• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제46권2호
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• pp.155-159
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• 2020

Chronic maxillary atelectasis (CMA) is a progressive alteration in the volume of the maxillary sinuses that may result in facial asymmetry. CMA in asymptomatic patients is known as silent sinus syndrome (SSS) and is a rare entity, especially in pediatric patients. This study reports a case of SSS in a pediatric patient who received an early diagnosis through cone-beam computed tomography (CBCT). An asymptomatic 12-year-old female patient in orthodontic treatment presented with opacification of the left maxillary sinus on a panoramic radiograph. Clinically, the patient had discrete hypoglobus and enophthalmos. CBCT and nasal video-endoscopy revealed ostiomeatal obstruction with bone deformity, leading to diagnosis of SSS. Endonasal endoscopic maxillary sinusotomy was performed. Two years later, the patient remained asymptomatic, and a second CBCT exam confirmed a stable condition. This case highlights the role of optimal radiographic interpretation for early diagnosis of maxillofacial alterations in pediatric patients.

• 재활복지
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• 제20권3호
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• pp.45-65
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• 2016

일차 진행성 실어증(Primary Progressive Aphasia, PPA) 환자군을 대상으로 한 효율적이고 체계적인 진단과 중재가 이루어지기 위해 기초연구가 많이 필요함에도 불구하고, 신경언어장애 내 치매 하위분야에서도 이들에 대한 연구는 부진한 편이다. 본 연구에서는 최근 10년간 국내외 관련 학술지에서 다루어진 PPA 연구논문의 동향을 분석하여 국내 PPA 연구의 향후 방향을 제시하는데 목적을 두었다. 일차적으로 선별된 171편의 논문을 대상으로 연구대상, 연구목적, 연구영역으로 나누고 연도별 연구동향에 대한 분석을 실시하였다. 연구대상은 국내외 모두 '실문법형'이 가장 많았고, 연구목적은 PPA의 전반적 특성이나 세 아형별 비교를 다룬 '특성연구'가 가장 많이 차지하고 있었다. 연구영역은 국외 연구에서는 의미(언어) 영역을 가장 많이 다루고 있으면서 '말'과 '기타'연구도 골고루 이루어져 있었던 반면, 우리나라는 '언어' 영역을 제외한 '말'과 '기타' 영역에 대한 연구가 아직 시행되지 않은 것으로 나타났다. 국외에서는 기존의 3가지 아형으로 나누어지던 PPA 분류에 말실행증(apraxia of speech) 분류가 추가되어 4가지 증상의 구별에 대한 연구가 활발히 모색되고 있는 반면, 국내는 환자 사례 발출이 어려워 이들이 보이는 증상이 의사소통장애에 상당히 초점이 맞춰져 있음에도 불구하고 시행된 연구가 거의 없었다. 기본적으로 관련 연구의 수가 절대적으로 부족하고 연구 영역의 다양성이 부족한 것으로 나타난 만큼, 향후 이에 대한 관심과 연구 확대가 필요하다.

• Physical Therapy Rehabilitation Science
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• 제5권2호
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• pp.106-112
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• 2016

Objective: This study was conducted to investigate the effects of resistant exercise on the gait performance of a patient with systemic lupus erythematosus (SLE) patient. Design: A case study. Methods: A 30-year-old male adult who had been diagnosed with systemic lupus erythmatosus (SLE) in April 2013, right middle cerebral artery infarction, and with left hemiplegia agreed to participate in this case study. Patient was unable to walk due to being affected with adynamia. Due to developing necrotizing vasculitis on the left lower extremity, patient underwent a myotomy on the left thigh. The patient was trained with a progressive resistant exercise program for 8 weeks. An intensity of 15 RM was used for the resistant exercises and the resistance level was increased progressively in order to improve the muscle power of the patient. Methods used to increase resistance included changing positions, providing mechanical resistance instead of manual resistance, transitioning from open kinetic chain to closed kinetic chain exercises, and changing the colors of the theraband to those with increase level of resistance. Outcome measures included the 5-repetition sit-to- stand test (5RSST), Timed Up & Go (TUG), and 10-meter walk test (10MWT). In addition, the GAITRite was used to assess the spatio-temporal gait variables, including gait speed, cadence, stride length of the left side, and double limb support pre and post-intervention. Results: The patient was able to perform sit-to- stand after two weeks of performing the resistant exercises. The patient was able to walk after 4 weeks, and the patient's overall gait performance had improved after 8 weeks. All of the variables had improved after each week. Conclusions: The results of this case study may be used to enhance future efforts to objectively evaluate resistant exercises during gait performance in persons affected by SLE.

• Journal of Acupuncture Research
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• 제28권4호
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• pp.127-135
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• 2011

Objectives : Ossification of the posterior longitudinal ligament (OPLL) is a cause of the progressive compression myelopahty or radiculopathy. More and more cases being reported in the field of western medicine, but very few cases have been reported in the field of oriental medicine. This study can make prove the effectiveness of oriental medicine about OPLL by acupotomy therpapy. Methods : A patient who is diagnosed to OPLL was participated in this study. The patient was treated by acupotomy therapy. After the treatment, patient was measured by VAS (visual analogue scale), questionnaires (NDI, J-OA score) and 5 Likert scale. Results : The results in the questionnaires (NDI, J-OA score) and VAS, ROM shows that the improving of OPLL pain and function. Conclusions : Acuptomy on OPLL was showed the effectiveness in pain and function of the patient.

