OBJECTIVE: Spinal epidural lipomatosis (SEDL) is a rare disorder often
associated with the administration of exogenous steroids or the eleva
tion of endogenous steroids. Spinal epidural lipomatosis develops in s
ome patients in the absence of elevated steroid levels. The limited in
formation known about idiopathic SEDL comes predominantly from isolate
d case reports. We proposed to study our experience with idiopathic SE
DL and to review the literature. METHODS: We identified eight symptoma
tic patients with idiopathic SEDL treated at our institution, which is
the largest series reported. AII patients were male and obese by body
mass index (>27.5 kg/m(2)). The mean age of the patients was 35.4 yea
rs. Idiopathic SEDL was equally distributed between the thoracic and l
umbar spine. Six patients underwent laminectomy and fat debulking with
good postoperative results; two patients were treated with a weight l
oss diet, which resulted in the relief of symptoms after losing >15 kg
each. RESULTS AND CONCLUSION: A review of our patients in conjunction
with other reported cases reveals the following: 1) idiopathic SEDL o
ccurs almost exclusively in the obese population; 2) idiopathic SEDL s
eems to occur with equal frequency between the thoracic and lumber spi
ne; 3) a strong male predominance exists; 4) thoracic SEDL presents at
an earlier age compared with lumbar SEDL; 5) surgical decompression r
emains the treatment of choice for the immediate relief of symptoms. O
ur experience suggests that idiopathic epidural lipomatosis may be a p
athological entity that has been underdiagnosed.