Nucleus pulposus (NP) embolism is an extremely rare cause of spinal cord infarction. To our knowledge, it has not been reported in pregnancy in the English literature. A 41-year-old pregnant woman presented with clinical symptoms initially attributed to a transverse myelitis. After a complicated clinical course, she expired, and was found at autopsy to have NP embolism to the spinal cord. In conclusion NP embolism is a rare cause of spinal cord infarction, and should be considered in the differential of a patient presenting with symptoms compatible with spinal cord infarction in the pregnant as well as nonpregnant state. Embolization of fibrocartilaginous material to the spinal cord vessels is a rare cause of spinal cord infarction. The etiology is unknown, although some cases have been reported to occur following trauma, which may be minor. To our knowledge, nucleus pulposus (NP) embolism to the spinal cord vessels has not been reported during pregnancy in the English language literature. We herein report such a case and review the salient literature on this topic.
CaseA 41-year-old G5P3105 woman presented to the labor and delivery service at 25 þ weeks gestational age with a chief complaint of sudden onset of lower extremity tingling, weakness, and inability to walk. The weakness developed in less than 30 min. She denied trauma, viral infection, contact with ill individuals, unusual food ingestion, or the use of alternate medicines. The patient had five other children, and her prior pregnancies were uneventful.On examination, she had decreased muscle tone, complete loss of strength, and absent deep tendon reflexes in the lower extremities. Plantar responses were absent. Sensory examination revealed the absence of perception to fine touch, pinprick, vibration, temperature, and joint position in the lower extremities below the T10 level. Rectal sphincter tone was absent. The remainder of the neurological examination was normal.Laboratory examination revealed normal serum chemistry and hematology. The patient's antithrombin-III level was mildly low at 74 (normal 85-120). Protein C, protein S, dilute Russell viper venom times (for lupus anticoagulant), and anticardiolipin antibody were normal. An Magnetic Resonance Imaging (MRI) of cervical, thoracic, and lumbar spine with and without contrast did not reveal any abnormalities, but showed mild disc protrusions at the C3-4 and C4-5 levels producing mild cervical stenosis and mild flattening of the thecal sac and cord. Lumbar puncture showed normal cerebrospinal fluid with one cell, protein 36 mg/dl, and glucose 62 mg/dl. The patient continued to be symptomatic, and an MRI of the spine was repeated a day later. Increased signal was noted within the cord from the conus to T6-7, compatible with either cord infarction or myelitis. An MRI of the brain with and without contrast was normal. Somatosensory evoked potentials to the right and left median nerve stimulations were normal. Cortical potentials were absent with right and left peroneal nerve stimulation. These findin...