• Title/Summary/Keyword: Muscle Weakness

검색결과 402건 처리시간 0.032초

Focal Atrophy of the Unilateral Masticatory Muscles Caused by Trigeminal Neuropathy from the Tumor in the Foramen Ovale

  • Juhyung Hong;Jin-Woo Chung
    • Journal of Oral Medicine and Pain
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    • 제47권4호
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    • pp.217-221
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    • 2022
  • Neurogenic muscular atrophy is muscle wasting and weakness caused by trauma or disease of the nerve that innervates the muscle. We describe a case of unilateral trigeminal neuropathy and neurogenic muscular atrophy of the masticatory muscle caused by a tumor in the foramen ovale. A 59-year-old man visited our clinic complaining of difficulty in right-sided mastication. There were no evident clinical signs and symptoms of temporomandibular disorder. However, severe atrophy of the right masseter and temporalis muscles and hypesthesia of the right side mandibular nerve area were confirmed. Through T1 and T2 signals on magnetic resonance imaging (MRI), a mass suspected of a neurogenic tumor was observed in the foramen ovale and cavernous sinus. Severe atrophy of all masticatory muscles on the right side was observed. This rare case shows trigeminal neuropathy caused by a tumor around the foramen ovale and atrophy of the ipsilateral masticatory muscles. For an accurate diagnosis, it is essential to identify the underlying cause of muscle atrophy with neurologic symptoms present. This can be done through a more detailed clinical examination, including sensory testing and brain MRI, and consider a referral to neurology or neurosurgery for the differential diagnosis of the intracranial disorder.

股關節外轉の時の中臀筋の筋力及び活動電位の變化に關する硏究 (A Myometric and Electromyographic Analysis of Hip Abductor Musculature in Healthy Right-Handed Persons)

  • 권혁철
    • 한국전문물리치료학회지
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    • 제5권4호
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    • pp.41-51
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    • 1998
  • The right hip abductor musculature has been reported to demonstrate "stretch weakness" attributable to chronic elongation imposed by standing posture common to right-handed healthy persons. Kendall and associates have described the concept of "stretch weakness",. The purpose of this study was to assess isometric hip abduction torque and surface electromyographic activity (using MYOMED 432) in a sample of 40 healthy right-handed persons (20 male, 20 female), all of whom agreed to participate in the study, and compare side difference in the hip abductor musculature. In order to assure the statistical significance of the results, the paired t test was applied at the .05 level of significance. The results were as follows: 1) The difference in apparent leg length of right and left legs was significant at the .05 level. 2) There was a significant difference between right and left pelvic height (standing position) at the 05 level measurements, and scapula height at the .05 level. 3) Power measurements and action potentials of right hip abductor were greater than the left hip abductor regardless of the range of joint motion (inner range, outer range) 4) The difference in muscle power and action potentials according to inner or outer range of both hip abductor were significant at the .05 level. 5) In supine during active left hip abduction, the appearance of action potentials in the right hip abductors is indicative of contra-lateral effect (p<.05) These results suggest: In healthy right-handed persons, the apparent leg length on the right is longer than on the left, and pelvic height is elevated on the right side. Muscle those and muscle action potentials of the right hip abductor are higher than those of the left hip abductor in the lengthened position. Therefore, the results in this study are contrary to Kendall's. This type of study should be carried out in many physical therapy departments.

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지대형 근이양증 (Limb-girdle Muscular Dystrophy)

