• 제목/요약/키워드: age at onset

검색결과 602건 처리시간 0.026초

식도암의 임상적 고찰 (A clinical Evaluation of Esophageal Cancer)

  • 이성윤;지행옥
    • Journal of Chest Surgery
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    • 제23권2호
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    • pp.285-298
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    • 1990
  • The records of 67 patients who had been operated as an esophageal cancer during the period from 1973 to 1989 at the Department of Thoracic and Cardiovascular Surgery, Hanyang University Hospital were reviewed retrospectively. The results were summarized as follows ; The age ranged from 28 years old to 80 years old. The highest incidence was 5th decades, then 6th decades, and the incidence of male was 10 times as the incidence of female[M:F= 10.16: 1]. The locations were lower esophagus 44%, middle esophagus 38.8%, upper esophagus 11.9% and cervical esophagus 4.4% The frequent symptoms were dysphagia [88%], epigastric or substernal pain and discomfort [29.8%], weight loss [20.8%], and laryngeal dryness [1.4%]. The most common interval between the onset of dysphagia and admission was 2-3 months; 82% of patients was within 6 months, The cancer consisted of stage I [3%], stage II [11.9%], stage III[47.6%], and stage IV [33.7%] The resectability of cancer was 67%. The organs of substitute were stomach in 21 cases, right colon 6 cases, and jejunum in 8 CRSCS. The relation between invasion of tumor and lymph node metastasis was analyzed: mucosal involvement: 1 case/2case, muscle invasion; 0/2 full thickness; 4/6, adjacent structure 7/12. Postoperative complications were pneumonia, pleural effusion, hoarseness, mediastinitis, anastomosis site leakage, reoperation due to stenosis, chylothorax, empyema, mechanical ileus, wound infection, meat impaction at anastomosis site, and repair of gastrostomy site leakage. Adjuvant therapies were irradiation [15cases], chemotherapy [14cases], and Bougie dilatation [4 cases],

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Glucose transport 1 deficiency presenting as infantile spasms with a mutation identified in exon 9 of SLC2A1

  • Lee, Hyun Hee;Hur, Yun Jung
    • Clinical and Experimental Pediatrics
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    • 제59권sup1호
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    • pp.29-31
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    • 2016
  • Glucose transport 1 (GLUT-1) deficiency is a rare syndrome caused by mutations in the glucose transporter 1 gene (SLC2A1) and is characterized by early-onset intractable epilepsy, delayed development, and movement disorder. De novo mutations and several hot spots in N34, G91, R126, R153, and R333 of exons 2, 3, 4, and 8 of SLC2A1 are associated with this condition. Seizures, one of the main clinical features of GLUT-1 deficiency, usually develop during infancy. Most patients experience brief and subtle myoclonic jerk and focal seizures that evolve into a mixture of different types of seizures, such as generalized tonic-clonic, absence, myoclonic, and complex partial seizures. Here, we describe the case of a patient with GLUT-1 deficiency who developed infantile spasms and showed delayed development at 6 months of age. She had intractable epilepsy despite receiving aggressive antiepileptic drug therapy, and underwent a metabolic workup. Cerebrospinal fluid (CSF) examination showed CSF-glucose-to-blood-glucose ratio of 0.38, with a normal lactate level. Bidirectional sequencing of SLC2A1 identified a missense mutation (c.1198C>T) at codon 400 (p.Arg400Cys) of exon 9.

Loss of Acquired Skills: Regression in Young Children With Autism Spectrum Disorders

  • Ye Rim Kim;Da-Yea Song;Guiyoung Bong;Jae Hyun Han;Hee Jeong Yoo
    • Journal of the Korean Academy of Child and Adolescent Psychiatry
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    • 제34권1호
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    • pp.51-56
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    • 2023
  • Objectives: Regression, while not a core symptom of autism spectrum disorder (ASD), has been suggested to be a distinct subtype by previous studies. Therefore, this study aimed to explore the prevalence and clinical differences between those with and without regression in children with ASD. Methods: This study includes data from toddlers and young children aged 2-7 years acquired from other projects at Seoul National University Bundang Hospital. The presence and characteristics of regression were explored using question items #11-28 from the Autism Diagnostic Interview-Revised. Chi-square and independent t-tests were used to compare various clinical measurements such as autistic symptoms, adaptative behavior, intelligence, and perinatal factors. Results: Data from 1438 young children (1020 with ASD) were analyzed. The overall prevalence rate of regression, which was mainly related to language-related skills, was 10.2% in the ASD group, with an onset age of 24 months. Regarding clinical characteristics, patients with ASD and regression experienced ASD symptoms, especially restricted and repetitive interests and behaviors, with greater severity than those without regression. Furthermore, there were significant associations between regression and hypertension/placenta previa. Conclusion: In-depth surveillance and proactive interventions targeted at young children with ASD and regression should focus on autistic symptoms and other areas of functioning.

