Author/Authors :
G, Balaji Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) - Pondicherry, India , P, Palaniappan Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) - Pondicherry, India , S, Nema Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) - Pondicherry, India , J, Menon Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) - Pondicherry, India
Abstract :
Osteochondroma arising from the tibial tuberosity is very rare. We report such a case which mimicked
OsgoodSchlatter’s disease in an adolescent. A 12 years-old boy presented with swelling over his right proximal tibia of one year duration associated with pain in the last three
months. Examination revealed a 4 x 2cm bony mass arising
from the proximal tibia. Radiographs revealed an
osteochondroma of the tibial tuberosity. Computer
tomography and magnetic resonance imaging confirmed the
continuity of the medulla of the bony mass to that of the
parent bone. Excision biopsy was done. At the final follow
up, he was asymptomatic and returned back to his daily
activities. We present this case for its rarity, challenges
involved in diagnosis and the difficulties encountered in
planning the surgery because of involvement of the
apophysis and extensor mechanism attachment in a skeletally immature boy.
Keywords :
Knee tibia , exostoses , osteochondroma , adolescent