• 대한두경부종양학회지
• /
• 제30권2호
• /
• pp.119-122
• /
• 2014

Rhabdomyosarcoma is the most common sarcoma in children less than 15 years of age. Two major histological subtypes are embryonal and alveolar. Embryonal rhabdomyosarcoma is diagnosed by immunopathology and treatments require coordinated management plans that include surgery, chemotherapy, and usually radiotherapy. 8-month-old male infant visited with swelling in left parotid area. Computed tomography scan showed a heterogeneous mass in the left parotid area and the result of fine-needle aspiration cytology was suspicious malignancy. Left total parotidectomy was performed and CSF leakage was noted and repaired. Confirmed by positive reactions to desmin and myogenin, the diagnosis was embryonal rhabdomyosarcoma. On postoperative brain MRI, extension along the meninges was noted and for treatment, chemotherapy and gamma knife radiosurgery were done. Five years after initial surgical resection(3 years and 10 months after completion of chemotherapy and gamma knife radiosurgery), the child did not show any evidence of local recurrence or distant metastasis.

• 한국방사선학회논문지
• /
• 제16권7호
• /
• pp.843-849
• /
• 2022

본 연구에서는 감마나이프를 이용한 방사선 수술 시 주변 정상 장기들의 피폭선량을 측정하여 2차 발암확률을 분석하고자 한다. 인체 조직 등가 물질로 구성된 소아 팬텀(Model 706-G, CIRS, USA)에 종양 볼륨은 0.25 cm³, 0.51 cm³, 1.01 cm³, 2.03 cm³ 총 4개로 설정하였으며, 평균 선량은 18.4 ± 3.4 Gy로 하였다. 감마나이프 수술 장비의 테이블위에 Rando phantom을 설치한 후에 OSLD nanoDot 선량계를 Right eye, Left eye, Thyroid, Thymus gland, Right lung, Left lung 에 위치시켜 각각의 피폭선량을 측정하였다. 청신경초종질환의 감마나이프 방사선 수술 시 주변 정상 장기들의 방사선 피폭으로 인한 암 발생확률은 종양 볼륨 2. 03 cm³에서 100,000명 당 4.08명의 암이 발생함을 알 수 있다. 본 연구는 정위적 방사선 수술 시 발생할 수 있는 2차 방사선 피폭선량의 위험성을 연구하여 향후 확률적 영향과 관련하여 유용한 자료로 활용될 것으로 사료된다.

• 한국방사선학회논문지
• /
• 제17권2호
• /
• pp.243-248
• /
• 2023

본 연구에서는 청신경초종 질환에서 방사선 수술 시 유리선량계를 이용하여 손상위험장기들의 피폭으로 인해 발생하는 2차 발암률을 분석하고자 한다. 인체 조직 등가 물질의 소아 팬텀을 사용하여, 종양의 체적은 0.506 cm³, 1.008 cm³, 2.032 cm³ 총 3개의 체적으로 설정하였고, 평균 선량은 18.4 ± 3.4 Gy로 방사선수술계획을 수립하였다. 수술 장비의 테이블에 인체 팬텀을 장착시킨 후 유리선량계를 우안, 좌안, 갑상샘, 흉선, 오른쪽 폐, 왼쪽 폐에 위치시켜 각각 피폭선량을 측정하였다. 본 연구에서 가장 큰 종양체적인 2.032 cm³의 청신경초종 질환에서 감마나이프 방사선 수술 시 손상위험장기의 피폭으로 인한 2차 암 발생률을 유리선량계로 측정한 그 결과는 10,000명 당 1.11명의 2차 암이 발생될 수 있는 것으로 계산되었다. 본 연구는 정위적 방사선 수술 시 발생할 수 있는 2차 방사선 피폭선량의 위험성을 연구하여 향후 방사선의 확률적 영향과 관련된 방사선 장해분야에 기초자료로 활용될 것이라 사료된다.

