J Neurol Surg A Cent Eur Neurosurg 2023; 84(03): 288-294
DOI: 10.1055/s-0041-1725960
Case Report

The Sensorineural Hearing Loss Related to a Rare Infratentorial Developmental Venous Angioma: A Case Report and Review of Literature

Kaveh Ebrahimzadeh
1   Department of Neurosurgery, Skull Base Research Center, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
,
1   Department of Neurosurgery, Skull Base Research Center, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
,
Seyed Ali Mousavinejad
1   Department of Neurosurgery, Skull Base Research Center, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
,
Mohammad Ansari
1   Department of Neurosurgery, Skull Base Research Center, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
,
Reyhaneh Kazemi
2   Medical Researcher, Skull Base Research Center, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
,
Hooman Bahrami-Motlagh
3   Department of Radiology, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
,
Reza Jalili Khoshnoud
4   Department of Neurosurgery, Functional Neurosurgery Research Center, Shahid Beheshti University of Medical Sciences, Shohada-e-Tajrish Hospital, Tehran, Iran
,
Guive Sharifi
1   Department of Neurosurgery, Skull Base Research Center, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
,
Mohammad Samadian
1   Department of Neurosurgery, Skull Base Research Center, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
,
Omidvar Rezaei
1   Department of Neurosurgery, Skull Base Research Center, Shahid Beheshti University of Medical Sciences, Loghman Hakim Hospital, Tehran, Iran
› Author Affiliations

Abstract

Background Developmental venous anomaly (DVA) is a benign venous abnormality draining normal brain parenchyma. It is mostly asymptomatic; however, rare complications such as hemorrhage may lead to symptomatic conditions. Headache and seizure are the most common symptoms. Hearing loss is an extremely rare presentation of DVA. To our knowledge, only five cases of DVA, presenting with hearing loss, had been reported so far.

Case Presentation We report the case of a 27-year-old woman who presented with a sensorineural hearing loss followed by facial paresis. Magnetic resonance imaging (MRI) and computed tomography (CT) angiography revealed hematoma with adjacent converging veins showing a typical “caput medusa” sign in the left middle cerebellar peduncle, in favor of DVA. Due to the compression effect of hematoma, she underwent surgery. Hearing loss and facial paresis improved significantly during the postoperative follow-up.

Conclusion Although DVA is mostly benign and asymptomatic, complications such as hemorrhage rarely occur. Hearing loss is an extremely rare presentation that can be attributable to the compression effect on the cranial nerve VII to VIII complex. In the case of compression effect or progression of symptoms, surgical intervention is necessary. A good clinical outcome could be expected postoperatively.



Publication History

Received: 21 August 2020

Accepted: 16 December 2020

Article published online:
14 June 2021

© 2021. Thieme. All rights reserved.

