Abstract
BACKGROUND: Infantile cartilaginous hamartoma of the rib is a rare condition occurring in newborn infants, with an incidence of 1 in 3,000 (0.03%) among primary bone tumor cases. Reports of this condition so far have presented 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 features and differential diagnosis are enumerated. CASE: A 1-month-old, male infant presented with a chest wall mass with a clinical diagnosis of osteochondroma. On fine needle aspiration cytology, a diagnosis 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 dealing with infantile chest wall masses to avoid an erroneous diagnosis of malignancy, owing to its ominous cytopathologic features.
Original language | English |
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Pages (from-to) | 69-73 |
Number of pages | 5 |
Journal | Acta Cytologica |
Volume | 45 |
Issue number | 1 |
Publication status | Published - 01-01-2001 |
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All Science Journal Classification (ASJC) codes
- Pathology and Forensic Medicine
- Histology
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Infantile cartilaginous hamartoma of the rib : A case report. / Rao, L.; Kini, A. C.; Valiathan, M.; Gurpur, C. R.; Rao, R. V.
In: Acta Cytologica, Vol. 45, No. 1, 01.01.2001, p. 69-73.Research output: Contribution to journal › Article
TY - JOUR
T1 - Infantile cartilaginous hamartoma of the rib
T2 - A case report
AU - Rao, L.
AU - Kini, A. C.
AU - Valiathan, M.
AU - Gurpur, C. R.
AU - Rao, R. V.
PY - 2001/1/1
Y1 - 2001/1/1
N2 - BACKGROUND: Infantile cartilaginous hamartoma of the rib is a rare condition occurring in newborn infants, with an incidence of 1 in 3,000 (0.03%) among primary bone tumor cases. Reports of this condition so far have presented 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 features and differential diagnosis are enumerated. CASE: A 1-month-old, male infant presented with a chest wall mass with a clinical diagnosis of osteochondroma. On fine needle aspiration cytology, a diagnosis 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 dealing with infantile chest wall masses to avoid an erroneous diagnosis of malignancy, owing to its ominous cytopathologic features.
AB - BACKGROUND: Infantile cartilaginous hamartoma of the rib is a rare condition occurring in newborn infants, with an incidence of 1 in 3,000 (0.03%) among primary bone tumor cases. Reports of this condition so far have presented 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 features and differential diagnosis are enumerated. CASE: A 1-month-old, male infant presented with a chest wall mass with a clinical diagnosis of osteochondroma. On fine needle aspiration cytology, a diagnosis 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 dealing with infantile chest wall masses to avoid an erroneous diagnosis of malignancy, owing to its ominous cytopathologic features.
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UR - http://www.scopus.com/inward/citedby.url?scp=0035142410&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0035142410
VL - 45
SP - 69
EP - 73
JO - Acta Cytologica
JF - Acta Cytologica
SN - 0001-5547
IS - 1
ER -