• Journal of Audiology & Otology
• /
• 제23권2호
• /
• pp.103-111
• /
• 2019

Background and Objectives: Dizzy patients with abnormal otolith function tests, despite a normal caloric response, are defined as having specific (isolated) otolith organ dysfunction. This study was performed to compare the differences in clinical presentation between isolated otolith dysfunction (iOD) patients with lab- and Sx-based iOD group and lab-based iOD symptoms. Subjects and Methods: The medical records of 23 iOD patients with normal caloric response but abnormal cervical vestibular evoked myogenic potential (VEMP), ocular VEMP, or subjective visual vertical were reviewed. Non-spinning vertigo was considered as otolith-related symptoms. The patients' age, onset of dizziness, Numeric Rating Scale on the severity of dizziness, and concomitant vestibular disorders were analyzed. Results: Patients in the lab-based iOD group were significantly older than those in the lab- and Sx-based iOD group. Known vestibular disorders were significantly more common in the lab-based iOD group (83.3%) compared to the lab- and Sx-based iOD group (18.2%). Despite the normal caloric response, catch-up saccade was found in the video head impulse test in more than half (54.5%) of the lab-based iOD group patients. There was no catch-up saccade in the lab- and Sx-based iOD group. There were no significant differences in gender ratio, frequency of dizziness attacks, and duration of illness. Conclusions: We propose new definitions of definite iOD (lab- and Sx-based iOD) and probable iOD (lab- or Sx-based iOD). These new definitions may help researchers to identify patients who are more likely to have true iOD, and facilitate comparisons of results between different studies.

• 대한청각학회지
• /
• 제23권2호
• /
• pp.103-111
• /
• 2019

Background and Objectives: Dizzy patients with abnormal otolith function tests, despite a normal caloric response, are defined as having specific (isolated) otolith organ dysfunction. This study was performed to compare the differences in clinical presentation between isolated otolith dysfunction (iOD) patients with lab- and Sx-based iOD group and lab-based iOD symptoms. Subjects and Methods: The medical records of 23 iOD patients with normal caloric response but abnormal cervical vestibular evoked myogenic potential (VEMP), ocular VEMP, or subjective visual vertical were reviewed. Non-spinning vertigo was considered as otolith-related symptoms. The patients' age, onset of dizziness, Numeric Rating Scale on the severity of dizziness, and concomitant vestibular disorders were analyzed. Results: Patients in the lab-based iOD group were significantly older than those in the lab- and Sx-based iOD group. Known vestibular disorders were significantly more common in the lab-based iOD group (83.3%) compared to the lab- and Sx-based iOD group (18.2%). Despite the normal caloric response, catch-up saccade was found in the video head impulse test in more than half (54.5%) of the lab-based iOD group patients. There was no catch-up saccade in the lab- and Sx-based iOD group. There were no significant differences in gender ratio, frequency of dizziness attacks, and duration of illness. Conclusions: We propose new definitions of definite iOD (lab- and Sx-based iOD) and probable iOD (lab- or Sx-based iOD). These new definitions may help researchers to identify patients who are more likely to have true iOD, and facilitate comparisons of results between different studies.

