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sentative

examples

are included

here.

-@llpatients

reported

have

l)eefl

examined

by

one

of

us

(R.D.M.).

Thirty

cases of osteoid

osteoma

were diagnosed

at this

institution

l)et\veen

1952

and

1974.

Of

these

patients,

22 (74%) were

2() @Tearsof age or

less@4 of the 22 were operated

on elsewhere

after

the clinical

diagnosis

had been

made

and are not

included

in this report.

Four

of the renlaining

18

1)atie1@tshave been

previously

reported

from

this

institution 1)\' Kendrick and Evarts and are not

included

in this report.

RESULTS

The

pertinent

features

of the

14 patients

reported

here

are summarized

in Table

I. These

patieilts

ranged

in age from 5 to 20 years.

In the

patients

reported

previously

from this institution

l)\' Kendrick

and Evarts,'

the \‘oungestwas 23

nionths

and the oldest was 62 @‘¿ears

of age. The sex

distribution

of our

patients

was

11 males

atid :3

females.

Pain

was

the

presenting

complaint

of

each patient.

The pain

was generally

of a boring

or aching nature and was characteristically worse

at night

than during

the day. In several

instances,

P@'@'@

would

abruptly

awaken

the patient.

Pain

had been

present

from

as little

as 1 month

to as

@ Rt'('ei\t'(l :\imgiist 13: dc('el)te(l for i@mblicatiomi .\ugust 18,

1976.)

ADDRESS FOR REPRIN1'S: R.1),\l.@ 1)epartment of Pedi atrics amid .@dolescemit \ledicine, The ( :les'el@tmid ( :limik' FolIo

datioll, 950() Euclid Avenue, Cleveland, ()hio 44106.

.\BSTR.@CT. Osteoid osteoma is a relatively coiiimon benign

tumor of bone ss'hich occurs most often in adolescents amid

\‘ounga(ltllts. The pattern of the pain svith its characteristic response to aspirin and the roemitgenogm'aphic findings niake

the clinical diagnosis easy and virtually certain. An example

is 1)resemited to help the pediatrician l)ecomfle familiar with the tumor amid its diagnosis. Pediatrics, 59:526—532, 1977,

OSTEOI I) O5TEOMA. BONE TUMORS.

Osteoid

osteonia

is a benign

tunior

of bone

which

is easily

diagnosed.

.‘\lthough approxi

matelv

70% of reported

instances

have

been

in

patients

20

@‘¿ears

old or \‘ounger, the disease

has

l)een

seldom

mentioned

in the

pediatric

litera

ture,

many

pediatricians

are

not

aware

of the

existence of such a disorder. The purpose of this

article

is to point

out the classic,

clinical

features

of osteoid osteoma

and the ease with which the

diagnosis

can be established.

The

treatment

and

the cure of osteoid

osteonia

is surgical

removal

of

the titnior.

MATERIALS AND METHODS

-.‘ coniputer search was niade of all instances of

osteoid

osteoma

diagnosed

at

The

Cleveland

Clinic

Foundation,

and this was conipared

with a

list

of all

pathologic

specimens

signed

out

as

osteoid

osteonias.

All charts

were

reviewed,

and

only those

cases with

biopsy-proven

diagnoses

were

included

in this stud@.

The

roentgenogranis

were

studied,

and repre

OsteoidOsteoma in Children and Young Adults

James P. Orlowski,M.D., and Robert D. Mercer, M.D.

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(:l('t('l(,,m(l(:li,1i('L(1U('(ItiOlI(Il1'()UU(latiOli.(;!(‘I('!(,?l(l

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(2)

Sijmptom.s’ 1)1,ration Aspirin Relief

Surgical Relief

1 M/19 Pain R hip I yr Yes No report No report R proximal femur Yes

2 M/1() Pain L thigh 8 mo Yes Yes, 2 cm Yes L femoral head Yes :3 XI I I 1 m2 Pain R knee I yr Yes Yes, 4 cm Yes R distal femur Yes

4 M/5 Pain L knee 2 yr Yes Yes, 4 cm Yes L distal femur Yes

5 MIS Pain R lower leg

and R foot

3#{189}yr Yes No report Yes II lateral

ctmnei-form

Yes

6 M/6 Pain L knee 3 mo Yes Yes, 2.5 cm Yes L distal femoral Yes

7 F/ 1 1

cond’,le

Pain R thigh 18 030 Ye5 Yes, 2 cmii Yes B femnoral neck Yes

S \1/15’2 Pain L ankle 6 mimo Yes No report Yes L distal tibia Yes 9 NI/ifi Pain L thigh 1 urn No report No No_report L femur midshaft Yes 10 M/2() Pain R knee and

