed and

first

time that proptosis was noticed. The periph­ ery o f the retina seemed to be normal and no angioma was present. T h e right eye was normal with vision of 2 0 / 3 0 .

Twenty-four

hours

later

the

dressings

were changed and the patient was discharged with a request to be in the cHnic in 24 hours.

In November, 1954, vision o f the right eye was 2 0 / 2 5 and the eye was still normal e x ­ cept for coarse nystagmus

both eyes were patched.

on looking to

either side and paralysis o f both elevators. The left eye turned out about 20 degrees

Dressings were changed every other day for four times. O n September 2, 1953 ( 1 0 days after o p ­ e r a t i o n ) , there was g o o d external

rotation

o f left e y e ; slight divergence was noted. O n

and slightly downward. There was complete

September 16th (three weeks postoperative)

paralysis o f both elevators and almost c o m ­

examination revealed 50 degrees' external r o ­

plete o f the medial rectus. There were four

tation o f the left eye.

mm. o f exophthalmos and a definite ptosis. The pupil reacted consensually but not di­ rectly. T h e veins o f the upper lid were en­

DIAMOX DR.

IN ACUTE GLAUCOMA

ALICE

R . D E U T S C H reported the case

gorged and so were those o f the temporal

of M r . J. C , aged 76 years, w h o gave the

region. T h e coiled, medusalike vessels on the

history o f having had recurrent severe eye

disc and surrounding it were approximately

inflammation all o f his life and stated that

the same as they had been two years previ­

he never saw well. H e also had many rounds

ously.

of sinus infection and bronchitis. H e was al­

PARALYTIC CONVERGENT S Q U I N T

after the use o f penicillin and the broad-

lergic to many drugs and had severe reactions DR.

B . W E I S B A U M reported the case o f an

spectrum antibiotics.

11-year-old N e g r o girl seen f o r the first time

A b o u t four years ago his vision began to

on July 22, 1953, with vision o f : O . D . ,

fail, especially in his right eye. A cataract

20/25,

O . S . , counting

fingers.

She

operation was performed in 1952 and was

showed a convergent squint,

J2;

fixating

only

complicated by intolerance to every kind o f

with the right eye. There was paralysis o f

mydriatic. A glaucoma operation had to be

the external rectus, O . S . , indicated by inabil­

performed several months later. Nevertheless

ity to abduct the left eye past the midline. A

the tension remained high, but could be con­

paresis o f the external

trolled with 0.1-percent D F P once a day at

rectus, O . D . , was

evidenced by weakness in external rotation.

bed time.

There was overaction o f the internal rectus,

T h e left eye showed dense macula corneae,

O . S . , with contractions. Measurements, us­

a normal anterior chamber, many posterior

ing the perimeter, were on three occasions

synechias, and a partial pupillary membrane.

25 degrees esotropia for near and 25 degrees

T h e pupil dilated incompletely and irregu­

esotropia for distance. Cycloplegic refraction

larly on 10-percent neosynephrine. A poste-

SOCIETY PROCEEDINGS

906

rior cortical cataract made fundus inspection

dent, w h o was admitted to the Baptist M e ­

difficult. Vision equalled 6 / 2 0 0 . T h e intra­

morial Hospital on April 1, 1954. H e had

ocular pressure was never higher than 18

been in good health until that day when he

mm. H g .

suddenly developed a left frontal headache

O n April 10, 1954, in the evening he in­

without history of trauma. H e went to the

advertently put one drop o f D F P in his left

John Gaston Hospital emergency room be­

eye. Severe headache started about 15 min­

cause o f this headache and was given Cafer-

utes later. The headache continued all night,

got without relief. S o o n after the Cafergot,

associated with nausea. H o w e v e r , he did not

the headache and the pain over the left eye

attribute this to his eye until the next morn­

became more severe. H e soon noticed some

ing when he noticed that he could not see.

difficulty with his speech, had some dizziness,

W h e n examined a f e w hours later the ciliary

and vomited. H e was brought to the Baptist

body o f the left eye was injected and the

Memorial Hospital where he was admitted

cornea edematous. T h e pupil was pinpoint

about 11:50 P . M .

and the anterior chamber shallow but there

At

was apparently no typical iris bombé. T h e

shortly

intraocular pressure was 80 mm. H g . H e was

equal and reacted to light. T h e r e was a hem­

admitted to the hospital.

the

time

after

o f the

first

admission, his

examination, pupils

were

orrhage in the left optic fundus. There was

Besides the local use o f 10-percent neo­

some mental confusion, probably due to his

synephrine and cyclogyl ( o n e percent), 250

mild aphasia. T h e cranial nerves were other­

mg. o f D i a m o x were given to him and re­

wise intact. There were no reflex, sensory,

peated after six hours, after which time the

o r motor changes. There was no stiffness o f

cornea was clearer and the tension 40 mm.

his neck.

