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H : 소장처정보

T : 목차정보

Case reports in medicine 548건

  1. [해외논문]   Occupational Protein Contact Dermatitis: Two Case Reports  

    Rocha, Joana (Department of Dermatology, Braga Hospital, Apartado 2242, 4701-965 Braga, Portugal ) , Pereira, Teresa (Department of Dermatology, Braga Hospital, Apartado 2242, 4701-965 Braga, Portugal ) , Sousa-Basto, Artur (Department of Dermatology, Braga Hospital, Apartado 2242, 4701-965 Braga, Portugal ) , Brito, Celeste (Department of Dermatology, Braga Hospital, Apartado 2242, 4701-965 Braga, Portugal)
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    Protein contact dermatitis (PCD) is a contact dermatitis caused by high-molecular-weight proteins. This entity has been reported with increasing frequency, most commonly as occupational hand dermatitis in food handlers. Clinically, it is characterized by a chronic and recurrent dermatitis with erythema, scaling, and fissures with acute exacerbations occurring a few minutes after contact with offending allergen. We report two cases in confectioners who presented with chronic hand dermatitis.

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    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.

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    Fig. 1 이미지
  2. [해외논문]   Tunga Penetrans: Painful Lesions on the Feet—The First Imported Case from Guinea-Bissau  

    Rosmaninho, A. (Serviço de Dermatologia, Centro Hospitalar do Porto, HSA, Edifício das Consultas Externas, Ex CICAP, Rua D. Manuel II, 4099-001 Oporto, Portugal ) , Vilaç (Serviço de Dermatologia, Centro Hospitalar do Porto, HSA, Edifício das Consultas Externas, Ex CICAP, Rua D. Manuel II, 4099-001 Oporto, Portugal ) , a, S. (Serviço de Dermatologia, Centro Hospitalar do Porto, HSA, Edifício das Consultas Externas, Ex CICAP, Rua D. Manuel II, 4099-001 Oporto, Portugal ) , Costa, V. (Serviço de Infecciologia, Hospital de São João, 4200-319 Oporto, Portugal ) , Sarmento, A. (Serviço de Dermatologia, Centro Hospitalar do Porto, HSA, Edifício das Consultas Externas, Ex CICAP, Rua D. Manuel II, 4099-001 Oporto, Portugal ) , Amorim, I. (Serviço de Dermatologia, Centro Hospitalar do Porto, HSA, Edifício das Consultas Externas, Ex CICAP, Rua D. Manuel II, 4099-001 Oporto, Portugal) , Selores, M.
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    Tungiasis is an endemic disease in certain poor areas around the world. Imported infestations in travelers are becoming more frequent and can lead to considerable morbidity. We report a case of a 50 year-old-man who returned from a trip to Guinea-Bissau with an infection caused by Tunga penetrans .

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    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]   The Rapunzel Syndrome: An Unusual Trichobezoar Presentation  

    Lopes, Luiz Roberto (Department of Surgery, School of Medicine, University of Campinas (Unicamp), Rua Tessália Vieira de Camargo, 126 - Cidade Universitária Zeferino Vaz, Campínas - SP - CEP: 13083-887, Brazil ) , Oliveira, Priscilla Sene Portel (Department of Surgery, School of Medicine, University of Campinas (Unicamp), Rua Tessália Vieira de Camargo, 126 - Cidade Universitária Zeferino Vaz, Campínas - SP - CEP: 13083-887, Brazil ) , Pracucho, Eduardo Marcucci (Department of Surgery, School of Medicine, University of Campinas (Unicamp), Rua Tessália Vieira de Camargo, 126 - Cidade Universitária Zeferino Vaz, Campínas - SP - CEP: 13083-887, Brazil ) , Camargo, Marcelo Amade (Department of Surgery, School of Medicine, University of Campinas (Unicamp), Rua Tessália Vieira de Camargo, 126 - Cidade Universitária Zeferino Vaz, Campínas - SP - CEP: 13083-887, Brazil ) , Coelho Neto, Joã (Department of Surgery, School of Medicine, University of Campinas (Unicamp), Rua Tessália Vieira de Camargo, 126 - Cidade Universitária Ze) , o de Souza , Andreollo, Nelson Adami
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    The Rapunzel syndrome is an unusual form of trichobezoar found in patients with a history of psychiatric disorders, trichotillomania (habit of hair pulling) and trichophagia (morbid habit of chewing the hair), consequently developing gastric bezoars. The principal symptoms are vomiting and epigastric pain. In this case report, we describe this syndrome in a young girl.

