A case report of Dyke Davidoff Masson syndrome which is diagnosed in advanced age

Year 2016, Volume: 8 Issue: 4, 222 - 226, 01.12.2016

Ümmü Serpil Sarı Ecenur Aydın Aşık Ayşin Kısabay Hatice Mavioğlu

https://doi.org/10.21601/ortadogutipdergisi.273597

Abstract

Major findings of
Dyke-Davidoff-Masson syndrome (DDMS) are unilateral cerebral atrophy,
contralateral hemiparesis and seizures. DDMS is a cranial malformation which is
described by Dyke and his colleagues in 1933. The etiology of DDMS are trauma,
inflamation, vascular malformations and occlusions. Computerized tomography and
magnetic resonance imaging are the gold standard for diagnosis of DDMS.

In this publication, we want to
emphasize DDMS once more with the rare case of a 55 years old female patient
who had a history of epilepsy since age of 4 
and has epilepsy and facial asymmetry, hemidystonia, mental retardation,
cranial hemiatrophy findings and DDMS diagnosis in advanced age. 

Keywords

Dyke Davidoff Masson syndrome, hemidystonia, seizure

İleri yaşta tanı konulan bir Dyke Davidoff Masson sendromu olgu sunumu

Abstract

Dyke-Davidoff-Masson sendromu (DDMS)
major bulguları unilateral serebral atrofi, kontrolateral hemiparazi ve
nöbetlerle karakterize, ilk kez Dyke  ve
arkadaşları tarafından 1933 yılında  
tanımlanan bir kranial malformasyondur. DDMS sendromunun etiyolojisi
travma, inflamasyon, vasküler malformasyonlar 
ve oklüzyonları içerir. Tanıda altın standart kranial bilgisayarlı
tomografi ve manyetik rezonans görüntülemedir.

Bu yazıda 4 yaşından
beri epilepsi tanısıyla tedavi gören 55 yaşındaki bayan hastanın epilepsiye
eşlik eden fasial asimetri,  hemiparezi,
hemidistoni, mental retardasyon, kraniyal hemiatrofi  bulguları ile ileri yaşta DDMS  tanısı alması nedeniyle nadiren görülen bu
sendromu olgu ve literatür eşliğinde vurgulamak istedik.

Keywords

Dyke Davidoff Masson sendromu, hemidistoni, nöbet

References

• Dyke CG, Davidoff LM, Masson CB: Cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses. Surg Gynecol Obstet 57:588-600, 1933)
• Ünalp A. , Aydoğan AÖ, Dyke-Davidof Masson sendromu- bir olgu sunumu, Ege Tıp Dergisi/ Ege Journal of medicine 46(2): 107-109, 2007)
• Afifi AK, Godersky JC, Menezes A, Smoker WR, Bell WE, Jacoby CG: Cerebral hemiatrophy, hypoplasia of internal carotid artery and intracranial aneurysm. A rare association occurring in an infant. Arch Neurol 44:232-235, 1987
• Ono K, Komai K, Ikeda T: Dyke-Davidoff-Masson syndrome manifested by seizure in late childhood: A case report. J Clin Neurosci 10:367-371, 2003
• Stred SE, Byrum CJ, Bove EL, Oliphant M: Coarctation of the midaortic arch presenting with monoparesis. Ann Thorac Surg 42:210-212, 1986
• Tasdemir HA, Incesu L, Yazicioglu AK, Belet U, Gungor L: Dyke-Davidoff-Masson syndrome. Clin Imaging 26:13-17, 2002
• Sener RN, Jinkins JR: MR of craniocerebral hemiatrophy. Clin Imaging 16:93-97, 1992
• Zilkha A: CT of cerebral hemiatrophy. AJR Am J Roentgenol 135:259-262, 1980
• Dähnert W. Dyke-Davidoff-Masson syndrome. In: Radiology Review Manual. (3th ed). Baltimore: Williams and Wilkins. A Waverly Company, 1996: 204.
• Shetty DS, Lakhkar NB, John JR. Dyke-Davidoff-Masson syndrome. Neurology India 2003; 51: 136-139.
• Winkler DT, Probst A, Wegmann W, Tolnay N. Dyke- Davidoff-Masson syndrome with crossed cerebellar atrophy: an old disease in a new millenium. Neuropathol Appl Neurobiol 2001; 27: 403-405.
• Romeo Araujo D, Pego Reigosa R, Branas Fernandez F, et al. Contralateral cerebellar atrophy in the Dyke- Davidoff-Masson syndrome. Neurologia 1999; 14: 320-321.
• Agular PH, Liu CW, Leitao H, et al. MR and CT imaging in the Dyke-Davidoff-Masson syndrome: report of three cases and contribution to pathogenesis an differential diagnosis. Arq Neuropsiquatr 1998; 56: 803-807.
• Ünal O, Tombul T, Çırak B ve ark. Left hemisphere and male sex dominance of cerebral hemiatrophy (Dyke–Davidoff–Masson Syndrome), Clinical imaging Volume 28,3 May–June 2004, Pages 163–165
• CE Parker, N Harris, J Mavalwala Dyke–Davidoff–Masson syndrome: five case studies and deductions from dermatoglyphics Clin Pediatr, 5 (1972), pp. 288–292
• AC Dean, G Solomon, C Harden, G Papakostas, DR Labar Left hemispheric dominance of epileptiform discharge Epilepsia, 38 (1997), pp. 503–505
• Nieman EA, Fullerton PM: Electroencephalographic findings in unilateral cerebral atrophy. Neurology 13:213-218, 1963
• Zúñiga-González EA, Molina-Carrión LE, Diego-Silva RC.Two cases of Dyke-Davidoff-Masson syndrome and adult cerebral hemiatrophy. Rev Med Inst Mex Seguro Soc. 2009 Mar-Apr;47(2):215-8.
• Feyza Sen MD, Mehmet Cabuk MD, Duygu Yoruk Atik MD, Aysun Unal MD, Hellenic Journal of Nuclear Medicine May - August 2010, 181-182