• Journal of Korean Neurosurgical Society
• /
• 제60권3호
• /
• pp.294-300
• /
• 2017

Hypothalamic hamartoma (HH) is a benign indolent lesion despite the presentation of refractory epilepsy. Behavioral disturbances and endocrine problems are additional critical symptoms that arise along with HHs. Due to its nature of generating epileptiform discharge and spreading to cortical region, various management strategies have been proposed and combined. Surgical approaches with open craniotomy or endoscopy, stereotactic approaches with radiosurgery and gamma knife surgery or radiofrequency thermos-coagulation, and laser ablation have been introduced. Topographical dimension and the surgeon's preference are key factors for treatment modalities. Endoscopic disconnection has been one of the most favorable options performed in treating HHs. Here we discuss presurgical evaluation, patient selection, surgical procedures, and complications.

• Journal of Korean Neurosurgical Society
• /
• 제56권4호
• /
• pp.356-360
• /
• 2014

The coexistence of moyamoya disease (MMD) with an arteriovenous malformation (AVM) is exceedingly rare. We report two cases of AVM associated with MMD. The first case was an incidental AVM diagnosed simultaneously with MMD. This AVM was managed expectantly after encephalo-duro-arterio-synangiosis (EDAS) as the main feeders stemmed from the internal carotid artery, which we believed would be obliterated with the progression of MMD. However, the AVM persisted with replacement of the internal carotid artery feeders by new external carotid artery feeders from the EDAS site. The AVM was eventually treated with gamma knife radiosurgery considering an increasing steal effect. The second case was a de novo AVM case. The patient was initially diagnosed with MMD, and acquired an AVM eight years later that was slowly fed by the reconstituted anterior cerebral artery. Because the patient remained asymptomatic, the AVM is currently being closely followed for more than 2 years without further surgical intervention. Possible differences in the pathogenesis and the radiologic presentation of these AVMs are discussed with a literature review. No solid consensus exists on the optimal treatment of MMD-associated AVMs. Gamma knife radiosurgery appears to be an effective treatment option for an incidental AVM. However, a de novo AVM may be managed expectantly considering the possible risks of damaging established collaterals, low flow characteristics, and probably low risks of rupture.

• Journal of Korean Neurosurgical Society
• /
• 제52권1호
• /
• pp.37-41
• /
• 2012

Objective : The aim of this study was to describe a single center's experience in the management of craniopharyngiomas in children over a 15-year period. Methods : The clinical records of pediatric patients treated for craniopharyngiomas between December 1995 and February 2011 were reviewed. Thirty-five pediatric patients diagnosed with craniopharyngioma were treated, and their medical records and imaging data were analyzed retrospectively. Results : The mean follow-up duration was 76 months (range, 10-195). Overall survival and local control rates at 10 years were $94.7{\pm}5.1%$ and $37.1{\pm}11.9%$, respectively. The female-to-male ratio was 16 : 19, and the mean age was 8.6 years (range, 1-17). Initially, gross total resection (GTR) was performed in 30 patients; subtotal resection (STR) followed by radiotherapy was performed in 5 patients. Of the 14 cases that showed recurrence after GTR, 5 patients were treated with GTR, 1 with radiation therapy (RT), 4 with gamma knife radiosurgery (GKRS), and 4 with subtotal resection followed by RT. No patients who underwent RT or GKRS had recurrences. Two cases with recurrence after STR followed by RT were treated with GTR. One patient died of hormonal insufficiency 64 months after the first surgery. The overall median time progression was 51.2 months (range, 3-182) : 49.7 months in the patients who underwent GTR and 60.2 months in the patients who underwent STR followed by RT. Conclusion : If safe resection is possible, GTR at the initial treatment should be attempted to reduce the tumor recurrence. However, if the tumor recurs after the first surgery, RT or GKRS with/without reoperation may be an effective salvage treatment for recurrent craniopharyngioma.