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    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]   Pulmonary Alveolar Microlithiasis: A Case Report with Emphasis on Imaging Findings  

    Abdalla, Guilherme (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , Marchiori, Edson (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , Zanetti, Glá (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , ucia (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , Mucillo, Antonio (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , Pereira, Mariana Leite (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , Ventura, Nina (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , Martins, Pedro (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , Constantino, Carolina Pesce Lamas (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ) , Canellas, Rodrigo (Department of Radiology, Rio de Janeiro Federal University, CEP 21941.913, Rio de Janeiro, Brazil ;) , Brandã , o, Viviane , Varella de Oliveira, Romulo
    Case reports in medicine v.2010 ,pp. 1 - 4 , 2010 , 1687-9627 ,

    초록

    Pulmonary alveolar microlithiasis (PAM) is a rare disease characterized by the presence of small calculi in the alveolar space. The authors report a case of a 21-year-old man with a 2-year history of shortness of breath on exertion and dry cough. Physical examination was altered only for crackles at auscultation. Pulmonary function revealed a mild restrictive ventilatory defect and the chest radiograph demonstrated paracardiac confluence of dense micronodular infiltrate. High-resolution CT scan revealed diffuse ground glass attenuation and septal thickening, more pronounced in lower pulmonary regions, with calcifications along the interlobar septa and subpleural regions. A transbronchial lung biopsy confirmed the diagnosis of PAM.

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    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.

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    Fig. 1 이미지
  5. [해외논문]   Bilateral Deep Peroneal Nerve Paralysis Following Kerosene Self-Injection into External Hemorrhoids  

    Rostami, Khalil (Department of Surgery, Ardabil University of Medical Sciences, Ardabil, Iran ) , Farzaneh, Esmaeil (Department of Medical Toxicology & Forensic Medicine, Ardabil University of Medical Sciences, Ardabil, Iran ) , Abolhassani, Hassan (Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran)
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    Along with conventional therapies, some abrogated traditional treatment had been used for hemorrhoids like local Kerosene injection especially for extremely irritated external hemorrhoids. We report a rare case of Kerosene self-injection into the hemorrhoid. Despite antibiotics therapy, extent debridement, and colostomy, the patient died after 24 hours because of heart attack. Moreover, we discuss here the case with contact or injection of hydrocarbon materials and early care action to decrease the extensions of injury and side effects.

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    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]   Ultrasonography and 3D-CT Follow-Up of Extrahepatic Portal Vein Aneurysm: A Case Report  

    Yukawa, Norio (Kamishirane Hospital, 2-65-1 Kamishirane, Asahi-ku, Yokohama 241-0002, Japan ) , Takahashi, Makoto (Kamishirane Hospital, 2-65-1 Kamishirane, Asahi-ku, Yokohama 241-0002, Japan ) , Sasaki, Kazuyoshi (Kamishirane Hospital, 2-65-1 Kamishirane, Asahi-ku, Yokohama 241-0002, Japan ) , Mori, Takuma (Kamishirane Hospital, 2-65-1 Kamishirane, Asahi-ku, Yokohama 241-0002, Japan ) , Matsuo, Ayumi (Kamishirane Hospital, 2-65-1 Kamishirane, Asahi-ku, Yokohama 241-0002, Japan ) , Ito, Kuniyasu (Kamishirane Hospital, 2-65-1 Kamishirane, Asahi-ku, Yokohama 241-0002, Japan ) , Kirikoshi, Hiroyuki (Department of Gastroenterology, Yokohama City University, Yokohama 236-0004, Japan ) , Ohya, Kiyoshi (Kamishirane Hospital, 2-65-1 Kamishirane, Asahi-ku, Yokohama 241-0002, Japan ) , Wada, Nobuyuki (Department of Surgery, Yokohama City University, 3-9 Fukuura, Kanazawa-ku, Yokohama 236-0004, Japan ) , Rino, Yasushi (Department of Surgery, Yokohama City University, 3-9 Fukuura, Kanazawa-ku, Yokohama 236-0004, Japan ) , Masuda, Munetaka (Department of Surgery, Yokohama City University, 3-9 Fukuura, Kanazawa-ku, Yokohama 236-0004, Japan)
    Case reports in medicine v.2010 ,pp. 1 - 6 , 2010 , 1687-9627 ,