• Clinical and Experimental Pediatrics
• /
• 제48권1호
• /
• pp.63-67
• /
• 2005

목 적 : HSP는 촉진성 피부 자반, 위장관 증상, 관절 증세, 신장침범을 특징으로 하는 전신성 혈관질환이다. 일반적으로 예후는 위장관 합병증과 신염의 중증도에 의해 결정된다. 본 연구에서는 위장관 증상과 다른 임상적 소견 및 검사소견과의 통계학적 상관관계를 분석하여 예후를 판정하고 복부초음파 검사소견을 알아보아 진단 및 합병증 발생, 특히 비전형적인 임상경과 시 조기 발견에 도움을 주고자 시행하였다. 방 법 : 1994년 1월부터 2004년 6월까지 원광대학교병원 소아과에서 치료받았던 177명의 환아를 대상으로 후향적으로 차트를 분석하여 위장관 증상이 있는 경우를 복부 양성군, 없는 경우를 복부 음성군으로 분류하여 통계적 분석을 시행하였으며 복부초음파 검사소견을 알아보았다. 결 과 : 대상 환아의 남녀 비는 1.5 : 1였고 주된 발생연령은 5-8세(53%)였다. 위장관 증세는 117례(66%)에서 호소하였으며 이 중 복통(98%)이 가장 흔하였으며 복부압통(38%), 구역과 구토(30%), 혈변(8.5%), 설사(3.4%), 반사압통(3.4%) 등이었고 장중첩증 5례, 급성 충수염 2례도 있었다. 복부 양성군에서 음성군에 비해 신장침범과 재발의 위험성이 증가하였으나 두 군간에 다른 임상적 및 검사 소견에서는 차이가 없었다. 복부 양성군에서 복부 초음파검사를 시행하였던 98례 중 소장 벽의 비후(71%)가 가장 흔하였고 십이지장, 공장, 회장 순으로 침범하였으며, 또한 소장 확장(42%), 림프절 비대(47%), 복수(25.5%) 등의 소견을 보였다. 결 론 : HSP 환아에서 위장관 증세는 신장침범이나 재발의 위험도를 증가시키며 복부초음파 검사는 비전형적 임상경과를 보이는 경우 조기진단과 중증의 위장관 합병증 발견에 도움 될 것으로 사료된다.

• Childhood Kidney Diseases
• /
• 제17권2호
• /
• pp.49-56
• /
• 2013

목적: 면역글로불린A(IgA) 신증은 다양한 임상양상을 보이는 가장 흔한 원발성 사구체 신염으로, 적극적인 치료로서 단백뇨와 사구체손상을 줄여야한다. 저자들은 학교 집단 요검사를 통해 진단된 IgA 신증의 특징을 알아보고자 하였다. 방법: ${\bigcirc\bigcirc}$대학교병원 소아청소년과에서 조직검사를 받고 IgA 신증으로 진단받은 환자 64명을 내원 당시의 증상 유무에 따라 두 군으로 나누어 후향적으로 연구하였다. 결과: 증상 없이 학교신검에 의해 진단된 37명과 혈뇨 등으로 내원하여 진단된 27명을 대상으로 하였다. 각 군의 평균 연령은 각각 $10.8{\pm}2.7$세 및 $9.5{\pm}3.4$세였고, 각 군 모두에서 남아가 많았다. 증상 발현 후 내원까지의 기간과 조직 검사까지의 기간은 증상군에서 더 짧았다. 임상 증상은 증상군에서 육안적 혈뇨(P<0.001)와 부종(P=0.008)이 더 많았다. 혈액검사에서 증상군의 백혈구 수가(P=0.007) 많았고, 혈색소 값은(P=0.007) 더 낮았으며 BUN과 크레아티닌 값은 차이가 없었다. 혈청 알부민 값은 증상군에서 학교신검군에 비해 더 낮았고(P=0.006), 두 군에서 치료기간은 차이가 없었고, 치료약제는 ACEI가 가장 많았다. 전체 환아군을 대상으로 광학적 신조직 검사분석 시, 육안적 혈뇨기왕력이 있는 군에서 없는 군에 비해 좀 더 심한 병변을 보였으며, 단백뇨의 중증도와 병변의 중증도와는 상관이 있었다. 결론: 학교신검군 및 증상군 모두 조기 진단된 IgA 신증으로 임상적 및 조직학적인 큰 차이를 볼 수 없었다. 학교신검은 조기에 IgA 신증을 선별하는데 유용하지만, 조기진단이 치료나 예후에 어떤 영향을 주는지는 향후 보다 많은 대상자들의 장기간 추적관찰이 더 필요할 것으로 생각된다.

