• 제목/요약/키워드: Abducens palsy

검색결과 35건 처리시간 0.023초

터어키안 주변종양에 대한 감마나이프 방사선 수술 (Gamma Knife Radiosurgery for Juxtasellar Tumors)

  • 장종희;장진우;박용구;정상섭
    • Journal of Korean Neurosurgical Society
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    • 제29권10호
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    • pp.1345-1351
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    • 2000
  • Objective : Around the sellar area, there are many important structures. But, the optimal radiation dosage for minimal toxicity to surrounding neural tissue has not been firmly established. The purpose of this study is to evaluate the radiosurgical outcome of juxtasellar tumors and to investigate the relationship between radiation dosage and toxicity to neural tissue. Method : Between May 1992 and June 2000, we treated 65 juxtasellar tumors by using the Leksell Gamma Knife. Among them, 52 patients who could be followed more than 1 year were included in this study. The radiosurgical dosage to the optic pathway, cavernous sinus, Meckel's cave, hypothalamus, pituitary gland and stalk, and brain stem was analyzed and correlated with clinical outcome. The mean follow-up period was 33.5 months(range 12.2- 99.0 months). Result : The clinical response rate was 69.2%. The volume response rate was 61.0% and the radiologic control rate was 92.7%. There were 4 complications(7.7%) of 2 trigeminal neuropathy, 1 abducens nerve palsy, and 1 trigeminal and transient abducens nerve palsy. The optic apparatus appeared to tolerate doses greater than 10Gy. The risk of cranial nerve complications in cavernous sinus seemed to be related to doses of more than 16Gy. In 3 of 4 patients who received more than 16Gy to cavernous sinus, the abducens or trigeminal neuropathy occurred. Also, one patient who received more than 15Gy to the Meckel's cave, trigeminal neuropathy developed. The hypothalamus, pituitary gland and stalk, and brain stem were relatively tolerable to radiation. Conclusion : Gamma Knife radiosurgery seems to be an effective method to control the growth of juxtasellar tumors. To avoid injury to surrounding important neural tissue, careful dose planning and further study for radiation toxicity to neural tissue were needed.

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Diplopia developed by cervical traction after cervical spine surgery

  • Kim, Ji-Yoon;Kim, Hyuna;Kang, So Jeong;Kim, Hyunjee;Lee, Young-Seok
    • Journal of Yeungnam Medical Science
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    • 제38권2호
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    • pp.152-156
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    • 2021
  • Diplopia is a rare complication of spine surgery. The abducens nerve is one of the cranial nerves most commonly related to diplopia caused by traction injury. We report a case of a 71-year-old woman who presented with diplopia developing from abducens nerve palsy after C1-C2 fixation and fusion due to atlantoaxial subluxation with cord compression. As soon as we discovered the symptoms, we suspected excessive traction by the instrument and subsequently performed reoperation. Subsequently, the patient's symptoms improved. In other reported cases we reviewed, most were transient. However, we thought that our rapid response also helped the patient's fast recovery in this case. The mechanisms by which postoperative diplopia develops vary and, thus, remain unclear. We should pay attention to the fact that the condition is sometimes an indicator of an underlying, life-threatening condition. Therefore, all patients with postoperative diplopia should undergo thorough ophthalmological and neurological evaluations as well as careful observation by a multidisciplinary team.

키아리 1형 기형을 동반한 고도 척추 측만증에서 수술 전 Halo-Pelvic 견인 후 발생한 6번 뇌신경(외전신경) 마비 (Sixth Cranial Nerve (Abducens Nerve) Palsy after Preoperative Halo-Pelvic Traction for Severe Scoliosis with Chiari I Malformation)

