본문 바로가기
HOME> 저널/프로시딩 > 저널/프로시딩 검색상세

저널/프로시딩 상세정보

권호별목차 / 소장처보기

H : 소장처정보

T : 목차정보

Case reports in pediatrics 81건

  1. [해외논문]   Recurrent Pneumonia due to Fibrosing Mediastinitis in a Teenage Girl: A Case Report with Long-Term Follow-Up  

    Hevroni, Avigdor (Institute of Pulmonology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel ) , Springer, Chaim (Institute of Pulmonology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel ) , Wasser, Oren (Institute of Pulmonology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel ) , Avital, Avraham (Institute of Pulmonology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel ) , Koplewitz, Benjamin Z. (Department of Radiology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel)
    Case reports in pediatrics v.2018 ,pp. 1 - 4 , 2018 , 2090-6803 ,

    초록

    A teenage girl was evaluated for recurrent right pneumonia. The evaluation revealed a calcified mediastinal mass that compressed the right intermediate and middle lobar bronchi, as well as the right pulmonary artery and veins. The clinical picture together with imaging studies and borderline positive serology testing suggested a diagnosis of fibrosing mediastinitis associated with histoplasmosis. This rare condition is characterized by the local proliferation of invasive fibrous tissue within the mediastinum due to a hyperimmune reaction to Histoplasma capsulatum . Antifungal and anti-inflammatory therapies are usually ineffective, and surgical intervention contains a high morbidity risk. Palliative surgery and stenting of the compressed airway have been suggested. In the past, the prognosis was thought to be poor, but recent studies demonstrate a more positive outcome. Our patient had been radiologically and functionally stable under follow-up for over thirteen years and has married and delivered two healthy children, both following an uneventful pregnancy.

    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]   A Case of Congenital Syphilis Presenting with Unusual Skin Eruptions  

    Leung, Alexander K. C. (Department of Pediatrics, Alberta Children's Hospital, University of Calgary, Calgary, AB, Canada T2M 0H5 ) , Leong, Kin Fon (Pediatric Institute, Kuala Lumpur General Hospital, Kuala Lumpur, Malaysia ) , Lam, Joseph M. (Department of Pediatrics, Department of Dermatology and Skin Sciences, University of British Columbia, Vancouver, BC, Canada V5Z 1K1)
    Case reports in pediatrics v.2018 ,pp. 1 - 4 , 2018 , 2090-6803 ,

    초록

    Once believed to be a rare disease in developed countries, recent data suggest that there is a surge in incidence of congenital syphilis in many developed countries. Diagnosis of congenital syphilis can be difficult because more than two-thirds of affected infants are asymptomatic at birth, and signs of symptomatic infants may be nonspecific or subtle. On top of this, some affected infants may have atypical presentations. Familiarity with the diverse presentations is essential to diagnosis. We report a 2-week-old male infant with congenital syphilis whose cutaneous manifestations included diffuse, erythematous keratoderma with desquamation and fissures on his hands and feet, multiple linear scaly fissures at the angles of his mouth, and onychauxis of the fingernails and toenails To our knowledge, diffuse, erythematous keratoderma of the hands and feet and thick nails have not been reported previously in congenital syphilis.

    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]   Difficulty in the Clinical Diagnosis of Tularemia: Highlighting the Importance of a Physical Exam  

    Kumar, Rupin (Department of Pediatrics, The Unterberg Children's Hospital at Monmouth Medical Center, Long Branch, NJ, USA ) , Mansour, Mohamed (Department of Pediatrics, The Unterberg Children's Hospital at Monmouth Medical Center, Long Branch, NJ, USA ) , Brunetto, Jacqueline (Department of Pediatrics, The Unterberg Children's Hospital at Monmouth Medical Center, Long Branch, NJ, USA ) , Verma, Renuka (Department of Pediatrics, The Unterberg Children's Hospital at Monmouth Medical Center, Long Branch, NJ, USA ) , Fisher, Margaret (Department of Pediatrics, The Unterberg Children's Hospital at Monmouth Medical Center, Long Branch, NJ, USA ) , Teitelbaum, Jonathan (Department of Pediatrics, The Unterberg Children's Hospital at Monmouth Medical Center, Long Branch, NJ, USA)
    Case reports in pediatrics v.2018 ,pp. 1 - 4 , 2018 , 2090-6803 ,

    초록

    We report an 18-month-old male who presented with fever and nonspecific symptoms. He was evaluated for multiple differential diagnoses including Kawasaki disease and JIA and received treatment for them. After he was readmitted, tularemia was considered based on the physical exam finding of an ulcer on the scalp and enlarged lymph nodes. Tularemia titers were positive, and the patient was given the appropriate antibiotic and was discharged home. Follow-up of the patient showed complete resolution of symptoms. This is a case that demonstrates the importance of physical exam in identifying rare diseases presenting with common signs and symptoms.