항전간제로 조절된 간질 환아에서 약물 중지 후 추적 관찰 - 재발위험인자 (A Follow-Up Study after Discontinuation of Antiepileptic Drug Therapy in Children with Well-Controlled Epilepsy : The Factors that Influence Recurrence)

  • 정사준;정혜전;최영미;조의현
    • Clinical and Experimental Pediatrics
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    • 제45권12호
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    • pp.1559-1570
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    • 2002
  • 목 적 : 간질 치료에 있어서 치료 중 무 발작 기간이 장기간 지속되는 환자에서 항전간제를 언제까지 투여할 것인가에 대한 답은 아직 확실히 제시된 바없다. 따라서 무 발작기간이 지속되는 환자들에서 항전간제 투여 중지 후 재발에 관계된 위험인자를 분석-평가함으로서 항전간제 중지시기에 대한 안내 지침에 도움이 되고자 본 연구를 시행하였다. 방 법 : 1993년부터 1998년 6월까지 경희대학교 의과대학 부속병원에서 간질로 진단받고 항전간제 투여 후 최소 2년 동안 무 발작으로 조절되어 약물투여가 중지된 환아 169명(남자 102명, 여자 67명)을 대상으로 하였다. 간질의 진단은 임상 병력, 신경학적 및 이학적 소견, 검사실 소견과 발작 간기에 기록한 뇌파를 기준으로 하였으며 필요한 경우 뇌의 구조병변의 유무를 규명하기 위하여 두부 전산화 촬영이나 자기공명상을 실시하였다. 재발 위험 인자는 성별, 초 발작 연령, 간질 가족력, 열성 경련의 병력, 간질의 원인, 발작형, 치료 전 발작 횟수, 신경학적 이상 여부, 발작 발생부터 치료 시작까지의 기간, 항전간제 사용에서 최종 발작까지의 기간, 총 약물 치료 기간, 약물 치료 중 재발여부, 항전간제 치료 중지 직전의 뇌파, 항전간제의 수, 항전간제 중지 시 연령, 무 발작 기간, 등 총 16가지를 선정하여 Kaplan-Meier 생존 분석에 의한 단 인자분석(전체, 특발성, 증후성)과 Cox-regression 모형에 의한 다 인자 분석을 각각 시행하였다. 결 과 : 대상 환아 총 169명 중 재발한 경우가 49명(28.9%)에서 나타났으며, 항전간제 치료기간은 평균 4.1년(2-13년)이었고 항전간제 치료 중지 후 평균 추적 관찰 기간은 4.1년, 무 발작 기간은 평균 3.3년(2-5년)이었다. 각 위험인자에 따른 단 인자 분석에서 초 발작 연령이 1세 미만인 경우, 간질의 원인이 증후성, 발작형이 영아연축 및 레녹스 증후군>부분 발작군>전신 발작군=롤락딕 발작군 순으로 재발률이 높았다. 또한 신경학적 이상을 보인 군과 발작 조절기간이 0인 경우보다 2년 이상인 군과 조절에 사용한 약물수가 2개 이상인 경우, 약물 중지 시 연령이 6세 이하인 군과 무 발작 기간이 2년>3-4년>4년 이상인 순으로 재발율이 높게 나타났다. 결 론 : 항전간제로 치료 시작 후 2년을 초과한 기간동안 무 발작이 계속되고 있는 6세 이상의 간질 환아에서는, 발작초발 연령이나 발작형, 사용하고 있는 항전간제의 수, 치료 시작 후 발작조절에 걸린 기간, 총 치료기간, 발작의 원인, 신경학적 이상 여부 등을 고려하여, 또 항전간제를 끊고자 하는 환아나 보호자의 의지 등에 따라 항전간제의 중단을 고려하여야 한다.