• 한방안이비인후피부과학회지
• /
• 제18권3호
• /
• pp.84-94
• /
• 2005

Objective: In order to help clinical approach on OME patient in progress observation and decision on improvement by clinical research results using tympanometry. Methods: Data was collected from 163 ears of 96 patients who were treated in Dept. of Oriental Medical Ophthalmology & Otolaryngology & Dermatology, Kyung-Hee Medical Center from 2001-2-12 to 2005-4-29 for Otitis Media with Effusion(OME). Tympanometry was applied to all patients and the test result was used to evaluate progress and improvement. F/U cases below 3 times were excluded. Results & conclusion: 1. Age and sex distribution was as follows: Mean Age 5.5years old(Standard deviation: 2.1), age distribution 2-61years old, below 10years old 151cases(92.6%) and above 10years old 12cases(7.4%). Male and female ratio was 1.81:1. 2. There were 67people(69.8%) with bilateral affected ear. Unilateral was 29people(30.2%). Affected ear distribution according to sex came out similarly. 3. Affected period distribution was as follows: over 12weeks 71cases(43.6%), under 12weeks 92cases(56.4%). Out of under 12weeks cases, 2-4weeks was 34cases(20.9%), 0-1weeks and 5-8weeks 20cases(12.3%), 9-12weeks 18cases(11.0%). There was evident difference about affected period between male and female. 4. All patients who served previous Tx in medical clinic(118 cases) took antibiotics. Only 6cases took tube insertion. The period of Taking antibiotics was as fellows: over 6weeks 42cases(35.6%), under 5weeks 37cases(31.4%). unknown 25cases(21.2%), jntermittent 14cases(11.9%). 5. In Period of Tx distribution, 5-6weeks showed 40cases(24.5%) which was highest number. In Improved cases(85cases), 3-4weeks and 5-6weeks each 22cases(25.9%) which was highest number. 1-2weeks 3cases(3.5%), 7-8weeks 12cases(14.1%), 9-10weeks 9cases(10.6%), 11-12weeks 10cases(11.8%), over 12weeks 7cases(8.2%). 6. The cases which have gastrointestinal Sx were 71cases(43.6%), the others 92cases(56.4%). Details of gastrointestinal Sx were as follows: Sx associated with appetite 47cases(47.5%), constipation 15cases(15.2%), abdominal pain and diarrhea 14cases(14.1%), frequent vomitting Teases(7.1%), etc 4cases(4.0%). 7. The cases which have accompanying disease were 116case(71.2%), the other 47cases(28.8%). Details a accompanying disease were as follows: sinusitis 57cases(35%), rhinitis 55cases(3.7%), allergic rhinitis 20cases(12.3%), atopic dermatitis 19cases(1.7%), urticaria 4cases(2.5%), asthma 3cases(1.8%), nasal polyp and conjunctivitis 2cases(1.2%) each, laryngitis 1case(0.6%).

• Journal of Chest Surgery
• /
• 제31권1호
• /
• pp.13-19
• /
• 1998

대동맥류는 예후가 좋지 못하고 사망률이 매우 높으며 외과적 치료 후에도 이환율과 사망률이 상대적으로 높은 질환이나 반면 발생 빈도는 점차로 증가하고 있는 추세에 있다. 고려대학교 부속 구로병원 흉부외과학 교실에서는 1986년 7월부터 1996년 7월까지 대동맥류로 수술한 25명의 환자들을 후향적 방법으로 임상 분석하였고, 환자들의 증상 발현부터 수술까지 소요된 시간과 입원부터 수술까지 소요된 시간, 수술 전 혈압 및 심박수의 변화 등과 사망률과의 관계를 통계 분석하였다. 대동맥류의 분류로는 해리성 대동맥류가 10례, 복부 대동맥류의 경우가 9례, Marfan씨 증후군 환자가 3례, 하행 흉부 대동맥류 환자가 3례이었고, 17례에서 인조 혈관 간치술을, 4례에서 Bentall씨 수기를 시행하였고, 2례에서는 대동맥류 우회술을, 2례에서는 대동맥 감싸기(Wrapping)를 시행하였다. 전체 수술 환자의 조기 사망은 7례로 전반기인 1988년부터 1992년 사이에 수술한 14례의 환자 중 6례의 환자에서 조기 사망하였고, 그 후에 수술한 11례의 환자 중에서는 1례의 환자에서 조기 사망을 경험하였다. 사인은 대량 출혈이 5례이고, 급성 신부전 및 호흡부전이 각각 1례씩이었다. 18례의 생존 환자군은 술 후 1개월부터 118개월까지(평균 50.6개월) 장기 추적 관찰을 시행하였고, 총 추적 관찰 기간은 911 환자-개월이었고, 수술 30개월 후에 발생한 혈변으로 인한 1례의 만기 사망을 경험하였다. 그외의 다른 모든 환자는 흉통이나 호흡 곤란 등의 증상없이 만족스러운 상태였다. 저자들의 경험의 경우 수술 전반기에 비해 후반기에 사망률이 낮았으며, 사망 환자의 주된 사인은 수술 중 혹은 수술 후 출혈이었다. 환자들의 증상 발현부터 수술까지 소요된 시간과 입원부터 수술까지 소요된 시간, 수술 전 혈압 및 심박수의 변화와 사망률과의 관계는 통계적으로 유의성을 보이지는 않았다.