• 동의신경정신과학회지
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• 제16권2호
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• pp.159-169
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• 2005

Amyotrophic lateral sclerosis (ALS) is characterised by progressive impairment of motor functions up to a complete loss of autonomy, and most of ALS patients are associated with the total preservation of mental state like depression. A patient in this case report had ALS and during progress of ALS had undergone depression and Hwabyung's Symptoms. This patient was treated with herb medication, acupuncture, psychotherapy(relaxation & councelling) primarily. During the 18 days of treatment from admission, the patient experienced much improvement of depression and Hwabyung's Symptoms. and ALS's symptom like weakness & numbness of lower limb had improved considerably, too.

• Journal of Korean Neurosurgical Society
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• 제47권1호
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• pp.55-57
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• 2010

Ossification of the posterior longitudinal ligament (OPLL) in the thoracic spine is rare, even in the Far East. A 45-year-old female presented with a 4month history of progressive motor weakness in the lower extremities, numbness below the midthoracic area, and spastic gait disturbance. Neuroradiological examinations revealed massive OPLLs at the T4-T6 levels with severe anterior compression of the spinal cord. Anterior decompressive corpectomies with bone grafts were performed from T4 to T6 using a trans-thoracic approach. After surgery, the patient made an uneventful recovery. However, eleven years after surgery, the patient developed recurrent lower extremity weakness and spastic gait disturbance. De novo OPLLs at the C6-T2 levels were responsible for the severe spinal cord compression on this occasion. After second surgery, paralysis in both legs was resolved. We present a rare case of late cervicothoracic OPLL in a patient surgically treated for thoracic OPLL.

• Archives of Plastic Surgery
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• 제45권3호
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• pp.271-274
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• 2018

The decision of which surgical approach to use for the treatment of a multifocal craniofacial abscess is still a controversial matter. A failure to control disease progress in the craniofacial region can potentially put the patient's life at risk. Therefore, understanding the various ways to approach the craniofacial region helps surgeons to obtain satisfactory results in such cases. In this report, we describe a patient who visited the emergency department with a large swelling in his right cheek. A blood test and computed tomography revealed odontogenic maxillary sinusitis. The patient developed sepsis due to a progressive multifocal abscess. An abscess was seen in the temporal muscle, infratemporal fossa, and interorbital region. To control this multifocal abscess, we used the facial dismasking flap (FDF) approach. After debridement using the FDF approach, we succeeded in obtaining sufficient drainage of the abscess, and the patient recovered from sepsis. The advantages of the FDF approach are that it provides a wide surgical field, extending from the parietal region to the mid-facial region, and that it leaves no aesthetically displeasing scars on the face. The FDF approach may be one of the best options to approach multifocal abscesses in the craniofacial region.

• 대한족부족관절학회지
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• 제23권2호
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• pp.71-73
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• 2019

Nearly one third of the world's population have active or latent tuberculosis, resulting in 1.5 million deaths annually. Tuberculosis involving the peripheral nerve is difficult to detect. Sural nerve tuberculoma is an extremely rare case of tuberculous involvement of the peripheral nerve that has attracted the attention of physicians. This paper reports a patient with sural nerve tuberculoma. A 58-year-old female patient presented with a palpable mass on the posterolateral calf with progressive tingling sensation on the distal area. The patient had no history of trauma and it was unclear whether the patient had any contact with individuals with active tuberculosis. The histopathologic findings revealed a granuloma-like lesion with caseous necrosis that was compatible with tuberculoma.

• Journal of Chest Surgery
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• 제21권5호
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• pp.929-934
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• 1988

Progressive systemic sclerosis is a disease of unknown origin and uncommon in the east area. We experienced one case of severe peptic esophageal stricture due to esophageal scleroderma. The patient`s life quality was improved with the esophageal reconstructive procedure using reversed tubed gastric pedicle and his body weight was normalized with regular diet.

• Journal of Korean Neurosurgical Society
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• 제40권4호
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• pp.289-292
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• 2006

Thoracic spinal actinomycosis causing epidural abscess and significant spinal cord compression is very rare. A case is presented of a 56-year-old woman with rapid progressive upper back pain and weakness in both legs without evidence of systemic infection. Magnetic resonance imaging revealed a thoracic epidural enhancing lesion at the T1-T5 level. After decompression by laminectomy, precise diagnosis was accomplished using specific histopathological studies of the surgical specimens. A histopathologic findings showing typical Actinomyces sulfur granules surrounded by acute inflammatory cells. The clinical radiological findings of spinal actinomycosis closely resemble metastatic tumors and other infectious processes. Delay in diagnosis and treatment can significantly worsen the condition of patient.