R hip

I yr Yes Yes, 2 cm Yes R femur mnidshaft Yes

11 \1/15 Pain L thigh No report Yes Yes, 3 cm No report L 1)roximiial femur Yes 12 M/612 Pain L knee :3 mo Yes Yes, 2 cmii Yes L femur midshaft

H proximmial femur Transverse process

(:-4 vertebra

Yes Yes Yes 1:3 M/12 Pain R knee 2 yr Yes No report Yes

14 F/1:3 Painful stiff neck 1 yr Yes No No TABLE I

OSTEOID OsTEomA

P(Iti(’Ilt Sux/ .‘ge (i,r)

long as :31/i 7ears before the diagnosis was made

and surgical relief provided. Pain was generalh’

located in the region of the bone tumor but was

referred to the thigh from lesions in the proximal feiiiur in cases 2, 3, and 1 1. It was referred to the

knee from lesions in the midshaft or proximal

femur in cases 10, 12, and 1:3.

Coiiiplete relief of pain with the use of aspirin ‘as a striking feature of the history in niost of the

l)atiellts. These patients found out on their own

that aspirin was needed almost every four hours.

Iii sonic instances, the demand for aspirin was insistent enough to suggest addiction. Patient 5

would steal aspirin from neighl)ors when his

parents tried to limit his consumption of this

drug. Patient 20 reported relief of pain with

aspirili l)Ut not with codeine. The relief of pain

with the use of aspirin is so specific that it is one of the diagnostic features of this disease.

The findings on physical examination were

usual1’ niiniiiial. Liniping was present when the

lesion was located in the lower extremities, as it

was in most of the patients reported here.

.-troph of muscle was also commonly present.

Pain on pressure over the area of the involved bone ‘as present, but it was relatively minimal.

Visible enlargement of the involved bone was

noted only in the one patient (case 8) in whom the

Atrop/mij Limp IA)C(ItiOfl of Tumor

osteoid osteoma was located in the distal part of

the til)ia.

The results of laboratory studies in these

patients were remarkable only in that they were

nornial. The ervthrocvte sedimentation rate

(ESR) was moderately elevated in one patient

(case 9). The white l)lood cell (WBC) count;

alkaline phosphatase, calcium, phosphorus, and

fibrinogen levels; and results of other laboratory

studies were normal in every patient.

CASE REPORT

There are at present more than 500 instances of

osteoid osteonia reported in the surgical and

radiological literature. Because of this

redun-dancv, only one case selected for teaching value is

described here in more detail.

Case 7

..‘ white girl, 1 1 years 3 months old, had complained of pain in her right thigh for 18 miionths. Aspirin relieved the

pain vithin niimiutes; she was taking approximately 6(X) mg

of aspirimi ever four to five hours. 11cr parents attempted to

Pre’emit her constant ingestion of aspirin, I)ut she would steal the drug froni her parents and from her neighbors. She attenipted to snitiggle a l)ottle of aspirin into the hospital l)eCatmse she was afraid she could not get it from her

(3)

Fmc. 1. .trophv of right thigh of 1 1-year-old girl with osteoid osteoma of right femnimr (case 7).

On 1)hvsical exaniination she sas found to be a hea1th child who walked with a slight limp. Localized pain amid temidermiess were pm’esemit at the mrmidportiomi of the right thigh.

The right thigh was 2.0 cm smiialler in circumference thami the

left thigh (Fig. I).The \‘BC cotimit, ESR, amid results of other

routimie lal)orator\ st udies sere nornial . Roemitgenogramus

demiionstrated a radiolucent area 1 .0 cmii in diamneter in the

neck of the right femur iFig. 2). A sniall miidus of increased

density commld be seen within the lucent area. Surgical curettage of this lesion with a homiiogenous bone graft m’esulted in promnpt amid complete relief of svmiiptoms.

There are earlier reports of patients which we

would now recognize as having osteoid osteoma.