장티브스에 관한 임상적 관찰 (Clinical review of Typhoid Fever Patients)

  • 최정신
    • 대한간호학회지
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    • 제6권1호
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    • pp.60-71
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    • 1976
  • The author reviewed the medical records of 96 typhoid fever patients who were diagnosed, admitted, and treated at Sea grave Memorial Hospital from January 1 , 1973 through August 31, 1975. Diagnosis was determined by clinical observation, aerology and bacteriology, eighty patients were treated medically, the remaining 16 patients required surgical intervention. The following results were obtained: 1) The age distribution of the patients revealed that 33.3% wert between 10 and 19 years old 21.9% were between 20 and 29, and 19.8% were between 30 and 39. The majority of patients were from these more active age groups. Male to female sex ratio was 1.3 : 1 2) Seasonal distribution was observed. Most illness occurred in the summer and autumn month 5. 3) 84. 3%of the patients came from farm families. 4) Duration between onset and admission averaged 16.0 days. The group without compilations was admitted after an average of 15. 1 days; The group with complications was ad-matted after an average of 19.4 days. 5) Methods of treatment before admission were as follows: 10.4% at medical clinics, 61, 5% at pharmacies (antibiotics 47.9%, other. drugs 13.5%), 7.3% by herb medications, 20.8% had no treatment. 6) Main clinical symptoms were as follows: fever 93.8%, headache 47.9%, abdominal pain 47.9%, chills 38.5%, cough 36.5%, general weakness 26.0%, nausea e vomiting 24.0% and generalized pain 21.9%. 7) Temperature of patients on admission: 22.9% were 39f or more, 67.6% were between 37℃ and 38℃, and 9.4% were 37℃ or less. 8) Occurrence of intensional bleeding after onset of disease averaged 9.3 days; perforation occurred at an average of 19. 1 days. 9) Interval between onset of major complication and surgical intervention averaged 2.8 days. 10) Among the 68 patients who underwent the bacteriological test the positive rate was 44.1% (30). The positive ,ales to, each separate culture method were as follows: 20.4% in the blood culture, 40.4% in the stool culture and 6.7% in the urine culture. Among these bacteriological positive patients 15 patients had a negative results or less than 160 titer of vidal reaction. 11) The initial vidal test of the total group showed a counts of 160 titer or more in 60.4% and less than 160 titer in 39.6%, 12) W. B. C. Counts in the uncomplicated group indicated that 32.5% were 6,000/㎣ or less, 47.5% were between 6,000 and 10,000, arid 20.0% were 10,000/㎣ or more. In the complicated group, 37.6% were 6,000/㎣ or less, 25,0% were 6,000-10,000/㎣ and 37.6% were 10,000/㎣ or more. 13) Duration of hospital stay of the patients averaged 6.4 days in the uncomplicated group and 12.7 days in the complicated group. 14) Subdiaphragmatic free air simple X-ray was found in 91.7% of the perforated cases. 15) Duration of antibiotic therapy until an febrile state was attained averaged 4.8 days in the uncomplicated group and 6.5 days in the complicated group. 16) Operative procedures were as follows: one layer simple closure of their perforation with or without debasement in 56.3%, drainage only in 6.3%, small bowel resection with primary anastomosis in 18.8% , externalization in 6.3%, cholecystectomy in 6.3%, The clinical findings of this study suggest the following recommendations. According to Top's report; 1% of typhoid fever patients treated with chlorarnphenicol and 2% of patients treated with other drugs become chronic carriers. Therefore, importance should be given to the strict control of these carriers. Immunization, improvement of sanitation and living standards are all needed for the prevention and treatment of disease, but a more serious problem is a lack of knowledge on the part of patients and their families. Thus it is most urgent to enlighten the citizens about the transmission and hygiene related to contagious disease. Legal restriction of sale of antibiotics at drug stores without a physician's prescription is an urgent matter for public health administrators. An even more important nursing responsibility is the reemphasis on health education both in the clinical setting and in the home.

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소아 스테로이드 반응성 신증후군에서 재발과 관련된 예측인자 (Predictive factors for Relapse in Children with Steroid Responsive Nephrotic Syndrome)

