Pathological intracranial extradural hematoma in a 10-year-old child [0.03%]
10岁儿童头皮下异物致进行性颅内硬膜外血肿一例报告
Abdul Rashid Bhat,Ashish Kumar Jain,A R Kirmani et al.
Abdul Rashid Bhat et al.
A nontraumatic spontaneous extradural hematoma, in a fully conscious 10-year-old male child, caused by a solitary eosinophilic granuloma of calvarium presented as a case of localized painful swelling of the head, which rapidly expanded and ...
Priyanka Kawal,Raj Kumar
Priyanka Kawal
Epidermoid cyst of the quadrigeminal cistern is uncommon, and its presentation as mutism as the main clinical finding with no other neurological finding is very rare. We report a case where the epidermoid cyst presented with progressive sym...
Encephalitis in a child with H1N1 infection: First case report from India [0.03%]
H1N1病毒感染儿童脑炎：印度首例报告
Rajesh Kulkarni,Aarti Kinikar
Rajesh Kulkarni
Neurological complications have been described with seasonal influenza infection. We report encephalitis manifesting as seizures in a child with confirmed H1N1 infection. Treatment with oseltamivir was started. Child was discharged without ...
Pavan Kumar Avadhanam,Sreedhar Vuyyur,Manas Kumar Panigrahi
Pavan Kumar Avadhanam
To report a rare occurrence of osteoblastoma involving the L4 vertebra in an 8-year-old female child with histological features suggestive of osteoblastoma with secondary aneurysmal changes. The mean age incidence of osteoblastoma is 20.4 y...
Spinal epidural lipomatosis: An unusual cause of relapsing and remitting paraparesis [0.03%]
脊髓硬膜下脂质瘤病：复发缓解性双下肢无力的不常见病因
Dinesh Rajput,Arun K Srivastava,Raj Kumar
Dinesh Rajput
Epidural lipomatosis is a rare entity to cause spinal cord compression and neurological deficits. This is usually associated with excess of steroids in the body either because of endogenous source as in Cushings disease or exogenous intake ...
Two female siblings with West syndrome: Familial idiopathic West syndrome with genetic susceptibility and variable phenotypic expression [0.03%]
两例婴儿姐妹手足徐动症的临床分析及基因检测
Ahmet Okay Caglayan,Hakan Gumus,Mitsuhiro Kato
Ahmet Okay Caglayan
The West syndrome (WS) is a characteristic form of epilepsy which usually begins in the first year of life. We describe two female siblings, aged 4 and 2 years, respectively, born from third degree consanguineous parents, with infantile spa...
Murat Altas,Omer Evirgen,Vefik Arica et al.
Murat Altas et al.
Brucellosis is an infectious disease, frequently encountered in developing countries. It may involve multiple organ systems of the human body. However, neurobrucellosis is a rare complication of brucellosis. The most frequent events of cran...
Supratentorial clear cell meningioma in a child: A rare tumor at unusual location [0.03%]
儿童幕上透明细胞脑膜瘤：罕见的肿瘤异常发生部位
Rakesh Ranjan,Shrividya Sethuraman
Rakesh Ranjan
Clear cell meningioma is a rare subtype of meningioma seen mainly in pediatric patients. Supratentorial location is an unusual site of occurrence and its natural history and prognosis are not well described in the literature. We present a u...
Klippel-Trenaunay and Sturge-Weber overlap syndrome with phakomatosis pigmentovascularis [0.03%]
血管瘢痕组织和色素异常综合征伴有眼球受累（phakomatosis pigmentovascularis）
Monika Chhajed,Sadbhavna Pandit,Neeraj Dhawan et al.
Monika Chhajed et al.
Klippel-Trenaunay syndrome and Sturge-Weber syndrome are rare disorders with neurologic and cutaneous signs of vascular origin. Phakomatosis pigmentovascularis represents the association of widespread, aberrant, and persistent nevus flammeu...
Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity [0.03%]
与背侧神经肠瘘相关的脊索裂综合征：一种罕见病症
Punit Srivastava,A N Gangopadhyay,D K Gupta et al.
Punit Srivastava et al.
Split notochord syndrome (SNS) is an extremely rare congenital malformation associated with anomalies of the vertebral column, gastrointestinal tract and central nervous system. Twenty cases of SNS associated with dorsal enteric fistula hav...