  • 김대성
    • Annals of Clinical Neurophysiology
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    • 제6권2호
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    • pp.65-74
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    • 2004
  • Limb-girdle muscular dystrophy (LGMD) is a heterogeneous group of inherited muscle disorders caused by the mutations of different genes encoding muscle proteins. In the past, when the molecular diagnostic techniques were not available, the subtypes of muscular dystrophies were classified by the pattern of muscle weakness and the mode of inheritance, and LGMD had been considered as a 'waste basket' of muscular dystrophy because many unrelated heterogeneous cases with 'limb-girdle' weakness were put into the category of LGMD. With the advent of molecular genetics at the end of the last century, it has been known that there are many subtypes of LGMD caused by the mutation of different genes, and now, LGMD is classified according to the results of the linkage analysis and the genes or proteins affected. Only small proportion (probably less than 10%) of LGMD is dominantly inherited, and autosomal dominant LGMD (AD-LGMD) consists of six subtypes (LGMD1A to 1F) so far. In autosomal recessive LGMD (AR-LGMD), more than 10 subtypes (LGMD2A to 2J) have been linked and most of the causative genes have been identified. Among AR-LGMDs, LGMD2A (calpain 3 deficiency), 2B (dysferlin deficiency), and sarcoglycanopathy (LGMD2C-2F) are major subtypes. The defective proteins in LGMDs are components of nuclear envelope, cytosol, sarcomere, or sarcolemma, and seem to play a different role in the pathogenesis of muscular dystrophy. It is notable that many causative genes of LGMDs are also responsible for other categories of muscular dystrophy or diseases affecting other tissue. However, by which mechanism they produce such a broad phenotypic variability is still unknown. The identification of mutation in the relevant gene is confirmative for the diagnosis, and is essential for genetic counseling and antenatal diagnosis of LGMD. Because many different genes are responsible for LGMD, differentiation of subtypes using immunohistochemistry and western blotting is the essential step toward the detection of mutation. For the effective research and medical care of the patients with muscular dystrophy in Korea, a research center with a medical facility supported by the government seems to be needed.

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견비통 치료 관련 선행연구에서 견비통의 유형 분류에 관한 연구 (Study on the Classificaition of Shoulder-Arm Pain in the Pre-Studies on Clinical Treatment of Shoulder-Arm Pain)

  • 김홍재;김명동
    • 동의생리병리학회지
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    • 제25권1호
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    • pp.8-18
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    • 2011
  • To have effective treatment for shoulder arm pain, we searched the cause, symptom, etiology, classification of the pain areas, acupuncture points, and muscles along the meridians, and acquired the following results. Shoulder-pain is mainly divided into the malfunction of viscera and entrails, damage due to the weakness of essence and qi, abnormal status of muscle function, change of joints, disease in the nerve and vessel, and the internal injury due to seven modes of emotions. Pain of shoulder joints are pain in the local area of shoulder joints, referred pain of shoulder, neck, and shoulder-arm, numbnes and swelling of muscle, and muslce weakness. Shoulder-arm pain is classified as four types of pain: shoulder-joint pain, shoulder-back pain, shoulder-chest pain, and shoulder-arm-elbow pain. And shoulder-arm-elbow pain is again divided into the shoulder-blade pain, shoulder-arm pain, shoulder-elbow pain. The related meridians on shoulder pain are the three yin meridians of hand, Kidney Meridian, Conception Meridian, three yang meridians of hand, Bladder Meridian, Governor Meridian Acupuncture points for shoulder pain are in the acupuncture points of the 10 meridians and a-shi points. Thre related meridian muscles on shoulder-pain are the three yin and yang meridians of hand, and their related muscles are the ones that are connected with the front, back, and chest side muscles of shoulder joints, and the ones that are connected with the front and back side muscles of arm.

고관절 외전시 중둔근의 근력 및 활동전위 변화에 관한 연구 (A Myometric and Electromyographic Analysis of Hip Abductor Musculature in Healthy Right-Handed Persons)

  • 권혁철
    • The Journal of Korean Physical Therapy
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    • 제2권1호
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    • pp.35-46
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    • 1990
  • The right hip adbuctor musculature has been reported to demonstrate 'stretch weakness' attributable to chronic elongation imposed by standing posture common to right-handed healthy persons. Kendall and associates have described the concept of 'stretch weakness'. The purpose of this study was to assess isometric hip abduction torque and surface electro-myographic activity (using MYOMED 432) in a sample of 40 healthy right-handed persons (20 male, 20 female), all of whom agreed to participate in the study, and compare side difference in the hip abductor musculature. In order to assure the statistical significance of the results, the paired t-test was applied at the .05 level of significance. The results were as follows : 1. The difference in apparent leg length of right and left legs was significant at the .05 leve1. 2. There was a significant difference between right and left pelvic height (standing position) at the .005 level measurements, and scapula height at the .05 level. 3. Power measurements and action potentials of right hip adbuctor were greater than the left hip adbuctor regardless of the range of joint motion (inner range, outer range). 4. The difference in muscle power and action potentials according to inner or outer range of both hip abductor were significant at the .05 level. 5. In supine during active left hip abduction, the appearance of action potentials in the right hip abductors is indicative of contra-lateral effect (p<.005). These results suggest : In healthy right-handed persons. the apparent leg length on the right is longer than on the left, and pelvic height is elevated on the right side. Muscle torque and muscle action potentials of the right hip adbuctor art higher than those of the hip abductor in the lengthened position. Therefore, the results in this study are contrary to Kendall's. This type of study should be carried out in many physical therapy departments.

