|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Evolving experiencewith prevention and treatment of splenic artery syndrome afterorthotopic liver transplantation 显示文摘 | Mogl MT Niissler NC Presser SJ | 2010 | Transpl Int2010，23，8： | 1 |
| 2 | Older liver graft transplantation,cholestasis and synthetic graft function 显示文摘 | Borchert D Glanemann M Mogl M | 2005 | Transpl Int2005，18，6： | 1 |
| 3 | Evolving experience with prevention and treatment of splenic artery syndrome after orthotopic liver transplantation显示文摘 | Mogl MT Nussler NC Presser SJ | 2010 | Transplant Int2010，23，8： | 1 |
| 4 | Emphusem-atous Pyelonephritis显示文摘 | Michaeli J Mogle P Perlberg S | | 0，，02： | 1 |
| 5 | Older liver graft transplantation,cholestasis and synthetic graft function显示文摘 | Borchert D Glanemann M Mogl M | 2005 | Transpl Int2005，18，6： | 1 |
| 6 | Adult liver transplantation using liver grafts from donors over 70 years of age 显示文摘 | Borchert DH Glanemann M Mogl M | 2005 | Transplant Proc2005，37，2： | 1 |
| 7 | Evolving experience with pervention and treatment of splenic artery syndrome after orthotopic liver transplantion显示文摘 | Mogl MT Nussler NC Presser SJ | 2010 | Transpl Int2010，23，8： | 1 |
| 8 | Multidetector computed tomography for preoperative assessment of hepatic vasculature and prediction of splenic artery steal syndrome in patients with liver cirrhosis before transplantation显示文摘 | Christian Grieser Timm Denecke Ingo G. Steffen Maria Avgenaki Vera Fr?hling Martina Mogl Dirk Schnapauff Lukas Lehmkuhl Lars Stelter Florian Streitparth Jan Langrehr Jan-Holger Rothe Bernd Hamm Enrique Lopez H?nninen | 2010 | European Radiology2010，，1： | 1 |
| 9 | Evolving experience with prevention and treatment of splenic artery syndrome after orthotopic liver transplantation显示文摘 | Mogl MT Nussler NC Presser SJ | 2010 | Transplant Int2010，23，8： | 1 |
| 10 | Older liver graft transplantation,cholestasis and synthetic graft function显示文摘 | Borchert D Glanemann M Mogl M | 2005 | Transpl Int2005，18，6： | 1 |
| 11 | Respiratory failure and multiple fractures in vitamin D-dependent rickets 显示文摘 | Alpan G Mogle P Patz D | 1985 | Acta Paediatr Scand1985，74，2： | 1 |
| 12 | General Method for Ultrashort Light Pulse Chirp Measurement显示文摘 | K Naganuma K Mogl H Y | 1989 | IEEE Journal of Quantum Electronics1989，25，6： | 1 |
| 13 | Evolving experience with prevention and treatment of splenic artery syndrome after orthotopic liver transplantation显示文摘 | Mogl MT Nussler NC Presser S J | 2010 | Transplant Int2010，23，8： | 1 |
| 14 | The normal width of the adult hip joint:the relationship to age,sex and obesity显示文摘 | Pogrund H Bloom R Mogle P | 1983 | Skeletal Radiol1983，10，1： | 1 |
| 15 | Safety and efficacy of new integrated bipolar and ultrasonic scissors compared to conventional laparoscopic 5-mm sealing and cutting instru- ments显示文摘 | Seehofer D Mogl M Boas-Knoop S | 2012 | Surg Endosc2012，26，： | 1 |
| 16 | Extraskeletal soft-tissue chondro- sarcoma显示文摘 | Amir D Amir G Mogle P | 1985 | Clin Orthop1985，198，： | 1 |
| 17 | An unhappy triad:Hemochromatosis, porphyria cutanea tarda and hepatocellular carcinoma-A case report显示文摘Liver fibrosis and cirrhosis are predisposing factors for the development of hepatocellular carcinoma (HCC). Hemosiderosis has also been described to trigger carcinogenesis. A significant iron overload, as found in hereditary hemochromatosis (HHC), is a risk factor for HCC and may also promote the symptoms of porphyria cutanea tarda (PCT). A 68-year old male patient presented to our clinic with a suspected HCC, elevated alpha-fetoprotein but normal liver function tests. He reported a 25 year-old history of vitiligo upon exposure to sunlight. The patient underwent an extended left hemihepatectomy, and the recovery was uneventful, with the exception of a persistent hyperbilirubinemia. Perfusion problems and extrahepatic cholestasis were ruled out by CT-scan with angiography and MR-cholangiopancreatography. However, MRI showed an iron overload. Histology confirmed the HCC (pT3, pN0, G3, R0) and revealed a portal fibrosis and hemosiderosis. Based on the skin lesions we suspected a PCT that was confirmed by laboratory tests showing elevated porphyrin, uroporphyrin, coproporphyrin and porphobilinogen. Concurrently, molecular diagnostics revealed homozygosity for the C282Y mutation within the hemochromatosis HFE gene. After phlebotomy and normalization of liver function tests the patient was discharged. This is the first case ever showing the unusual combination of HCC in a fibrotic liver with HHC and PCT. This diagnosis not only warrants oncological follow-up but also symptomatic therapy to normalize iron metabolism and thereby improve liver function and alleviate the symptoms of HHC and PCT. Thus progression of fibrosis may be prevented and liver regeneration supported. | Martina T Mogl Andreas Pascher Sabine J Presser Michael Schwabe Peter Neuhaus Natascha C Nuessler | 2007 | World Journal of Gastroenterology2007，13，13： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员