Background:
Spinal hydatidosis is a rare manifestation of cystic echinococcosis caused by Echinococcus granulosus, endemic in Peru and other regions of South America, the Mediterranean, Africa, and Asia. Vertebral involvement accounts for 0.5–2% of cases and is associated with high morbidity, neurological compromise, and frequent recurrence.
Case Presentation:
A 28-year-old woman from Huacho, Peru, with prior T12 hydatid cyst surgery presented with six months of progressive dorsal pain, lower limb paresthesias, urinary retention, and worsening paraparesis. Examination showed paraparesis (MRC 3+/5, left predominance), hyperreflexia, a sensory level at T10, and partial sphincter dysfunction.
MRI revealed a multiloculated cystic lesion at T12 with vertebral body lysis and >50% canal compromise. CT demonstrated ≈80% destruction of the T12 vertebral body with dorsolumbar instability. After one week of albendazole (400 mg twice daily), she underwent T12 corpectomy, cyst excision, decompression, and reconstruction with a titanium mesh cage and T11–L1 fixation. Intraoperative rupture occurred; hypertonic saline irrigation was applied. Histopathology confirmed echinococcosis.
Postoperatively, she completed a 4-month rehabilitation program, achieving recovery of sphincter control and motor improvement to 4/5. At discharge, she could walk short distances with a walker and required partial assistance.
At 12 months post-surgery, she remained stable, with no radiological recurrence. She ambulated with minimal assistance and had functional urinary continence, with mild residual weakness.
Conclusion:
Recurrent spinal hydatidosis requires aggressive surgical resection and prolonged antihelminthic therapy. Multicystic lesions increase the risk of rupture and recurrence. Early diagnosis, radical excision, stabilization, and close follow-up are essential to optimize neurological outcomes.