• Journal of Korean Neurosurgical Society
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• 제52권2호
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• pp.138-143
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• 2012

Objective : This is a retrospective review of 22 surgically treated benign and malignant tumors of brachial plexus region to describe clinical presentation, the characteristics of brachial plexus tumor and clinical outcomes with a literature review. Methods : Twenty-one patients with consecutive 22 surgeries for primary brachial plexus tumors were enrolled between February 2002 and November 2011 were included in this study. The medical records of all patients were reviewed. Results : Eleven male and 10 female patients were enrolled. Mean age was 39 years. Three patients had brachial plexus tumor associated with neurofibromatosis (13.6%). Presenting signs and symptoms included parenthesis and numbness (54.5%), radiating pain (22.7%), direct tenderness and pain (27.2%), palpable mass (77.3%). Twelve patients presented preoperative sensory deficit (54.5%) and 9 patients presented preoperative motor deficit (40.9%). Twenty tumors (90.9%) were benign and 2 tumors (9.1%) were malignant. Benign tumors included 15 schwannomas (68.2%), 4 neurofibromas (18.2%) and 1 granular cell tumor (4.5%). There were 1 malignant peripheral nerve sheath tumor (MPNST) and 1 malignant granular cell tumor. Gross total resection was achieved in 16 patients (72.7%), including all schwannomas, 1 neurofibroma. Subtotal resection was performed in 6 tumors (27.3%), including 3 neurofibromatosis associated with brachial plexus neurofibromas, 1 MPNST and 2 granular cell tumor in one patient. Conclusion : Resection of tumor is the choice of tumor in the most of benign and malignant brachial plexus tumors. Postoperative outcomes are related to grade of resection at surgery and pathological features of tumor.

• Advances in pediatric surgery
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• 제15권1호
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• pp.27-37
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• 2009

Neuroblastoma is the most common extracranial solid tumor in children. We retrospectively analyzed the results of neuroblastoma treatment of 191 patients (116 males and 75 females) treated between January 1986 and December 2005 at the Department of Pediatric Surgery and the Department of Pediatrics, Seoul National University Children's Hospital. The mean age at diagnosis was 3.1 years (0.1 yrs - 13.5 yrs). Forty-seven patients were under 1 year of age. The mean follow-up period was 57.3 months (24 days - 19.1 yrs). Patients were classified into two groups according to the completeness of resection of the primary tumor; (1) gross total resection (GTR) and (2) incomplete resection (IR). The number of patients in stages I, II, III, IV, IV-S were 17 (8.9 %), 12 (6.3 %), 43 (22.5 %), 114 (59.7 %), 4 (2.1 %), respectively. GTR was achieved in 120 patients and IR in 71 (22 stage III, 47 stage IV, 1 stage IV-S, 1 brain). Overall survival (OS) was 65.2 % and event-free survival (EFS) was 48.6 %. EFS were 100 %, 75 %, 66.8 %, 31.3 %, 75 % at stage I, II, III, IV, IV-S, respectively. There was no significant difference in EFS according to the completeness of resection. EFS was improved in GTR group (p=ns) of stage III, but by contrast, stage IV patients showed worse EFS in GTR group. EFS was improved significantly after the introduction of autologous stem cell transplantation (ASCT) (58.1% vs. 40.6%, p=.029). The EFS improved significantly after the introduction of ASCT in IR group (p=.009) rather than GTR group (p=ns). The EFS of the patients under 1 year of age (N=47) was better than the patients over 1 year of age (N=144) significantly (75.5 % vs. 39.4 %, p=.0034). The prognosis of neuroblastoma was related to the INSS stage and age at diagnosis. The survival of IR group significantly improved after ASCT.

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

• Radiation Oncology Journal
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• 제16권4호
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• pp.389-398
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• 1998

