Journal of the Korean Association of Oral and Maxillofacial Surgeons

The Korean Association of Oral and Maxillofacial Surgeons (대한구강악안면외과학회)
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Classical oral manifestations of Dyke-Davidoff-Masson syndrome: a case report with review of the literature

  • Kalaskar, Ritesh (Department of Pediatric & Preventive Dentistry, Government Dental College & Hospital) ;
  • Kalaskar, Ashita Ritesh (Department of Oral Medicine & Radiology, Government Dental College & Hospital)
  • Received : 2017.06.17
  • Accepted : 2017.08.16
  • Published : 2018.08.31
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Abstract

Dyke-Davidoff-Masson syndrome is a non-inherited rare condition that presents during childhood and is characterized by seizures, hemiplegia, mental retardation, cerebral hemiatrophy, calvarial thickening, and hyperpneumatization of the frontal sinuses. The present article highlights a case of a 12-year-old male child with additional clinical findings of $caf{\acute{e}}$-au-late pigmentation and ocular lipodermoid. This is the first case report of DykeDavidoff-Masson syndrome to describe oral manifestations, such as unilateral delayed eruption of teeth, hypoplasia, and taurodontism, which could be unique and characteristic of this condition. Oral health care providers and physicians should be aware of these oral observations as dental referrals could warrant early dental prophylactic care and can be useful in diagnosing the possible time of injury and type of Dyke-Davidoff-Masson syndrome.

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References

  1. Dyke CG, Davidoff LM, Masson CB. Cerebral hemiatrophy and homolateral hypertrophy of the skull and sinuses. Surg Gynecol Obstet 1933;57:588-600.
  2. Aguiar PH, Liu CW, Leitao H, Issa F, Lepski G, Figueiredo EG, et al. MR and CT imaging in the Dyke-Davidoff-Masson syndrome. Report of three cases and contribution to pathogenesis and differential diagnosis. Arq Neuropsiquiatr 1998;56:803-7. https://doi.org/10.1590/S0004-282X1998000500016
  3. Singh P, Saggar K, Ahluwalia A. Dyke-Davidoff-Masson syndrome: classical imaging findings. J Pediatr Neurosci 2010;5:124-5. https://doi.org/10.4103/1817-1745.76108
  4. Sener RN, Jinkins JR. MR of craniocerebral hemiatrophy. Clin Imaging 1992;16:93-7. https://doi.org/10.1016/0899-7071(92)90119-T
  5. Stred SE, Byrum CJ, Bove EL, Oliphant M. Coarctation of midaortic arch presenting with monoparesis. Ann Thorac Surg 1986;42:210-2. https://doi.org/10.1016/S0003-4975(10)60522-X
  6. Demir Y, Surucu E, Cilingir V, Bulut MD, Tombul T. Dyke-Davidoff-Masson syndrome with cerebral hypometabolism and unique crossed cerebellar diaschisis in 18F-FDG PET/CT. Clin Nucl Med 2015;40:757-8. https://doi.org/10.1097/RLU.0000000000000890
  7. Shrestha B. Acquired cerebral hemiatrophy: Dyke-Davidoff-Masson syndrome--a case report. Turk Neurosurg 2013;23:117-21.
  8. Solomon GE, Hilal SK, Gold AP, Carter S. Natural history of acute hemiplegia of childhood. Brain 1970;93:107-20. https://doi.org/10.1093/brain/93.1.107
  9. Uduma FU, Emejulu JK, Motah M, Okere PC, Ongolo PC, Muna W. Differential diagnoses of cerebral hemiatrophy in childhood: a review of literature with illustrative report of two cases. Glob J Health Sci 2013;5:195-207.
  10. Arora R, Rani JY. Dyke-Davidoff-Masson syndrome: imaging features with illustration of two cases. Quant Imaging Med Surg 2015;5:469-71.
  11. Dutta A, Bose S, Sen K, Pandit N, Sharma S. Refractory seizure in childhood: Dyke-Davidoff-Masson syndrome revisited. Oman Med J 2016;31:304-8. https://doi.org/10.5001/omj.2016.58
  12. Kumar NV, Gugapriya TS, Guru AT, Kumari SN. Dyke-Davidoff-Masson syndrome. Int J Appl Basic Med Res 2016;6:57-9. https://doi.org/10.4103/2229-516X.174016
  13. Jain D, Aggarwal HK, Goyal S, Mittal A. Dyke-Davidoff-Masson syndrome: a rare case report. Iran J Neurol 2014;13:255-6.
  14. Shen WC, Chen CC, Lee SK, Ho YJ, Lee KR. Magnetic resonance imaging of cerebral hemiatrophy. J Formos Med Assoc 1993;92:995-1000.
  15. Roy U, Panwar A, Mukherjee A, Biswas D. Adult presentation of Dyke-Davidoff-Masson syndrome: a case report. Case Rep Neurol 2016;8:20-6. https://doi.org/10.1159/000443521
  16. Behera MR, Patnaik S, Mohanty AK. Dyke-Davidoff-Masson syndrome. J Neurosci Rural Pract 2012;3:411-3. https://doi.org/10.4103/0976-3147.102646
  17. Kumar LSV. Cafe au lait spot: case report. J Adv Clin Res Insights 2014;1:106-7. https://doi.org/10.15713/ins.jcri.27
  18. Bhallil S, Benatiya I, El Abdouni O, Mahjoubi B, Hicham T. Goldenhar syndrome: ocular features. Bull Soc Belge Ophtalmol 2010:17-9.
  19. Sethi NK, Sethi PK, Torgovnick J, Arsura E. Acquired Dyke-Davidoff-Masson syndrome: a clinicoradiographic correlation. Eastern J Med 2011;16:269-71.
  20. Witkop CJ Jr, Keenan KM, Cervenka J, Jaspers MT. Taurodontism: an anomaly of teeth reflecting disruptive developmental homeostasis. Am J Med Genet Suppl 1988;4:85-97.
  21. Varghese B, Aneesh M, Singh N, Gilwaz P. A case of rasmussen encephalitis: the differential diagnoses and role of diagnostic imaging. Oman Med J 2014;29:67-70. https://doi.org/10.5001/omj.2014.15
  22. Auvin S, Bellavoine V, Merdariu D, Delanoe C, Elmaleh- Berges M, Gressens P, et al. Hemiconvulsion-hemiplegia-epilepsy syndrome: current understandings. Eur J Paediatr Neurol 2012;16:413-21. https://doi.org/10.1016/j.ejpn.2012.01.007
  23. Qiu BP, Shi CH. Silver-Russel syndrome: a case report. World J Pediatr 2007;3:68-70.
  24. Moon WK, Chang KH, Kim IO, Han MH, Choi CG, Suh DC, et al. Germinomas of the basal ganglia and thalamus: MR findings and a comparison between MR and CT. AJR Am J Roentgenol 1994;162:1413-7. https://doi.org/10.2214/ajr.162.6.8192009
  25. Amor DJ, Kornberg AJ, Smith LJ. Encephalocraniocutaneous lipomatosis (Fishman syndrome): a rare neurocutaneous syndrome. J Paediatr Child Health 2000;36:603-5. https://doi.org/10.1046/j.1440-1754.2000.00541.x
  26. Jacoby CG, Go RT, Hahn FJ. Computed tomography in cerebral hemiatrophy. AJR Am J Roentgenol 1977;129:5-9. https://doi.org/10.2214/ajr.129.1.5

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