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  • References

  • 1 Numaguchi Y, Kitamura K, Fukui M. et al. Intracranial venous angiomas. Surg Neurol 1982; 18 (03) 193-202
  • 2 Rigamonti D, Spetzler RF, Drayer BP. et al. Appearance of venous malformations on magnetic resonance imaging. J Neurosurg 1988; 69 (04) 535-539
  • 3 Roux A, Edjlali M, Porelli S. et al. Developmental venous anomaly in adult patients with diffuse glioma: a clinically relevant coexistence?. Neurology 2019; 92 (01) e55-e62
  • 4 Sarwar M, McCormick WF. Intracerebral venous angioma. Case report and review. Arch Neurol 1978; 35 (05) 323-325
  • 5 Garner TB, Del Curling Jr O, Kelly Jr DL, Laster DW. The natural history of intracranial venous angiomas. J Neurosurg 1991; 75 (05) 715-722
  • 6 Rigamonti D, Spetzler RF, Medina M, Rigamonti K, Geckle DS, Pappas C. Cerebral venous malformations. J Neurosurg 1990; 73 (04) 560-564
  • 7 Li X, Wang Y, Chen W. et al. Intracerebral hemorrhage due to developmental venous anomalies. J Clin Neurosci 2016; 26: 95-100
  • 8 Robert T, Villard J, Oumarou G, Daniel RT, Pollo C, Uské A. Intracerebellar hemorrhage caused by developmental venous anomaly, from diagnosis to treatment. J Neurol Surg A Cent Eur Neurosurg 2013; 74 (01, Suppl 1): e275-e278
  • 9 McLaughlin MR, Kondziolka D, Flickinger JC, Lunsford S, Lunsford LD. The prospective natural history of cerebral venous malformations. Neurosurgery 1998; 43 (02) 195-200 , discussion 200–201
  • 10 Ruíz DS, Yilmaz H, Gailloud P. Cerebral developmental venous anomalies: current concepts. Ann Neurol 2009; 66 (03) 271-283
  • 11 Fierstien SB, Pribram HW, Hieshima G. Angiography and computed tomography in the evaluation of cerebral venous malformations. Neuroradiology 1979; 17 (03) 137-148
  • 12 Valavanis A, Wellauer J, Yaşargil MG. The radiological diagnosis of cerebral venous angioma: cerebral angiography and computed tomography. Neuroradiology 1983; 24 (04) 193-199
  • 13 Aoki R, Srivatanakul K. Developmental venous anomaly: benign or not benign. Neurol Med Chirur 2016; 56 (09) 534-543
  • 14 Senegor M, Dohrmann GJ, Wollmann RL. Venous angiomas of the posterior fossa should be considered as anomalous venous drainage. Surg Neurol 1983; 19 (01) 26-32
  • 15 Ferrante L, Acqui M, Trillò G, Antonio M, Nardacci B, Celli P. Cavernous angioma of the VIIIth cranial nerve. A case report. Neurosurg Rev 1998; 21 (04) 270-276
  • 16 Malinvaud D, Lecanu J-B, Halimi P, Avan P, Bonfils P. Tinnitus and cerebellar developmental venous anomaly. Arch Otolaryngol Head Neck Surg 2006; 132 (05) 550-553
  • 17 Entezami P, Boulos A, Yamamoto J, Adamo M. Paediatric presentation of intracranial haemorrhage due to thrombosis of a developmental venous anomaly. BMJ Case Rep 2019; 12 (01) bcr-2018-bcr-227362
  • 18 Wu B, Liu W, Zhao Y. Coexistence of extra-axial cavernous malformation and cerebellar developmental venous anomaly in the cerebellopontine angle. World Neurosurg 2012; 78 (3–4): 375.e5-375.e9
  • 19 Rothfus WE, Albright AL, Casey KF, Latchaw RE, Roppolo HM. Cerebellar venous angioma: “benign” entity?. AJNR Am J Neuroradiol 1984; 5 (01) 61-66
  • 20 Huber G, Henkes H, Hermes M, Felber S, Terstegge K, Piepgras U. Regional association of developmental venous anomalies with angiographically occult vascular malformations. Eur Radiol 1996; 6 (01) 30-37
  • 21 San Millán Ruíz D, Delavelle J, Yilmaz H. et al. Parenchymal abnormalities associated with developmental venous anomalies. Neuroradiology 2007; 49 (12) 987-995
  • 22 Sehgal V, Delproposto Z, Haacke EM. et al. Clinical applications of neuroimaging with susceptibility-weighted imaging. J Magn Reson Imaging 2005; 22 (04) 439-450
  • 23 Kim H-T, Lee J-M, Koh E-J, Choi H-Y. Surgery versus conservative treatment for spontaneous supratentorial intracerebral hemorrhage in spot sign positive patients. J Korean Neurosurg Soc 2015; 58 (04) 309-315
  • 24 Kalani MYS, Yagmurlu K, Martirosyan NL, Cavalcanti DD, Spetzler RF. Approach selection for intrinsic brainstem pathologies. J Neurosurg 2016; 125 (06) 1596-1607
  • 25 Cavalcanti DD, Preul MC, Kalani MYS, Spetzler RF. Microsurgical anatomy of safe entry zones to the brainstem. J Neurosurg 2016; 124 (05) 1359-1376
  • 26 Recalde RJ, Figueiredo EG, de Oliveira E. Microsurgical anatomy of the safe entry zones on the anterolateral brainstem related to surgical approaches to cavernous malformations. Neurosurgery 2008; 62(03, Suppl 1):9–15, discussion 15–17
  • 27 Hebb MO, Spetzler RF. Lateral transpeduncular approach to intrinsic lesions of the rostral pons. Neurosurgery 2010; 66(3, Suppl Operative):26–29, discussion 29
  • 28 Baghai P, Vries JK, Bechtel PC. Retromastoid approach for biopsy of brain stem tumors. Neurosurgery 1982; 10 (05) 574-579
  • 29 Bricolo A, Turazzi S. Surgery for gliomas and other mass lesions of the brainstem. In: Simon L, Calliauw L. Cohadon. eds. Advances and technical standards in neurosurgery. New York, NY: Springer; 1995: 261-341
  • 30 Kyoshima K, Kobayashi S, Gibo H, Kuroyanagi T. A study of safe entry zones via the floor of the fourth ventricle for brain-stem lesions. Report of three cases. J Neurosurg 1993; 78 (06) 987-993