Surgical management of myelopathy caused by a solitary spinal osteochondroma in a young cat

Case summary A 10-month-old, male castrated, domestic shorthair cat was presented with fast-progressing ataxia of the pelvic limbs. MRI and CT were performed, revealing a bony proliferation at T11, with mass effect and laterodorsal compression of the spinal cord. After hemilaminectomy and the removal of the bony mass, the cat recovered uneventfully. At the 1 year follow-up, the cat did not show any neurological deficits or signs of recurrence. Relevance and novel information Solitary osteochondroma as a cause of neurological deficits in the pelvic limb has been described in dogs and humans, but, to the best of our knowledge, there are no reported feline cases described in the literature, in which CT and MRI were performed in combination with the successful removal of the lesion and an excellent outcome for the patient.

Long-term outcomes in primary spinal osteochondroma: a multicenter study of 27 patients

OBJECT Clinical outcomes in patients with primary spinal osteochondromas are limited to small series and sporadic case reports. The authors present data on the first long-term investigation of spinal osteochondroma cases. METHODS An international, multicenter ambispective study on primary spinal osteochondroma was performed. Patients were included if they were diagnosed with an osteochondroma of the spine and received surgical treatment between October 1996 and June 2012 with at least 1 follow-up. Perioperative prognostic variables, including patient age, tumor size, spinal level, and resection, were analyzed in reference to long-term local recurrence and survival. Tumor resections were compared using Enneking appropriate (EA) or Enneking inappropriate surgical margins. RESULTS Osteochondromas were diagnosed in 27 patients at an average age of 37 years. Twenty-two lesions were found in the mobile spine (cervical, thoracic, or lumbar) and 5 in the fixed spine (sacrum). Twenty-three cases (88%) were benign tumors (Enneking tumor Stages 1–3), whereas 3 (12%) exhibited malignant changes (Enneking tumor Stages IA–IIB). Sixteen patients (62%) underwent en bloc treatment—that is, wide or marginal resection—and 10 (38%) underwent intralesional resection. Twenty-four operations (92%) followed EA margins. No one received adjuvant therapy. Two patients (8%) experienced recurrences: one in the fixed spine and one in the mobile spine. Both recurrences occurred in latent Stage 1 tumors following en bloc resection. No osteochondroma-related deaths were observed. CONCLUSIONS In the present study, most patients underwent en bloc resection and were treated as EA cases. Both recurrences occurred in the Stage 1 tumor cohort. Therefore, although benign in character, osteochondromas still require careful management and thorough follow-up.