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복시(複視)(Diplopia)를 호소하는 Guillain-Barre Syndrome(GBS) 환자 치험 1례 증례보고 (A Clinical Case Report on Guillain-Barre Syndrome with diplopia)

  • 강성욱;문미현;홍석훈;황충연;강정란;박준영
    • 한방안이비인후피부과학회지
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    • 제18권3호
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    • pp.102-107
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    • 2005
  • Guillain-Barre Syndrome (GBS) is an acute inflammatory demyelinating polyneuropathy. It is disorder in which the body's immune system, attacks parts of the peripheral nervous system. It is characterized by the rapid onset of weakness, paralysis of the legs, arms, breathing muscles and face. But the analysis of CSF and electrical tests on nerve and muscle function can be performed to confirm the diagnosis. Most cases occur shortly after a viral infection. This is a clinical ease report on Cuillain-Barre Syndrome with diplopia. The patient, a 52-year-old man had a weakness in both legs and diplopia. His weakness and diplopia improved after oriental medical treatment, so this is reported as a potential treatment. Objective: This study was designed to evaluate the effects on oriental medicine therapy on Guillain-Barre Syndrome with diplopia. Methods & Result: The Clinical data was analyzed on a patient with Cuillain-Barre Syndrome whose main symptoms were diplopia. The patient was treated by acupuncture and oriental medicine. As a result, symptoms was improved remarkably. Conclusion: The patient showed weakness and diplopia. After acupuncture and oriental medicine treatment, weakness and diplopia was improved in 4weeks after visit to clinic. The study suggests that oriental medicine treatment is effective on Cuillain-Barre Syndrome.

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소아기 피부근염의 임상적 고찰; 진단시 임상증상을 중심으로 한 고찰 (A clinical analysis of juvenile dermatomyositis; focus on clinical manifestations at diagnosis)

  • 이소영;방지석;김희석;김중곤
    • Clinical and Experimental Pediatrics
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    • 제50권11호
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    • pp.1116-1124
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    • 2007
  • 목 적 : 소아기 피부근염은 피부와 근육을 침범하는 만성 염증성 질환으로 비교적 드문 질환이다. 우리 나라에서는 산발적인 증례 보고는 있어 왔으나 종합적인 분석은 두가지의 보고가 있을 뿐이다. 이에 저자들은 진단 당시에 소아기 피부근염 환자들의 임상적 증상 및 검사 소견을 분석하였다. 방 법 : 1985년 1월부터 2007년 5월까지 서울대학교병원 소아과 면역 질환 분과에서 소아기 피부근염으로 진단받거나 타병원에서 진단 후 전원된 환아 47명을 대상으로 하여 연령 및 성병분포, 초기 임상 증상, 증상 발현으로부터 진단까지의 시간, 혈청근효소, 자가항체, 근전도, 근생검, 자기공명영상, 합병증 등을 분석하였다. 결 과 : 대상 환아들은 모두 47명으로 남자가 25명 여자가 22명으로 남녀 비율은 1.14:1이었다. 진단 당시 연령은 $6.51{\pm}0.88$세(1.5-13.25세)였다. 피부 발진은 모든 환아에서 나타났으나 3례의 환아에서는 진단 후 발생하였고, 얼굴 발진이 가장 많았다. 진단 당시 근쇠약감은 44례의 환아에서 나타났으며, 2례는 진단 후 나타났다. 근위부 근쇠약감은 계단을 잘 오르지 못하는 것이 가장 흔한 증상이었다. 질병 활성도는 평균 10.8점(3-17점)이었으며, 근쇠약감은 평균 4.91점(0-9점), 피부 병변은 평균 5.89점(0-9점)이었다. 피부와 근육의 증상 이외의 증상은 43%에서 관찰되었고, 석회증이 30%, 관절 구축이 21%, 흡인성 폐렴이 13 %로 관찰되었다. 석회증이 발생한 환아 중 47%는 진단 당시부터 관찰되었고 석회증이 발생한 위치는 골반과 둔부가 50%에 해당하였다. 혈청 근효소의 상승은 LDH가 96%, AST가 80%였다. 자가 항체 중 항핵항체가 59%로 가장 많은 양성을 나타내었으며, 이중 반점 모양이 58%에서 관찰되었다. 근전도는 88%에서 근염에 합당한 소견을 보였고, 근생검은 91%에서 피부근염에 합당한 소견을 보였다. 자기공명영상은 9례에서 시행되었고 모두 T2 강조 영상에서 고신호 강도 변화를 보여 근염에 합당하였다. 결 론 : 소아기 피부근염을 진단하기 위해서는 여러가지 진단 방법이 사용되고 있으나, 얼굴 발진, Gottron 발진, heliotrope 발진과 같은 피부 발진과 상하지 근위부 근육의 쇠약감과 같은 임상증상이 중요할 것으로 생각된다.

