1.Analysis According to Characteristics of 18 Cases of Brachial Plexus Tumors : A Review of Surgical Treatment Experience
In Ho JUNG ; Kyeong Wook YOON ; Young Jin KIM ; Sang Koo LEE
Journal of Korean Neurosurgical Society 2018;61(5):625-632
		                        		
		                        			
		                        			OBJECTIVE: Because the anatomical structure of the brachial plexus is very complex, surgical treatment of tumors in this region is challenging. Therefore, a lot of clinical and surgical experience is required for successful treatment; however, many neurosurgeons have difficulty accumulating this experience owing to the rarity of brachial plexus tumors. The purpose of this report is to share our surgical experience with brachial plexus tumor with other neurosurgeons.METHODS: The records of 18 consecutive patients with brachial plexus tumors who underwent surgical treatment between January 2010 and December 2017 in a single institution were retrospectively reviewed. The surgical approach was determined according to the tumor location and size, and intraoperative neurophysiological monitoring (IONM) was used in most of cases to prevent iatrogenic nerve injury during surgery. In addition, to evaluate the differences in tumor characteristics according to pathologic diagnosis, the tumors were divided twice into two groups, based on two separate classifications, and statistical analysis was performed.RESULTS: The 18 brachial plexus tumors comprised 15 (83.3%) benign peripheral nerve sheath tumors including schwannoma and neurofibroma, one (5.6%) malignant peripheral nerve sheath tumor, one (5.6%) benign tumor of non-neural sheath origin (neurogenic cyst), and one (5.6%) metastatic tumor (papillary carcinoma). The authors analyzed relationship between tumor size/location and tumor characteristic parameters such as age, size, right-left, and pathology. There were no statistically significant differences except a tendency of bigger tumor size in young age.CONCLUSION: For a successful surgical outcome, an appropriate surgical approach is essential, and the appropriate surgical approach is determined by the location and size of the tumor. Furthermore, applying IONM may prevent postoperative complications and it is favorable option for brachial plexus tumors surgery.
		                        		
		                        		
		                        		
		                        			Brachial Plexus Neuropathies
		                        			;
		                        		
		                        			Brachial Plexus
		                        			;
		                        		
		                        			Classification
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Intraoperative Neurophysiological Monitoring
		                        			;
		                        		
		                        			Monitoring, Intraoperative
		                        			;
		                        		
		                        			Nerve Sheath Neoplasms
		                        			;
		                        		
		                        			Neurilemmoma
		                        			;
		                        		
		                        			Neurofibroma
		                        			;
		                        		
		                        			Neurosurgeons
		                        			;
		                        		
		                        			Pathology
		                        			;
		                        		
		                        			Peripheral Nerves
		                        			;
		                        		
		                        			Postoperative Complications
		                        			;
		                        		
		                        			Retrospective Studies
		                        			
		                        		
		                        	
2.Subfrontal Schwannoma Extended Broadly to Nasal Cavity Treated by Gamma Knife Radiosurgery Following Surgical Excision: A Case Report.
Soo Hee KIM ; Jung Hwan LEE ; Soon Ki SUNG ; Chang Hwa CHOI
Brain Tumor Research and Treatment 2017;5(2):116-119
		                        		
		                        			
		                        			Subfrontal schwannomas are rarely reported. They are usually found only in the subfrontal area, but some extend to the nasal cavity. In these cases, prevention of postoperative cerebrospinal fluid (CSF) leakage through thinned or eroded anterior skull base is important. A 51-year-old female with anosmia and mild nausea was diagnosed as subfrontal extraaxial mass with nasal cavity extension. This mass was initially thought to be an olfactory groove meningioma. We performed a bifrontal craniotomy for surgical excision. We did not totally remove the tumor, as we wanted to prevent a skull base defect. The histopathological diagnosis was a schwannoma. There was no postoperative complication such as CSF leakage. The residual tumor was treated with gamma knife radiosurgery. The nasal cavity mass has not grown as of five years after radiosurgery.
		                        		