  • 황재광;이춘성;최신우;김정환
    • 대한정형외과학회지
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    • 제55권6호
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    • pp.534-539
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    • 2020
  • 고도 척추 측만증의 치료는 척추외과 의사에게 어려운 과제로 남아있다. 고도 척추 측만증의 수술 시 급격한 교정은 신경학적 손상이나 기구 실패 등의 수술 중 합병증의 위험을 증가시킬 수 있다. 이러한 합병증을 최소화하기 위해 최종 수술을 시행하기에 앞서 부분 교정을 얻기 위한 다양한 수술 전 견인법들이 사용되고 있다. 하지만 이전 연구에 의하면 halo 견인과 관련한 합병증의 하나로 뇌신경 마비가 발생할 수 있으며 대표적으로 6번 뇌신경(외전신경)의 마비가 가장 흔하게 나타난다. 이러한 합병증을 줄이기 위해 견인 무게의 점진적 증량이나 세심한 신경학적 검진이 필요하며 특히 이전에 뇌수술이나 경추부 수술을 시행한 경우에는 더욱 주의가 필요할 수 있다. 저자들은 이전에 키아리 1형 기형과 관련하여 감압술을 시행했던 고도 척추 측만증에서 수술 전 halo-pelvic 견인에 의한 6번 뇌신경 마비의 증례를 경험하였기에 문헌 고찰과 함께 보고하고자 한다.

Oral findings and dental management of a patient with Moebius syndrome: a case report

  • Lee, Eunkyoung;Kim, Youngjin;Kim, Hyunjung;Nam, Soonhyeun
    • 대한장애인치과학회지
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    • 제10권2호
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    • pp.101-105
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    • 2014
  • Moebius syndrome is a rare, congenital neurological disease involving facial paralysis and limitation of eye movements. It results from maldevelopment of the sixth and seventh cranial nerves. Dental features of this syndrome include micrognathia, microstomia, tongue deformity, cleft palate, hypoplasia of the teeth, and congenital missing teeth. A 7-year-old female with Moebius syndrome was referred from a local dental clinic for caries treatment. She presented with facial paralysis and microstomia. Oral findings included multiple caries with enamel hypoplasia, congenital missing teeth, and tongue deformity. Dental treatments including restorative and preventive procedures were performed. Oral findings and management aspects of Moebius syndrome for this case are discussed. Early evaluation and multidisciplinary care are needed for children with Moebius syndrome.

Sixth Cranial Nerve Palsy Caused by Gastric Adenocarcinoma Metastasis to the Clivus

  • Lee, Aleum;Chang, Kee-Hyun;Hong, Hyunsook;Kim, Heekyung
    • Journal of Korean Neurosurgical Society
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    • 제57권3호
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    • pp.208-210
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    • 2015
  • Tumors of the clivus and metastases to the clivus are very rare. Metastasis involving the clivus has previously been described in only two case reports. In skull metastasis, the breast and prostate are the most common primary foci, while metastasis from gastric carcinoma is extremely rare. A review of the English literature revealed only one published case of clivus metastases from gastric adenocarcinoma. There is no literature thoroughly explaining the differential diagnosis between chordoma and metastasis. Here we report a rare case of metastasis to the clivus from a gastric adenocarcinoma in a 42-year-old female patient with sudden blurry vision, presenting as bilateral cranial nerve VI palsy.

밀러-피셔 증후군 환자의 양안 외전신경마비 치험 1례 (A Case Report of Miller-Fisher Syndrome with Bilateral Abducens Nerve Palsy)

  • 윤석영;노민영;감은영;강은정;김종한;최정화;박수연;정민영;이지현
    • 한방안이비인후피부과학회지
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    • 제33권4호
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    • pp.133-144
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    • 2020
  • Objectives : The purpose of this study is to report the effect of Korean medicine treatment on limitation of eye movement in Miller-Fisher Syndrome. Methods : A patient was treated with herbal medicines, acupuncture(including electropuncture, phamacopuncture), Moxibustion and cupping therapy. To evaluate the result of this treatment, we used photographs of eye movement, Scott and Kraft score of both eye, length of eyeball movement and visual analogue scale(VAS) for subjective symptoms. Results : After treatment, the limitation of eye movement and diplopia were remarkably improved. Also, other symptoms such as dizziness, gait disturbance, facial nerve disorder were disappeared. Conclusions : This study suggests that Korean medicine treatments are effective for patient with limitation of eye movement in Miller-Fisher Syndrome.