The first clear recognition that this was a disease

separate from localized osteoniyelitis and

belong-ing in a class of “benign osteoblastic

osteoid-tissue-forniing tumors” was the report by Milch in

19:34. \Iilch described lesions in the right radius

of a 22-year-old man, the left astragalus of a

23-year-old man, the left fibula of a 15-year-old boy,

and the distal phalanx of the third right toe of a

20-year-old woman. Much felt that the history,

clinical findings. and roentgenograms were

pathognomonic of this condition and he advised

that the tuilior be treated by complete excision.

Jaffe in 1935 introduced the term

“osteoid-osteonia. ‘

He redescrihed three of the patients

reported by Milch and added two more. Jaffe is

often given credit for the original description of

osteoid osteonia. His article is a classic description

of the pathologic anatomy of this disease. He

pointed out that there was no evidence to support

the concept of inflammatory origin of the lesion,

Fm;. 2. Osteoid osteomima of neck of temnur svitli curt ical thickemiimmg case

and he concluded that this ssas a l)enign hone

neoplasul. Iii 19:36, Jaffe’ suirimarized the

prin-cipal clinical and roentgenographic features of

osteoid osteoiiia as follovs:

a) The l)ttiemits ssere all adolescemits or votmng adults

1)) The )m’imi(.’ipal(‘OmilI)laimit\vas local paimi

C,) Umiiformnlv. the lesion originated in songv bone areas

(1) As observed radiographicallv. the )athological areas

sere roumidish and .‘learly cirdumflscril)ed

e) The lesions were smuall amid (‘Ioselv simnilar in size f) Imi ever case operation svas performed on the

assuniption that the lesion vas an inflamnmnatorv one

g) Comuplete eradicatiomi resimlted in the evemitual disap-pearamice of all svmrII)tonis. vithout rt’(’1mrremu’t- of the local

lesiomi.

B\ 1940, jaffe and Lichtenstein were able to

report on a total of33 patients. and 1w 1945, jaffe’

had data on 62 pioveu instances. The generally

voting age of the patients. the preponderance of

niales over feniales, and the relief of pain 1w the

use of aspirin had been noted. The lesion had been

ol)served within and adjacent to the cortex as vell

as in the spongiosa of l)one. The pathologic

anatonlv and roentgenogra)h ic features were

svell described. Since 1945 there has beeii a flood

of reports on osteoid osteoma, and hundreds of

(4)

I76

I55 I 75

t50

25-H

2

75-,

2 50-’

95

CLINICAL FEATURES

25-33

29

AGE IN YEARS

Fi;. :3, .ge distribution of 647 cases of osteoid osteoma collected from the literature.

reports are in the orthopedic, roentgenographic, and )atliologic literature. The pediatric literature

has been strangely devoid of reports on this

disease of adolescents and young adults. The

solitary report that we have been aI)le to find is

that of Purcell et a!. in l952. They surveyed the

findings iii 1:3 children froni 22 months to 15 years

of age from the records of the Mayo Clinic, and,

in an addenduni they mentioned a patient in

vhoni there were probably two separate osteoid osteoirias.

Osteoid osteoma occurs iiiainly in older

chil-dren, adolescents, and young adults. It is

unconinion l)eyond the age of 30 years. A survey

of 674 patients reported in the literature showed

that 66.8#{176}4of theni were less than 20 years of age,

and 80.9% were less than 25 ‘ears of age. Half the

patients were between ages 1 1 and 20 ‘ears (Fig.

3). Seventy percent of these reported patients

were niale. The lesion is not rare in the general

population, l)lIt it is rare in blacks.’

Pain is the chief complaint of nearly all

patients. The pain is moderate or mild; neverthe-less. it is often severe enough to cause the patient

to cry. It is described as a boring pain, or “like a

toothache,

‘‘

and it generally appears to lessen

svitli activity and to l)ecome vorse with rest. It is

often niore intense at night and interferes with

rest. “Starting pain” is frequently described. This

terni is used when the patient awakens suddenly

at night. crying out in pain.

Iii our experience, niassage and the application

of heat were iiot helpful in the relief of pain. The

response to aspirin was proiiipt and dramatic. The

unusual response to aspirin was noted as early as 194() b’ jaffe and Lichtensteiii, and it has

subse-quentlv been confiriiied and conimented on by

iiianv authors.

Pain is usually located in the approximate

position of the tumor, and it may be localized

with extreme I)recision by the patient. However,

referral of pain to a nearby joint is not unusual.

.‘\trophv of niuscie is a common occurrence

when the osteoid osteoma involves an extreniity.

