SavedAdd your journal

Journals / Şişli Etfal Hastanesi Tıp Bülteni / 2005 / Cilt: 39 - Sayı: 4

Magnetic resonance imaging in Dyke-Davidoff-Masson syndrome presented with epilepsy

Epilepsi ile başvuran Dyke-Davidoff-Masson sendromlu olguda manyetik rezonans görüntüleme

Nuran YILMAZ
Ender UYSAL
A. Deniz KAHRAMAN
Hakan YILDIRIM
Handan TOROSLU
Muzaffer BAŞAK
Pages
52–56
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

In this study we have presented Dyke-Davidoff-Masson syndrome in a 22 years old male patient with medically intractable epilepsy and discussed clinical appearance, pathology and the value of the magnetic resonance imaging in the diagnosis of this syndrome.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Dyke-Davidoff-Masson syndrome, clinically characterized by intractable epileptic seizures, facial asymmetry, mental retardation and cerebral hemiatrophy is very rare and that might cause resistant seizures.
📊
Key Findings & Data:Magnetic Resonance Imaging (MR!) is one of the imaging methods of choice to demonstrate the etiology of epilepsy.
💡
Conclusion & Impact:In this study we have presented Dyke-Davidoff-Masson syndrome in a 22 years old male patient with medically intractable epilepsy and discussed clinical appearance, pathology and the value of the magnetic resonance imaging in the diagnosis of this syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Erişkin · Manyetik rezonans görüntüleme · Erkek

Abstract

Dyke-Davidoff-Masson syndrome, clinically characterized by intractable epileptic seizures, facial asymmetry, mental retardation and cerebral hemiatrophy is very rare and that might cause resistant seizures. Magnetic Resonance Imaging (MR!) is one of the imaging methods of choice to demonstrate the etiology of epilepsy. In this study we have presented Dyke-Davidoff-Masson syndrome in a 22 years old male patient with medically intractable epilepsy and discussed clinical appearance, pathology and the value of the magnetic resonance imaging in the diagnosis of this syndrome.

Özet

Klinik olarak dirençli epileptik nöbetler, fasial asimetri, mental retardasyon ve serehral hemiatrofi ile karakterize bir sendrom olan Dyke-Davidoff-Masson sendromu (DDMS) oldukça nadir görülmektedir. Manyetik rezonans görüntüleme (MRG), epilepsi etyolojisinin değerlendirilmesinde tercih edilen etkin görüntüleme yöntemlerinden birisidir. Biz olgu sunumumuzda, kliniğimize dirençli epilepsi tanısı ile refere edilen 22 yaşındaki erkek hastada DDMS sendromunu gösterdik ve bu sendromun klinik görünümünü, patolojisini ve tanısında MRG yönteminin değerini tartıştık.

🔖

Cite This Article

YILMAZ, N., UYSAL, E., KAHRAMAN, A. D., YILDIRIM, H., TOROSLU, H., BAŞAK, M. (2005). Magnetic resonance imaging in Dyke-Davidoff-Masson syndrome presented with epilepsy. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 39 - Sayı: 4, 52–56. https://ajindex.com/articles/363591

References (13)

  1. Alp Recep, İlhan Selen, Koçer Abdülkadir, Türk Börü Ülkü. Dirençli epilepsi nedenleri arasında unutulmaması gereken bir tanı: Dyke-Davidoff-Masson sendromu, iki olgu sunumu. Genel Tıp Derg 2004; 14 (3): 113-116
  2. C. G. Dyke, L. M. Davidoff, C. B. Masson: Cerebral he- miatrophy with homolateral hypertrophy of the skull and sinuses. Surgery, Gynecology and Obstetrics, Chicago, 1933;57: 588-600.
  3. Sener RN, Jinkins JR. MR of cranjocerebral hemiat­ rophy. Clin Imaging. 1992; 16:93-7. Zilka A. CT of cerebral hemiatrophy AJR 1980; 135:259- 62 Shetty DS, Lakhkar BN, Joh JR. Dyke-Davidoff-Masson syndrome. Neurology India 2003; 51 (1):136 Lerner AM, Gadoth N, Streifler J et al. Radiological case of the month. AJDC 1988; 142: 303-404.
  4. Paşaoğlu E, Damgacı L, Sakman B ve ark Dyke -Davi- doff-Masson sendromu: BT ve MRG bulguları. Tanısal ve Girişimsel Radyoloji 2000; 6: 237 -241. Aguiar PH, Liu CW, Leitao H, et all. MR and CT ima­ ging in the Dyke-Davidoff-Masson syndrome. Report of three cases and contribution to pathogenesis and differen­ tial diagnosis. Arq Neuropsiquiatr. 1998;56:803-7.
  5. Zeiss J, Brinker RA. Imaging of cerebral hemiatrophy. J Comput Assit Tomogr. 1988;12:640-3
  6. Bronen RA, Fulbright RK, Spencer DD, Kim JH, Lange RC, Sutilla C (1996) Refractory epilepsy: comparison of MR imaging, CT, and histopathologic findings in 117 pa­ tients. Radiology 201:97-105
  7. Bronen RA (1992) Epilepsy: the role of MR imaging. AJR 159:1165-1174
  8. Jack CR Jr (1993) Epilepsy: surgery and imaging. Radi­ ology 189: 635-646
  9. Taveras JM, Wood EH, Diagnostic Radiology, 2nd ed. Baltimore,Williams and Wilkins Comp 1976
  10. S. Çakırer, M. Başak, A. Mutlu, G. M. Galip. MR ima­ ging in epilepsy that is refractory to medical therapy. Eur. Radiol. (2002) 12:549-558
  11. Unal O, Tombul T, Cirak B, Anlar O, incesu L, Kayan M. Left hemisphere and male sex dominance of cerebral hemiatrofy (Dyke-Davidoff-Masson Syndrome). Clin Imaging. 2004 May-Jun; 28(3): 163-5.
  12. Alkan A, Baysal T, Kıroğlu Y, Sığırcı A, Okran İ. Dyke- Davidoff-Masson Sendromunda MRG bulguları. İnönü Üniversitesi Tıp Fakültesi Derg 200L; 8-37-40.
  13. Grossman Robert I, Yousem David M. Neuroradiology. 2nd ed.2003;454.