		                        		
		                        		
		                        			Cerebrospinal Fluid
		                        			;
		                        		
		                        			Cerebrospinal Fluid Leak
		                        			;
		                        		
		                        			Craniotomy
		                        			;
		                        		
		                        			Cytochrome P-450 CYP1A1
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Meningioma
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Nasal Cavity*
		                        			;
		                        		
		                        			Nausea
		                        			;
		                        		
		                        			Neoplasm, Residual
		                        			;
		                        		
		                        			Neurilemmoma*
		                        			;
		                        		
		                        			Olfaction Disorders
		                        			;
		                        		
		                        			Olfactory Nerve
		                        			;
		                        		
		                        			Postoperative Complications
		                        			;
		                        		
		                        			Radiosurgery*
		                        			;
		                        		
		                        			Skull Base
		                        			
		                        		
		                        	
3.One Stage Posterior Minimal Laminectomy and Video-Assisted Thoracoscopic Surgery (VATS) for Removal of Thoracic Dumbbell Tumor.
Kyoung Hyup NAM ; Hyo Yeoung AHN ; Jeong Su CHO ; Yeoung Dae KIM ; Byung Kwan CHOI ; In Ho HAN
Journal of Korean Neurosurgical Society 2017;60(2):257-261
		                        		
		                        			
		                        			OBJECTIVE: This study was conducted to assess the surgical results of one-stage posterior minimal laminectomy and video-assisted thoracoscopic surgery (VATS) for the treatment of thoracic dumbbell tumor and to describe its precise technique. In addition, we investigated the technique's usefulness and limitations. METHODS: Seven cases of thoracic dumbbell tumor (two men and five women, mean age, 43 years) were analyzed retrospectively. Pathological findings included schwannoma in four patients, neurofibroma in two patients, and hemangioma in one patient. The location of tumors varied from T2/3 to T12/L1. Dumbbell tumors were resected by one-stage operation using posterior laminectomy followed by VATS without instrumentation. Clinical data were reviewed. RESULTS: The mean follow-up period was 25 months (range, 3–58 months), and the operative time ranged from 255 to 385 min (mean, 331 min), with estimated blood loss ranging from 110 to 930 mL (mean, 348 mL). The tumor was completely resected without instrumentation and postoperative instability in all cases. Postoperative complications included atelectasis and facial anhydrosis in one case each. CONCLUSION: One-stage posterior minimal laminectomy and VATS may be a safe and less invasive technique for removal of thoracic dumbbell tumor without instability. This method has the advantage of early ambulation and rapid recovery because it reduces blood loss and postoperative pain.
		                        		
		                        		
		                        		
		                        			Early Ambulation
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Hemangioma
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Laminectomy*
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Methods
		                        			;
		                        		
		                        			Neurilemmoma
		                        			;
		                        		
		                        			Neurofibroma
		                        			;
		                        		
		                        			Operative Time
		                        			;
		                        		
		                        			Pain, Postoperative
		                        			;
		                        		
		                        			Postoperative Complications
		                        			;
		                        		
		                        			Pulmonary Atelectasis
		                        			;
		                        		
		                        			Retrospective Studies
		                        			;
		                        		
		                        			Thoracic Surgery, Video-Assisted*
		                        			
		                        		
		                        	
4.Schwannoma of the Orbit.
Kwang Seog KIM ; Jin Woo JUNG ; Kyung Chul YOON ; Yu Jin KWON ; Jae Ha HWANG ; Sam Yong LEE
Archives of Craniofacial Surgery 2015;16(2):67-72
		                        		