Significant atr01)h’ was noted in eight of our

patients. \Ve regard atrophy as a significant

diagnostic feature of this disease. Limping is also

present ss’hen the osteoid osteoma occurs in an

extreniity. Palpable swelling ma’ l)e present

when the lesion has produced cortical

thicken-ing.

Osteoid osteoma has been described in virtually

every l)one iii the body, including the skull.’’ In

roost patients, the lesion has been found in the

lower extremities. A review of 94 patients

reported in the pediatric age group,7’m”

includ-ing our patients, showed that 34 occurred in the

feimir and 35 in the tibia, for a total of 73.4% of all

patients.

\Then osteoid osteoma occurs near or within a

joint, special prOl)lems of diagnosis and prognosis

arise. Sherman’7 iii 1947 was the first to comment

on this situation. She described one case in which

a 16-year-old girl had an osteoid osteoma of the

neck of the feiiiur. There were mild degenerative

changes of the hip joint, and the synovial

nieml)ralie showed severe villous proliferation

and intense chronic inflammation. Sherman’s

second patient was a 13-year-old boy with osteoid

osteoma of the olecranon fossa. The synovial

IlielTnl)rane of the elbow joint was injected and thickened, and showed a chronic inflammatory

reaction. Sherman felt that these cases

repre-sented a secondary reaction to the nearby osteoid

osteoma.

Flahertv et (ii. S mentioned three patients in

whoni there were degenerative changes in the hip

associated with a tumor in the femoral neck. Others have emphasized the diagnostic

prob-lems,’’” the changes in the joints,m and the

concern that intraarticular osteoid osteoma in a

child can lead to serious disturbances of growth

(5)

func-Fi;. 4. Ostenid osteommia of neck of femnur vitli calcification of

nidims.

tion.

Th ree patients vith intraarticular osteoid

osteomua have re’ittsi l)een reported froni this inst iti it IOU .

Osteoid osteonia of the spine is not particularly

tinconinion. Recently. Keim and Reina0 stated

that there ‘ere more than 50 patients with

osteoid osteonia of the spine described in the

literature, and tlie’ added nine patients.

Osteoid osteoma of the spine is usually

asso-ciated svitli painful scoliosis. The coiiiplaint of

1)ainful scoliosis is unusual in voting people and

must always be considered with extrenie care.

This is I)artic11lt1lY true when there are no

associated signs of inflammation and when the

In”’ is strikingly relieved with the use of aspirin.

Scoliosis has also been seen vith osteoid osteoma

of the ril)S.’ \Vhen osteoid osteonia is present in

the spine, there is often localized tenderness,

restriction of motion, spasni of paravertebral

nuiscies, and sonietinies an awkward gait. A head

tilt iua be seen in osteoid osteoma of the cervical

sl)ine. Radicular pain down the arni or down the

leg may l)e present and can be confused with the

P1’ of a protruding disc. If patients with benign

osteoblastoma are excluded. significant cord

compression with transverse mvelit is has not l)een

described as a result of osteoid osteoma of the

spine.

The treatnient of osteoid osteoma of the spine

is surgical excision of the lesion. Complete

renioval of the nidus results in complete relief of

pain. The tumor niav recur following incomPlete

removal of the nidus.

In niost instances of recurrent osteoi(l osteoma,

n-iost likely the nidus was not completely

renioved. Of niore interest are those ratients in

whoni the tumor has reappeared after what seems

to have been complete renioval of die nidus.

Dunlop et (ii. o: described a maii who had en 1)1o(’

excision of an osteoid osteoiiia at the base of the

right second metacarpal. .\ second resection was

needed a sear and a half later, and a central nidus

was again identified. Nineteen months later. a

third large excision was required for return of

svmptonis. \Vorland et a!. recentl’ described a

23-month-old girl with an osteoid osteoma of the

proxiiiial part of the left tibia. The tumor

recurred one year after the first en bloc excision,

and recurred for the second tinle eight ‘ears after

the second en bloc excision.

Multifocal osteoid osteonias ma also occur and

account for some of the reported recurrences of

this tumor.

The concept that l)enign osteol)lastoma is an

entity distinct froni osteoid osteonia has been

confusing since the original description of what

we would not terni l)enign osteol)lastonia l)\ jaffe

and NIaver in 19:32.-s This is a tumor

characteris-tically larger than osteoid osteonia. It tends to

occur in the spine or long l)ones. The pain pattern

is less t’pical, and roentgenogranis demonstrate

less sclerosis than those of osteoid osteonia.

