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dc.creatorPaterakis K., Brotis A., Bakopoulou M., Rountas C., Dardiotis E., Hadjigeorgiou G.M., Fountas K.N., Karantanas A.en
dc.date.accessioned2023-01-31T09:46:14Z
dc.date.available2023-01-31T09:46:14Z
dc.date.issued2019
dc.identifier10.1016/j.wneu.2019.02.222
dc.identifier.issn18788750
dc.identifier.urihttp://hdl.handle.net/11615/77974
dc.description.abstractBackground: 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.en
dc.language.isoenen
dc.sourceWorld Neurosurgeryen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85064317017&doi=10.1016%2fj.wneu.2019.02.222&partnerID=40&md5=94801c463a0a9098569524829713bb04
dc.subjectcontrast mediumen
dc.subjectabdominal radiographyen
dc.subjectadulten
dc.subjectArticleen
dc.subjectcase reporten
dc.subjectcerebrospinal fluid drainageen
dc.subjectclinical articleen
dc.subjectcomputer assisted tomographyen
dc.subjectcontrast enhancementen
dc.subjectdura materen
dc.subjectfemaleen
dc.subjectfifth lumbar vertebraen
dc.subjectgiant Tarlov cysten
dc.subjecthumanen
dc.subjecthydronephrosisen
dc.subjecthypesthesiaen
dc.subjectlaminectomyen
dc.subjectlumbar spineen
dc.subjectlumbosacral regionen
dc.subjectMarfan syndromeen
dc.subjectmeningoceleen
dc.subjectnephrostomyen
dc.subjectnuclear magnetic resonance imagingen
dc.subjectparaspinal muscleen
dc.subjectsacral vertebraen
dc.subjectscoliosisen
dc.subjectspinal rooten
dc.subjectTarlov cysten
dc.subjectthree dimensional imagingen
dc.subjectureter dilatationen
dc.subjectureter obstructionen
dc.subjectwound closureen
dc.subjectcomplicationen
dc.subjectdiagnostic imagingen
dc.subjecthydronephrosisen
dc.subjectlumbosacral plexusen
dc.subjectMarfan syndromeen
dc.subjectmotor evoked potentialen
dc.subjectpathophysiologyen
dc.subjectpercutaneous nephrostomyen
dc.subjectsymptom assessmenten
dc.subjectTarlov cysten
dc.subjectureter obstructionen
dc.subjectx-ray computed tomographyen
dc.subjectAdulten
dc.subjectEvoked Potentials, Motoren
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectHydronephrosisen
dc.subjectLumbosacral Plexusen
dc.subjectMagnetic Resonance Imagingen
dc.subjectMarfan Syndromeen
dc.subjectNephrostomy, Percutaneousen
dc.subjectSymptom Assessmenten
dc.subjectTarlov Cystsen
dc.subjectTomography, X-Ray Computeden
dc.subjectUreteral Obstructionen
dc.subjectWound Closure Techniquesen
dc.subjectElsevier Inc.en
dc.titleA Giant Tarlov Cyst Presenting with Hydronephrosis in a Patient with Marfan Syndrome: A Case Report and Review of the Literatureen
dc.typejournalArticleen


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