• Title/Summary/Keyword: Case review form

Search Result 282, Processing Time 0.026 seconds

The Features of the Hypotheses Generated by Pre-service Elementary Teachers Using the Form of Peirce's Abduction (Peirce의 귀추법 양식을 이용한 교육 대학생들이 생성한 가설의 특징 분석)

  • Joung Yong-Jae;Song Jin-Woong
    • Journal of Korean Elementary Science Education
    • /
    • v.25 no.2
    • /
    • pp.126-140
    • /
    • 2006
  • The purpose of this study was to design a 'Form of Abduction' which is the 'guide form used in generating hypothesis through abduction', and to analyze the features of the hypotheses generated with the 'Form of Abduction' compared with those generated without any special guide form. Through a review of Peirce's literature regarding the meaning and frame of abduction, a 'Form of Abduction' was designed as a three step format as follows: (i) writing down what is doubted, (ii) wiling tentative explanations which replace what is doubted with what is believed, (iii) writing the tentative explanations as hypotheses. The thirty four pre-service elementary teachers were asked to generate hypotheses without a 'Form of Abduction' at first, and then were asked to do so again using the form. The results of analysing the features of the hypotheses were as follows: in the case of using a 'Form of Abduction', firstly, the types of misunderstanding or mis-adapting the meaning of hypothesis were found to be rare, and secondly, the types of 'giving explanation about the cause of problematic situations through analogical inferencing from the existing knowledge' were found to be double the rate of when no special guide form was used. In conclusion, the hypotheses generated with the 'Form of Abduction' had the features of satisfying the original meaning of hypothesis, i.e. 'explaining the cause of phenomenon and leading to knowledge expansion'. These results also showed that using a 'Form of Abduction', although its form was simple, could be a way of helping students generate hypothesis properly in science classes.

  • PDF

A Case of Scimitar Syndrome (Adult Form) (성인형 Scimitar 증후군 1예)

  • Kim, Woo-Gyu;Kim, Jeong-Kyung;Jeon, Seong-Hee;Lim, Dal-Soo;Min, Cheol-Hong;Park, Hun-Sik;Lim, Byung-Sung;Hong, Suk-Keun;Hwang, Hweung-Kon;Kim, Mi-Young
    • Tuberculosis and Respiratory Diseases
    • /
    • v.47 no.2
    • /
    • pp.259-264
    • /
    • 1999
  • The scimitar syndrome, a rare complex anomaly, is defined as an anomalous right pulmonary venous drainage, partial or complete, to the inferior vena cava. The shape of the Turkish curved sword (scimitar) has provided the name of this syndrome. Additional characteristics of this syndrome such as hypoplasia of the right lung and of the right pulmonary arterial tree, anomalous arterial supply of the right lung from the aorta, dextrocardia and bronchial anomalies are common. Recently we experienced a case of scimitar syndrome (adult form) in a 19-year-old woman patient, so we report the case with a brief review of the literature.

  • PDF

A CASE REPORT OF ACTINOMYCOSIS IN THE LEFT TMJ (좌측 하악 과두부에 발생한 방선균증의 증례보고)

  • Kim, Ki-Yeob;Yoon, Kyoo-Ho;Jun, In-Sung;Kim, Tae-Youl;Jang, Jung-Yong;Ban, Jae-Hyurk
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
    • /
    • v.30 no.3
    • /
    • pp.234-236
    • /
    • 2004
  • Actinomycosis is a rare form of disease that is caused by Actinomyces such as A. israelii and A. bovis, which may take the form of chronic, purulent inflammation of deep tissue evolves with necrosis, formation of sinuses and fibrotic mass. This disease arises in the head and neck area mainly in 55% and other places like that chest and the gastrointestinal tract occurs in 45%. Actinomycosis can present in a variety of forms and may mimic other infections or even neoplasms. Our case was 44-year-old man having painful indurated mass in his left TMJ area, otorrhea in his left ear and trismus. He was treated with surgical excision and biopsy confirmed actinomycosis. And after that, he was cured successfully with antibiotic therapy. We report this case of actinomycosis that developed in the left TMJ area with review articles.