    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]   Cholangiocarcinoma in a Child with Progressive Abdominal Distension and Secondary Hypercalcemia  

    Monsereenusorn, Chalinee (Division of Hematology/Oncology, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand ) , Satayasoontorn, Kantang (Department of Pathology, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand ) , Rujkijyanont, Piya (Division of Hematology/Oncology, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand ) , Traivaree, Chanchai (Division of Hematology/Oncology, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand)
    Case reports in pediatrics v.2018 ,pp. 1 - 5 , 2018 , 2090-6803 ,

    초록

    Cholangiocarcinoma is extremely rare in childhood and has been reported in association with other underlying diseases. The survival and prognosis are dismal especially in patients with unresectable or advanced stage cholangiocarcinoma. Overall survival in patients with metastatic cholangiocarcinoma could be increased by using combination chemotherapy with cisplatin and gemcitabine. A case of childhood cholangiocarcinoma was hereby reported.

    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]   Bilateral Giant Hydronephrosis in a Ten-Year-Old Male  

    Kamath, Sowmini P. (Department of Pediatrics, Kasturba Medical College (Constituent Unit of Manipal Academy of Higher Education), Mangaluru 575001, India ) , Ganesh Pai, K. (Department of Pediatric Surgery, Kasturba Medical College (Constituent Unit of Manipal Academy of Higher Education), Mangalore 575001, India ) , Baliga, B. Shantharam (Department of Pediatrics, Kasturba Medical College (Constituent Unit of Manipal Academy of Higher Education), Mangaluru 575001, India)
    Case reports in pediatrics v.2018 ,pp. 1 - 3 , 2018 , 2090-6803 ,

    초록

    We describe a ten-year-old male with bilateral giant hydronephrosis due to pelviureteric junction obstruction presenting with abdominal distension and renal failure. The diagnosis was confirmed on computed tomography and required a two-stage procedure, initially percutaneous nephrostomy followed by Anderson–Hynes pyeloplasty with recovery of kidney function.

    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]   Same Phenotype in Children with Growth Hormone Deficiency and Resistance  

    Ioimo, Irene (University of Pavia, Piazzale Golgi 2, 27100 Pavia, Italy ) , Guarracino, Carmen (University of Pavia, Piazzale Golgi 2, 27100 Pavia, Italy ) , Meazza, Cristina (University of Pavia, Piazzale Golgi 2, 27100 Pavia, Italy ) , Domené (Centro de Investigaciones Endocrinológicas “Dr. César Bergadá” (CEDIE) CONICET-FEI, División de Endocrinología, Hospital de Niños “Ricardo Gutiérrez”, Buenos Aires, Argentina ) , , Horacio M. (University of Pavia, Piazzale Golgi 2, 27100 Pavia, Italy) , Bozzola, Mauro
    Case reports in pediatrics v.2018 ,pp. 1 - 4 , 2018 , 2090-6803 ,

    초록

    By definition, about 2.5% of children show a short stature due to several causes. Two clinical conditions are characterized by serum IGF-I low levels, idiopathic GH deficiency (IGHD), and GH insensitivity (GHI), and the phenotypic appearance of these patients may be very similar. We studied two children with short stature and similar phenotypes. The first case showed frontal bossing, doll face, acromicria, and truncal obesity, with a GH peak GH1 gene, type IA idiopathic GHD was diagnosed. The second case had cranium hypoplasia, a large head, protruding forehead, saddle nose, underdeveloped mandible, and a micropenis. Basal GH levels were high (28.4 ng/ml) while serum IGF-I levels were low and unchangeable during the IGF-I generation test. Laron syndrome was confirmed after the molecular analysis of the GH receptor ( GHR ) gene. IGHD type IA and Laron syndrome is characterized by opposite circulating levels of GH, while both have reduced levels of IGF-I, with an overlapping clinical phenotype, lacking the effects of IGF-I on cartilage. These classical cases show the importance of differential diagnosis in children with severe short stature.

    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 Utilization of Mechanical Thrombectomy in a Presentation of Pediatric Acute Ischemic Stroke  

    Kim, Esther S. (Department of Emergency Medicine, Lehigh Valley Health Network/USF MCOM, CC & I-78, Allentown, PA 18103, USA ) , Mason, Erica K. (Department of Emergency Medicine, Lehigh Valley Health Network/USF MCOM, CC & I-78, Allentown, PA 18103, USA ) , Koons, Andrew (Department of Emergency Medicine, Lehigh Valley Health Network/USF MCOM, CC & I-78, Allentown, PA 18103, USA ) , Quinn, Shawn M. (Department of Emergency Medicine, Lehigh Valley Health Network/USF MCOM, CC & I-78, Allentown, PA 18103, USA ) , Williams, Robert L. (Diagnostic Radiology, Section of Neuroradiology, Lehigh Valley Health Network/USF MCOM, CC & I-78, Allentown, PA 18103, USA)
    Case reports in pediatrics v.2018 ,pp. 1 - 3 , 2018 , 2090-6803 ,

    초록

    Guidelines regarding the management of acute ischemic stroke (AIS) in the pediatric population using mechanical recanalization procedures are lacking. We present a case of a 14-year-old male diagnosed in the Emergency Department with an acute onset stroke who underwent successful mechanical clot removal by interventional radiology.

