Dyke–Davidoff–Masson syndrome: A rare cause of cerebral hemiatrophy in children

2020 ◽  
Vol 17 (3) ◽  
pp. 58-60
Author(s):  
Surendar Penumuri ◽  
Keyword(s):  
1998 ◽  
Vol 56 (4) ◽  
pp. 803-807 ◽  
Author(s):  
PAULO HENRIQUE AGUIAR ◽  
WEI LIU CHING ◽  
HELIO LEITÃO ◽  
F. ISSA ◽  
GUILHERME LEPSKI ◽  
...  

Cerebral hemiatrophy or Dyke-Davidoff-Masson syndrome is a condition characterized by seizures, facial asymmetry, contralateral hemiplegia or hemiparesis, and mental retardation. These findings are due to cerebral injury that may occur early in life or in utero. The radiological features are unilateral loss of cerebral volume and associated compensatory bone alterations in the calvarium, like thickening, hyperpneumatization of the paranasal sinuses and mastoid cells and elevation of the petrous ridge. The authors describe three cases. Classical findings of the syndrome are present in variable degrees according to the extent of the brain injury. Pathogenesis is commented.


2002 ◽  
Vol 12 (10) ◽  
pp. 2542-2547 ◽  
Author(s):  
Katsumi Hayakawa ◽  
Toyoko Kanda ◽  
Yuriko Yamori
Keyword(s):  

1988 ◽  
Vol 12 (4) ◽  
pp. 640-643 ◽  
Author(s):  
Jacob Zeiss ◽  
Ray A. Brinker

2013 ◽  
Vol 5 (2) ◽  
pp. 111-113
Author(s):  
Mohammad Ibrahim Khalil ◽  
Maliha Hakim ◽  
Afzal Momin ◽  
Abu Nayeem ◽  
Md. Mohitul Islam ◽  
...  

Dyke-Davidoff-Masson Syndrome (DDMS), also known as cerebral hemiatrophy, is a rare clinical condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia or hemiparesis, with learning difficulties and behavioral changes. It is commonly diagnosed in presence of clinical feature associated radiological findings which include cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses. In this present case report a 12 year old teenager female patient was diagnosed as DDMS with recurrent generalized seizures, learning difficulties and right sided hemiparesis. Magnetic resonance imaging (MRI) of the brain showed hemiatrophy involving the left cerebral hemisphere and EEG showed generalized epileptiform discharged. An X-ray of the paranasal air sinuses was normal.DOI: http://dx.doi.org/10.3329/jssmc.v5i2.20768J Shaheed Suhrawardy Med Coll 2013;5(2):111-113


2012 ◽  
Vol 10 (1) ◽  
pp. 71-74 ◽  
Author(s):  
Sumit Thakar ◽  
Yasha T. Chickabasaviah ◽  
Alangar S. Hegde

Invasive craniocerebral aspergillosis, often encountered in an immunocompromised setting, is almost uniformly fatal despite radical surgical and medical management, and is frequently a necropsy finding. The authors report a unique, self-resolving clinical course of this aggressive infection in a 10-month-old infant. The infant was brought to the emergency services in altered sensorium with a 1-week history of left-sided hemiparesis, excessive irritability, and vomiting. An MRI study of the brain revealed multiple, heterogeneously enhancing lesions in the right cerebral hemisphere with mass effect. The largest lesion in the frontotemporal cortical and subcortical regions was decompressed on an emergent basis. Histopathological findings were suggestive of invasive aspergillosis, although there was no evidence of the infection in the lungs or paranasal sinuses. Computed tomography–guided aspiration of the remaining lesions and follow-up antifungal therapy were recommended. The parents, however, requested discharge without further treatment. The child was seen at a follow-up visit 3 years later without having received any antifungal treatment. Imaging showed resolution of the infection and features of Dyke-Davidoff-Masson syndrome (cerebral hemiatrophy). This report of invasive cerebral aspergillosis resolving without medical therapy is the first of its kind. Its clinicoradiological aspects are discussed in light of previously reported cases.


2001 ◽  
Vol 25 (2) ◽  
pp. 82-85 ◽  
Author(s):  
Akira Uchino ◽  
Akihiro Sawada ◽  
Yukinori Takase ◽  
Masamitsu Abe ◽  
Sho Kudo

1949 ◽  
Vol 16 (1) ◽  
pp. 17-20
Author(s):  
R. M. GEIST ◽  
C. R. HUGHES
Keyword(s):  

2013 ◽  
Vol 5 (3) ◽  
Author(s):  
Felix Uduma Uduma ◽  
Jude-Kennedy C. Emejulu ◽  
Mathieu Motah ◽  
Philip C. N. Okere ◽  
Pierre C. Ongolo ◽  
...  

1996 ◽  
Vol 20 (1-2) ◽  
pp. 231-234 ◽  
Author(s):  
William G. Honer ◽  
Lili C. Kopala ◽  
Jake J. Locke ◽  
Jocelyne S. Lapointe
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document