• 대한핵의학회지
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• 제37권4호
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• pp.229-234
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• 2003

목적: 홍역 감염 후 속발되는 뇌염은 사망률이 높아 조기진단 및 적극적인 치료가 예후에 중요하다. 저자들은 홍역 후 발생된 뇌염에 대한 Tc-99m ECD 뇌혈류 SPECT와 뇌핵자기공명영상(MRI)의 진단 성능을 비교하였고 뇌혈류 SPECT상 중등도 이상의 심한 뇌혈류 감소가 호발하는 부위를 알아보았다. 대상 및 방법: 홍역으로 진단받은 112명 중에서 의식저하, 경련, 마비 등의 임상증상과 혈청 및 뇌척수액에서 홍역 특이항체가 관찰되어 홍역 후 급성 뇌염으로 진단받고 Tc-99m ECD 뇌혈류 SPECT와 MRI를 시행받은 11명(M : F=4 : 7, 연령 $1.6{\sim}14$세)을 대상으로 하였다. SPECT상 관찰되는 뇌혈류는 0(정상)에서 3(결손)으로 점수화하였고 2점 이상인 경우를 중등도 뇌혈류 감소로 정의하였다. 홍역 후 발생된 뇌염 환아에서 MRI와 SPECT의 두부병소 진단 성능과 중등도 뇌혈류 감소의 호발부위를 알아보았다. 결과: MRI 시행결과 7명(63.6%)에서 T2-강조영상에서 회백질의 고강도 변화가 관찰되었으나, SPECT상 11명(100%) 모두에서 뇌혈류 감소 부위가 관찰되었다. 중등도 뇌혈류 감소는 전두엽(81.8%), 측두엽(72.7%), 후두엽(27.3%), 기저핵(27.3%), 두정엽(9.1%) 순서로 호발하였다. 결론: 홍역 후 발생된 뇌염 환아에서 두부병소를 진단하는데 MRI에 비하여 Tc-99m ECD 뇌혈류 SPECT가 좀더 도움이 될 것으로 사료된다.

• Journal of Korean Neurosurgical Society
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• 제59권2호
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• pp.168-171
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• 2016

Choroidal fissure cysts are often incidentally discovered. They are usually asymptomatic. The authors report a case of growing and hemorrhagic choroidal fissure cyst which was treated surgically. A 22-year-old female presented with headache. Cranial MRI showed a left-sided choroidal fissure cyst. Follow-up MRI showed that the size of the cyst had increased gradually. Twenty months later, the patient was admitted to our emergency department with severe headache. MRI and CT showed an intracystic hematoma. Although such cysts usually have a benign course without symptoms and progression, they may rarely present with intracystic hemorrhage, enlargement of the cyst and increasing symptomatology.

• 대한핵의학회:학술대회논문집
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• 대한핵의학회 2000년도 2nd Korea-China Congress of Nuclear Medicine and 39th Annual Spring Meeting if the Korea SOciety Nuclear Medicine
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• pp.58.1-58.1
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• 2000

• Journal of Korean Neurosurgical Society
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• 제38권5호
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• pp.387-389
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• 2005

Primary atypical teratoid/rhabdoid tumor[AT/RT] of the central nervous system is a recently described, highly malignant neoplasm that usually occur in the posterior fossa of children. Although AT/RT usually occurs in young children, AT/RT is being recognized in adults with increasing frequency. The authors report 49-year-old man with multiple AT/RT lesions [right lateral ventricle, right temporal lobe and right cerebellum]. Histopathologic findings showed typical rhabdoid cells with eccentric nuclei and prominent nucleoli. Eventhough the tumor was removed, a patient was dead in one month after surgery due to recurrence and rapid regrowth of the tumor.