Bilateral Localized Tenosynovial Giant Cell Tumor Causing Patellofemoral Pain Syndrome (슬개대퇴 통증 증후군을 초래한 양측성 건활막 거대세포종)

  • Chung, Whan-Yong;Shin, Sung-Chul;Yi, Sang-Yeop;Sung, Seung-Yong
    • Journal of the Korean Orthopaedic Association
    • /
    • v.56 no.6
    • /
    • pp.525-529
    • /
    • 2021
  • A localized tenosynovial giant cell tumor rarely affects the bilateral knee joint compared to the diffuse form. Only a few cases can be found in the literature, and there is no case report of the bilateral localized form of giant cell tumor causing patellofemoral pain syndrome in Korea. This study experienced a case of bilateral localized giant cell tumor, causing patellofemoral pain syndrome. The tumor was excised arthroscopically and confirmed pathologically. This paper reports this case with a review of the relevant literature.

Review on Cases Applying Hwangryunhaedok-tang External Agent in Korea (황련해독탕(黃連解毒湯) 외용제를 적용한 국내 치험례 고찰)

  • Choi, Min-A;Kim, Kyu-Seok
    • The Journal of Korean Medicine Ophthalmology and Otolaryngology and Dermatology
    • /
    • v.35 no.1
    • /
    • pp.48-57
    • /
    • 2022
  • Objectives : The purpose of this review study is to identify clinical indications of Hwangryunhaedok-tang(HHT) external application and to suggest directions for future research and treatment by analyzing domestic cases applying HHT external treatment except for pharmacopuncture research. Methods : We searched 235 studies published in Korean since 2000 from four domestic databases: Oriental Medicine Advanced Searching Integrated System(OASIS), Research Information Sharing Service(RISS), Korean Traditional Knowledge Portal(KTKP), and Korean studies Information Service Systems(KISS) using keywords such as 'HTT and external use', 'HHT and external agent' 'HHT and wet dressing', or 'HHT and case'. We excluded duplicate papers, papers related to acupuncture including pharmacopuncture, or papers not related to the topic. Results : We selected and analyzed seven case reports. HHT external agent was used alone in one case, as main treatment in two cases, and as adjuvant treatment in four cases. HHT external application was applied to various skin diseases accompanied by inflammation mainly in the form of wet dressings. Conclusion : HHT external agent may be effective on various skin diseases accompanied by inflammation when applied alone or in combination with other agents according to the treatment stage. Based on this results, further studies will be needed to establish the primary clinical indication of HHT external agent.

Ciliated Foregut Cyst and Accessory Spleen in the Pancreas: A Case Report and Literature Review (췌장에서 발생한 부비장과 동반된 섬모성 전장낭: 증례 보고와 문헌고찰)

  • Hyun Jin Kim;Heejin Kwon;Kyungjae Lim;Jinhan Cho;Min Gyoung Pak;Kwan Woo Kim
    • Journal of the Korean Society of Radiology
    • /
    • v.84 no.1
    • /
    • pp.263-269
    • /
    • 2023
  • Ciliated foregut cyst is a relatively rare disease; thus, most reports are in the form of case studies. This benign cyst is usually found in the mediastinum and account for approximately 20% of all mediastinal masses. However, it is rarely found in the hepatobiliary and peripancreatic regions. Approximately 20 cases of ciliated foregut cysts involving the pancreas have been reported in the Enlgish literature. Here, we present a case of ciliated foregut cyst that occurred in the tail of the pancreas in a 29-year-old female. The patient's ultrasonography, CT, and MRI findings are presented, along with a review of the literature.