Benign osteoblastoma was described as

“os-teogenic fibroma” by Lichtenstein in 1951,’ and

Golding and Sissons in 1954. Dahlin and

John-son’ ‘ used the term “giant osteoid osteoma” in

1954, and, in 1956, Lichtenstein and Jaffe’

independently proposed the name

‘benign

osteo-blastonia. ‘ ‘ This has l)ecome the accepted

desig-nation in the irianv case reports that have

followed. \Iarsh et a!. have recently thoroughly

reviewe(l the range of nianifestations of this

tumor. They report the characteristics of 1 72

patients with I)enign osteOI)ldstollia found in the

literature and add 25 new patients of their own.

The histologic similarit between benign

osteo-l)lastonia and osteoid osteonia was noted as early

as 19:32 when jaffe and \Iayei (lescril)ed the

(6)

recognized that tile pathologic findings were of

the sanie nature as the l)atients described by

Bergstrand Patie11ts that we would now accept

a.s having classic osteoid osteomas. Schajowicz

and Lemnos ‘ and (leSouza Dias and Frost ‘ ‘

#{149}

believe that both lesions represent a COflhIiiOii

basic P1cess. deSotiza Dias and Frost suggest that

these (lisorders I)e classified according to their

location in l)One, since the location determines

the nature of the reaction evoked in the

surround-ing hea1th’ i)one and also the size: (1 ) cortical

osteobiastonia, (2) spongious osteoblastoma, (:3) I)e1iStecul osteoblastoma, and (4) iiiultifocal

osteo-l)lastOiiia.

ROENTGENOGRAPHIC FINDINGS

The characteristic 1)icttlre of an osteoid

O5teOIflt is that of a sniall, rounded nidus

stirFOUll(ie(l i)\’ a reactive layer of sclerotic l)One

amid associated with thickening of the cortex (Fig.

4). The iiidtis is small and usual1’ not more than

0.5 ciii in diameter. It is most often radiolucent, bitt it may l)e calcified. Calcification of the nidus il-lay l)e s1)ott\’, 01 it iiia i)e uniformly dense.

There is no apparent relationship i)et’Veen the

age of the lesion and its appearance. At times, a nidus niav l)e 1)Ie5e1lt svith no sclerotic rini around

it. l)llt ill most instances it is surrounded by a zone

of sclerotic l)Olie. The sclerosis surrounding a

nidus miia’ l)e uneven iii distribution. ‘

Osteoid osteonia is characteristically associated \vi tii l)eriOsteal ile\V l)one format ion, causing

cortical thickening. The cortical thickening is

usually fusiform and niav be extensive, with its

greatest svidth in relation to the site of the osteoid osteonia. The l)e1istetl reaction is greatest \shen the osteoid osteoma is located l)eneatll the

perios-teumu OI vithin the cortex, and least or even

al)sent ss’iien the osteoid osteonia is located within

cancellous l)one. The new bone max’ have a

lalilinate(l 1l)I)ear1n1’e, and erosion of the cortex

can occur. Osteoid osteonia never produces the

irregular infiltrative areas of hone destruction

associated svith malignant l)one ttllilors.s

The importance of obtaining roentgenograms

of high (ItlalitY and I)ersistellce in the search for a

nidus must l)e stressed. Laminograph’ is by far

the most satisfactory method of depicting

morphologic (letail . As Freiburger amid

co-work-ers have suggested, roentgenographic

localiza-tioii of the tunior in the operating rooni to

facilitate 1)k’(’ renioval and examination of the

excised bone l)lock to confirm the presence of a

nidims aie valtial)le I)1oced11Ies.

. .,. .

-

,,

‘.:---.-.

-

i-.-:‘‘! S

..--‘_.4

‘r

-

-

-

- - - -- -.7’ .-. ‘.*.---

----.“..- -

:,,

-- .

:;:4::z.:’

;

: , ;‘ --- - .

-

- ;- -, -- _.J_

-Fmc. 5. Osteoid osteonia renioved en bloc. Smmiall tumnor is

clearly demnarcated fromii heal thy bomie. Tumimor nieasmmres 0.5 x 0:3 cmii.

