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465 LETTERS TO THE EDITOR

ment, I would be very interested in hearing

views of other Academy members who have

studied the Statement.

DANIEL A. LAcozzlNo, M.D.

3030 Hoyt

Everett, Washington 98201

School Absenteeism and Child Health

To ma EDITOR:

Drs. Moore and Frank have reported that

the rate of school absenteeism in Charlestown,

Massachusetts, increased subsequent to the

establishment of a comprehensive health center

in the area.’ One might speculate that the

presence of the center itseff was responsible

for part or all of this increase. Many children

who were not acutely ill and who would not

ordinarily have visited the doctor might have

been absent from school in order to keep

ap-pointments for follow-up or maintenance care

or for social or other ancillary services. The

more comprehensive the services provided at

the center, the more such visits a well child

would be likely to make and the more school

he might miss as a consequence.

This suggests that, under some

circum-stances, school absenteeism may not be an

ap-propriate measure of the level of health in a

group of children. It serves, too, as a reminder

to the pediatrician that a visit to the doctor

may mean a day’s absence from school-a fact

we may tend sometimes to overlook in

sche-duling appointments.

DANIEL S. BLUMENTHAL, M.D.

Field Operations Branch

Nutrition Program

Center for Disease Control U.S. Public Health Service Atlanta, Georgia 30333

REFERENCE

1. Moore, C. T., and Frank, K.: Comprehensive health services for children : An exploratory study of benefit. Pediatrics, 51 :17, 1973.

EDITOR’S Norx:

Drs. Moore and Frank commented as

fol-lows:

The possible confounding association

be-tween health center utilization and

absentee-ism for well child problems is similar to some

of the possible causes of bias which we

out-lined in the discussion of our article. A

condi-lion of selection for the study was that each

child have a complete checkup at the health

center prior to inclusion in the study. To some

degree, this may have decreased the effect of

the bias which Dr. Blumenthal describes.

However, we agree that this is a possible cause

of our findings and support his contention that

medical care may occasionally serve to disrupt

the child’s daily activities.

GORDON T. MOORE, MD.

KENNETH Fix, M.D.

Cambridge Hospital

Cambridge, Massachusetts 02139

Thyroid Abscess in Childhood

To THE EDITOR:

In a recent article by Kirkland et al’

de-scribing the nature of solitary thyroid nodules

in 30 children, one child with thyroid abscess

was reported. The authors reviewed 35 cases

of abscesses in childhood, four of which were

reported after 1950. We recently studied a

child with thyroid abscess in whom the clinical

course was characterized by multiple

recur-rences.

The patient was a 5 4/12 year-old-girl who

developed progressive swelling in the anterior

portion of the neck two weeks after the onset

of intermittent low grade fever, rhinorrhea, and

cough. There were no complaints of pain,

dysphagia, dyspnea, or hoarseness.

On admission, temperature was 103 F;

pulse, 120/minute; blood pressure, 110/80

mm Hg; weight, 35 pounds (weight age 3 6/

12 years) ; and height, 43 inches (height age

4 10/12 years) . A tender, erythematous, hard,

nonfluctuant, midline mass measuring 5 by 3

cm was palpated in the anterior neck just

below the thyroid cartilage. The left

submandi-bular lymph nodes were also markedly

en-larged and tender.

Laboratory data showed a hemoglobin of

11.8 gm/100 ml, leukocyte count of 19,700/

cu mm with 75% segmented neutrophils, 17%

lymphocytes, and 8% monocytes, and

erythro-cyte sedimentation rate of 63 mm/mm. Two

blood cultures showed no growth and throat

culture grew normal flora. Tine test was

nega-tive. Thyroid function tests are shown in Table

I (first occurrence).