A case report and literature review of osseous choristoma on the tongue. (혀에서 골성 이소종(osseous choristoma)에 대한 증례 보고 및 문헌 고찰)

  • Park, Yun-Ha;Baek, Jin-A
    • The Journal of the Korean dental association
    • /
    • v.56 no.10
    • /
    • pp.548-554
    • /
    • 2018
  • Choristoma is a growth of normal tissue that occurs at an abnormal region. In the oral cavity, osseous choristoma that has a normal bone feature mainly has been appeared. It is mainly occurred on the tongue. So, It can be found in dental practice or in discomfort in the mouth. Osseous choristoma in the oral cavity is extremely rare. But It can be treated excisional biopsy under local anesthesia. The prognosis is very good. This case is a report of osseous choristoma on the dorsal surface of the tongue. A 17-year-old female patient presented with a foreign body sensation of the tongue. A diameter of the mass is 0.7cm, and there is no pain. Panoramic radiographs showed a radiopaque image in the form of a double image. An excisional biopsy was performed and diagnosed as an osseous choristoma. 12 months after the resection, there were no signs of recurrence. Intraoral osseous choristoma is very rare, but it is clinically very simple and can be found in dental radiographs. We present this case because of Dentists who examine the oral cavity of the patient can easily diagnose the lesion and treat it by simple resection.

  • PDF

A Case of Trichloroethylene Poisoning (삼염화에틸렌 중독 1 례)

  • Jean, Jae-Cheon;Jang, Sung-Won;Yang, Seung-Joan;Lee, Jae-Won;Jin, Sang-Chan;Joo, Myeong-Don;Choi, Woo-Ik
    • Journal of The Korean Society of Clinical Toxicology
    • /
    • v.5 no.1
    • /
    • pp.61-66
    • /
    • 2007
  • Trichloroethylene (TCE) is an unsaturated chlorinated hydrocarbon in the form of a colorless, volatile liquid, which is used as an industrial organic solvent for spot removal and for metal degreasing. In general, the primary complications of TCE poisoning result from involvement of the central nervous and respiratory systems, including aspiration pneumonia. A case is reported of a 54-year-old man who presented in a comatose state after accidental ingestion of 100 ml of TCE, and who recovered after conservative treatment and mechanical ventilation. We discuss this case and present a literature review.

  • PDF

A Case of Primary Squamous Cell Carcinoma of the Thyroid Gland (갑상선에 발생한 원발성 편평세포암 1예)

  • Seol, Jeong-Hun;Kim, Hong-Jun;Hong, Jae-Min;Rho, Kyung-Jin;Hong, Hyun-Jun
    • Korean Journal of Head & Neck Oncology
    • /
    • v.26 no.2
    • /
    • pp.240-242
    • /
    • 2010
  • Primary squamous cell carcinoma of the thyroid gland is a very rare event, representing much less than 1% of all malignant tumors of the thyroid gland. The cancer is characterized by rapidly progressive clinical course in spite of its differentiated morphologic features. In most cases, a squamous epithelium is believed to be a result of metaplasia of a follicular epithelium, although in rare exceptions, it can originate from a remnant of the thyroglossal duct or ultimobranchial body. Squamous cell carcinoma of the thyroid gland can occur in a pure form or mixed with adenocarcinoma. Because their clinical behavior is more aggressive than that of other malignant neoplasm of thyroid gland, the tumor should be treated more vigorously at its initial stage. Recently, authors experienced one case of primary squamous cell carcinoma of the thyroid gland. We report our case with a brief review of literature.

A Case of Canavan Disease (Canavan Disease 1례)

  • Son, Young Ho;Hwang, Tae Gyu;Sinn, Jong Beom
    • Clinical and Experimental Pediatrics
    • /
    • v.46 no.9
    • /
    • pp.934-938
    • /
    • 2003
  • Canavan disease, also known as van Bogaert-Bertrand disease, is a rare autosomal recessive disorder characterized by early an onset and a progressive spongyform degeneration of the brain, associated with an edema of the central nerve system, intramyelinic swelling and neurologic symptoms. This disorder is most prevalent in people of Ashkenazi Jewish descent but has been observed in other ethnic groups. Patients have severe mental retardation, poor head control, macrocephaly and seizures. Canavan disease is caused by the accumulation of N-acetylaspartic acid(NAA) in the brain as the result of a deficiency of aspartoacylase(ASPA) activity. Most children are reported to have the infantile form, becoming symptomatic between three and six month of age, after unremarkable prenatal and perinatal course. We experienced a case of Canavan disease in a six day old female newborn baby, associated with seizure, degeneration of brain white matter and markedly elevated urine N-acetylaspartic acid(NAA) level. So, we report the case with a brief review of the related literature.