		                        			
		                        			BACKGROUND: A schwannoma is a benign, slow-growing peripheral nerve sheath tumor that originates from Schwann cells. Orbital schwannomas are rare, accounting for only 1% of all orbital neoplasms. In this study, we retrospectively review orbital schwannomas and characterize clinical, radiologic, and histologic features of this rare entity. METHODS: A retrospective review was performed to identify patients with histologically confirmed orbital schwannoma, among a list of 437 patients who had visited our hospital with soft tissue masses within the orbit as the primary presentation between 2010 and 2014. Patient charts and medical records were reviewed for demographic information, relevant medical and family history, physical examination findings relating to ocular and extraocular sensorimotor function, operative details, postoperative complications, pathologic report, and recurrence. RESULTS: Five patients (5/437, 1.1%) were identified as having histologically confirmed orbital schwannoma and underwent complete excision. Both computed tomography (CT) and magnetic resonance imaging (MRI) studies were not consistent in predicting histologic diagnosis. There were no complications, and none of the patients experienced significant scar formation. In two cases, patients exhibited a mild postoperative numbness of the forehead, but the patients demonstrated full recovery of sensation within 3 months after the operation. None of the five patients have experienced recurrence. CONCLUSION: Orbital schwannomas are relatively rare tumors. Preoperative diagnosis is difficult because of its variable presentation and location. Appropriate early assessment of orbital tumors by CT or MRI and prompt management is warranted to prevent the development of severe complications. Therefore, orbital schwannomas should be considered in the differential diagnosis of slow-growing orbital masses.
		                        		
		                        		
		                        		
		                        			Cicatrix
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Diagnosis, Differential
		                        			;
		                        		
		                        			Forehead
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Hypesthesia
		                        			;
		                        		
		                        			Magnetic Resonance Imaging
		                        			;
		                        		
		                        			Medical Records
		                        			;
		                        		
		                        			Neurilemmoma*
		                        			;
		                        		
		                        			Orbit*
		                        			;
		                        		
		                        			Orbital Neoplasms
		                        			;
		                        		
		                        			Peripheral Nerves
		                        			;
		                        		
		                        			Physical Examination
		                        			;
		                        		
		                        			Postoperative Complications
		                        			;
		                        		
		                        			Recurrence
		                        			;
		                        		
		                        			Retrospective Studies
		                        			;
		                        		
		                        			Schwann Cells
		                        			;
		                        		
		                        			Sensation
		                        			
		                        		
		                        	
5.Retrospective Analysis of Thoracoscopic Surgery for Esophageal Submucosal Tumors.
Seung Ku KANG ; Ju Sik YUN ; Sang Hyung KIM ; Sang Yun SONG ; Yochun JUNG ; Kook Joo NA
The Korean Journal of Thoracic and Cardiovascular Surgery 2015;48(1):40-45
		                        		
		                        			
		                        			BACKGROUND: Surgical enucleation is the treatment of choice for esophageal submucosal tumors (SMTs) with symptomatic, larger, or ill-defined lesions. The enucleation of SMTs has traditionally been performed via thoracotomy. However, minimally invasive approaches have recently been introduced and successfully applied. In this study, we present our experiences with the thoracotomic and thoracoscopic approaches to treating SMTs. METHODS: We retrospectively reviewed 53 patients with SMTs who underwent surgical enucleation between August 1996 and July 2013. Demographic and clinical features, tumor-related factors, the surgical approach, and outcomes were analyzed. RESULTS: There were 36 males (67.9%) and 17 females (32.1%); the mean age was 49.2+/-11.8 years (range, 16 to 79 years). Histology revealed leiomyoma in 51 patients, a gastrointestinal stromal tumor in one patient, and schwannoma in one patient. Eighteen patients (34.0%) were symptomatic. Fourteen patients underwent a planned thoracotomic enucleation. Of the 39 patients for whom a thoracoscopic approach was planned, six patients required conversion to thoracotomy because of overly small tumors or poor visualization in five patients and accidental mucosal injury in one patient. No mortality or major postoperative complications occurred. Compared to thoracotomy, the thoracoscopic approach had a slightly shorter operation time, but this difference was not statistically significant (120.0+/-45.6 minutes vs. 161.5+/-71.1 minutes, p=0.08). A significant difference was found in the length of the hospital stay (9.0+/-3.2 days vs. 16.5+/-5.4 days, p<0.001). CONCLUSION: The thoracoscopic enucleation of submucosal esophageal tumors is safe and is associated with a shorter length of hospital stay compared to thoracotomic approaches.
		                        		
