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  1. Article ; Online: Trans-cystic tube drainage a more viable option than T-tube for hepatic resection with cholecystectomy if external biliary drainage is desired.

    Nuamah, Nabil M

    Updates in surgery

    2017  Volume 69, Issue 4, Page(s) 553–554

    MeSH term(s) Cholecystectomy ; Drainage ; Liver
    Language English
    Publishing date 2017
    Publishing country Italy
    Document type Letter ; Comment
    ZDB-ID 2572692-4
    ISSN 2038-3312 ; 2038-131X
    ISSN (online) 2038-3312
    ISSN 2038-131X
    DOI 10.1007/s13304-017-0430-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.B 101: Show issues Location:
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  2. Article: A new variant of double common bile duct associated with choledochal cyst.

    Nuamah, Nabil M / Ekiz, Feza / Kartal, Gulbiz / Sunamak, Oguzhan / Şahiner, Ibrahim Tayfun

    Journal of surgical case reports

    2020  Volume 2020, Issue 6, Page(s) rjaa147

    Abstract: Extrahepatic bile duct duplication is a rare biliary anomaly often associated with conditions like cholecysto-choledocholithiasis, choledochal cyst and malignancy. Precise preoperative diagnosis using conventional radiologic imaging still remains a ... ...

    Abstract Extrahepatic bile duct duplication is a rare biliary anomaly often associated with conditions like cholecysto-choledocholithiasis, choledochal cyst and malignancy. Precise preoperative diagnosis using conventional radiologic imaging still remains a challenge and use of existing classification system is equally confusing. A female patient diagnosed with choledochal cyst by magnetic resonance cholangiopancreatography was found to have an associated new variant of double common bile duct during surgery. The variant discovered could not be classified by existing classification systems and was missed by preoperative imaging. Recognition of existence of this anomaly that warrants careful dissection during biliary surgery is necessary to avoid inadvertent biliary injury as preoperative diagnosis still remains a challenge. Review of existing classification systems is required to include newly discovered variants.
    Language English
    Publishing date 2020-06-15
    Publishing country England
    Document type Case Reports
    ISSN 2042-8812
    ISSN 2042-8812
    DOI 10.1093/jscr/rjaa147
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Duplicated common bile duct: a recipe for biliary injury. Report of a new variant.

    Nuamah, Nabil M / Ibis, Cem / Gok, Ali F K / Ekiz, Feza / Acunas, Bulent

    Journal of surgical case reports

    2017  Volume 2017, Issue 2, Page(s) rjx021

    Abstract: Duplicated common bile duct, often associated with conditions like lithiasis, biliary cysts and pancreatobiliary maljunction, could result in highly morbid and potentially fatal biliary injuries. Precise preoperative diagnosis and classification still ... ...

    Abstract Duplicated common bile duct, often associated with conditions like lithiasis, biliary cysts and pancreatobiliary maljunction, could result in highly morbid and potentially fatal biliary injuries. Precise preoperative diagnosis and classification still remain a challenge. A female patient undergoing emergency laparoscopic cholecystectomy for acute calculous cholecystitis sustained iatrogenic bile duct injury. A drainage tube was placed into the injured duct for post-operative conservative management. Post-operative tube cholangiogram revealed a double common bile duct with cystic duct opening distally. This was identified as a new variant not previously reported or classified. However rare, duplicated common bile duct could result in serious iatrogenic bile duct injury if unidentified during surgery. Knowledge of its existence is essential to avoid such injuries as preoperative diagnosis still remains a challenge. A thorough clinical and morphological study of previously reported variants is needed for a comprehensive classification to encompass newly discovered variants.
    Language English
    Publishing date 2017-02-10
    Publishing country England
    Document type Case Reports
    ISSN 2042-8812
    ISSN 2042-8812
    DOI 10.1093/jscr/rjx021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Hepatic focal nodular hyperplasia developing in a Fanconi anemia patient: a case report and literature review.

    Nuamah, Nabil M / Hamaloglu, Erhan / Ozdemir, Arif / Ozenc, Ahmet / Sozseker, Chava / Sokmensuer, Cenk

    Haematologica

    2006  Volume 91, Issue 8 Suppl, Page(s) ECR39

    Abstract: Fanconi anemia, an autosomal recessive and X-linked disorder, is known to be associated with a variety of neoplasms. Liver tumors are one of the most frequently observed neoplasms but the association between the two disorders remains obscure. We present ... ...