목적 : 천막상부 약성 신경교종의 치료로서 수술 후 방사선 치료의 역할을 생존율을 중심으로 평가하며 그 예후 인자를 분석한다. 대상 및 방법 : 1985년 9월부터 1997년 3월까지 수술 후 방사선 치료를 받은 69례의 환자를 대상으로 분석하였고 나이의 범위는 7세에서 66세이며 중앙값은 47세였다. 42례(61$\%$)는 다형성 교모세포종 이었고 27례(39$\%$)는 악성 성상세포종이었다. 20례(29$\%$)는 Karnofsky 역할수행능력 점수가 80점 이상이었다. 43례(62$\%$)는 수술 전 3개월 이내에 증상을 호소하였다. 24례 (35$\%$)는 육안 상 완전 절제를, 40례(58$\%$)는 부분 절제를, 나머지 5례(7$\%$)에서는 뇌정위 조직검사만 시행하였다. 총 방사선 조사량은 50.4-61.2Gy(중앙값, 55.8; 최빈값, 59.4)로 하루 1.8-2.0 Gy 씩 33-83일 동안(중앙값, 48) 치료하였다. 단 3례는 수술 후 전신 상태의 불량으로 하루 3.0Gy 씩 각각 33, 36, 39Gy 까지 치료하였다. 추적 관찰율은 93$\%$였고 중앙간은 14개월이었다. 결과 : 전체 환자의 2년 및 3년 생존율과 중앙 생존기간은 각각 38$\%$, 20$\%$, 16개월이었다. 악성 성상세포종과 다형성 교모세포종의 중앙생존기간은 각각 34, 14개월이었다(p=0.0001). 완전절제, 부분절제, 뇌정위 조직검사군에서의 3년 생존율은 각각 38$\%$, 11$\%$, 0$\%$였다(p=0.02). 연령이 40세 미만, 40-59, 60세 이상 군의 3년 생존율은 각각 52$\%$, 8$\%$, 0$\%$였다(p=0.0007). 역할수행 능력점수 80점 이상과 80점 미만군의 3년 생존율은 각각 53$\%$, 9$\%$였파(p=0.008). 상기와 같이 절제 정도에 따른 3개의 수술 군과 3개의 연령 군을 포함한 다요인 분석에서 병리학적등급, 수술 정도, 연령이 유의한 인자였다. 그러나 2개의 수술 군(완전절제와 비완전 절제)과 2개의 연령 군(50세 미만과 50세 이상)을 공변량으로한 다요인 분석에서 연령대신 병리학적 등급, 수술 정도, 역할수행 능력이 유의한 인자였고, 이들 세 가지 요인을 갖춘 5례는 치료와 관련한 심각한 부작용 없이 3년 누적생존율이 100$\%$로 생존하고 있다. 결론 : 악성 신경교종의 치료에서 수술 후 방사선치료를 추가함으로써 기존의 수술 단독의 생존율을 향상시키는 역할을 확인할 수 있었다. 악성 성상세포종 환자 중, 특히 양호한 역할수행 능력과 완전 절제를 받은 환자군의 생존율이 가장 양호하였다. 다형성 교모세포종 환자에서는 특히 젊은 나이인 경우 적절한 신경학적 기능보존과 함께 최대한의 종양 절제가 선행되어야 할 것으로 생각된다. 그러나 양호한 예후 인자를 갖지 못한 대부분의 다형성 교모세포종 환자군의 생존율은 여전히 좋지 않아 이 환자 군에서는 수술 후 통상적인 방사선 치료보다는 다른 적극적인 치료가 추가 또는 시도되어야 할 것으로 생각된다.

• Clinical and Experimental Pediatrics
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• 제63권5호
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• pp.171-177
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• 2020

Low-grade epilepsy-associated neuroepithelial tumors (LEATs) are responsible for drug-resistant chronic focal epilepsy, and are the second-most common reason for epilepsy surgery in children. LEATs are extremely responsive to surgical treatment, and therefore epilepsy surgery should be considered as a treatment option for LEATs. However, the optimal time for surgery remains controversial, and surgeries are often delayed. In this review, we reviewed published article on the factors associated with seizure and cognitive outcomes after epilepsy surgery for LEATs in children to help clinicians in their decision whether to pursue epilepsy surgery for LEATs. The achievement of gross total resection may be the most important prognostic factor for seizure freedom. A shorter duration of epilepsy, a younger age at surgery, and extended resection of temporal lobe tumors have also been suggested as favorable prognostic factors in terms of seizure control. Poor cognitive function in children with LEATs is associated with a longer duration of epilepsy and a younger age at seizure onset.

• Radiation Oncology Journal
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• 제22권2호
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• pp.91-97
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• 2004

목적 : 두개 내 다형성아교모세포종 환자의 방사선치료 후 생존율을 조사하고 그 예후 인자의 중요성을 알아보고자 하였다. 대상 및 방법: 1994년부터 2003년까지 삼성서울병원에서 병리학적으로 다형성아교모세포종으로 확진된 환자 중 근치적 목적으로 방사선치료를 시행한 120명을 대상으로 분석하였다. 남자는 64명(53$\%$), 여자는 56명(47$\%$)이었으며, 20례(17$\%$)의 종양은 다발성이었다. 수술은 육안적 완전 절제, 부분 절제 및 조직검사를 각각 22례(18$\%$), 59례(58$\%$), 29례(24$\%$)에서 시행하였고, 방사선치료는 4$\~$10 WV 선형가속기를 이용하여 54$\~$72Gy (중앙값 60 Gy)를 조사하였다. 대상 환자의 추적관찰기간은 2개월에서 62개월(중앙값 12개월)이었다. 결과 : 전체 환자군의 1년 및 2년 생존율은 52$\%$와 14$\%$이었으며, 중앙생존기간은 13개월이었다. 예후 인자에 따른 1년 생존율은 50세 미만은 64$\%$, 50세 이상은 41$\%$ (p<0.01), 수술 전 활동도가 ECOG 0 혹은 1인 경우 는 57$\%$, 2 이상은 44$\%$ (p=0.03)였다. 두개 내 병변 수에 따른 1년 생존율은 단일병변은 57$\%$, 다발성 병변은 23$\%$ (p=0.02)이었으며, 절제정도에 따른 생존율은 육안적 완전 절제, 부분 절제, 조직검사만 시행한 경우에 각각 67$\%$, 48$\%$, 47$\%$ (p=0.04)였다. 다변량 분석에 따른 예후인자로는 여자(p<0.01), 50세 미만(p<0.01), 활동도가 ECOG 0 혹은 1 (p=0.05), 육안적 완전절제(p=0.05)가 좋은 예후 인자이었다 결론 : 근치적 목적으로 방사선치료를 시행한 두개 내 다형성아교모세포종 환자의 중앙생존기간은 13개월로 기존의 문헌보고와 비슷한 수준이었다. 치료성적의 향상을 위하여 다양한 방사선치료 기술의 적용을 통한 방사선량의 증가와 효과적인 항암화학요법 약제의 개발 및 사용 등의 연구가 필요하고, 환자의 예후인자에 따라 개별화된 치료방법이 적용되어야 할 것으로 판단된다

