IntroductionWith a worldwide incidence of 0.4% [1], gout is a prevalent metabolic disorder that results from the inappropriate metabolism of uric acid and deposition of monosodium urate crystals in tissues [2]. While gout is typically associated with an inflammatory arthritis of the peripheral joints, gouty involvement of the axial spine is a well-known and underreported source of back pain, radiculopathy, myelopathy, and even paraplegia [1][2][3][4]. Since Koskoff et al. described the first case of extradural gout causing paraplegia [5], the radiographic prevalence of axial spine gout has been estimated to be between 14% and 35% in patients with poorly controlled hyperuricemia [2,[6][7][8].Though spinal gout can involve any portion of the spine, the preponderance of lesions occur in the lumbar spine [1,2,4,7,8], and more than 80% of patients with gout may harbor multiple gouty lesions [2,4]. The clinical diagnosis of spinal gout remains a challenge because the common presenting findings such as fever, leukocytosis, and elevated systemic inflammatory markers such as sedimentation rate more commonly suggest infection [9][10][11][12]. Fortunately, characteristic findings on magnetic resonance imaging (MRI) [13,14], computed tomography (CT) [15,16], or ultrasound [17] serve as useful adjuncts for proper diagnosis of spinal gout. Successful medical and surgical management of spinal gout has been previously described in the literature [1,4,[18][19][20].Whereas tophaceous gout of the calvarium [21], infratemporal fossa [22], middle ear [22,23], and cervicomedullary junction with involvement of lower cranial nerves [24] have been reported in the past, to our knowledge, intradural tophaceous gout has not been described. We present the first case of an individual with gouty tophi involving the cavernous sinus and the intradural spinal compartment.
Case PresentationA 61-year-old, African-American male with stage 1 chronic kidney disease, hypertension, and gout (uric acid levels <7.0 mg/dL maintained on allopurinol) presented to the outpatient neurosurgery clinic with headaches, diplopia, masticatory difficulty, and neuralgia along the third division of the left trigeminal nerve. On examination, he was found to have left abducens palsy, weakness of the left masseter, and trismus. MRI of the brain revealed a large lesion in the lateral wall of the left cavernous sinus and Meckel's cave as well as an incidental lipoma. The lesion appeared hypointense on T1-and T2-weighted images and demonstrated contrast enhancement. The soft tissue mass extended into the infratemporal and pterygopalatine fossae via the foramina ovale and rotundum, respectively ( Figure 1A-1C). Marked denervation atrophy of the masticator and pterygoid muscles was also noted. Follow-up MRI of the brain demonstrated further extension of the mass into the left superior orbital fissure. Surgical resection via a trans-Sylvian corridor was undertaken to prevent permanent ophthalmoplegia and blindness. Intra-operatively the cavernous sinus dura appeared thickened...