Abstract
Summary: We report a case of cauda equina syndrome caused by Gnathostoma spinigerum, which was confirmed by an immunoblotting test. MR imaging of the lumbosacral spine showed long, segmented hyperintensity along the cauda equina with irregular enhancement on the postcontrast study. The conus medullaris was slightly enlarged with abnormal enhancement. The patient was treated with corticosteroids, and her clinical condition improved. MR imaging, 9 months after treatment, showed the condition to be completely resolved.
Gnathostomiasis (Gnathostoma spinigerum infestation) is commonly found in Thailand and Japan and is caused mainly by eating raw infested fish. Most cases present with cutaneous involvement (migratory swelling or urticaria) and neurologic findings (i.e., radiculitis, myelitis, subarachnoid hemorrhage, or intracerebral hemorrhage).
MR imaging of the affected area of the nervous system may help in assessing severity, and revealing the presence of gnathostomiasis and assessing the severity of disease (1). We report a case with involvement of the cauda equina.
Case History
A 56-year-old woman presented with sudden and severe radicular pain from the buttocks to both legs followed by weakness in her legs. She had urinary incontinence 7 days before admission. She recalled no history of migratory swelling, trauma to the back, or having eaten raw fish. On physical examination, she was afebrile and had no migratory swelling or creeping eruption. She was oriented and had paraparesis (hip flexor grade III/V; hip extensor grade II/V; knee flexor grade I/V; knee extensor grade IV/V; ankle flexor and extensor grade IV/V; and extensor hallucis longus grade III/V, bilaterally). She also had decreased pinprick sensation in the perianal area and saddle anesthesia, and the tone of the anal sphincter was decreased with a positive anal wink and bulbocarvernosus reflex. The patient’s quadriceps reflex was 1+ on both sides. The blood count revealed eosinophilia with normal platelet count. Prothrombin time, activated partial thrombin time, and findings on lumbosacral spine radiographs were normal. MR imaging of the lumbosacral spine showed a long, segmental hyperintensity along the cauda equina on T1-weighted (Fig 1A, B) and T2-weighted (Fig 1C, D) images. Postgadolinium injection with fat suppression images showed a long, segmental linear enhancement along the cauda equina and increased enhancement of the conus medullaris (Fig 1E), while the axial images showed irregular enhancement of both the cauda equina (Fig 1F) and the conus medullaris (Fig 1G).
Lumbar puncture showed xanthochromic CSF. The CSF opening pressure was 180 mm H2O; the white blood cell count, 750 cells/mm3 (lymphocytes 63%, eosinophils 27%, neutrophils 7%); the red blood cell count, 5650 cells/mm3; protein, 182 mg/dL; and glucose, 11 mg/dL (plasma glucose, 119 mg/dL), or 9% compared with plasma glucose. No bacteria or fungi were cultured. The serum was found to be positive for Gnathostoma spinigerum after immunoblotting by using the 24-kDa diagnostic band and negative for Angiostrongylus cantonensis (the same technique but by using the 31-kDa diagnostic band).
The patient received prednisolone 1 mg/kg/dose for 3 weeks and felt relief from the severe radicular pain. One month after treatment with rehabilitation and bladder training, the patient gradually improved motor control and urinary continence. After 6 months, she had no noticeable motor weakness or incontinence. MR imaging of the lumbosacral spine at 9-month follow-up showed improvement (Fig 2). The long hyperintensity along the cauda equina disappeared on T1- and T2-weighted images (Fig 2A, B). The roots of the cauda equina appeared clumped together on T2-weighted images (Fig 2B). Postgadolinium imaging showed contrast enhancement of cauda equina (Fig 2C).
Discussion
The clinical manifestation of this patient corresponded with a cauda equina syndrome, and MR imaging showed a long segmental hyperintensity along the cauda equina. Postgadolinium injection showed irregular-shaped enhancement at the cauda equina and conus medullaris. These findings suggested a subacute hemorrhage at the cauda equina and an inflammatory process at the terminus of the cord.
Differential causes of bleeding in the cauda equina include bleeding diathesis (2), parasitic infestation (gnathostomiasis), or bleeding tumor (3). The patient did not have any other bleeding disorder or evidence of malignancy. The sudden sacral pain with radicular pain to both legs is not characteristic of tumor pain (4, 5) and was consistent with gnathostomiasis infection. The mechanisms of bleeding caused by Gnathostoma spinigerum include tissue and vascular injury (6, 7).
A lumbar puncture, which demonstrated xanthochromic CSF with eosinophils (>10%) suggested gnathostomiasis (1, 8). The diagnosis was confirmed through the positive serum immunoblotting test by using the 24-kDa diagnostic band.
The presence of eosinophils in the CSF can be caused by Angiostrongylus cantonensis. We therefore performed immunoblotting for A. cantonensis as well, but the result was negative. There is, in fact, no report of any case of spinal cord lesion or bleeding tracts from Angiostronyliasis, probably because it is a smaller organism than Gnathostoma spinigerum. The enhancement of the terminal lumbar cord with enhancement was similar with a previous report of spinal gnathostomiasis (1). The eosinophilia at the initial presentation supported the diagnosis of this tissue parasite.
Antihelmintics, such as albendazole, or corticosteroids, have not been proved effective against neurologic gnathostomiasis (6, 9). Corticosteroids are believed to reduce the inflammatory process in damaged tissue (6). We therefore treated the patient with prednisolone (1 mg/kg/d) for 3 weeks, and she gradually improved. In 1 month, her severe radicular pain was relieved followed by recovery of motor strength and sensory acuity, and, after 4 months, she regained urinary continence. At 9 months, the MR imaging of lumbosacral region improved (Fig 2) and she had no residual neurologic deficit.
Acknowledgments
The authors thank the patient for allowing us to report the case and Mr. Bryan Roderick Hamman for assistance with the English-language presentation of the manuscript.
References
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