Journals / Balkan Medical Journal / 2016 / Cilt: 33 - Sayı: 6

Frequency of Nerve Root Sleeve Cysts in Autosomal Dominant Polycystic Kidney Disease

Pages
652–656
Publication Date
2022-10-11
DOI
—
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Results: Spinal meningeal cysts were more numerous and larger in patients than in controls (14.8±11.6 vs. 6.4±4.6 cysts respectively, p

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Objective & Hypothesis:Background: There is sporadic data about the occurrence of spinal meningeal cysts in patients with autosomal dominant polycystic kidney disease (ADPKD).
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Key Findings & Data:Methods: We enrolled 50 patients with ADPKD and 37 healthy volunteers.
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Conclusion & Impact:Results: Spinal meningeal cysts were more numerous and larger in patients than in controls (14.8±11.6 vs. 6.4±4.6 cysts respectively, p
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background: There is sporadic data about the occurrence of spinal meningeal cysts in patients with autosomal dominant polycystic kidney disease (ADPKD). We suggest that there is a relationship with the frequency and size of spinal meningeal cysts and headache, intracranial aneurysms, and cerebrospinal fluid leakage in patients with ADPKD. Aim: To investigate the relationship with spinal meningeal cyst, cerebrospinal fluid leakage, and headache in patients with ADPKD. Study Design: Cross-sectional study. Methods: We enrolled 50 patients with ADPKD and 37 healthy volunteers. This cross-sectional study included patients with ADPKD and matched healthy volunteers. Magnetic resonance imaging myelography was performed using the 3D-T2 HASTE technique in an MRI scanner. We questioned our subjects regarding presence of headache and evaluated headache severity using a visual analog scale. The relationship between the number and size of spinal meningeal cysts with headache, intracranial aneurysms, and liver cysts was also investigated. Results: Spinal meningeal cysts were more numerous and larger in patients than in controls (14.8±11.6 vs. 6.4±4.6 cysts respectively, p

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Cite This Article

ALTIPARMAK, M. R., CEYHAN, E., ALBAYRAM, S., IŞIK, Z. H., AKALIN, N., TUNÇ, N., AŞIK, M., AKPINAR, T. S., ECDER, T., TUFAN, F. (2022). Frequency of Nerve Root Sleeve Cysts in Autosomal Dominant Polycystic Kidney Disease. Balkan Medical Journal, Cilt: 33 - Sayı: 6, 652–656. https://ajindex.com/articles/461345

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References (3)

  1. Ecder T F-BG, Schrier RW. Polycystic kidney disease. In: Schri- er RW, ed. Diseases of the kidney and urinary tract. Philadel- phia: Williams & Wilkins; 2007:502-39.
  2. Schievink WI, Torres VE. Spinal meningeal diverticula in autosomal dominant polycystic kidney disease. Lancet 1997;349:1223-4. [CrossRef] Albayram S, Baş A, Ozer H, Dikici S, Gulertan SY, Yuksel A. Spontaneous intracranial hypotension syndrome in a patient with marfan syndrome and autosomal dominant polycystic kid- ney disease. Headache 2008;48:632-6. [CrossRef] Schievink WI, Meyer FB, Atkinson JLD, Mokri B. Spontaneous spinal cerebrospinal fluid leaks and intracranial hypotension. J Neurosurg 1996;84:598-605. [CrossRef] Schievink WI, Ebersold MJ, Atkinson JL. Roller-coast- er headache due to spinal cerebrospinal fluid leak. Lancet 1996;347:1409. [CrossRef] Gabow PA. Autosomal dominant polycystic kidney disease- -more than a renal disease. Am J Kidney Dis 1990;16:403-13. [CrossRef] Igarashi P, Somlo S. Genetics and pathogenesis of polycystic kidney disease. J Am Soc Nephrol 2002;13:2384-98. [CrossRef] Torres VE, Harris PC, Pirson Y. Autosomal dominant polycystic kidney disease. Lancet 2007;369:1287-301. [CrossRef] Takagi H, Umemoto T. Matrix metalloproteinases synthesized in autosomal dominant polycystic kidney disease play a role in development of a concurrent abdominal aortic aneurysm. Med Hypotheses 2005;64:778-81. [CrossRef] Hateboer N, v Dijk MA, Bogdanova N, Coto E, Saggar-Malik AK, San Millan JL, et al. Comparison of phenotypes of polycys- tic kidney disease types 1 and 2. European PKD1-PKD2 Study Group. Lancet 1999;353:103-7. [CrossRef] Romao EA, Moyses Neto M, Teixeira SR, Muglia VF, Vieira- Neto OM, Dantas M. Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease. Braz J Med Biol Res 2006;39:533-8. [CrossRef] Chauveau D, Fakhouri F, Grunfeld JP. Liver involvement in autosomal-dominant polycystic kidney disease: therapeutic di- lemma. J Am Soc Nephrol 2000;11:1767-75.
  3. Itai Y, Ebihara R, Eguchi N, Saida Y, Kurosaki Y, Minami M, et al. Hepatobiliary cysts in patients with autosomal dominant polycystic kidney disease: prevalence and CT findings. AJR Am J Roentgenol 1995;164:339-42. [CrossRef] Tahvanainen E, Tahvanainen P, Kaariainen H, Höckerstedt K. Polycystic liver and kidney diseases. Ann Med 2005;37:546-55. [CrossRef] Xu HW, Yu SQ, Mei CL, Li MH. Screening for intracranial aneurysm in 355 patients with autosomal-dominant polycystic kidney disease. Stroke