  • 조민현;이동원;이태호;고철우
    • Childhood Kidney Diseases
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    • 제9권2호
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    • pp.167-174
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    • 2005
  • 목 적 : 스테로이드 반응성 신증후군 환아들의 초기 치료 중에 나타나는 임상경과 중 재발빈도와 관련되는 자료들을 선별하여, 재발에 대한 예측인자로서의 의의를 확인하기 위해 본 연구를 시행하였다. 방 법 : 대상환아는 1996년부터 2001년까지 6년간 경북대학교 병원 소아과에서 스테로이드 반응성 신증후군으로 진단되어 2년 이상 추적관찰이 가능하였던 73례로 하였고, 이 환아들을 대상으로 성별, 발병연령, 신장조직 검사결과, 각종 검사실 성적, 첫 치료 후 관해까지의 기간, 첫 치료 후 재발까지의 기간, 재발빈도 등을 의무기록지를 통해 후향적으로 고찰하였으며, 재발빈도와 다른 자료들간의 상관관계를 통계적으로 분석하였다. 결 과 : 대상환아의 신증후군 진단 당시 평균 연령은 $4.53{\pm}2.53$세였으며 남녀비는 52:21로 남아가 많았다. 첫 치료 후 완해까지의 기간은 $10.2{\pm}7.4$일이었고 대부분(77$\%$)은 2주 이내에 완해됨을 알 수 있었다. 재발은 전체의 78$\%$인 57명에서 나타났는데, 첫 1년간은 $2.6{\pm}1.4$회, 2년째는 $1.9{\pm}1.3$회를 재발하였으며, 이 중 23$\%$인 13명이 "빈발 재발형"으로 진단되었다. 재발이 있었던 환아들은 첫 치료 후 $4.7{\pm}3.5$개월 후에 첫 재발이 있었다. 진단 당시 시행한 혈액검사 및 요단백-크레아티닌 비, 24시간 요단백배설량, 진단 당시 연령, 성별, 혈뇨의 동반 유무와 재발빈도 간에는 유의한 상관관계를 발견할 수 없었다. 그러나, 첫 치료 후 완해까지의 기간과 재발빈도 간에는 유의한 상관관계를 발견할 수 있었으며, 7일 이내에 완해가 온 군은 7일 이후에 완해가 온 군에 비해, 첫 치료 후 1년간의 재발횟수가 통계적으로 유의하게 적었다($0.93{\pm}1.28\;vs\;2.22{\pm}1.60$, P=0.006). 또한, Kaplan-Meier 모형을 이용한 누적완해율의 분석에서도 두 군간의 유의한 차이를 확인할 수 있었다(P=0.0017). 결 론 : 스테로이드 반응성 신증후군 환아에서 첫 발병 당시 경구 스테로이드 투여 후 완해까지의 기간은 이후 재발빈도를 추정할 수 있는 예측인자로 가능성이 있으며 이를 증명하기 위해서는 대규모의 전향적인 연구가 필요하다고 생각된다.

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여드름에 관한 임상적 연구 (A Clinical study of Recurrent Acne in the Oriental Medicine)

  • 최인화
    • 한방안이비인후피부과학회지
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    • 제13권2호
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    • pp.140-151
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    • 2000
  • Acne is a common chronic disease which most frequently affects the face, appearing in both males and females near puberty, and in most cases becomes less active as adolescence ends. The intensity and duration of activity vary for each individual. The disease may be minor, with only a few comedones or papules, or it may occur as the highly inflammatory and diffusely scarring acne conglobation. Permanent scarring of the skin and psyche can result from such inaction. The disease, however, has implications far beyond the few marks that may appear on the face. The lesions cannot be hidden under clothing; each is prominently displayed and detracts significantly from one's personal appearance and self-esteem. Recently many of acne patients are visiting to Oriental Medicine Hospitals. They want to receive the treatment of acne related another disease and causes, or worry about side effects of antibiotics and hormone therapy. This study was performed at Pundang Cha Oriental Medicine Hospital Department of Dermatology from March 1, 1997 to February 29, 2000 in 31 patients with recurrent acne. We investigated the clinical findings, included distribution of age & sex, severity of acne, sites on face, related causes, duration of disease and causes of visiting Oriental Medicine Hospital and so on. The results were as follows : The peak age at onset was 20-29 years old in females with 16 cases reported. The 22 total cases patients had severe signs with most frequently sites being forehead & chin. They visited Oriental Medicine Hospital because they want to take the treatment of acne related with another body problems(12 cases) and worry about side effects of antibiotics. Twenty cases were diagnosed 肺熱血熱(20 cases). And given acupuncture treatment, herb-medication and sometimes we used external applications. Relatively, their satisfaction grade was high. Dermatologists are trying to treat new methods in order to remove scar and decrease sebaceous gland secretion,. And we, Oriental Medicine doctors, have to develop and offer to patients the most effective management and successful treatment of this disease.