Guilain-Barre Syndrome 환자에 대한 한방치료 1례 (A case report of Guillain-Barre syndrome)

  • 허건;이옥진;이정민;오민석
    • 혜화의학회지
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    • 제23권1호
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    • pp.137-148
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    • 2014
  • Objective : This is clinical about the Wei syndrome(痿證)-patient diagnosed as Guillian-Barre Syndrome(GBS). GBS, What is called acute inflammatory plolyneuritis, is a disorder in which the body's immune system attacks parts of peripheral nerve system. It is characterized by the rapid onset of weakness, paralysis of the legs, arms, breathing muscles and face. But the analysis of CSF and electical tests on nerve and muscle function can be performed to confirm the diagnosis. Most cases occur shortly after a viral infection. Methods & Result : This is the clinical report about the one patient diagnosed as Guillain-Barre Syndrome. The patient, 46-year-old men had weakness in both legs and arms after divertculitis. His weakness and general condition improved after oriental medical treatment and acupuncture. As a result, symptoms were improved remarkably. Conclusion : We report that we had good effects of oriental medical treatment on Guillain-Barre Syndrome.

Guillain-Barre syndrome으로 추정되는 계증 치험 1례(例) (A case of the patient with Wei symptom suspected Guillain-Barre syndrome)

  • 정병무;신원용;최은영;윤철호;정지천;현민경
    • 대한한방내과학회지
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    • 제25권4호
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    • pp.450-456
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    • 2004
  • Guillain-Barre syndrome, or acute inflammatory polyneuritis, is a disorder in which the body's immune system attacks parts of the peripheral nervous system. The causes and mechanisms of this syndrome are unknown. Typically, Guillain-Barre syndrome can be diagnosed from the patient's symptoms and physical examination such as the rapid onset of weakness, paralysis and loss of reflexes. The analysis of CSF and electrical tests on nerve and muscle function can be performed to confirm the diagnosis. Most cases occur shortly after a viral infection. This is a clinical report about one patient suspected as having Guillain-Barre syndrome. The patient, a 62-year-old man had weakness in both legs after gastroduodenal disease. His weakness and general condition improved after Korean medical treatments, so this is reported as a potential treatment.

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길랑바레 증후군 호전 이후 재발한 사지무력 증상에 대한 한방 복합치료 1예: 증례보고 (A Case of Combined Korean Medicine Treatment for Recurrent Limb Weakness after Guillain-Barré Syndrome Improvement: Case Report)

  • 박송미;조성우
    • 한방재활의학과학회지
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    • 제29권4호
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    • pp.135-142
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    • 2019
  • The objective of this study is to propose Korean Medicine treatment for recurrent limb weakness after Guillain-Barre syndrome (GBS) improvement by intraveinous immunoglobulin, and to report its effectiveness. Manual muscle test (MMT), Korean modified Bathel index (K-MBI), and tendon reflex were used to evaluate the patient. The patient was improved hip joint, knee joint, ankle joint MMT from grade 3-/3- to grade 5/5 and in the upper limb the patient can do big joint exercise but cannot do micromovement like writing or using cell phone. When discharge date the patient's wrist joint MMT grade is improved grade 5-/5- to grade 5/5. The K-MBI score is improved from 71 to 86 and there was a big change in walking and chair/bed transfer, there was no change in tendon reflex. This study suggests that Korean Medicine can be effective for patients who have recurrent limb weakness after GBS improvement.