• Journal of Korean Neurosurgical Society
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• 제49권4호
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• pp.226-228
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• 2011

We report a case of spontaneous right carotid-cavernous fistula (CCF) in a proximal segment of persistent primitive trigeminal artery (PPTA) and combined vascular anomalies such as left duplicated hypoplastic proximal posterior cerebral arteries and a variation of anterior choroidal artery supplying temporal and occipital lobe. A 45-year-old male presented with progressive right exophthalmos, diplopia, and ocular pain. With manual compression of the internal carotid artery, a cerebral angiography revealed a right CCF from a PPTA. Treatment involved the placement of detachable non-fibered and fibered coils, and use of a hyperglide balloon to protect against coil herniation into the internal carotid artery. A final angiograph revealed complete occlusion of PPTA resulted in no contrast filling of CCF.

• Journal of Korean Neurosurgical Society
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• 제29권5호
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• pp.688-692
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• 2000

The authors report a case of ganglioglioma in unusual site, the hypothalamus. The tumor was completely removed and no recurrence was noted on the follow up. Ganglioglioma usually occurs in the temporal and frontal lobe, but is rarely found on the hypothalamus. We report this case with pertinent literatual reviews.

• Journal of Korean Neurosurgical Society
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• 제40권5호
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• pp.373-376
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• 2006

An astroblastoma is a rare primary glial tumor occurring preferentially in young adults. It is characterized by a perivascular arrangement of the tumor cells forming perivascular pseudorosettes mimicking ependymomas. The histogenesis of astroblastoma is unclear, despite a number of studies to determine its possible cellular origin. We have experienced a case of astroblastoma located at the temporal lobe. It presented as a large, well-circumscribed, and highly enhanced mass lesion on magnetic resonance images[MRI]. The tumor was well demarcated and did not infiltrate the brain, which made complete removal possible. Here, we report and discuss the characteristic histological and radiological features of this case.

• Journal of Korean Neurosurgical Society
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• 제59권3호
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• pp.302-305
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• 2016

Gliofibroma is an extremely rare biphasic tumor with an astrocytic and benign mesenchymal component, which commonly occurs within the first two decades of life. The exact biological behavior of the tumor is not fully understood. Therefore, it is not listed as a distinct entity in the current World Health Organization classification of central nervous system tumors. Here, we describe a rare case of gliofibroma, which was located on the medial temporal lobe in a 61-year-old woman. Preoperatively, we misdiagnosed it as a meningioma because it was a well-demarcated and well-enhanced extra-axial mass with calcification and bony destruction. On the histopathological and immunohistochemical examination, the tumor consisted of a mixture of glial tissue and mesenchymal tissue and it was finally diagnosed as a gliofibroma. To our knowledge, this case of intracranial gliofibroma is in the oldest patient ever reported.

• Journal of Korean Neurosurgical Society
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• 제58권6호
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• pp.554-556
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• 2015

Primary intracranial malignant melanoma is a very rare and highly aggressive tumor with poor prognosis. A 66-year-old female patient presented a headache that had been slowly progressing for several months. A large benign pigmented skin lesion was found on her back. A brain MRI showed multiple linear signal changes with branching pattern and strong enhancement in the temporal lobe. The cytological and immunohiostochemical cerebrospinal fluid examination confirmed malignant melanoma. A biopsy confirmed that the pigmented skin lesion on the back and the conjunctiva were benign nevi. We report a case of primary intracranial malignant melanoma and review relevant literatures.

• Journal of Korean Neurosurgical Society
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• 제52권6호
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• pp.555-557
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• 2012

We report an uncommon case of a 45-year-old woman who presented with spontaneous rhinorrhea. A computed tomography (CT) scan of the head revealed an abnormally large sphenoid sinus associated with a parasellar bony defect (Sternberg's canal) through which magnetic resonance imaging could detect an encephalocele of the right temporal lobe. An endoscope-assisted trans-sphenoidal approach was performed and, with the aid of image guided surgery, reduction of the encephalocele was obtained and followed by surgical repair of the dural and bony defects. The postoperative course was uneventful and the cerebrospinal fluid fistula was closed as confirmed by the postoperative CT scan and by the absence of rhinorrhea. After three years of monitoring the patient remained asymptomatic.