HISTOLOGIC FEATURES

The typical osteoid osteonia is a small, round,

or oval tumor-like nidus composed of osteoid and

miniature. irregularly niineralized trabeculae of

newly formed 1)Ofle developing within a

sul)stra-tiii-ii of highly vascularized osteogenic connective

tissue (Fig. 5). Tins’ unmvelinated nerve fibers

accompanying 1)100(1 vessels miia’ l)e seen in the

periphery i#{149}witiiii-i the muatrix of the nidus. The

pain of these lesions is )rol)al)ly niediated by the autonoiiiic nervous system via these fibers.

Varia-tions in the proportion of osteoid and in the

calcification of newly formed trai)eculae account

for the fact that the nidus is sometimes

radiolu-cent and sometiiiies dense. Scattered foci of

osteol)lastic reabsorption of bone max’ be

observed. Between the ttmnior nodule and the

surrounding l)OIie is a zone of loosely arranged

cellular and vascularized connective tissue. Less

niineralization is present toward the periphery of

the tunior. The surrounding host I)one varies froni

slighti thickened to densely sclerotic i)one tissue.

\Vhere thickened cortex exists, it is composed of a

layer of niore oi less transfornied original cortex

and a layer of compacted, newl’ deposited

pen-osteal l)oiie.

CONCLUSION

Osteoid osteonia is a l)enign tumor of bone that

com lm)nlv occurs in cli ildren and adolescents.

Pediatricians should 1)e familiar with the

s’nip-toms of this tumor. They should suspect the

presence of the tumor on the basis of the clinical

symptoms and confirm its presence

roentgeno-graphically. Because the average length of time

l)etWeen onset of symptoms and

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(7)

i(. diagnosis is about two ‘ears, the importance of persistence in the search for roentgenographic evidence of the tumor is stressed. Four important

aspects of osteoid osteonia in children are

empha-sized: ( 1 ) The prompt and dramatic relief of pain

l)\’ the use of aspirin is so striking that it is a

diagnostic feature of the disease. (2) “Starting

pain” at night, which suddenly avakens the child,

is a characteristic feature of the disease. (3)

Because pain ma\ l)e referred to a nearby joint,

the entire extremity should l)e examined by

roentgenographv if osteoid osteonia is suspected.

(4) Painful scoliosis iii vhich the pain is relieved 1w aspirin is suggestive of osteoid osteoma.

Surgical excision of the lesion effects

imme-diate and lasting relief from pain if the nidus is conipletelv nenioved.

REFERENCES

I. Kendrick JI, Evarts C\l: Osteoid-osteomua: A critical

amial’sis of 40 ttmmnors. Clin Orthop 54:51. 1967.

2. \lik’h II : Osteoid-tissmme-tormnimig tumimor simnulating

annular sequestriumn. J Bone Joint Stirg 16:681,

19:34.

:3. Jaffe IlL: “Osteoid-osteomna: A 1)emugn osteoblastic tumnor (‘omupused of osteoid and atypical bone. .rch

Smmrg :31:709. 193.5.

4. JaHe I IL: Osteoid osteomna. .ni j Pathol 12:796, 1936.

5. Jaffe II L, Lichtemisteimi L: ()steoid-osteomna: Further

experiemice vith this bemiigmi tiLmilor of 1)omie. j Bomie joint Simmg 22:645, 1940.

6. JaHe IlL: Osteoid-osteommma of bone. Radiolog’ 45:319,

1943.

7. Purcell 11\t. \Iills Sl). Lipscomnb PR: Osteoid-osteommma in childhood. Pediatrics 9:293. 1932.

8. Fmeiberger 1111. Loitmmman BS. Ilelpern \l. Thomupson TC:

Osteoid-osteomiia: A report omi 80 cases. .Amn J

1)emitgema)l 52: 194. 1939.

9. \Immnk j. Pevser E. Gellei B: Osteoid osteomiia of the

frontal bone. Br j Radiol :3:3:328, 196().

10. Dtl J(: Osteoid-osteomna of the skull. Br J Radiol

46:392, 197:3.

1 1. deSouza DM5 L. Frost I l\1: Osteoid

osteomna-osteohlas-tomna. (:mmic&r :3:3: 1073. 1974.

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1977;59;526

Pediatrics

James P. Orlowski and Robert D. Mercer

Osteoid Osteoma in Children and Young Adults

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Pediatrics

James P. Orlowski and Robert D. Mercer

Osteoid Osteoma in Children and Young Adults

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