J Neurol Surg B Skull Base 2018; 79(06): 614-620
DOI: 10.1055/s-0038-1651501
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Skull Base Dural Thickness and Relationship to Demographic Features: A Postmortem Study and Literature Review

Maged D. Fam
1   Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States
,
Andrea Potash
2   Department of Otolaryngology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States
,
Martin Potash
3   Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States
,
Robert Robinson
3   Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States
,
Lucy Karnell
2   Department of Otolaryngology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States
,
Erin O'Brien
4   Department of Otorhinolaryngology, Mayo Clinic, Rochester, Minnesota, United States
,
Jeremy D. W. Greenlee
1   Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States
› Author Affiliations
Further Information

Publication History

16 December 2017

31 March 2018

Publication Date:
05 June 2018 (online)

Abstract

Dural membrane is an important anatomic structure that surrounds and protects the entire central nervous system. Physical properties of the dura have many pathophysiological and therapeutic implications in cranial surgery, especially skull base disorders. The aim of this study is to investigate variation in skull base dural thickness and correlation with different demographic parameters. At the time of autopsy, the petrous apex dura with the underlying bone of 20 cadavers was harvested. Dural thickness was independently measured by two pathologists at the thinnest and thickest segments in the specimen. Correlational analyses were then performed to compare dural thickness with gender, age, neck circumference, height, weight, and body mass index (BMI). Mean, minimum, and maximum skull base dural thickness in our study was 0.36, 0.27, and 0.46 mm, respectively. Age demonstrated a negative correlation with dural thickness with significantly thinner dura in the older subjects, p = 0.01. There was a trend toward thinner dura in females that approached statistical significance, p = 0.06. No strong correlation could be found with body weight, height, neck circumference, or BMI. Our findings show a considerable intersubject and intrasubject variability in skull base dural thickness. Some demographic parameters also seem to impact dural thickness. Additional histological studies are needed for better understanding of the pathophysiological mechanisms pertaining to the tensile properties of the dural membrane.

 
  • References

  • 1 Mack J, Squier W, Eastman JT. Anatomy and development of the meninges: implications for subdural collections and CSF circulation. Pediatr Radiol 2009; 39 (03) 200-210
  • 2 Squier W, Lindberg E, Mack J, Darby S. Demonstration of fluid channels in human dura and their relationship to age and intradural bleeding. Childs Nerv Syst 2009; 25 (08) 925-931
  • 3 Yew M, Dubbs B, Tong O. , et al. Arachnoid granulations of the temporal bone: a histologic study of dural and osseous penetration. Otol Neurotol 2011; 32 (04) 602-609
  • 4 Gacek RR. Arachnoid granulation cerebrospinal fluid otorrhea. Ann Otol Rhinol Laryngol 1990; 99 (11) 854-862
  • 5 Gacek RR, Gacek MR. Arachnoid granulations of the temporal bone. Am J Otol 1999; 20 (03) 405-406
  • 6 Bech RA, Waldemar G, Gjerris F, Klinken L, Juhler M. Shunting effects in patients with idiopathic normal pressure hydrocephalus; correlation with cerebral and leptomeningeal biopsy findings. Acta Neurochir (Wien) 1999; 141 (06) 633-639
  • 7 LeVay AJ, Kveton JF. Relationship between obesity, obstructive sleep apnea, and spontaneous cerebrospinal fluid otorrhea. Laryngoscope 2008; 118 (02) 275-278
  • 8 Schlosser RJ, Wilensky EM, Grady MS, Bolger WE. Elevated intracranial pressures in spontaneous cerebrospinal fluid leaks. Am J Rhinol 2003; 17 (04) 191-195
  • 9 Schlosser RJ, Woodworth BA, Wilensky EM, Grady MS, Bolger WE. Spontaneous cerebrospinal fluid leaks: a variant of benign intracranial hypertension. Ann Otol Rhinol Laryngol 2006; 115 (07) 495-500
  • 10 Scurry Jr WC, Ort SA, Peterson WM, Sheehan JM, Isaacson JE. Idiopathic temporal bone encephaloceles in the obese patient. Otolaryngol Head Neck Surg 2007; 136 (06) 961-965
  • 11 Seth R, Rajasekaran III K, Luong A, Benninger MS, Batra PS. Spontaneous CSF leaks: factors predictive of additional interventions. Laryngoscope 2010; 120 (11) 2141-2146
  • 12 Stucken EZ, Selesnick SH, Brown KD. The role of obesity in spontaneous temporal bone encephaloceles and CSF leak. Otol Neurotol 2012; 33 (08) 1412-1417
  • 13 Kuchiwaki H, Inao S, Ishii N, Ogura Y, Gu SP. Human dural thickness measured by ultrasonographic method: reflection of intracranial pressure. J Ultrasound Med 1997; 16 (11) 725-730
  • 14 Qureshi AI, Lobanova I, Ullah N. , et al. Prevalence of and factors associated with dural thickness in patients with mild cognitive impairment and Alzheimer's disease. J Vasc Interv Neurol 2015; 8 (03) 68-73
  • 15 Reina MA, Dittmann M, López Garcia A, van Zundert A. New perspectives in the microscopic structure of human dura mater in the dorsolumbar region. Reg Anesth 1997; 22 (02) 161-166
  • 16 Reina MA, López-García A, Dittmann M, de Andrés JA. Structural analysis of the thickness of human dura mater with scanning electron microscopy [in Spanish]. Rev Esp Anestesiol Reanim 1996; 43 (04) 135-137
  • 17 Patin DJ, Eckstein EC, Harum K, Pallares VS. Anatomic and biomechanical properties of human lumbar dura mater. Anesth Analg 1993; 76 (03) 535-540
  • 18 Vandenabeele F, Creemers J, Lambrichts I. Ultrastructure of the human spinal arachnoid mater and dura mater. J Anat 1996; 189 (Pt 2): 417-430
  • 19 Willatt DJ, Yung MW, Helliwell TR. A correlation of the surgical anatomy of the dura to head and neck surgery. Arch Otorhinolaryngol 1987; 243 (06) 403-406
  • 20 Kwon S, Suh SW, Kim D. , et al. Analysis of dural sac thickness in the human cervical spine. Anat Sci Int 2018; 93 (02) 284-290
  • 21 Hong JY, Suh SW, Park SY. , et al. Analysis of dural sac thickness in human spine-cadaver study with confocal infrared laser microscope. Spine J 2011; 11 (12) 1121-1127
  • 22 Maikos JT, Elias RA, Shreiber DI. Mechanical properties of dura mater from the rat brain and spinal cord. J Neurotrauma 2008; 25 (01) 38-51
  • 23 Ivan ME, Iorgulescu JB, El-Sayed I. , et al. Risk factors for postoperative cerebrospinal fluid leak and meningitis after expanded endoscopic endonasal surgery. J Clin Neurosci 2015; 22 (01) 48-54
  • 24 Boling CC, Karnezis TT, Baker AB. , et al. Multi-institutional study of risk factors for perioperative morbidity following transnasal endoscopic pituitary adenoma surgery. Int Forum Allergy Rhinol 2016; 6 (01) 101-107