본문 바로가기
HOME> 저널/프로시딩 > 저널/프로시딩 검색상세

저널/프로시딩 상세정보

권호별목차 / 소장처보기

H : 소장처정보

T : 목차정보

Case reports in medicine 548건

  1. [해외논문]   A Management Dilemma: Infectious Keratitis Associated with Soft Contact Lens Use and Dubious Treatment Compliance  

    Tsaousis, Konstantinos T. (Department of Ophthalmology, “Hippokration” General Hospital, 54642 Thessaloniki, Greece ) , Sakkias, Georgios (Department of Ophthalmology, “Hippokration” General Hospital, 54642 Thessaloniki, Greece ) , Kozeis, Nikolaos (Department of Ophthalmology, “Hippokration” General Hospital, 54642 Thessaloniki, Greece ) , Tahiaos, Periklis (Department of Ophthalmology, “Hippokration” General Hospital, 54642 Thessaloniki, Greece)
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    Purpose . To present a case of infectious keratitis caused by the microorganism Serratia marcescens in a contact lens user and further to confer on the most advantageous management of comparable situations. Case . After altering the routine that she used for contact lens disinfection, a 24-year-old patient presented with pain and conjunctival redness in both eyes. Slit-lamp examination revealed two infiltrates in the inferior part of the cornea in the right eye and five smaller infiltrates in the superior half of the left cornea. Appropriate treatment, after hospitalization, improved the symptoms while culture of the contact lens material revealed Serratia marcescens as the responsible infectious factor. Conclusion . Enhancing the availability of information with respect to contact lens users and customized analysis regarding treatment for a particular complication could be beneficial in order to reduce the frequency of admission to the eye clinic due to infectious keratitis. In addition, rapid laboratory testing of the infected materials should be a priority for selection of the optimal treatment regimen.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  2. [해외논문]   An Unusual Case of Aplastic Anemia Caused by Temozolomide  

    Comez, Gazi (Department of Internal Medicine, Faculty of Medicine, University of Gaziantep, 27310 Gaziantep, Turkey ) , Sevinc, Alper (Department of Medical Oncology, Faculty of Medicine, University of Gaziantep, 27310 Gaziantep, Turkey ) , Sever, Ozlem Nuray (Department of Medical Oncology, Faculty of Medicine, University of Gaziantep, 27310 Gaziantep, Turkey ) , Babacan, Taner (Department of Internal Medicine, Faculty of Medicine, University of Gaziantep, 27310 Gaziantep, Turkey ) , Sarı, Ibrahim (Department of Pathology, Faculty of Medicine, University of Gaziantep, 27310 Gaziantep, Turkey ) , Camci, Celalettin (Department of Medical Oncology, Faculty of Medicine, University of Gaziantep, 27310 Gaziantep, Turkey)
    Case reports in medicine v.2010 ,pp. 1 - 2 , 2010 , 1687-9627 ,

    초록

    Radiotherapy and concomitant/adjuvant therapy with temozolomide are a common treatment regimen for children and adults with high-grade glioma. Although temozolomide is generally safe, it can rarely cause life-threatening complications. Here we report a case of a 31-year-old female patient who underwent surgical resection followed by radiotherapy plus concomitant temozolomide. She developed pancytopenia after adjuvant treatment with temozolomide. A bone marrow aspiration and biopsy showed hypocellularity with very few erythroid and myeloid cells, consistent with aplastic anemia. In the English literature, aplastic anemia due to temozolomide is extremely rare.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  3. [해외논문]   Popliteal Artery Entrapment Syndrome Presenting with Acute Limb Ischaemia: A Case Report  

    Soobrah, Ramawad (Department of General Surgery, Northwick Park Hospital, Watford Road, Harrow HA1 3UW, UK ) , Nawaz, Adam (Faculty of Medicine, Imperial College London, South Kensington Campus, London SW7 2AZ, UK ) , Hussain, Tahir (Department of General Surgery, Northwick Park Hospital, Watford Road, Harrow HA1 3UW, UK)
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    Popliteal artery entrapment syndrome (PAES) is a relatively rare condition that occurs in young patients as a result of anomalous anatomic relationships between the popliteal artery and the surrounding musculotendinous structures. Patients usually lack atherogenic risk factors and most commonly present with intermittent claudication in the early stages. In the later stages of undiagnosed PAES, acute ischaemia can occur as a result of complete arterial occlusion or embolism. Hence, early diagnosis and surgical release of the entrapment is crucial for good operative outcome and to prevent limb loss.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  4. [해외논문]   Deoxycorticosterone Producing Tumor as a Cause of Resistant Hypertension  

