Spontaneous Regression of Osteochondroma – A Rare Phenomenon

Background: Osteochondroma is a common benign bone tumour, but its spontaneous regression is a rare occurrence. The first case was reported by Hunter in 1786. And only 30 cases were found in literature to date. Spontaneous regression of osteochondroma usually occurs in paediatric age group prior to skeletal maturation without any sequelae. The exact pathophysiology of its spontaneous regression is still not fully understood. We report a case of spontaneous regression of osteochondroma in a child after a 6-year period of follow up without needing any surgical intervention.International Journal of Human and Health Sciences Vol. 05 No. 03 July’21 Page: 372-374

Iliac wing osteochondroma in a 16-year-old boy: a case report

<p class="abstract">Osteochondroma is the most common benign bone tumour. Commonly seen in the long bones of the lower extremity. Ilium is a rare site. We present a 16-year-old boy with swelling in the right groin for 8 months. After clinical and radiological evaluation, it was diagnosed as osteochondroma of right iliac wing. Patient underwent en-bloc excision of the lesion and histopathology confirmed the diagnosis. Pelvic osteochondroma is a rare entity but not unusual. Extra periosteal en-bloc excision is the management of choice in patients with cosmetic deformity, neurovascular compression and malignant transformation with very low recurrence rate.</p>

Osteochondroma of acromioclavicular joint

Osteochondroma is the most common type of benign bone tumour. It is a benign chondrogenic lesion derived from aberrant cartilage from the perichondral ring, and it commonly presents in the proximal humerus, proximal femur and knee. Osteochondroma is usually solitary but can be multiple with patients with hereditary multiple exostoses. Malignant changes happen in approximately 1% of cases. Osteochondroma usually causes local pain or swelling. We discuss a unique case of an osteochondroma that highlights the fact that osteochondroma can occur in the most unlikely places, and they should be properly visualised via radiography to evaluate any extensions and compromised surrounding structures before surgical intervention.

Hallux Osteoid Osteoma: A Case Report and Literature Review

Osteoid osteoma is a benign bone tumour that mostly affects males in the second and third decade of their life. The lesion mainly occurs in long bones, usually in the femur and tibia, causing severe localized pain that is worse at night and responds to nonsteroidal anti-inflammatory drugs (NSAIDs). Diagnosis is usually made on the basis of history and radiographic findings. However, in more unusual locations as the hand and foot, diagnostic issues can arise. Treatment often includes complete removal of the tumor. We present a 22 year old male with osteoid osteoma involving the distal phalanx of the hallux. To our knowledge very few cases of great toe osteoid osteoma have been reported in the literature.

Pseudoaneurysm of the popliteal artery due to osteochondroma of the distal femur

Osteochondroma is the most common type of benign bone tumour, and is most often found in the knee region. The lesion is usually clinically silent although it may cause different complications such as fractures of the tumour, bone deformities, neurological disorders, malignant transformation and in rare cases vascular disorders. Vascular disorders include stenosis, occlusions, thrombosis, arteriovenous fistula and in rare cases pseudoaneurysm formation. A delay in diagnosis especially of pseudoaneurysm formation may result in life-threatening situations, extensive operations and lengthy hospital stays. We report the case of a 22-year-old woman with an osteochondroma of the distal femur which caused pseudoaneurysm of the popliteal artery.