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right leg about 4 months previously but had not told anyone. Funthenmore, he reported

Fic. 1. Case 1. Atrophy of the right leg.

PzrnmIcs, November 1961

AMERICAN

ACADEMY

OF

PEDIATRICS

847

CLINICAL

CONFERENCE

BONY

LESIONS

OF

THE

LOWER

EXTREMITIES

SIMULATING

CENTRAL

NERVOUS

SYSTEM

DISEASE

Irving H. Rozenfeld, M.D.

Sarah Morris Hospital for Children, Chicago

W

E HAVE recently seen two youngsters whose pnesenting complaints were

highly suggestive of spinal cord disease but

whose lesions were far removed from this

area. We believe this deserves emphasis.

Case 1

CASE REPORTS

The first patient was seen initially when he was 143k years old, complaining of vague pains in his night knee and thigh. This pain

was intermittent, slightly worse at night,

but did not interfere with the patient’s ac-tivities. Physical examination was entirely

negative. There was no local tenderness,

limitation of motion or limp.

Roentgeno-grams of the knee, thigh and hip were

in-terpreted as negative, and the patient was

advised to limit activity temporarily.

Although he was subsequently seen for

minor respiratory infections, there was no

further mention of pain. Eighteen months

later, the patient’s mother called to say that

she had just noticed that the right leg was

thinner than the left.

When seen, however, the patient, now 16

years old, reported that pain in the leg had

continued during the 18-month period.

There was no specific localization of the

pain; it was worse at night and responded

to heat, massage and aspirin. He had pain

occasionally during the day and had limped for the preceding several months. This how-even did not stop him from playing football

and baseball. He reported further that he

first became aware of the thinness of the

Presented as part of a Clinical Conference for the Annual Meeting of the American Academy of

Pediatrics, October, 1960, under Chairmanship of Dr. Jack Metcoff.

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FIG. 2. Case 1. Tomograms, revealing a lesion in the upper part of the patella.

an 11-lb weight loss during this 4-month

period.

848 BONY LESIONS

On

examination,

there was marked

at-rophy of the entire right leg, as shown in

Figure 1. The hamstring, quadriceps and

gastrocnemius muscles were equally

in-volved. The circumference of the right

thigh, 8 in. above the patella, was 2 in. less than that of the left; the circumference of the right calf, 8 in. below the tibial tubercle, was almost 1 in. less than that of the left. Incidentally, the boy was night-handed. There was no local tenderness on palpation

of the leg, but the patient complained of

pain in the knee on extreme flexion of the

knee joint. There was no limitation of

mo-tion.

Neurologic examination revealed

hyper-activity of the deep tendon reflexes and

ankle clonus present on the right and an

area of hypasthesia over the medial aspect

as negative. Lumbar puncture revealed

non-ma! fluid dynamics, and the protein and

cellular components were with normal limits. Electromyography revealed no fibrillation

potentials and a marked decrease in the

total number of potentials. These findings

were interpreted as compatible with upper

neurone disease.

Because of the persistent complaint of

pain in the knee, associated with forced

flexion of the knee, tomograms were taken;

these revealed a lesion in the upper pole

of the patella (Fig. 2). The central nidus

with a surrounding area of sclerosis is typ-ical of an osteoid osteoma. A

hemipatallec-tomy was done, with complete subsidence

of pain. Four months later the patient has

a slight limp, complete range of motion and some return of muscle mass. The

hemipatel-lectomy was done instead of a total

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FIG. 3. Case 2. Atrophy of the left leg.

CLINICAL CONFERENCE 849

vealed the presence of mild pain of 6 months

duration in the left knee. Upon further

in-vestigation it was found that the youngster’s

basketball coach had been aware of the

atrophy and pain for approximately 6

months, but since the pain was relieved by

the activity of playing basketball, and since the atrophy did not interfere with the boy’s

ability as a basketball player, the coach

ignored the whole thing.

Physical examination showed the atrophy of the left leg, and little else (Fig. 3). There

was very little muscle weakness, and again

the marked discrepancy between the

de-gree of atrophy and the muscle weakness

was noticable. There was no local

tender-ness in the leg and no limitation of motion.

The circumference of the left thigh was 1i.

in. less than that of the right, and the

cir-cumference of the left gastrocnemius was

1 in. less than that on the right. There were no pathologic reflexes.

A roentgenognam of the knee revealed a

flattening of the lateral tibia! condylar an-ticulating surface, with multicystic irnegu-lanities of the bone. A diagnosis of

osteo-chondnitis dissecans was made. The

pa-tient is under therapy at the time of this

writing.

COMMENT

These two cases are presented to

demon-strate that relatively small lesions in and

around the knee, with only slight pain,

ap-panently can cause enough reflex splinting

of the muscle groups around the knee to

produce an atrophy of disuse. This

oc-curred despite the fact that the patients not

only walked but actively participated in

sports. If the reflex spasm of the muscle

groups is great enough, abnormal

neuro-logic signs such as ankle clonus and

in-creased deep tendon reflexes may be

dem-onstrated.

This clinical situation is neither stressed

nor mentioned in the standard pediatric,

orthopedic or neurologic textbooks; yet it

is striking when it occurs. Emphasizing this syndrome might increase ones index of

suspicion, which is always important in

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1961;28;847

Pediatrics

Irving H. Rozenfeld

SIMULATING CENTRAL NERVOUS SYSTEM DISEASE

CLINICAL CONFERENCE: BONY LESIONS OF THE LOWER EXTREMITIES

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(5)

1961;28;847

Pediatrics

Irving H. Rozenfeld

SIMULATING CENTRAL NERVOUS SYSTEM DISEASE

CLINICAL CONFERENCE: BONY LESIONS OF THE LOWER EXTREMITIES

http://pediatrics.aappublications.org/content/28/5/847

the World Wide Web at:

The online version of this article, along with updated information and services, is located on

American Academy of Pediatrics. All rights reserved. Print ISSN: 1073-0397.

References

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