lumbosacral lipoma
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Author(s):  
Dominic N. P. Thompson ◽  
Jochem Spoor ◽  
Martje Schotman ◽  
Susan Maestri ◽  
Claudia L. Craven ◽  
...  
Keyword(s):  

2021 ◽  
pp. 39-45
Author(s):  
A.A. SUFIANOV ◽  
◽  
I.S. SHELYAGIN ◽  
M.R. GIZATULLIN ◽  
A.A. SUFIANOV ◽  
...  

To assess the effectiveness of reconstructive plasty of the dura mater in patients with lumbosacral lipomas (LSL) using an original method for controlling the patency of the spinal spaces.


2020 ◽  
Vol 17 (4) ◽  
pp. 77-84
Author(s):  
Albert Akramovich Sufianov ◽  
Marat Rimovich Gizatullin ◽  
Ivan Sergeyevich Sheliagin ◽  
Valentina Vasilyevna Sidorenko

Author(s):  
Yumiko Komori ◽  
Masahiro Nonaka ◽  
Takamasa Kamei ◽  
Junichi Takeda ◽  
Tetsuo Hashiba ◽  
...  

The authors present the case of a 1-month-old girl with a lumbosacral lipoma who then developed an extracanalicular syrinx and experienced rapid deterioration. The patient’s initial MRI study, obtained before she became symptomatic, revealed a spinal lipoma with a syrinx in contact with the lipoma-cord interface. She was initially asymptomatic but developed loss of motor function in the left leg 14 days after MRI. Emergency surgery was performed. Intraoperative findings revealed a swollen spinal cord. Lipomatous tissue on the caudal side of the conus was removed subtotally, and the central canal was opened. Expansion of the syrinx was observed intraoperatively. Postoperatively, the patient’s left leg paresis remained. Postoperative MRI revealed rostral and extracanalicular expansion of the syrinx. This is the first report on the rapid deterioration of a conus lipoma due to extracanalicular expansion of a syrinx. Careful follow-up and repeat MRI should be considered for patients with spinal lipomas with syringomyelia, especially when the syrinx is attached to the lipoma-cord interface.


2019 ◽  
Vol 35 (11) ◽  
pp. 2163-2169 ◽  
Author(s):  
Hugo Layard Horsfall ◽  
Aswin Chari ◽  
Terhi Huttunen ◽  
Clare Simcock ◽  
Felice D’Arco ◽  
...  

Abstract Purpose Lumbosacral lipoma (LSL) is a severe occult spinal dysraphism, frequently associated with neurological, urological and orthopaedic complications. Whole spine imaging is typically performed to identify concomitant, but spatially separate, congenital anomalies. Our hypothesis: the incidence of additional, clinically significant abnormalities of the neuraxis is low; thus, imaging should be optimised at the lumbosacral region. We aim to assess the prevalence and relevance of LSL-associated lesions. Method A single-centre, retrospective, radiological review using a prospectively maintained operative database. Inclusion criteria: children (< 16 years) with confirmed diagnosis of LSL and received whole spine MRI. Fatty filum, syndromic cases and cutaneous stigmata above lesion level were excluded. Data was extracted from radiological imaging, reports and clinical correspondence. Results One hundred twelve patients (40:72, M:F) aged 0.5 years (0.2–2.7) (median ± IQR) with LSL had whole spine MRI between 2001 and 2017. Classification of LSL: transitional 48 (43%); dorsal 30 (27%); caudal 28 (25%) and chaotic 6 (5%). Additional anomalies included syringohydromyelia 44 (39%), subcutaneous tract 19 (17%), abnormal vertebral segmentation 18 (16%), dermoid cyst 1 and 1 Chiari I deformity. There were no Chiari II malformations. No child required surgery for an associated lesion. Binary logistic regression revealed no factors associated with predicting secondary lesions. Conclusions In congenital LSL, additional anomalies of the neuraxis are typically loco-regional rather than pan-CNS and additional lesions are rarely clinically significant. The loco-regional distribution of anomalies suggests that only lumbosacral spinal imaging is required in the initial evaluation of LSL. Such a policy would lessen the anaesthetic/sedation time for children and reduce imaging cost per patient. MRI protocols could be refined to optimise imaging quality at the region of interest.


2019 ◽  
Vol 35 (9) ◽  
pp. 1591-1597
Author(s):  
Sangjoon Chong ◽  
Ji Yeoun Lee ◽  
Kyung Hyun Kim ◽  
Hyung-Ik Shin ◽  
Keewon Kim ◽  
...  

2019 ◽  
Vol 90 (3) ◽  
pp. e27.1-e27
Author(s):  
HL Horsfall ◽  
C Simcock ◽  
F D’Arco ◽  
D Thompson

ObjectivesPaediatric lumbosacral lipomas are commonly assessed by whole spine MRI, which is costly, time consuming and reduces imaging detail at the region of interest. This study evaluates the utility of whole spine vs local spine MRI in paediatric lumbosacral lipoma (LSL).DesignSingle centre, retrospective, radiological review.Subjects119 patients (77F:46M) aged 0.8 years (0.2–3.9) (median ±IQR) with complex LSL who had whole spine MRI between 2001–2017.MethodsLumbosacral lipomas were identified from a prospectively collected database. Cases where whole spine MRI was available were included. Type of lipoma and any associated spinal anomalies were recorded.Results347 patients had LSL, of which 119 (34%) patients had whole spine MRI. 3% were excluded due diagnosis of fatty filum terminale. 13% scans were unavailable. 119 patients were studied: 77F:46M aged 0.8 years at scan. Type of LML: transitional 36%; caudal 18%; dorsal 19%; unclassified 26%. Additional imaging abnormalities included: syrinx 18%; Chiari 1%; dermal sinus tract 13%; vertebral segmentation 13%; other 2%. None were associated with clinical symptoms nor required surgical treatment. Investigating the cost-benefit analysis of modality, lumbar spine required less MR time and cost less (40 vs 20 mins; £228.69 vs £282.39).ConclusionsThe low incidence of clinically relevant secondary lesions suggests that lumbosacral MRI only is necessary in the assessment of LSL. Imaging quality of the ROI can be optimised and MRI time and costs reduced.


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