    Gupta, Saurabh (Department of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA ) , Melendez, Jose (Department of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA ) , Khanna, Apurv (Department of Medicine, Division of Nephrology, SUNY Upstate Medical University, Syracuse, NY 13210, USA)
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    We describe a young woman with longstanding resistant hypertension. Evaluation for renal artery stenosis and primary aldosteronism was unrevealing. In this setting of a suppressed plasma aldosterone concentration (PAC) and a suppressed plasma renin activity (PRA), a differential diagnosis of a deoxycorticosterone (DOC) producing tumor was entertained. Biochemical and imaging studies confirmed this diagnosis. Rare and novel DOC producing tumors are an important cause of resistant hypertension.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  5. [해외논문]   Pulmonary Embolism Revealing Idiopathic Membranous Glomerulonephritis  

    Hamzaoui, A. (Departement of Internal Medicine, Fattouma Bourguiba Hospital, 5000 Monastir, Tunisia ) , Harzallah, O. (Departement of Internal Medicine, Fattouma Bourguiba Hospital, 5000 Monastir, Tunisia ) , Klii, R. (Departement of Internal Medicine, Fattouma Bourguiba Hospital, 5000 Monastir, Tunisia ) , Njim, L. (Department of Anatomopathology, Fattouma Bourguiba Hospital, 5000 Monastir, Tunisia ) , Mahjoub, S. (Departement of Internal Medicine, Fattouma Bourguiba Hospital, 5000 Monastir, Tunisia)
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    We describe a case of a 55-year-old man who presented with pulmonary embolism and who was found to have nephrotic syndrome due to idiopathic membranous nephropathy. There are no other signs of nephrotic syndrome such as edema.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  6. [해외논문]   Vitreous Humour Extrusion after Suxamethonium Induction of Anaesthesia in a Polytraumatized Patient: A Case Report  

    Amadasun, Frederick Ebegue (Department of Anaesthesiology, University of Benin Teaching Hospital, PMB 1111, Benin City, Nigeria ) , Isesele, Theodore Ojeide (Department of Anaesthesiology, University of Benin Teaching Hospital, PMB 1111, Benin City, Nigeria)
    Case reports in medicine v.2010 ,pp. 1 - 4 , 2010 , 1687-9627 ,

    초록

    Introduction . Suxamethonium, a deepolarizing muscle relaxant, increases intraocular pressure. It is therefore advised to be avoided in open globe surgery, for fear of extruding ocular contents. Several anecdotal reports support this fear. Some workers however, dispute this claim. There is as yet no formal case report in the literature on the subject. Case Presentation . A 34-year old Nigerian male, was involved in a road traffic accident. He presented at the Accident & Emergency Unit of our hospital about 2 hours after the accident. Clinical examination revealed right corneal laceration (with intact ocular contents) and intra-abdominal visceral injury. Emergency laparotomy was scheduled, to be followed with corneal repair. Anaesthesia was induced with 10 mg midazolam, 100 mg ketamine, and 100 mg suxamethonium given intravenously in sequence. After laparotomy, the ophthalmologists reported for the corneal repair, only to find that the vitreous humour has been extruded. Conclusion . The fear about the use of suxamethonium in open globe situations is real. It will be good clinical judgment to use alternative drugs and techniques to effect rapid muscle relaxation, in the anaesthetic management of the open globe patient. This would be of interest to anaesthetists, ophthalmologists and clinical pharmacologists among others.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  7. [해외논문]   Successful Treatment of Cisplatin Overdose with Plasma Exchange  

