Progressive multifocal leukoencephalopathy (PML) is a demyelination disease caused by opportunistic infection of the ubiquitous, usually nonpathogenic neurotropic papovavirus (JC virus). The virus infects and destroys myelin-producing oligodendrocytes, thereby causing patchy areas of demyelination in the cerebral white matter. It is exclusively a disease of immunosuppressed individuals. We report a case of an immunocompetent child patient with pathologically-proven PML and with a survival over 3 years after diagnosis. Serial follow up of neuroimaging study including brain MRI, MRS, SPECT and PET was obtained.ope
Prader-Willi syndrome (PWS) is a rare neurodevelopmental disease caused by abnormality of chromosome...
Fine needle aspiration (FNA) cytology is the decisive test in the preoperative diagnostics of thyroi...
Myoepithelial tumor is a mixed tumor which is commonly developed at the exocrine gland such as saliv...
Leigh syndrome (LS) is a genetically and clinically heterogeneous disorder caused by metabolic defec...
Pachydermoperiostosis is a rare hereditary syndrome characterized by finger clubbing, periosteal new...
Cerebral sparganosis is a rare intracranial parasitic infectious disease. The best treatment seems t...
Uterine sarcomas are rare tumors of mesodermal origin and constitute 2-6% of uterine malignancies. T...
This study was designed to evaluate the influence of cultured epidermal tissue graft and the adminis...
Chronic intestinal pseudo-obstruction syndrome is a rare, severe and disabling disorder characterize...
X-linked Charcot-Marie-Tooth (CMTX) disease is a clinically heterogeneous hereditary motor and senso...
Limbic encephalitis has been reported usually as an autoimmune complication related to onconeuronal ...
A 58-years-old man came to the hospital because of progressive intellectual deterioration, gait dist...
Primary mucinous cystadenomas of the retroperitoneum is extremely rare, and its histogenesis and bio...
A 54-yr-old male, who was treated by chemotherapy for gastric cancer 15 months ago, presented to Yon...
Rhabdomyosarcoma is the most common soft tissue sarcoma in childhood and young adult. Rhabdomyosarco...
Prader-Willi syndrome (PWS) is a rare neurodevelopmental disease caused by abnormality of chromosome...
Fine needle aspiration (FNA) cytology is the decisive test in the preoperative diagnostics of thyroi...
Myoepithelial tumor is a mixed tumor which is commonly developed at the exocrine gland such as saliv...
Leigh syndrome (LS) is a genetically and clinically heterogeneous disorder caused by metabolic defec...
Pachydermoperiostosis is a rare hereditary syndrome characterized by finger clubbing, periosteal new...
Cerebral sparganosis is a rare intracranial parasitic infectious disease. The best treatment seems t...
Uterine sarcomas are rare tumors of mesodermal origin and constitute 2-6% of uterine malignancies. T...
This study was designed to evaluate the influence of cultured epidermal tissue graft and the adminis...
Chronic intestinal pseudo-obstruction syndrome is a rare, severe and disabling disorder characterize...
X-linked Charcot-Marie-Tooth (CMTX) disease is a clinically heterogeneous hereditary motor and senso...
Limbic encephalitis has been reported usually as an autoimmune complication related to onconeuronal ...
A 58-years-old man came to the hospital because of progressive intellectual deterioration, gait dist...
Primary mucinous cystadenomas of the retroperitoneum is extremely rare, and its histogenesis and bio...
A 54-yr-old male, who was treated by chemotherapy for gastric cancer 15 months ago, presented to Yon...
Rhabdomyosarcoma is the most common soft tissue sarcoma in childhood and young adult. Rhabdomyosarco...
Prader-Willi syndrome (PWS) is a rare neurodevelopmental disease caused by abnormality of chromosome...
Fine needle aspiration (FNA) cytology is the decisive test in the preoperative diagnostics of thyroi...
Myoepithelial tumor is a mixed tumor which is commonly developed at the exocrine gland such as saliv...