Journals / Epilepsi / 2017 / Cilt: 23 - Sayı: 3

İki Dyke-Davidoff Masson Sendromu Olgusu

Two Cases of Dyke-Davidoff Masson Syndrome

Journal
Epilepsi
Pages
131–134
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Biz burada manyetik rezonans görüntüleme ile yetişkinlikte tanısı koyulan iki DDMS olgusunu tanımladık.

📌 3 Key Takeaways

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Objective & Hypothesis:Dyke-Davidoff Masson Sendromu (DDMS) nöbetler, fasiyal asimetri ve kontralateral hemiparezi ye da hemipleji ile karakterize nadir görülen bir sendromdur.
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Key Findings & Data:Dyke-Davidoff Masson Sendromu ilk defa 1933 yılında, serebral hemiatrofi ile birlikte ipsilateral kemik ve sinüs hipertrofisi gibi karakteristik radyolojik bulgularla tanımlanmıştır.
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Conclusion & Impact:Biz burada manyetik rezonans görüntüleme ile yetişkinlikte tanısı koyulan iki DDMS olgusunu tanımladık.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Dyke-Davidoff Masson Sendromu (DDMS) nöbetler, fasiyal asimetri ve kontralateral hemiparezi ye da hemipleji ile karakterize nadir görülen bir sendromdur. Dyke-Davidoff Masson Sendromu ilk defa 1933 yılında, serebral hemiatrofi ile birlikte ipsilateral kemik ve sinüs hipertrofisi gibi karakteristik radyolojik bulgularla tanımlanmıştır. Dyke-Davidoff Masson Sendromu tanısının yetişkinlikte koyulması oldukça nadirdir. Biz burada manyetik rezonans görüntüleme ile yetişkinlikte tanısı koyulan iki DDMS olgusunu tanımladık.

Özet

Dyke-Davidoff Masson Syndrome (DDMS) is a rare syndrome characterized by seizures, facial asymmetry, and contralateral hemiplegia or hemiparesis. The typical radiological features of DDMS include cerebral hemiatrophy with ipsilateral hypertrophy of the skull and sinuses. It is usually diagnosed in childhood. Presently described are 2 rare cases of DDMS that were diagnosed in adults based on magnetic resonance imaging of the brain.

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Cite This Article

TEZCAN, S., ULUKAN, Ç., ERDOĞAN, Ş., PEKER, E., AYDIN, N. (2017). İki Dyke-Davidoff Masson Sendromu Olgusu. Epilepsi, Cilt: 23 - Sayı: 3, 131–134. https://ajindex.com/articles/157438

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References (14)

  1. Sato N, Yagishita A, Oba H, Miki Y, Nakata Y, Yamashita F, et al. Hemimegalencephaly: a study of abnormalities occurring outside the involved hemisphere. AJNR Am J Neuroradiol 2007;28(4):678–82
  2. Behera MR, Patnaik S, Mohanty AK. Dyke-Davidoff-Masson syn-drome. J Neurosci Rural Pract 2012;3(3):411–3
  3. Geller E, Faerber EN, Legido A, Melvin JJ, Hunter JV, Wang Z, et al. Rasmussen encephalitis: complementary role of multitech-nique neuroimaging. AJNR Am J Neuroradiol 1998;19(3):445–9
  4. Lin DD, Barker PB, Kraut MA, Comi A. Early characteristics of Sturge-Weber syndrome shown by perfusion MR imaging and proton MR spectroscopic imaging. AJNR Am J Neuroradiol 2003;24(9):1912–5
  5. Osborn AG, Salzman KL, Barkovich AJ. Diagnostic Imaging: Brain. 2nd ed. Canada: Amirsys; 2010
  6. Hsin YL, Chuang MF, Shen TW, Harnod T. Temporo-spatial analyses define epileptogenic and functional zones in a case of Dyke-Davidoff-Masson syndrome. Seizure 2011;20(9):713–6
  7. Pendse NA, Bapna P, Menghani V, Diwan A. Dyke-Davidoff-Mas-son syndrome (DDMS). Indian J Pediatr 2004;71(10):943
  8. Malik P, Garg R, Gulia AK, Kario J. Dyke-Davidoff-Masson Syn-drome- a rare cause of refractory epilepsy. Iran J Psychiatry 2014;9(1):42–4
  9. Zilkha A. CT of cerebral hemiatrophy. AJR Am J Roentgenol 1980;135:259–62
  10. Parker CE, Harris N, Mavalwala J. Dyke-Davidoff-Masson syn-drome. Five case studies and deductions from dermatoglyphics. Clin Pediatr (Phila) 1972;11(5):288–92
  11. Biçici V, Ekiz T, Bingöl I, Hatipoğlu C. Dyke-Davidoff-Masson syndrome in adulthood: A 50-year diagnostic delay. Neurology 2014;83(12):1121
  12. Stoevesandt D, Stock K, Spielmann RP, Heine HJ, Paulsen F, Bräuer L. Postmortal diagnosis of a Dyke-Davidoff-Masson syndrome in a 75-year-old woman-a case report. Ann Anat 2009;191(2):225–7
  13. Shrestha B. Acquired cerebral hemiatrophy: Dyke-Dav-idoff-Masson Syndrome - a case report. Turk Neurosurg 2013;23(1):117–21
  14. Dyke CG, Davidoff LM, Masson CB. Cerebral hemiatrophy and homolateral hypertrophy of the skull and sinuses. Surg Gyne-col Obstet 1933;57:588–600.