• Asian Pacific Journal of Cancer Prevention
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• 제15권17호
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• pp.7241-7244
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• 2014

Background: To determine the accuracy of preoperative urinary symptoms, urinalysis, computed tomography (CT) and cystoscopic findings for the diagnosis of urinary bladder invasion in patients with colorectal cancer. Materials and Methods: Records of patients with colorectal cancer and a suspicion of bladder invasion, who underwent tumor resection with partial or total cystectomy between 2002 and 2013 at the Faculty of Medicine Siriraj Hospital, were reviewed. Correlations between preoperative urinary symptoms, urinalysis, cystoscopic finding, CT imaging and final pathological reports were analyzed. Results: This study included 90 eligible cases (71% male). The most common site of primary colorectal cancer was the sigmoid colon (44%), followed by the rectum (33%). Final pathological reports showed definite bladder invasion in 53 cases (59%). Significant features for predicting definite tumor invasion were gross hematuria (OR 13.6, sensitivity 39%, specificity 73%), and visible tumor during cystoscopy (OR 5.33, sensitivity 50%, specificity 84%). Predictive signs in CT imaging were gross tumor invasion (OR 7.07, sensitivity 89%, specificity 46%), abnormal enhancing mass at bladder wall (OR 4.09, sensitivity 68%, specificity 66%), irregular bladder mucosa (OR 3.53, sensitivity 70%, specificity 60% ), and loss of perivesical fat plane (OR 3.17, sensitivity 81%, specificity 43%). However, urinary analysis and other urinary tract symptoms were poor predictors of bladder involvement. Conclusions: The present study demonstrated that the most relevant preoperative predictors of definite bladder invasion in patients with colorectal cancer are gross hematuria, a visible tumor during cystoscopy, and abnormal CT findings.

• Journal of Korean Neurosurgical Society
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• 제46권1호
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• pp.74-76
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• 2009

We present an extremely rare case of the atypical choroid plexus papilloma in an adult which developed at the trigone of right lateral ventricle. A 62-year-old woman presented with the history of intermittent and gradually progressive headache and left side hemiparesis for 6 months. The brain magnetic resonance image showed highly enhanced and well demarcated mass at the trigone of lateral ventricle attached to the choroid plexus. Gross total resection was performed by transcortical approach via the middle temporal gyrus. The tumor was diagnosed as an atypical choroid plexus papilloma. She had no neurologic deficit after the surgery. We report a case of atypical choroid plexus papilloma in adult and introduce newly classified pathologic characteristics of this tumor.

• Journal of Korean Neurosurgical Society
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• 제37권3호
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• pp.232-234
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• 2005

We report a rare case of a patient with meningeal solitary fibrous tumor. A 60-year-old woman presented with right leg monoparesis. Brain magnetic resonance imaging demonstrates a well enhancing huge mass, located in left parietal lobe. Cerebral angiography demonstrating increased vascularity in area of the tumor, which had feeder vessels extending from the internal carotid artery and external carotid artery. A presumptive diagnosis of meningioma or hemangiopericytoma was considered. At surgery, the consistency was firm and had destroyed the dura and skull. A gross total resection was performed. Immunohistochemically, tumor was strongly, and widely, positive for CD34 and vimentin. There was no staining for epithelial membrane antigen(EMA), S-100 protein, cytokeratin, and glial fibrillary acidic protein (GFAP). Differential diagnosis of intracranial solitary fibrous tumor includes fibroblastic meningioma, meningeal hemangiopericytoma, neurofibroma, and schwannoma.

• Journal of Korean Neurosurgical Society
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• 제54권6호
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• pp.521-524
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• 2013

Ependymoma can spread via cerebrospinal fluid, but late spinal recurrences of intracranial tumor are very rare. We describe a case of a 33-year-old male who presented with multiple, delayed, recurrent lesions in the spinal cord from an intracranial ependymoma. The patient underwent gross total resection and postoperative radiation therapy 14 years prior to visit for a low grade ependymoma in the 4th ventricle. The large thoraco-lumbar intradural-extramedullary spinal cord tumor was surgically removed and the pathologic diagnosis was an anaplastic ependymoma. An adjuvant whole-spine radiation therapy for residual spine lesions was performed. After completion of radiation therapy, a MRI showed a near complete response and the disease was stable for three years.