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Correlation between the morning hypertension on ambulatory blood pressure monitoring and the left ventricular mass in children

  • Kim, Hyun Jung;Kim, Kyung Hee;Kil, Hong Ryang
    • Clinical and Experimental Pediatrics
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    • 제57권9호
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    • pp.403-409
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    • 2014
  • Purpose: Although high morning blood pressure (BP) is known to be associated with the onset of cardiovascular events in adults, data on its effects in children with hypertension are limited. Our retrospective study aimed to define the clinical characteristics of children with morning hypertension (MH) and to determine its associated factors. Methods: We reviewed 31 consecutive patients with hypertension, confirmed by the ambulatory blood pressure monitoring (ABPM). We divided these patients into 2 groups: the MH group (n=21, 67.7%), morning BP above the 95th percentile for age and height (2 hours on average after waking up) and the normal morning BP group (n=10, 32.3%). We compared the clinical manifestations, laboratory results, and echocardiographic findings including left ventricular hypertrophy (LVH) between the groups. Results: The early/atrial (E/A) mitral flow velocity ratio in the MH group was significantly lower than that in the normal morning BP group. In addition, LV mass was higher in the MH group than in the normal morning BP group, although the difference was not statistically significant. The age at the time of hypertension diagnosis was significantly higher in the MH group than in the normal morning BP group (P =0.003). The incidence of hyperuricemia was significantly higher in the MH group than in the normal morning BP group. Conclusion: Older patients and those with hyperuricemia are at higher risk for MH. The rise in BP in the morning is an important factor influencing the development of abnormal relaxation, as assessed by echocardiography. Clinical trials with longer follow-up periods and larger sample sizes are needed to clarify the clinical significance of MH.

Successful and safe treatment of hemangioma with oral propranolol in a single institution

  • Chung, Sun-Hee;Park, Dong-Hyuk;Jung, Hye-Lim;Shim, Jae-Won;Kim, Deok-Soo;Shim, Jung-Yeon;Park, Moon-Soo;Koo, Hong-Hoe
    • Clinical and Experimental Pediatrics
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    • 제55권5호
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    • pp.164-170
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    • 2012
  • Purpose: Dramatic improvement of hemangioma to propranolol has been recently reported; however, details on dose and duration of treatment, potential risks, and monitoring have not been determined. The objective of this study is to describe and analyze the use of propranolol as a first-line treatment or as a single therapy in management of complicated hemangioma. Methods: A retrospective chart review of eight patients diagnosed with hemangioma and treated with propranolol in Kangbuk Samsung Hospital from February 2010 to April 2011 was performed. Results: Eight patients with hemangioma with functional impairment, cosmetic disfigurement, or rapid growth were treated with propranolol. Five patients had solitary facial hemangioma. The mean age of symptoms at onset was 5 weeks. The median age for starting propranolol treatment was 5.5 months. Propranolol at 2 mg/kg/day was finally administered in divided doses with a gradual increase. Significant regression was observed in seven patients, and shrinkage in size, softening in consistency, and decrease in redness were evident within 4 weeks. Among them, six patients were still taking propranolol, and one patient had stopped after 12 months. Other one patient did not show significant improvement with satisfactory result after 3 months of propranolol use. Treatment with propranolol was well tolerated and had few side effects. No rebound growth was observed in any of the patients. Conclusion: We observed that use of propranolol was very effective in treatment of hemangioma without obvious adverse effects or relapse.

구안괘사(口眼喎斜)환자의 일반적 특성 및 비수(肥瘦)에 따른 임상적 고찰 (Clinical Studies on the General Features and the Obesity-Skinniness of Patients with Bell's Palsy)

  • 최규호;장수영;신현철
    • 대한한방내과학회지
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    • 제30권1호
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    • pp.129-143
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    • 2009
  • Objective : This study was aimed to investigate the general features and differences between obesity and skinniness of patients with Bell's palsy. Methods : We measured the sex, age. BMI. pulse diagnosis and HBGS (House-Brackmann Grading System) of 234 patients who were diagnosed with Bell's palsy. Results and Conclusions : The results with statistical significance were as follows (1) The distribution of age revealed that 40s was the most at 30.8 %: (2) The improvement period in facial palsy patients with sub-paralysis was shorter than whole-paralysis. And in one part the more we treated, the shorter the improvement period was: (3) In distribution of fat rate in facial palsy patients, obesity was the most at 61.37%, low weight 15.88%. So we found that the fatter the patients was. the higher the onset rate was: (4) In distribution of pulse diagnosis in facial palsy patients with obesity. the ratio of Xu mai (虛脈) was 67.06%. Shi mai (實脈) 32.94%. The Xu mai was similar to Qi xu (氣虛). So we found that the facial palsy patients with obesity were more Qi xu than with low weight. In distribution of pulse diagnosis in facial palsy patients with skinniness, the ratio of Chi mai (遲脈) was none. Shuo mai (數脈) was most: (5) In distribution of region in facial palsy patients with obesity-Xu mai. the ratio of left was 45.10%, right 54.90%, but this result was not statistically significant.

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