Epidural blood patch treatment of diplopia that developed after headache resolution in a patient with spontaneous intracranial hypotension

  • Lee, Myung-Su;Lee, Sookyung;Seo, Dong-Kyun;Yoon, Syn-Hae;Choi, Seong-Soo
    • Journal of Dental Anesthesia and Pain Medicine
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    • 제18권4호
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    • pp.255-259
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    • 2018
  • Sudden headache onset may rarely be caused by spontaneous intracranial hypotension (SIH). Other associated symptoms in patients with SIH are nausea, vomiting, vertigo, hearing alteration, and visual disturbance. This case report describes a 43-year-old female diagnosed with SIH who developed diplopia after resolution of an abrupt-onset headache, which was managed with conservative treatments, including bed rest and hydration. She was also diagnosed with secondary right sixth cranial nerve palsy. Although conservative management relieved her headache, the diplopia was not fully relieved. Application of an autologous epidural blood patch successfully relieved her diplopia, even after 14 days from the onset of visual impairment.

Möbius Syndrome Demonstrated by the High-Resolution MR Imaging: a Case Report and Review of Literature

  • Hwang, Minhee;Baek, Hye Jin;Ryu, Kyeong Hwa;Choi, Bo Hwa;Ha, Ji Young;Do, Hyun Jung
    • Investigative Magnetic Resonance Imaging
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    • 제23권2호
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    • pp.167-171
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    • 2019
  • $M\ddot{o}bius$ syndrome is a rare congenital condition, characterized by abducens and facial nerve palsy, resulting in limitation of lateral gaze movement and facial diplegia. However, to our knowledge, there have been few studies on evaluation of cranial nerves, on MR imaging in $M\ddot{o}bius$ syndrome. Herein, we describe a rare case of $M\ddot{o}bius$ syndrome representing limitation of lateral gaze, and weakness of facial expression, since the neonatal period. In this case, high-resolution MR imaging played a key role in diagnosing $M\ddot{o}bius$ syndrome, by direct visualization of corresponding cranial nerves abnormalities.

마비사시 소아 환자에 대한 증례 보고 1례 (A Case Report of Paralytic Strabismus in Childhood)

  • 권지현;김경민;유선애
    • 대한한방소아과학회지
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    • 제34권1호
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    • pp.61-70
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    • 2020
  • Objectives The purpose of this study is to report the effectiveness of Korean medicine on treating paralytic strabismus in childhood. Methods We treated a 4-years-old patient who was diagnosed with paralytic strabismus with herbal medicine, laser acupuncture, T-acupuncture and moxibustion. Results After 5 months of the Korean medicine treatment, the child's strabismus, diplopia, and limitation of abduction were improved. There was no recurrence of the symptoms for 1 year and 4 months. Conclusions Korean medicine treatment can be effective in improving symptoms of paralytic strabismus. However, further studies are needed to demonstrate the treatment benefits to abducens nerve palsy.

뫼비우스 증후군에서 측두근 전위술을 이용한 역동적 재건 (Dynamic Reconstruction with Temporalis Muscle Transfer in Mobius Syndrome)

  • 김백규;이윤호
    • Archives of Plastic Surgery
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    • 제34권3호
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    • pp.325-329
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    • 2007
  • Purpose: Mobius syndrome is a rare congenital disorder characterized by facial diplegia and bilateral abducens palsy, which occasionally combines with other cranial nerve dysfunction. The inability to show happiness, sadness or anger by facial expression frequently results in social dysfunction. The classic concept of cross facial nerve grafting and free muscle transplantation, which is standard in unilateral developmental facial palsy, cannot be used in these patients without special consideration. Our experience in the treatment of three patients with this syndrome using transfer of muscles innervated by trigeminal nerve showed rewarding results. Methods: We used bilateral temporalis muscle elevated from the bony temporal fossa. Muscles and their attached fascia were folded down over the anterior surface of the zygomatic arch. The divided strips from the attached fascia were passed subcutaneously and anchored to the medial canthus and the nasolabial crease for smiling and competence of mouth and eyelids. For the recent 13 years the authors applied this method in 3 Mobius syndrome cases- 45 year-old man and 13 year-old boy, 8 year-old girl. Results: One month after the surgery the patients had good support and already showed voluntary movement at the corner of their mouth. They showed full closure of both eyelids. There was no scleral showing during eyelid closure. Also full closure of the mouth was achieved. After six months, the reconstructed movements of face were maintained. Conclusion: Temporalis muscle transfer for Mobius syndrome is an excellent method for bilateral reconstruction at one stage, is easy to perform, and has a wide range of reconstruction and reproducibility.