		                        		
		                        		
		                        			Female
		                        			;
		                        		
		                        			Gastrointestinal Stromal Tumors
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Leiomyoma
		                        			;
		                        		
		                        			Length of Stay
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Mortality
		                        			;
		                        		
		                        			Neurilemmoma
		                        			;
		                        		
		                        			Postoperative Complications
		                        			;
		                        		
		                        			Retrospective Studies*
		                        			;
		                        		
		                        			Thoracoscopy*
		                        			;
		                        		
		                        			Thoracotomy
		                        			
		                        		
		                        	
6.The management of facial nerve tumors involving the internal auditory canal.
Xiaoan ZHANG ; Yu LI ; Chunfu DAI
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2015;29(14):1235-1238
		                        		
		                        			OBJECTIVE:
		                        			10 summarize tne clinical features of the facial nerve tumors involving the internal auditory canal and promote the management of facial nerve tumor.
		                        		
		                        			METHOD:
		                        			We retrospectively reviewed the clinical manifestations, the experiences of diagnosis and treatment of the facial nerve tumor involving the internal auditory canal. All these 5 cases were enrolled during January 2013 to Apr 2015.
		                        		
		                        			RESULT:
		                        			Among the 5 cases, 3 cases were facial neurilemmoma and the others were facial neurofibroma. The main symptoms of facial nerve tumors involving the internal auditory canal most commonly were facial paralysis companied with hearing loss. All the patients accepted the surgical treatment with various approaches, 3 cases of translabyrinthine approach, 1 case of middle fossa approach, and 1 case of combination of translabyrinthine and transotic approach. Total tumor resection were achieved in all 5 cases. Facial-hypoglossal nerve anastomosis was performed in one case, another case was undergone great auricular nerve graft.
		                        		
		                        			CONCLUSION
		                        			Surgical intervention for patients with facial neuroma involving internal auditory canal should be considered when facial weakness has deteriorated to grade 4. The management should be based on the patient's hearing, facial nerve function, tumor size and invasive extension to select the appropriate surgical procedures.
		                        		
		                        		
		                        		
		                        			Anastomosis, Surgical
		                        			;
		                        		
		                        			Cranial Nerve Neoplasms
		                        			;
		                        		
		                        			diagnosis
		                        			;
		                        		
		                        			surgery
		                        			;
		                        		
		                        			Facial Nerve
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			surgery
		                        			;
		                        		
		                        			Facial Nerve Diseases
		                        			;
		                        		
		                        			diagnosis
		                        			;
		                        		
		                        			surgery
		                        			;
		                        		
		                        			Facial Paralysis
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			Hearing Loss
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Hypoglossal Nerve
		                        			;
		                        		
		                        			surgery
		                        			;
		                        		
		                        			Neurilemmoma
		                        			;
		                        		
		                        			diagnosis
		                        			;
		                        		
		                        			Neurofibroma
		                        			;
		                        		
		                        			diagnosis
		                        			;
		                        		
		                        			Retrospective Studies
		                        			
		                        		
		                        	
7.Laparoscopic resection for 125 gastroduodenal submucosal tumors.
Dong Jin KIM ; Jun Hyun LEE ; Wook KIM
Annals of Surgical Treatment and Research 2014;86(4):199-205
		                        		
