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  1. AU="Essaidi, Zakaria"
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  3. AU=Epstein Marina
  4. AU="Meier, Nicole"
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  6. AU="Fadwa M. AlKhulaifi"
  7. AU="Ghazal, Mohammed"
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  1. Artikel: Non-functional retroperitoneal paraganglioma: A report of case with literature review.

    Hajri, Amal / Ballati, Ahmed / Essaidi, Zakaria / Errguibi, Driss / Boufettal, Rachid / Rifki El Jai, Saad / Chehab, Farid

    Annals of medicine and surgery (2012)

    2021  Band 65, Seite(n) 102360

    Abstract: Introduction: Retroperitoneal paragangliomas are rare tumors, they arise from ganglia along the sympathetic and parasympathetic chain. We report a rare case of a non functional paraganglioma in whom surgical resection was performed.: Presentation of ... ...

    Abstract Introduction: Retroperitoneal paragangliomas are rare tumors, they arise from ganglia along the sympathetic and parasympathetic chain. We report a rare case of a non functional paraganglioma in whom surgical resection was performed.
    Presentation of case: A 35 years-old female presented with chronic abdominal pain, A contrast magnetic resonance imaging (MRI) of abdomen showed a well-defined Left latero-aortic cystic retro-peritoneal surgical resection using laparotomy was performed, The patiente recovered well and was discharged three days after surgery. Histological examination and immunohistochemical revealed a retroperitoneal paraganglioma.
    Discussion and conclusion: Non-functioning retroperitoneal paragangliomas are rare and are most often Isolated. Radiological techniques including, Contrast-enhanced computed tomography (CT) and Magnetic resonance imaging (MRI) are useful for identifying and locating retroperitoneal paragangliomas. surgical excision is still the most effective treatment when it possible.
    Sprache Englisch
    Erscheinungsdatum 2021-04-28
    Erscheinungsland England
    Dokumenttyp Case Reports
    ZDB-ID 2745440-X
    ISSN 2049-0801
    ISSN 2049-0801
    DOI 10.1016/j.amsu.2021.102360
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: A gastrointestinal stromal tumor of stomach presenting with an intratumoral abscess: A case report.

    Ballati, Ahmed / Essaidi, Zakaria / El Attar, Layla / Errguibi, Driss / Hajri, Amal / Boufettal, Rachid / El Jai, Saad Rifki / Chehab, Farid

    Annals of medicine and surgery (2012)

    2021  Band 63, Seite(n) 102143

    Abstract: Introduction: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors in the gastrointestinal tract, GISTs of the stomach presenting as an intratumoral abscess are extremely rare, which necessitates emergency surgery, we report a ... ...

    Abstract Introduction: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors in the gastrointestinal tract, GISTs of the stomach presenting as an intratumoral abscess are extremely rare, which necessitates emergency surgery, we report a case of a stomach GIST developing an intratumoral abscess, in whom emergency surgery was performed.
    Presentation of case: A 68-year-old man presented with severe abdominal pain and a fever. Laboratory data showed an elevated white blood cell count and C-reactive protein level. Computed to mography scan showed a 15 × 10 cm cystic mass adjacent to greater curvature of the stomach, which contained air. Emergency laparotomy revealed A giant cystic gastric mass was observed. Sleeve gastrectomy were performed. Immunohistochemically, the tumor was diagnosed as a Gastric high risk GIST,and imatinib mesylate was initiated, The patient had an uneventful postoperative course and remains well.
    Discussion and conclusion: Such rare cases can be diagnosed and treated properly with careful clinical evaluation, surgical resection and adjuvant chemotherapy with imatinib mesylate is still the mainstay and most effective treatment for GISTs to date.
    Sprache Englisch
    Erscheinungsdatum 2021-02-02
    Erscheinungsland England
    Dokumenttyp Case Reports
    ZDB-ID 2745440-X
    ISSN 2049-0801
    ISSN 2049-0801
    DOI 10.1016/j.amsu.2021.01.091
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel: Chromophobe renal cell carcinoma: A case report and literature review.

    Ballati, Ahmed / Essaidi, Zakaria / El Jai, Saad Rifki / Hajri, Amal / Errguibi, Driss / Boufettal, Rachid / Chehab, Farid

    Annals of medicine and surgery (2012)

    2021  Band 68, Seite(n) 102643

    Abstract: Introduction: Chromophobe renal cell carcinoma, a distinct subtype of renal cell carcinoma (RCC) with characteristic light microscopic, histochemical, and ultrastructural features, typically has a favorable clinical course.: Presentation of case: A ... ...

    Abstract Introduction: Chromophobe renal cell carcinoma, a distinct subtype of renal cell carcinoma (RCC) with characteristic light microscopic, histochemical, and ultrastructural features, typically has a favorable clinical course.
    Presentation of case: A 45-year-old femele presented with abdominal pain. A physical examination found a palpable mass in the left upper quadrant of the abdomen. A CT scan of the abdomen showed a heterogeneously enhancing mass, with necrosis and calcifications contents betwen the liver and the right kidney. she underwent surgical resection. Partial nephrectomy was performed. Pathological diagnosis was Chromophobe renal cell carcinoma.
    Discussion and conclusion: Chromophobe RCC is a rare variety of kidney neoplasm that has recently been better characterized from a molecular and genetic perspective. Overall, it is considered to have a better prognosis, and is associated with earlier stage tumors and longer overall survival compared with clear cell RCC.
    Sprache Englisch
    Erscheinungsdatum 2021-07-28
    Erscheinungsland England
    Dokumenttyp Case Reports
    ZDB-ID 2745440-X
    ISSN 2049-0801
    ISSN 2049-0801
    DOI 10.1016/j.amsu.2021.102643
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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    Kategorien

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