    Yamada, Yasuhiro (Department of Hematology & Infectious Diseases, Kumamoto University School of Medicine, Kumamoto 860-8556, Japan ) , Ikuta, Yoshiaki (Department of Gastroenterological Surgery, Kumamoto University School of Medicine, Kumamoto 860-8556, Japan ) , Nosaka, Kisato (Department of Hematology & Infectious Diseases, Kumamoto University School of Medicine, Kumamoto 860-8556, Japan ) , Miyanari, Nobutomo (Department of Gastroenterological Surgery, Kumamoto University School of Medicine, Kumamoto 860-8556, Japan ) , Hayashi, Naoko (Department of Gastroenterological Surgery, Kumamoto University School of Medicine, Kumamoto 860-8556, Japan ) , Mitsuya, Hiroaki (Department of Hematology & Infectious Diseases, Kumamoto University School of Medicine, Kumamoto 860-8556, Japan ) , Baba, Hideo (Department of Gastroenterological Surgery, Kumamoto University School of Medicine, Kumamoto 860-8556, Japan)
    Case reports in medicine v.2010 ,pp. 1 - 4 , 2010 , 1687-9627 ,

    초록

    Accidental cisplatin overdose has been occurring with an increasing frequency due to expanding usage of the agent. However, the optimal strategy to treat such patients remains to be established. Here, we report a case of large cisplatin overdose, successfully managed by plasma exchange, intravenous hydration, granulocyte colony-stimulating factor (G-CSF) administration, and other supportive care. A 67-year-old man with esophageal carcinoma received a large cisplatin overdose of 240 , when he received adjuvant therapy following subtotal esophagectomy. On day 4, he experienced frank cisplatin toxicities and emergency plasma exchange was initiated. With 7 cycles of plasma exchange, the cisplatin concentration decreased from 2,350 to 110 ng/mL. Severe bone marrow suppression with high fever ensued on day 10, which was successfully treated with G-CSF and antibiotics. Despite moderate hearing sense reduction, he recovered without significant complications. Immediate plasma exchange with hydration and other care was efficacious in quickly lowering cisplatin concentrations.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  8. [해외논문]   Leiomyosarcoma Arising in the Pancreatic Duct: A Case Report and Review of the Current Literature  

    Riddle, Nicole D. (Department of Pathology and Cell Biology, University of South Florida College of Medicine, 12901 Bruce B. Downs Blvd, MDC 11, Tampa, FL 33612, USA ) , Quigley, Brian C. (Department of Pathology and Cell Biology, University of South Florida College of Medicine, 12901 Bruce B. Downs Blvd, MDC 11, Tampa, FL 33612, USA ) , Browarsky, Irwin (Department of Pathology and Cell Biology, University of South Florida College of Medicine, 12901 Bruce B. Downs Blvd, MDC 11, Tampa, FL 33612, USA ) , Bui, Marilyn M. (Department of Pathology and Cell Biology, University of South Florida College of Medicine, 12901 Bruce B. Downs Blvd, MDC 11, Tampa, FL 33612, USA)
    Case reports in medicine v.2010 ,pp. 1 - 4 , 2010 , 1687-9627 ,

    초록

    Context . Leiomyosarcomas are rare malignant smooth muscle tumors that may arise in any organ or tissue that contains smooth muscle, commonly within the gastrointestinal tract. They are most often found in the stomach, large and small intestines, and retroperitoneum. Primary pancreatic leiomyosarcoma is extremely rare, and to the best of our knowledge only 30 cases have been reported in the world literature since 1951. Our case represents the first to have a clear origin from the main pancreatic duct. Case Report . This case was diagnosed in a large, tertiary care center in Tampa, Florida. Pertinent information was obtained from chart review and interdepartmental collaboration. A mass in the tail of the pancreas was identified with large pleomorphic and spindle-shaped cells. Immunohistochemistry for vimentin, smooth muscle actin, and desmin was positive. All remaining immunohistochemical markers performed were negative. The tumor clearly originated from the pancreatic duct wall, filled and expanded the duct lumen, and was covered with a layer of benign biliary epithelium. Conclusion . Leiomyosarcoma of the pancreas is an extremely rare malignancy with few reported cases in the literature. The prognosis is poor, and treatment consists of alleviating symptoms and pain management. To our knowledge, this represents the first reported case demonstrating clear origin of a leiomyosarcoma from the pancreatic duct.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  9. [해외논문]   Cervicothoracic Intradural Arachnoid Cyst Misdiagnosed as Motor Neuron Disease  

