BACKGROUND: Infantile cartilaginous hamartoma of the rib is a rare conditio
n occurring in newborn infants, with an incidence of 1 in 3,000 (0.03%) amo
ng primary bone tumor cases. Reports of this condition so far have presente
d the clinical, radiologic and histopathologic-features. To the best of our
knowledge, reports of the cytopathologic features have not been documented
. In the present case report, clinical, radiologic and cytopathologic featu
res and differential diagnosis are enumerated.
CASE: A 1-month-old, male infant presented with a chest wall mass with a cl
inical diagnosis of osteochondroma. On fine needle aspiration cytology, a d
iagnosis of infantile cartilaginous hamartoma of the rib was suggested; it
was supplemented by the clinical history and radiologic findings.
CONCLUSION: Although rare, this condition ought to be kept in mind while de
aling with infantile chest wall masses to avoid an erroneous diagnosis of m
alignancy, owing to its ominous cytopathologic features.