• 대한물리치료과학회지
• /
• 제9권2호
• /
• pp.159-170
• /
• 2002

Parkinson's disease(PD) is a progressive neurodegenerative disease that affects the functioning of the basal ganglia, a brain area that contributes to the control of movement. The disease is caused by the death of nerve cells in the brain that produce dopamine, a chemical messenger. The cells affected usually produce a neurotransmitter(a chemical that transmits nerver impulses) called dopamine, which acts with acetylcholine, another neurotransmitter, to fine-tune muscle control. In Parkinson's disease, the level of dopamine relative to acetylcholine is reduced, adversely affecting muscle control. When the supply of dopamine is depleted, the function of the basal ganglia is disrupted and its ability to control movement-deteriorates. The result is that PD patients experience moderate rigidity, difficulty in initiating movements and slowness in executing them, and a rhythmical tremor at rest. Although the cause of Parkinson's disease is not known, genetic factors may be involved. About 3 in 10 people with the disorder have an affected family member. About 1 in 100 people over the age of 60 in the US have Parkinson's disease. And Parkinson's disease is slightly more common in men. The course of the disease is variable, but drags may be the best effective in treating the symptoms and improving quality of life. But, The doctor may arrange physical therapy to help with physical mobility problems. It is important to continue to exercise and take care of your general health. Try to take a walk each day. Stretching exercises can help you maintain your strength and mobility. So, This papers will serve about the information of PD for clinical physical therapist. Finally, The aim of review is increasing approach method and technique for PD patients by the view of physical therapy.

• 대한정형도수물리치료학회지
• /
• 제8권2호
• /
• pp.73-87
• /
• 2002

Parkinson's disease(PD) is a progressive neurodegenerative disease that affects the functioning of the basal ganglia, a brain area that contributes to the control of movement. The disease is caused by the death of nerve cells in the brain that produce dopamine, a chemical messenger. The cells affected usually produce a neurotransmitter(a chemical that transmits nerver impulses) called dopamine, which acts with acetylcholine, another neurotransmitter, to fine-tune muscle control. In Parkinson's disease, the level of dopamine relative to acetylcholine is reduced, adversely affecting muscle control. When the supply of dopamine is depleted, the function of the basal ganglia is disrupted and its ability to control movement deteriorates. The result is that PD patients experience moderate rigidity, difficulty in initiating movements and slowness in executing them, and a rhythmical tremor at rest. Although the cause of Parkinson's disease is not known, genetic factors may be involved. About 3 in 10 people with the disorder have an affected family member. About 1 in 100 people over the age of 60 in the US have Parkinson's disease. And Parkinson's disease is slightly more common in men. The course of the disease is variable, but drugs may be the best effective in treating the symptoms and improving quality of life. But, The doctor may arrange physical therapy to help with physical mobility problems. It is important to continue to exercise and take care of your general health. Try to take a walk each day. Stretching exercises can help you maintain your strength and mobility. So, This papers will serve about the information of PD for clinical physical therapist. Finally, The aim of review is increasing approach method and technique for PD patients by the view of physical therapy.