		                        			
		                        			PURPOSE: The present study aims to elucidate the treatment strategies of laparoscopic resection for gastroduodenal submucosal tumors (SMTs). METHODS: Data of 125 gastroduodenal STMs were collected retrospectively resected from August, 2004 to February, 2013. Surgical outcomes according to tumor locations, pathologic results and survival data for gastrointestinal stromal tumors (GISTs) were collected and analyzed. RESULTS: There were 55 male and 70 female patients with mean age 57.9 +/- 12.7 years old. Mean tumor size of gastric SMTs was 2.7 +/- 1.64 cm (range, 0.4-8.5 cm). GIST was the most common (n = 70, 56%). Regarding the tumor location, all the fundic lesions were GISTs and leiomyoma was occurred 58.8% of cardiac lesions. Ectopic pancreas and schwannomas were mostly located at body portion, 73% and 80%, respectively. SMTs located at duodenal bulb comprise 4 GISTs and 3 carcinoids. Surgical results comparing between lesions located at cardia, near-pylorus and else had no difference in operation time, hospital stay and complications. In terms of outcome of GIST, all patients underwent curative resection except one case of peritoneal sarcomatosis. There was one recurrence in a high risk group following resection. The cumulative 5-year disease free survival rate was 93.5% in all GISTs. There were two postoperative complications, one gastric outlet obstruction and one leakage following wedge resection. CONCLUSION: Laparoscopic wedge resection is a safe and feasible procedure for the small to medium sized gastroduodenal SMTs even their locations are near cardia or pylorus.
		                        		
		                        		
		                        		
		                        			Carcinoid Tumor
		                        			;
		                        		
		                        			Cardia
		                        			;
		                        		
		                        			Disease-Free Survival
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Gastric Outlet Obstruction
		                        			;
		                        		
		                        			Gastrointestinal Stromal Tumors
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Laparoscopy
		                        			;
		                        		
		                        			Leiomyoma
		                        			;
		                        		
		                        			Length of Stay
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Neurilemmoma
		                        			;
		                        		
		                        			Pancreas
		                        			;
		                        		
		                        			Postoperative Complications
		                        			;
		                        		
		                        			Pylorus
		                        			;
		                        		
		                        			Recurrence
		                        			;
		                        		
		                        			Retrospective Studies
		                        			;
		                        		
		                        			Stomach Neoplasms
		                        			
		                        		
		                        	
8.Schwannoma of Ansa Cervicalis in the Submandibular Space.
Ji Hye PARK ; Dongbin AHN ; Ki Ha HWANG ; Ji Yun JEONG
Korean Journal of Otolaryngology - Head and Neck Surgery 2014;57(9):616-619
		                        		
		                        			
		                        			Although schwannomas can arise from all types of nerves except the optic and olfactory nerves, those that arise from the ansa cervicalis is extremely rare, with only four cases having been reported worldwide. Because of their rarity, ansa cervicalis schwannomas are rarely considered in patients presenting with schwannomas of the neck region. In the present case, we did not consider ansa cervicalis as the nerve of origin preoperatively, but during the surgery, found a mass originating from the ansa cervicalis by identifying a contracture of the strap muscles. We thus address the need to consider ansa cervicalis as a possible original site in the evaluation and management of schwannomas of the neck region. In addition, surgeons should focus on the intraoperative findings to determine the nerve of origin and to anticipate postoperative complications, as well as performing appropriate preoperative imaging studies.
		                        		
		                        		
		                        		
		                        			Contracture
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Muscles
		                        			;
		                        		
		                        			Neck
		                        			;
		                        		
		                        			Neurilemmoma*
		                        			;
		                        		
		                        			Olfactory Nerve
		                        			;
		                        		
		                        			Postoperative Complications
		                        			;
		                        		
		                        			Submandibular Gland
		                        			
		                        		
		                        	
9.The management of facial nerve tumor manifested as facial paralysis.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2014;29(8):716-719
		                        		
		                        			OBJECTIVE:
		                        			To heighten the awareness of the facial nerve tumors.
		                        		