She responded to intravenous aqueous

peni-cillin, 250,000 units every six hours for four

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LETTERS TO THE EDITOR 466

TABLE I

THYROID FUNCTION TESTS

Fifst Occurrence Second Occurrence Asymptomatic Third Occurrence

PB! og/l00 ml 9.7 8.1 8.0 8.7

F4! (D)* g/100 ml 35 4.8 6.2 4.8

TSHoU/ml - - 8.7

Antithyroglobulin <1:16 - <1:16 <1:16

antibody

Antithyroid - - Neg

-antibody (Coons)t

RAI Uptake

Pre TSH 4 hr 12% - 7%

-24hr 17% - 14%

-Post TSHt 4 hr - 30%

-Thyroid Scan

Pre TSH No uptake

L lobe

- No uptake

L lobe

-Post TSH - - No uptake

L lobe

-* Thyroxine determination by Murphy-Pattee method and expressed as iodine (Bioscience Laboratories).

t Antithyroglobulin antibody (Coons) determination through the courtesy of Robert M. Blizzard. M.D.

t

Bovine TSH 10 units qd X 2.

in the size of the mass. She was discharged six

days after admission on oral potassium

phen-oxymethyl penicillin, 400,000 units every six

hours.

Ten days after discharge from the hospital,

while still receiving oral penicillin, the mass increased in size and again became

erythema-tous. It remained nonfluctuant. There was no

fever, and she was clinically euthyroid.

Ther-apy was changed to oral dicloxacillin, 200 mg

every six hours. Four days later, she was again

hospitalized with a fluctuant, 3 by 4 cm, tender

erythematous mass in the anterior neck and she

was afebrile. She was maintained on the same

dose of dicloxacillin, and on the next hospital

day, she underwent incision and drainage of the

mass, under general anesthesia. Surgery

reveal-ed bloody, purulent material which on gram

stain showed very few gram-positive cocci.

Bac-terial culture grew Streptoccocus viridans. Acid

fast and fungal cultures showed no growth. Her

thyroid function tests were as shown in Table

I (second occurrence) . She was discharged on

the fourth hospital day and continued on oral

dicloxacillin, 200 mg every six hours for an

additional two weeks.

Two weeks after therapy had been

discon-tinued, there was slight erythema around the

incision but no induration. She had remained

afebrile and was clinically euthyroid. Table I

(asymptomatic) shows the results of thyroid function tests.

After three months without therapy, she

de-veloped a 3 by 3 cm area of induration and

erythema around the incision with no local or

constitutional symptom. She received a ten-day

course of oral potassium phenoxymethyl peni-cillin, 400,000 units every six hours, with

re-gression of swelling and erythema. In Table I

(

third occurrence) are shown the thyroid func-tion tests during this relapse. When last seen

three weeks after this course of therapy, she was euthyroid, and there was minimal

indura-tion without erythema around the incision.

In contrast to the patient described by

Kirk-land et al.,’ our patient showed constitutional symptoms during her initial presentation. Most

of the reported cases follow this clinical

pat-tern.” 2 J addition, the clinical course in our

patient was characterized by recurrences as has been previously reported.” With each

episode of suppuration, there was an increase

in the protein bound iodine (PBI - thyroxine

iodine (T4I) difference (Table I) .

Antihyro-globulin antibody and antithyroid antibody

(Coons) were not detectable. Even though the radioiodine uptake (RAT) was normal and

in-creased with thyrotropin (TSH)

administra-tion (Table I) , the left lobe of the thyroid

gland remained nonfunctional.

N. OLATUNJI OLAMBIWONNU, M.D.

ROBERT PENNY, M.D.

S. DOUGLAS FRASIER, M.D.

(3)

467 LETTERS TO THE EDITOR

The University of Southern California School of Medicine

and the Los Angeles County

-USC Medical Center 1129 North State Street

Los Angeles, California 90033

(EDIToR’s Nom: Although we try to limit

letters to 300 words, as stated in the box on

page 462, this one seemed to merit extra space.)

REFERENCES

1. Kirkland, R. T., Kirkland, J L., Rosenberg, H.

S., Harberg, F. J., Librik, L., and Clayton,

C. W. : Solitary thyroid nodules in 30

chil-dren and report of a child with a thyroid

ab-scess. Pediatrics, 51 :85, 1973.

