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A Giant Tarlov Cyst Presenting with Hydronephrosis in a Patient with Marfan Syndrome: A Case Report and Review of the Literature

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Συγγραφέας
Paterakis K., Brotis A., Bakopoulou M., Rountas C., Dardiotis E., Hadjigeorgiou G.M., Fountas K.N., Karantanas A.
Ημερομηνία
2019
Γλώσσα
en
DOI
10.1016/j.wneu.2019.02.222
Λέξη-κλειδί
contrast medium
abdominal radiography
adult
Article
case report
cerebrospinal fluid drainage
clinical article
computer assisted tomography
contrast enhancement
dura mater
female
fifth lumbar vertebra
giant Tarlov cyst
human
hydronephrosis
hypesthesia
laminectomy
lumbar spine
lumbosacral region
Marfan syndrome
meningocele
nephrostomy
nuclear magnetic resonance imaging
paraspinal muscle
sacral vertebra
scoliosis
spinal root
Tarlov cyst
three dimensional imaging
ureter dilatation
ureter obstruction
wound closure
complication
diagnostic imaging
hydronephrosis
lumbosacral plexus
Marfan syndrome
motor evoked potential
pathophysiology
percutaneous nephrostomy
symptom assessment
Tarlov cyst
ureter obstruction
x-ray computed tomography
Adult
Evoked Potentials, Motor
Female
Humans
Hydronephrosis
Lumbosacral Plexus
Magnetic Resonance Imaging
Marfan Syndrome
Nephrostomy, Percutaneous
Symptom Assessment
Tarlov Cysts
Tomography, X-Ray Computed
Ureteral Obstruction
Wound Closure Techniques
Elsevier Inc.
Εμφάνιση Μεταδεδομένων
Επιτομή
Background: Giant Tarlov cysts are always symptomatic and mimic many serious pathologic entities. We present the largest, to our knowledge, reported Tarlov cyst. Case Description: A 33-year-old woman with Marfan syndrome suffered from right kidney hydronephrosis because of ureter obstruction, for which she was treated with nephrostomy. Her neurologic examination was unremarkable. The role of magnetic resonance imaging in the management of this case is described. Absence of intractranial hypotension symptoms after cerebrospinal fluid (CSF) overdrainage suggested the presence of a valve-like mechanism. The patient was planned for surgical cyst remodeling by the application of titanium clips. The cyst's neck was exposed through an L5-S2 laminectomy. L5 and S1 laminae were severely eroded. CSF leaked out of the underlying, bulging, and thinned dura at each attempt for clip application. Intraoperatively, multiple responses from the S1, S2, and S3 roots were simultaneously recorded at each stimulation. Therefore, we decided to abandon this technique and performed a nonwatertight duroplasty followed by a layered wound closure instead. A week later, the patient received a lumbar-peritoneal shunt. The patient remained neurologically intact, the cyst shrunk, and the nephrostomy was removed. Conclusions: Indirect evidence was helpful to assess for the presence of a valve-like mechanism. Intraoperatively, the surgeon must keep on high alert for sacral erosion to avoid inadvertent dural tear and rootlet injury. Finally, lumboperitoneal diversion remains a valid alternative in the management of our giant Tarlov cyst because it reduced the intracystic pressure that resulted in cyst regression. © 2019 Elsevier Inc.
URI
http://hdl.handle.net/11615/77974
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