    초록

    Extrahepatic portal vein aneurysm is a rare disorder. From 1956 to 2008, we found only 43 published English-language reports, including 67 cases, using Pub Med. We report a case of a 77-year-old woman who had complaints of lower abdominal fullness and residual urine. We performed ultrasonography (US), which demonstrated a congenital extrahepatic portal vein aneurysm. She had no obvious symptoms of the extrahepatic portal vein aneurysm. She had undergone gastrectomy without blood transfusion for gastric ulcer more than 20 years ago. Physical examination revealed no abnormal findings. US revealed a2.2×1.8 cm, round shaped hypoechogenic lesion at the hepatic hilum. Color Doppler US showed bidirectional colors due to circular flow within this lesion. 3D-CT and CT angiography demonstrated that the saccular aneurysm at the hepatic hilum was 3.0 cm in diameter and was enhanced equal to that of portal vein.Twenty-six months after the diagnosis, the aneurysm had not grown in size. Since our patient had no serious complaints or liver disease, surgical procedures had not been employed. US and 3D-CT are noninvasive diagnostic techniques and are helpful in the diagnosis and follow-up of extrahepatic portal vein aneurysms.

    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]   A Man with an Umbilicated Papule of the Hand: What Is Your Diagnosis?  

    Sarma, Deba P. , Cox, Meredith , Walter, Paige , Crisler, William , Huerter, Christopher
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    Extrahepatic portal vein aneurysm is a rare disorder. From 1956 to 2008, we found only 43 published English-language reports, including 67 cases, using Pub Med. We report a case of a 77-year-old woman who had complaints of lower abdominal fullness and residual urine. We performed ultrasonography (US), which demonstrated a congenital extrahepatic portal vein aneurysm. She had no obvious symptoms of the extrahepatic portal vein aneurysm. She had undergone gastrectomy without blood transfusion for gastric ulcer more than 20 years ago. Physical examination revealed no abnormal findings. US revealed a2.2×1.8 cm, round shaped hypoechogenic lesion at the hepatic hilum. Color Doppler US showed bidirectional colors due to circular flow within this lesion. 3D-CT and CT angiography demonstrated that the saccular aneurysm at the hepatic hilum was 3.0 cm in diameter and was enhanced equal to that of portal vein.Twenty-six months after the diagnosis, the aneurysm had not grown in size. Since our patient had no serious complaints or liver disease, surgical procedures had not been employed. US and 3D-CT are noninvasive diagnostic techniques and are helpful in the diagnosis and follow-up of extrahepatic portal vein aneurysms.

    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]   Reversible Cortical Blindness as a Prominent Manifestation of Cerebral Embolism due to Infective Endocarditis  

    Kranidiotis, Georgios P. (Department of Clinical Therapeutics, School of Medicine, University of Athens, “Alexandra” Hospital, 80 Vasilissis Sofias Av. 115 28 Athens, Greece ) , Gougoutsi, Alexandra N. (Department of Clinical Therapeutics, School of Medicine, University of Athens, “Alexandra” Hospital, 80 Vasilissis Sofias Av. 115 28 Athens, Greece ) , Retsas, Theodoros A. (Department of Clinical Therapeutics, School of Medicine, University of Athens, “Alexandra” Hospital, 80 Vasilissis Sofias Av. 115 28 Athens, Greece ) , Anastasiou-Nana, Maria I. (Department of Clinical Therapeutics, School of Medicine, University of Athens, “Alexandra” Hospital, 80 Vasilissis Sofias Av. 115 28 Athens, Greece)
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    Introduction . Infective endocarditis in the left heart may be complicated by stroke, due to embolisation from infectious valvular vegetations. Infarction of both occipital lobes, which are supplied by the posterior cerebral arteries, is infrequent, and is the cause of cortical blindness from lesion of the visual cortex. Cortical blindness is characterized by intact pupillary reflexes, a normal fundoscopy, and, rarely, denial of visual loss. Case Presentation . We report the case of a 58-year-old woman, recipient of a mechanical aortic valve, who presented with fever, multiple organ dysfunction, and cortical blindness. Transesophageal echocardiography and blood cultures confirmed the diagnosis of infective endocarditis caused by methicillin-sensitive Staphylococcus aureus . Computed tomography of the brain without contrast revealed the presence of infarctions in both occipital lobes. It is noteworthy that the visual loss resolved after treatment of endocarditis. Conclusions . A stroke occurring in a patient presenting with fever and a history of valvular heart disease strongly suggests the presence of infective endocarditis. Bilateral thromboembolic infarcts of the occipital lobes cause cortical blindness, that can resolve after treatment of endocarditis.

