• Title/Summary/Keyword: Subependymal giant cell astrocytoma

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Endoscopic Surgery of a Subependymal Giant Cell Astrocytoma Associated with Tuberous Sclerosis - Case Report - (결절성 경화증에 동반된 상의하 거대 세포 성상세포종의 내시경적 수술 - 증 례 보 고 -)

  • Lim, Jeong-Hwan;Song, Jun-Hyeok;Kim, Myung-Hyun;Park, Hyang-Kwon;Kim, Sung-Hak;Shin, Kyu-Man;Park, Dong-Been
    • Journal of Korean Neurosurgical Society
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    • v.29 no.4
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    • pp.564-568
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    • 2000
  • The authors present a rare case of subependymal giant cell astrocytoma which successfully treated with endoscopic tumor resection. A 15-year-old boy was presented with multiple episode of generalized seizure and intermittent headache for 5 years. The patient had facial adenoma sebaceum, multiple nevi on his back, and mental retardation. Cerebral MRI scans showed a round tumor located at the frontal horn of right ventricle near the foramen monro. The tumor was totally removed with endoscopic procedure and histologically confirmed as a subependymal giant cell astrocytoma. Subependymal giant cell astrocytomas can cause all the clinical problems that are associated with other types of intracranial tumor. However, surgical indication is not well standardized, because of the lack of basic knowledge about the tumor and the likelihood of surgical morbidity. We believe that endoscopic surgery, a minimally invasive technique, can circumvent the surgical disadvantage while achieving the surgical goal.

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Subependymal Giant Cell Astrocytoma in the Tuberous Sclerosis (결정성 경화증에서의 상의하 거대 성상세포종)

  • Park, Jin-Han;Kim, Seong-Ho;Han, Dong-Ro;Bae, Jang-Ho;Ko, Sam-Kyu;Kim, Oh-Lyung;Chok, Byung-Yeam;Cho, Soo-He
    • Journal of Yeungnam Medical Science
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    • v.11 no.2
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    • pp.221-229
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    • 1994
  • Tuberous sclerosis is reported rarely and is associated with systemic lesions including central nervous system, skin, heart, eye and kidney. Approximately 5-15% of individuals with tuberous sclerosis will develope brain neoplasia, almost invariably subependymal giant-cell astrocytoma (SGCA). We experienced a case of SGCA with tuberous sclerosis operated by the transcallosal approach and report with literature review.

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A Case of Tuberous Sclerosis with Multiple Fibroma on Scalp and Extremity (두피 및 사지에 다발성 섬유종을 동반한 결절성 경화증)

  • Kim, Hyoung Suk;Jeong, Hii Sun;Shin, Keuk Shun;Lee, Sang Yeob;Song, Ji Sun
    • Archives of Plastic Surgery
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    • v.35 no.3
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    • pp.341-344
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    • 2008
  • Purpose: Tuberous sclerosis is an autosomal dominant multisystemic neurocutaneous syndrome characterized by the development of multiple hamartoma distributed through the body, skin, brain, heart, kidney, and lung. The classic triad is seizure, mental retardation, and facial angiofibroma. We experienced a case of a tuberous sclerosis associated with the facial lesion and multiple masses on scalp, forehead, and right lower extremity. Methods: This a 34-year-old male patient had subependymal giant cell astrocytoma in brain and multiple angiomyolipoma in both kidneys. Tangential excision with razor blade and dermabrasion were done on the centrofacial area. We excised other lesions and the mass on scalp was excised and covered with split thickness skin graft. Results: The histopathological finding revealed that the facial lesion was angiofibroma and the others were multiple fibroma. Conclusion: In our case of tuberous sclerosis, we chose the tangential excision to remove the large nodules of angiofibroma, and then dermabrasion was used to smooth the final contour. The patient appeared to have a good results from this treatment modality. But, tuberous sclerosis is an disease that needs long term follow-up to check up the recurrence of skin problem.