    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]   A Rare Case of Lemierre-Like Syndrome: A Case Report and Literature Review  

    Ibrahim, Judy (Department of Academic Affairs, Tawam Hospital, Al Ain, UAE ) , Noureddin, Muhammad Bassel (Pediatrics Department, General Pediatrics Division, Tawam Hospital, Al Ain, UAE ) , Lootah, Ali (Department of Academic Affairs, Tawam Hospital, Al Ain, UAE ) , Al Khalidi, Aisha (Pediatrics Department, Pediatric Infectious Diseases Division, Tawam Hospital, Al Ain, UAE ) , Ghatasheh, Ghassan (Pediatrics Department, Pediatric Infectious Diseases Division, Tawam Hospital, Al Ain, UAE ) , Al Tatari, Hossam (Pediatrics Department, Pediatric Infectious Diseases Division, Tawam Hospital, Al Ain, UAE)
    Case reports in pediatrics v.2018 ,pp. 1 - 3 , 2018 , 2090-6803 ,

    초록

    Lemierre's syndrome (LS) is a serious rare complication of oropharyngeal infections. It is characterized by thrombosis of internal jugular vein that rapidly progresses into sepsis and is typically caused by anaerobes. Most of the reported cases have been linked to Fusobacterium necrophorum ; however, there are a handful of reported cases due to aerobes. It is primarily the disease of healthy young adults and can present in school-aged children. The early recognition and treatment of this complication results in resolution of the illness; nevertheless, there have been some concerns about chronic venous insufficiency as a long-term complication. We report a case of a 6-year-old boy, who presented with fever and headache with a history of sore throat. His blood culture was positive for group A Streptococcus (GAS) and was subsequently found to have internal jugular vein, sigmoid, and transverse sinus vein thrombosis.

    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]   An Atypical Case of Bartonella henselae Osteomyelitis and Hepatic Disease  

    Mathews, Dionna M. (Our Lady of the Lake Children's Hospital, Baton Rouge, LA, USA ) , Vance, Katie M. (Division of Academic Affairs, Our Lady of the Lake Regional Medical Center, Baton Rouge, LA, USA ) , McMahon, Pamela M. (Division of Academic Affairs, Our Lady of the Lake Regional Medical Center, Baton Rouge, LA, USA ) , Boston, Catherine (Pediatric Hematology/Oncology, Our Lady of the Lake Children's Hospital/St. Jude Affiliate Baton Rouge, Baton Rouge, LA, USA ) , Bolton, Michael T. (Pediatric Infectious Diseases, Our Lady of the Lake Children's Hospital, Baton Rouge, LA, USA)
    Case reports in pediatrics v.2018 ,pp. 1 - 3 , 2018 , 2090-6803 ,

    초록

    Bartonella henselae is a Gram-negative bacterium and the causative agent of cat scratch disease (CSD). Atypical presentations of B. henselae that involve the musculoskeletal, hepatosplenic, cardiac, or neurologic systems are rare. In this case report, we describe a case of B. henselae osteomyelitis involving bilateral iliac bones complicated by hepatic lesions in a 12-year-old immunocompetent female patient. Although B. henselae is a rare cause of osteomyelitis, it should be considered when patients who present with fever, pain, and lymphadenopathy do not respond to routine osteomyelitis therapy.

    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]   Septate Uterus in a Girl with Rubinstein–Taybi Syndrome  

    de Castro Coelho, Filipa (Department of Gynecology and Obstetrics, Hospital Dr. Nélio Mendonça, Serviço de Saúde da Região Autónoma da Madeira, E.P.E. (SESARAM), Funchal, Portugal ) , Câ (Department of Gynecology and Obstetrics, Hospital Dr. Nélio Mendonça, Serviço de Saúde da Região Autónoma da Madeira, E.P.E. (SESARAM), Funchal, Portugal ) , mara, Sara (Department of Radiology, Hospital Dr. Nélio Mendonça, Serviço de Saúde da Região Autónoma da Madeira, E.P.E. (SESARAM), Funchal, Portugal ) , Alves, Inê (Department of Gynecology and Obstetrics, Hospital Dr. Nélio Mendonça, Serviço de Saúde da Região Autónoma da Madeira, E.P.E. (SESARAM), Funchal, Portugal) , s , Brazã , o, Kathleen
    Case reports in pediatrics v.2018 ,pp. 1 - 4 , 2018 , 2090-6803 ,

    초록

    Rubinstein–Taybi syndrome is an extremely rare plurimalformative condition that can affect any organ. However, reports regarding gynecological problems are unusual. We report the first case of a septate uterus in an adolescent with this syndrome, in agreement with the American Society for Reproductive Medicine (ASRM) and the Congenital Uterine Malformations by Expert (CUME) criteria for uterine septum. Additional studies are required to determine whether there is an increased frequency of mUllerian duct anomalies with the condition. Our report extends the data on the clinical phenotype associated with Rubinstein–Taybi syndrome.

    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