    Sä (Max Planck Institute of Psychiatry, Kraepelinstraße 2-10, 80804 Munich, Germany ) , mann, P. G. (Max Planck Institute of Psychiatry, Kraepelinstraße 2-10, 80804 Munich, Germany ) , Himmerich, H. (Max Planck Institute of Psychiatry, Kraepelinstraße 2-10, 80804 Munich, Germany ) , Merl, T. (Department of Neurosurgery, Klinikum Großhadern, Ludwig Maximilians University, Marchioninistraße 15, 81377 Munich, Germany ) , Erö (Max Planck Institute of Psychiatry, Kraepelinstraße 2-10, 80804 Munich, Germany ) , s, C. (Department of Neurosurgery, Klinikum Großhadern, Ludwig Maximilians University, Marchioninistraße 15, 81377 Munich, Germany ) , Mü (Max Planck Institute of Psychiatry, Kraepelinstraße 2-10, 80804 Munich, Germany) , ller, M. B. , Tonn, J. C. , Buchwald, B.
    Case reports in medicine v.2010 ,pp. 1 - 4 , 2010 , 1687-9627 ,

    초록

    Recognizing syndromes which mimic ALS is crucial both to avoid giving this diagnosis erroneously and since there may be appropriate treatments. We report a 63-year-old woman diagnosed with possible ALS five years ago based on upper and lower motor neuron signs with typical electrophysiology and normal cranial MRI. At reassessment, spinal MRI revealed a cervicothoracic cyst with cord compression that was successfully treated neurosurgically. Histopathology confirmed an arachnoid origin as suspected from MRI. Spinal cysts may mimic ALS and need to be thoroughly excluded by appropriate imaging.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지
  10. [해외논문]   48XXYY Syndrome in an Adult with Type 2 Diabetes Mellitus, Unilateral Renal Aplasia, and Pigmentary Retinitis  

    Zantour, Baha (Department of Endocrinology and Internal Medicine, Tahar Sfar Hospital, Hiboune, Mahdia 5100, Tunisia ) , Sfar, Mohamed Habib (Department of Endocrinology and Internal Medicine, Tahar Sfar Hospital, Hiboune, Mahdia 5100, Tunisia ) , Younes, Samia (Department of Endocrinology and Internal Medicine, Tahar Sfar Hospital, Hiboune, Mahdia 5100, Tunisia ) , Alaya, Wafa (Department of Endocrinology and Internal Medicine, Tahar Sfar Hospital, Hiboune, Mahdia 5100, Tunisia ) , Kamoun, Mahdi (Department of Endocrinology and Internal Medicine, Tahar Sfar Hospital, Hiboune, Mahdia 5100, Tunisia ) , Mkaouar, Emna (Department of Molecular Human Genetics, Faculty of Medicine, Avenue Majida BOULILA, Sfax 3029, Tunisia ) , Jerbi, Saida (Department of Radiology, Tahar Sfar Hospital, Hiboune, Mahdia 5100, Tunisia)
    Case reports in medicine v.2010 ,pp. 1 - 5 , 2010 , 1687-9627 ,

    초록

    A 45-year-old male was referred for diabetes mellitus. Clinical examination found a family history of multiple precocious deaths, strong consanguinity, personal history of seizures during childhood, small testicles, small penis, sparse body hair, long arms and legs, dysmorphic features, mental retardation, dysarthria, tremor, and mild gait ataxia. Investigations found pigmentary retinitis, metabolic syndrome, unilateral renal aplasia, and hypergonadotropic hypogonadism, and ruled out mitochondrial cytopathy and leucodystrophy. Karyotype study showed a 48XXYY chromosomal type. Renal aplasia and pigmentary retinitis have not been described in 48XXYY patients. They may be related to the chromosomal sex aneuploidy, or caused by other genetic aberrations in light of the high consanguinity rate in the patient's family.

    원문보기

    원문보기
    무료다운로드 유료다운로드

    회원님의 원문열람 권한에 따라 열람이 불가능 할 수 있으며 권한이 없는 경우 해당 사이트의 정책에 따라 회원가입 및 유료구매가 필요할 수 있습니다.이동하는 사이트에서의 모든 정보이용은 NDSL과 무관합니다.

    NDSL에서는 해당 원문을 복사서비스하고 있습니다. 아래의 원문복사신청 또는 장바구니담기를 통하여 원문복사서비스 이용이 가능합니다.

    이미지

    Fig. 1 이미지

논문관련 이미지