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    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]   Fibromatous Uterus in a 16-Year-Old Girl: A Case Report  

    Tsili, Athina C. (Department of Clinical Radiology, University Hospital of Ioannina, 45110 Ioannina, Greece ) , Lentoudi, Ekaterini D. (Department of Clinical Radiology, University Hospital of Ioannina, 45110 Ioannina, Greece ) , Argyropoulou, Maria I. (Department of Clinical Radiology, University Hospital of Ioannina, 45110 Ioannina, Greece ) , Dalkalitsis, Nikolaos (Department of Obstetrics & Gynaecology, University Hospital of Ioannina, 45110 Ioannina, Greece ) , Batistatou, Anna (Department of Pathology, University Hospital of Ioannina, 45110 Ioannina, Greece ) , Paraskevaidis, Evangelos (Department of Obstetrics & Gynaecology, University Hospital of Ioannina, 45110 Ioannina, Greece ) , Tsampoulas, Konstantine (Department of Clinical Radiology, University Hospital of Ioannina, 45110 Ioannina, Greece)
    Case reports in medicine v.2010 ,pp. 1 - 5 , 2010 , 1687-9627 ,

    초록

    Although uterine leiomyomas are the most common neoplasms of the female genital tract, this is not the case when referring to women under the age of 20. Only a few cases of uterus leiomyomas have been reported in this age. Preoperative imaging evaluation is mandatory in adolescent women for the accurate detection, localization, and characterization of uterus leiomyomas. We report a case of a 16-year-old girl admitted to our hospital for pain and abdominal distention. The patient underwent multidetector CT examination of the abdomen and MR examination of the pelvis. Both imaging modalities revealed uterine enlargement and the presence of innumerable variably sized leiomyomas. Histopathologic examination following exploratory laparotomy confirmed the presence of uterus leiomyomas. The patient underwent laparoscopic myomectomy two years after the first operation, following MR examination of the pelvis.

    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]   Detection of BCR-ABL Positive Cells in an Asymptomatic Patient: A Case Report and Literature Review  

    Bayraktar, Soley (Slyvester Comprehensive Cancer Center, 1475 NW Ave, Suite 3300, Miami, FL 33136, USA ) , Goodman, Mark (Slyvester Comprehensive Cancer Center, 1475 NW Ave, Suite 3300, Miami, FL 33136, USA)
    Case reports in medicine v.2010 ,pp. 1 - 3 , 2010 , 1687-9627 ,

    초록

    We report a case of an asymptomatic 39-year-old male who was incidentally found to have a white blood cell count of 15 000/ associated with a positive BCR-ABL/ t (9;22)(q34;q11) chromosomal translocation detected in 51/300 of cells by FISH and RT-PCR from peripheral blood. Within the next 3 months, leukocytosis spontaneously subsided; however, BCR-ABL by RT-PCR and FISH was persistent both in peripheral blood and bone marrow. The patient was not started on any therapy and is being followed regularly with laboratory checkup and physical examination for monitoring signs and symptoms of chronic myeloid leukemia (CML) and biological behavior of his BCR-ABL transcripts. At 1 year of surveillance, he is disease free; however he has persistent detection of BCR-ABL fusion gene. Our case is challenging because actual risk of developing CML in BCR-ABL positive healthy, asymptomatic patients is not known.

    원문보기

    원문보기
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    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.

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    Fig. 1 이미지

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