Mesenchymal hamartoma of the chest wall is a rare tumor with about 53 repor
ted cases in the English literature. We reviewed six chest wall mesenchymal
hamartomas in four patients, including two cases with multiple lesions, wi
th specific focus on the radiologic and pathologic correlation. All cases o
ccurred in neonates or infants with ages ranging from seven hours to seven
months. They were diagnosed with plain chest radiographs (n=6), ultrasonogr
aphy (n=2), chest CT scan (n=6), whole body bone scan (n=2) and MRI (n=3).
All cases except a small one without cystic change showed the typical featu
res of mesenchymal hamartoma radiographically and pathologically. Radiologi
cally they were well-circumscribed masses with solid and cystic components
with multiple fluid-fluid levels in association with single or multiple rib
destruction or change. The CT scan showed the typical findings of chest wa
ll homartoma, and the MR showed heterogeneous signal intensities of che mas
s on T1- and T2-weighted images. The MR also revealed more concisely a seco
ndary aneurysmal bone cyst formation with multiple fluid-fluid levels on th
e T2-weighted image. Microscopically, they showed alternating areas of cart
ilaginous islands and primitive appearing mesenchymal proliferation, which
corresponded well with the solid component on the radiologic findings. The
areas of bone formation and blood-tilled cystic spaces matched the calcifie
d or ossified densities and the cystic components, respectively. A small ca
se without cystic change showed peculiar radiological and pathological find
ings resembling an osteochondroma. In conclusion, mesenchymal hamartoma of
the chest wall in infancy is quite rare and sometimes can be misdiagnosed a
s malignancy due to to he bone-destroying radiographic appearance and the h
ighly cellular and mitotically active microscopic features, unless the radi
ologists and pathologists are aware of the characteristic clinical, radiolo
gical, and pathological findings. Imaging studies can usually make a correc
t diagnosis with good correlation to the pathologic findings.