1.Pineal Cavernous Malformations: Report of Two Cases.
Dong Seok KIM ; Kyu Won SHIM ; Tae Gon KIM ; Jong Hee CHANG ; Yong Gou PARK ; Joong Uhn CHOI
Yonsei Medical Journal 2005;46(6):851-858
Pineal hemorrhage only occurs in rare cases, and this known to have several different causes such as germ cell tumors, pineal cysts and vascular malformations, including the cavernous malformations. Pineal cavernous malformations are extremely rare: to date only fifteen cases have been reported worldwide. Although the diagnosis of pineal cavernous malformation is not easy because of the extreme rareness of this condition, the presence of this lesion can be suspected based on its typical radiological findings. Case 1. A 42-year- old man presented with a limitation in his upward gazing. Radiologic examinations showed acute hemorrhage in the pineal region. He underwent ventriculo-peritoneal (VP) shunting but the patient's condition deteriorated after the shunting surgery. We operated and totally removed the tumor and the hemorrhages via an occipital-transtentorial approach. Case 2. A 37-year-old man presented with diplopia. Radiologic examinations showed acute hemorrhage in the third ventricle. He underwent VP shunting, and after this procedure the diplopia was aggravated. We operated and totally removed the tumor and the hemorrhages via an occipital-transtentorial approach. If there is no doubt about the pineal cavernous malformation on MR imaging, we strongly recommend early surgical intervention without performing a risky biopsy. In this study, we describe our experiences for the diagnosis of cavernous malformations in the pineal region with special emphasis on the radiological aspects and the clinical course of this disease.
Tomography, X-Ray Computed
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*Pineal Gland/blood supply
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Male
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Magnetic Resonance Imaging
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Intracranial Hemorrhages/diagnosis/pathology/*radiography
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Humans
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Hematoma/diagnosis/pathology/*radiography
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Diplopia/diagnosis
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Central Nervous System Vascular Malformations/diagnosis/pathology/*radiography
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Angiography
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Adult
2.MR imaging findings of moyamoya disease.
Kee Hyun CHANG ; Jeong Geun YI ; Moon Hee HAN ; In One KIM
Journal of Korean Medical Science 1990;5(2):85-90
The brain MR images of 23 patients with angiographically proved moyamoya disease were reviewed to evaluate the capability of MR to demonstrate vascular and parenchymal abnormalities. All the MR images were obtained on a 2.0 T superconducting system and included T1-weighted sagittal and T2-weighted axial images without implementation of flow compensation (FC). The vascular abnormalities demonstrated on MR images were narrowing of the cavernous internal carotid artery (ICA) (73%), narrowing or occlusion of the supraclinoid ICA (87%) and proximal middle cerebral artery (MCA) (91%), and multiple collateral vessels in the basal ganglia and/or thalamus (96%). The parenchymal abnormalities included ischemic infarctions (74%), predominantly located in watershed areas, hemorrhagic infarctions (26%), intracerebral hematomas (13%), and intraventricular hemorrhage (13%). In conclusion, MR imaging was a useful diagnostic modality for detecting both vascular and parenchymal abnormalities associated with moyamoya disease. This may obviate the need for invasive angiography as far as the diagnosis is wanted at the non-quantitative level.
Adolescent
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Adult
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Basal Ganglia/pathology/radiography
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Carotid Artery, Internal/pathology/radiography
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Cerebral Angiography
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Child
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Female
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Hematoma/complications/diagnosis/pathology
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Humans
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Magnetic Resonance Imaging
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Male
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Moyamoya Disease/complications/*diagnosis/pathology
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Myocardial Infarction/complications/diagnosis/pathology
3.Aortic Dissection Presenting with Secondary Pulmonary Hypertension Caused by Compression of the Pulmonary Artery by Dissecting Hematoma: A Case Report.
Dong Hun KIM ; Sang Wan RYU ; Yong Sun CHOI ; Byoung Hee AHN
Korean Journal of Radiology 2004;5(2):139-142
The rupture of an acute dissection of the ascending aorta into the space surrounding the pulmonary artery is an uncommon occurrence. No previous cases of transient pulmonary hypertension caused by a hematoma surrounding the pulmonary artery have been documented in the literature. Herein, we report a case of acute aortic dissection presenting as secondary pulmonary hypertension.
Aortic Aneurysm/*complications/diagnosis
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Aortic Rupture/*complications/diagnosis
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Constriction, Pathologic
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Female
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Hematoma/*complications
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Human
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Hypertension, Pulmonary/*etiology
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Middle Aged
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Pulmonary Artery/pathology/radiography
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Tomography, X-Ray Computed
4.MR Imaging in a Child with Scurvy: a Case Report.
Seung Woo CHOI ; Sun Won PARK ; Young Se KWON ; In Suk OH ; Myung Kwan LIM ; Won Hong KIM ; Chang Hae SUH
Korean Journal of Radiology 2007;8(5):443-447
Scurvy is very rare disease in industrialized societies. Nevertheless, it still exists in higher risk groups including economically disadvantaged populations with poor nutrition, such as the elderly and chronic alcoholics. The incidence of scurvy in the pediatric population is very low. This study reports a case of scurvy in a 5-year-old girl with cerebral palsy and developmental delay based on MRI findings.
Ascorbic Acid/blood/therapeutic use
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Bone Diseases, Metabolic/etiology
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Cerebral Palsy/complications
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Child, Preschool
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Cholecalciferol/blood
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Developmental Disabilities/complications
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Drainage
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Female
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Femur/pathology/radionuclide imaging/surgery
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Fever/etiology
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Follow-Up Studies
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Hematoma/diagnosis/etiology/surgery
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Humans
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Knee/radiography
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Magnetic Resonance Imaging/*methods
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Muscle Weakness/etiology
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Rare Diseases
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Scurvy/complications/*diagnosis/drug therapy
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Thigh/pathology
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Vitamins/therapeutic use