2. Cochrane, R. C., and Nowak, S. J. C. : Acute

thyroiditis with report of ten cases. New Eng. J- Med., 210:935, 1934.

3. Szego, P. L., and Levy, R. P. : Recurrent acute suppurative thydroiditis. Canad. Med. Assoc.

J., 103:631, 1970.

Lead Poisoning: Status

of the

FEP and Other Tests

To THE EDITOR:

The recent articles by Piomelli et al.’ and

Chisolm2 represent another welcomed

investi-gation and discussion on the use of free

eryth-rocyte porphyrin (FEP) test in the control of

lead poisoning. These investigators, however,

have greatly overstated the potential of this

test as a primary screening tool in community

lead control programs.

The policy statement of the Surgeon General

of the Public Health Service, developed in

con-sultation with Dr. Chisolm, has established

that “The prime goal of screening programs is

the prevention of lead poisoning” [emphasis

added].3 For this purpose, a blood lead level of 40&g/100 ml has been judged to be the

most reliable indicator of recent or current

ex-cess exposure to lead; and it can be used to

initiate preventive environmental controls to

reduce the exposure before toxicity results.

As Piomelli at al.’ and Chisolm2 have

ob-served, the FEP concentration in blood is an

index of metabolic toxicity due to lead and not

a measure of early exposure to lead. When

blood FEP is elevated, an adverse response to

lead has already occurred. This is a most

im-portant distinction and further evaluation of

the data collected by Piomelli et al’

demon-strates the consequences of using the FEP test

in primary screening of children for lead

ex-posure. Of the 568 children in the New York

study with undue lead absorption (40g/100

ml) , only 354 or 62.3% had positive FEP tests. If the FEP test had been used as the primary

screening method, the other 214 children or

37.7% would have been missed and preventive

services through control of their hazardous

en-vironments denied them. The aim of all health

professionals, epidemiologists, and clinicians

alike, must be the prevention of this childhood

disease.

It must also be recognized that the

discus-sion of the advantages of the FEP analysis as

a “pre-screening test” is based on an

admin-istrative decision of the New York City Health

Department which does not provide for routine

medical or environmental follow-up of

chil-dren with blood lead levels below 60g/100

ml. This decision is contrary to the

recommen-dations of both the Surgeon General3 and the

American Academy of Pediatrics and should

not be advocated for general use in other corn-munities without this clear understanding.

It is desirable for a laboratory test to be

simple, accurate, and economical, but it must

above all else provide information necessary to

accomplish the primary objectives of a screen-ing program. While the FEP test may be used in certain phases of a childhood lead control

program, it is not now a suitable alternative

to blood lead tests as the primary screening

in a preventive community program.

ROBERT D. FISCHER, M.D.

Medical Advisor

Department of Health, Education, and Welfare

Bureau of Community Environmental

Management

Parklawn Building, Room 16-79

5600 Fishers Lane

Rockville, Maryland 20852

References

1. Piomelli, S., Davidow, B., Guinee, V. F.,

Young, P., and Gay, C.: The FEP (free

erythrocyte porphyrins) test: A screening

micromethod for lead poisoning. Pediatrics, 51:254, 1973.

2. Chisolm, J. J.: Screening for lead poisoning in

children. Pediatrics, 51 :280, 1973.

3. U_S. Public Health Service: Medical aspects of childhood lead poisoning. The Surgeon

General’s policy statement. Pediatrics, 48:

464, 1971.

(4)

1973;52;465

Pediatrics

N. Olatunji Olambiwonnu, Robert Penny and S. Douglas Frasier

Thyroid Abscess in Childhood

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(5)

1973;52;465

Pediatrics

N. Olatunji Olambiwonnu, Robert Penny and S. Douglas Frasier

Thyroid Abscess in Childhood

http://pediatrics.aappublications.org/content/52/3/465.3

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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