    Abstract Fanconi anemia, an autosomal recessive and X-linked disorder, is known to be associated with a variety of neoplasms. Liver tumors are one of the most frequently observed neoplasms but the association between the two disorders remains obscure. We present a case of a 27-year old female Fanconi anemia patient diagnosed with a mass on the right lobe of the liver measuring 90x75x60 mm. Histopathological examination of the mass after right hepatic lobectomy revealed focal nodular hyperplasia. This appears to be the first reported case of a hepatic focal nodular hyperplasia of such proportion associated with Fanconi anemia. Previously reported cases of liver tumors in association with Fanconi anemia in the English Literature were either hepatocellular carcinomas or hepatic adenomas.
    MeSH term(s) Adult ; Carcinoma, Hepatocellular/etiology ; Carcinoma, Hepatocellular/surgery ; Fanconi Anemia/complications ; Female ; Focal Nodular Hyperplasia/etiology ; Humans ; Liver Neoplasms/etiology ; Liver Neoplasms/surgery ; Review Literature as Topic
    Language English
    Publishing date 2006-08
    Publishing country Italy
    Document type Case Reports ; Journal Article
    ZDB-ID 2333-4
    ISSN 1592-8721 ; 0017-6567 ; 0390-6078
    ISSN (online) 1592-8721
    ISSN 0017-6567 ; 0390-6078
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Uh III Zs.76: Show issues Location:
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  5. Article ; Online: Spontaneous splenic rupture in a healthy allogeneic donor of peripheral-blood stem cell following the administration of granulocyte colony-stimulating factor (g-csf). A case report and review of the literature.

    Nuamah, Nabil M / Goker, Hakan / Kilic, Yusuf A / Dagmoura, Hassen / Cakmak, Atilla

    Haematologica

    2006  Volume 91, Issue 5 Suppl, Page(s) ECR08

    Abstract: Human granulocyte colony-stimulating factor (G-CSF) is a hematopoietic hormone promoting the growth, proliferation, differentiation and maturation of myeloid and leukocytic lineages. G-csfs have been used to improve granulocyte count in neutropenic ... ...

    Abstract Human granulocyte colony-stimulating factor (G-CSF) is a hematopoietic hormone promoting the growth, proliferation, differentiation and maturation of myeloid and leukocytic lineages. G-csfs have been used to improve granulocyte count in neutropenic patients, reduce the incidence and duration of neutropenia in patients receiving cytotoxic chemotherapy and to mobilize peripheral blood stem cells prior to leukapheresis for using in both autologous and allogeneic hematopoietic cell transplantation. In general, side-effects are mild to moderate and life threatening side-effects like splenic rupture are very rare. We herein, report a case of spontaneous splenic rupture secondary to high-dose G-CSF use (20 mcg/kg/day), in a healthy female allogeneic donor of peripheral-blood stem cell (PBSC) .
    MeSH term(s) Abdominal Pain/etiology ; Adult ; Female ; Filgrastim ; Granulocyte Colony-Stimulating Factor/adverse effects ; Hematopoietic Stem Cell Mobilization/adverse effects ; Hemoperitoneum/etiology ; Humans ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/surgery ; Living Donors ; Male ; Peripheral Blood Stem Cell Transplantation ; Recombinant Proteins ; Rupture, Spontaneous ; Splenectomy ; Splenic Rupture/diagnosis ; Splenic Rupture/etiology ; Splenic Rupture/surgery ; Splenomegaly/chemically induced
    Chemical Substances Recombinant Proteins ; Granulocyte Colony-Stimulating Factor (143011-72-7) ; Filgrastim (PVI5M0M1GW)
    Language English
    Publishing date 2006-05
    Publishing country Italy
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 2333-4
    ISSN 1592-8721 ; 0017-6567 ; 0390-6078
    ISSN (online) 1592-8721
    ISSN 0017-6567 ; 0390-6078
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Kategorien

    In stock of ZB MED Cologne/Königswinter

    Uh III Zs.76: Show issues Location:
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