H g . T h e third dose o f D i a m o x was given

The possibility o f a subarachnoid hemor­

after eight hours after which time the ten­

rhage was considered but a lumbar puncture

sion dropped to 21 mm. H g in spite o f the

was not done at the time o f his admission.

fact that the pupil was still pinpoint. D i a m o x

T h e following morning X - r a y films o f his

was continued every 12 hours f o r two doses

skull were obtained and thought to be within

and again after 24 hours until 1.5 gm. was

the limits o f normal. H e was examined by

given. Neosynephrine was continued.

an ophthalmologist w h o also thought spon­

It was not until after the third day that

taneous subarachnoid hemorrhage was a pos­

the pupil showed some dilatation. The intra­

sibility. Subsequent to this a lumbar punc­

ocular pressure varied from 18 to 21 mm.

ture revealed bloody spinal fluid under in­

Hg.

creased pressure.

Epinephrine-bitartrate

ointment

was

used three times a day for one week and then discontinued. W h e n the patient was last

B y A p r i l 8th, he had improved clinically and a lumbar

puncture

revealed that the

seen on April 15th, the pupil was o f normal

spinal fluid was only faintly xanthochromic

size and the pupillary membrane seemed to

without gross blood. W e felt that bilateral

be denser; the intraocular pressure was nor­

carotid arteriograms should be done in an

mal and the vision, 6 / 2 0 0 . D i a m o x seemed

attempt to locate the suspected

to be a definite help in the handling o f this

carotid arteriograms, to our surprise, were

case.

negative f o r aneurysm. W e thought that the

aneurysm;

middle cerebral complex on the left SUBARACHNOID HEMORRHAGE W I T H ALOID

SUBHY­

HEMORRHAGE

slightly elevated and the anterior

was

cerebral

artery was pushed slightly to the right. These presented

findings, coupled with the fact that this stu­

the case o f C. K., a 26-year-old medical stu­

dent was not making the clinical progress w e

DR.

RICHARD

L. DESAUSSURE

SOCIETY PROCEEDINGS had hoped for, made us suspect an cerebral hematoma.

infra-

O n April 13th, a ventriculogram demon­ strated a shift o f the ventricular system to the right. A t operation, an intracerebral he­ matoma in the left temporal lobe was dis­ closed. It involved almost the entire left temporal lobe. T h e hematoma was evacuated and the edges o f the brain adjacent to the hematoma were biopsied but there was n o evidence o f tumor in the biopsy specimens. W e did not find the bleeding point; there was n o evidence o f an aneurysm, heman­ gioma, or tumor. Postoperatively, this student did quite well except that the subtemporal decompression became tense and papilledema increased. It was our feeling that the intracerebral swell­ ing was probably the result o f operative trauma and not the result of further bleed­ ing, although this was considered as a possi­ bility. B y A p r i l 2Sth, the subtemporal de­ compression had become soft and he was discharged from the hospital. A t the time o f his discharge he had some aphasia and, in particular, had difficulty understanding writ­ ten words. H e was re-examined on April 30, 1954, at which time his decompression had become much softer, the papilledema was subsiding, and the vision o f the left eye was improved. This is the eye in which the hemorrhage had occurred. H e was re-examined on M a y 14th and showed further improvement. This student falls within the group ( d e ­ scribed by Margolis, O d o m , Woodhall, and Bloor in 1951) o f individuals with intra­ cerebral hematomas due to small angioma­ tous malformations. These occurred in y o u n g individuals with no history o f predisposing factors. Their headaches occurred suddenly;

907

generally, the patient became unconscious at a later date. Bleeding occurred in the white matter and, usually, the bleeding -point could not be demonstrated. In a few cases minute angiomatous malformations were discovered. These authors felt that, in the other cases, the angiomas had been destroyed by the he­ matomas. Subhyaloid hemorrhages have been re­ ported in association with subarachnoid hem­ orrhage. H o w e v e r , it seems that they are usually associated with intracerebral hema­ tomas. In a recent review. Golden, O d o m , and W o o d h a l l found that o f 321 cases o f subarachnoid hemorrhage only 15 had associ­ ated subhyaloid hemorrhages. In 51 cases o f intracerebral hematoma without subarach­ noid hemorrhage, seven had subhyaloid hem­ orrhage; however, in 13 cases o f subarach­ noid and subdural hemorrhage, six had sub­ hyaloid hemorrhages. This gives a percentage of five percent for the pure subarachnoid hemorrhages, 14 percent for the intracerebral hematomas alone, and ^ 2 percent for the subarachnoid plus subdural hematomas. T h e mechanism by which the preretinal or subhyaloid hemorrhage is produced is still debated but the consensus seems to be that it is due to occlusion o f the venous channels and is not a direct extension o f the hemor­ rhage into the subhyaloid space. This is usu­ ally caused by sudden increase in intracranial pressure. This case serves to illustrate: ( 1 ) W h e n a subhyaloid hemorrhage is noted in the presence o f subarachnoid hemorrhage, a space-occupying lesion should be suspected and searched f o r ; ( 2 ) the lack o f nuchal rigidity does not exclude subarachnoid hem­ orrhage. Daniel F. Fisher, Recorder for the Eye Section.