		                        			METHOD:
		                        			The clinical data of twenty-three patients complaining of facial paralysis who were diagnosed postoperatively as facial nerve tumors were analyzed. The hearing assessment of all patients was based on pure tone audiometry at the frequency of 0. 5, 1, 2, 4 kHz. Temporal bone high resolution CT scan and temporal bone MRI with gadolinium enhancement were conducted on all patients. Facial nerve function was assessed with the House-Brackmann (HB) grading system. Facial electroneurography (ENoG) was conducted on 20 patients to quantify the degree of nerve degeneration preoperatively. The pathological types of tumor were determined by postoperative pathological reports.
		                        		
		                        			RESULT:
		                        			Nineteen out of 23 cases presented hearing loss (82.6%), 10 cases suffered from tinnitus (43.5%), otalgia (17.4%) affected 4 cases, 3 cases manifested otorrhea (13.0%), and 2 cases presented vertigo (8.7%). Geniculate ganglion was the most commonly involved site (20 cases, 87.0%), followed by tympanic segments (18 cases, 78.3%), pyramid segment (16 cases, 69.6%), mastoid segment (10 cases, 43.5%), labyrinthine segment (9 cases, 39.1%), internal auditory canal segment and parotid gland segment (5 cases, 21.7%, respectively). Twenty-one cases (91.3%) of schwannomas, 1 case (4.3%) of neurofibroma and 1 case (4.3%) of hemangiomas were identified with histopathology postoperatively. The tumors were all completely excised, and the facial nerve function could recovered to HB III at the best after facial nerve repairment.
		                        		
		                        			CONCLUSION
		                        			Facial nerve tumor is a rare and often misdiagnosed disease which was commonly manifested as facial nerve paralysis. Temporal bone CT and MRI can help to clarify the diagnosis preoperatively. Pure tone audiometry and electroneurography also plays a some certain roles in the diagnosis of facial nerve tumors. The tumors should be completely resected and the surgical approaches were determined based on tumor size, facial nerve function and preoperative auditory function.
		                        		
		                        		
		                        		
		                        			Cranial Nerve Neoplasms
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			Facial Nerve
		                        			;
		                        		
		                        			pathology
		                        			;
		                        		
		                        			Facial Nerve Diseases
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			Facial Paralysis
		                        			;
		                        		
		                        			etiology
		                        			;
		                        		
		                        			Hearing Loss
		                        			;
		                        		
		                        			Hemangioma
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Neurilemmoma
		                        			;
		                        		
		                        			Temporal Bone
		                        			
		                        		
		                        	
10.1 case of vocal cord plexiform schwannoma.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2014;28(23):1898-1899
		                        		
		                        			
		                        			Summary A 36 years old patient with hoarseness for 2 years and got worsen for one month, electronic laryngoscopy showed a red smooth-faced wide based neoplasm on the posterior 2/3 of the right side of the vocal cords. The neoplasm was excised under suspension laryngoscope . The pathologic results showed:Cells were weave patterned, infiltrative growth, mitotic figure was rare. Immunohistochemical results showed CD34 (-), SMA (-), DM (-), S - 100 (+). The pathological diagnosis was plexiform schwannoma.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Hoarseness
		                        			;
		                        		
		                        			etiology
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Laryngeal Neoplasms
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			diagnosis
		                        			;
		                        		
		                        			surgery
		                        			;
		                        		
		                        			Laryngoscopes
		                        			;
		                        		
		                        			Laryngoscopy
		                        			;
		                        		
		                        			Neurilemmoma
		                        			;
		                        		
		                        			complications
		                        			;
		                        		
		                        			diagnosis
		                        			;
		                        		
		                        			surgery
		                        			;
		                        		
		                        			Syndrome
		                        			;
		                        		
		                        			Vocal Cords
		                        			;
		                        		
		                        			pathology
		                        			
		                        		
		                        	
            
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