• 대한유전성대사질환학회지
• /
• 제11권1호
• /
• pp.88-98
• /
• 2011

Lesch-Nyhan syndrome is a X-linked recessive disorder caused by a deficiency of the enzyme hypoxanthine-guanidine phosphoribosyltransferase (HPRT), enzyme to recycle purines. Case history: born induced vaginal delivery at 40 weeks complicated by premature membrane ruputure, body weight 2.820 gm. He showed failure to thrive showing severe protein aversion like milk products and pink daper. Developmental delay revealing rolling over at 10.5 month, followed by regression. Seizure at 2 months, His poor oral feeding was lifelong problem. Weak crying, spastic, choreoathetoid movement. Self mutilating behavior noted and diagnosed at age 3 years. No family history of consanguinity and neurological disorders. Method: Laboratory test, physical exam, imaging study and molecular. Clinical follow up Treat ment with allopurinol. Result: uric acid 10.5 mg/dL (N 3.5-7.9), APRT 151.1uM/ min/ml pro(25.7-101), HPRT 7.6 (N 233.5-701) and c.151C>T hemizygote (p,Arg51X). Abdominal sonogram showed staghorn calculi in both kidneys, brain MRI brain atrophy. Clinical follow up showed, seizure at 2 mo, developmental delay (head control and, rolling over at at 11mo, pointing body part at 2 yr 7 mo, eye hand coordination at 2 y 11mo,creeping at 3 y 7 mo, speaking words at 6 y 6 mo ),and developmental regression at 3 yr of age. Sleeping problem including insomnia and severe constipation. Self mutilating behavior (lip bite) started at 2.5 yr, neurologic sx including intermittent upward gaze accompanied by swallowing difficulty at 3 y 7 mo grand mal seizure at 4.5 yr and spastic extremity and trunchal hypotonia and choleoathetoid movement and ataxia at 6.5 yr. Scoliosis with severe spasticity at 9 yr 9 mo. Acute life threatening episode with irregular breathing at 9 yr and 9 mo, Emaciation and nephrolithiasis and recurrent pneumonia. Died suddenly at 10 yr 3 mo. Conclusion: life long feeding problem, chronic gut motility dysfunction, sleeping difficulty and progressing neurologic deterioration and nephrolithiasis despite normal serum uric acid maintence by allopurinol treatment.

• Journal of Yeungnam Medical Science
• /
• 제5권2호
• /
• pp.87-93
• /
• 1988

저자등은 최근 5년동안 본원 신경과 외래와 입원 환자중 CT상 특징적인 뇌교소노위축을 보이고 그에 따른 임상적 증상을 보인 OPCA 환자 12예에서 다음과 같은 결과를 얻었다. 1. 연령분포는 49세에서 72세이며 주로 50대에서 60대에 많았다. 성별분포는 암자에서 약 4.5배 더 빈발하였다. 가족력이 있는 것으로 추정이 되는 1예에서는 발병연령이 보다 빨랐다. 2. 증상의 발현부터 진단까지의 기간은 대부분 1년에서 6년 사이였다. 3. 초기증상으로는 현기증(58%), 운동실조(33%) 등이 흔하였고 그 외에도 지전, 하지무력감, 구음장애, 두통, 뇨실금 등이었다. 또 진단당시 임상적 특징으로는 소뇌기능장애(100%), 구음장애(83%), 심부건반사항진(58%) 등이 주요 소견이었다. 4. CT소견으로 소뇌홈은 전례에서 1mm이상 확장되어 있었고 4예에서는 2mm이었다. 소뇌뇌교뇌조의 폭은 대부분이 3mm 내지 4mm이며 2예에서는 5mm였다. 제 4 뇌실은 전후 직경이 4mm, 좌우직경이 4mm 내지 8mm까지 확장된 소견을 보였으며 전례에서 전뇌교뇌조와 사구외조의 확장이 나타났다. 6예에서는 대뇌위축도 동반 되었음이 발견되었다.