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Information Journal Paper

Title

An unusual diagnosis for persistent diarrhoea and vomiting (CLINICAL QUIZ)

Pages

  73-74

Keywords

Not Registered.

Abstract

 Pheochromocytomas are rare and often sporadic tumours of catecholamine-secreting chromaffin cells, usually present within the adrenal medulla, but also may occur elsewhere. A 45-year-old female was referred by her general practitioner with a 5-year history of increasingly frequent episodes of cyclical diarrhoea, vomiting, abdominal pain and intermittent palpitations. Contrast CT Abdomen/Pelvis revealed a 36x33x46 mm mass in the aorto caval region of her retro-peritoneum, just above the bifurcation. On the basis of her symptoms, CT findings and an elevated plasma metanephrine level of 2314pmol/L (normal range 80 – 510pmol/L), it was at this point a likely diagnosis of a Phaeochromocytoma was made. The retroperitoneal mass was successfully resected, and the histology confirmed a Phaeochromocytoma. Her symptoms rapidly improved and she made a good recovery. This unusual case highlights some of the dilemmas that arise when investigating patients with chronic and recurrent diarrhoea and vomiting.

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  • Cite

    APA: Copy

    Nott, James, Khan, Asad, Madhotra, Ravi, MacFaul, George, & ROSTAMI, KAMRAN. (2017). An unusual diagnosis for persistent diarrhoea and vomiting (CLINICAL QUIZ). GASTROENTEROLOGY AND HEPATOLOGY FROM BED TO BENCH, 10(1), 73-74. SID. https://sid.ir/paper/324836/en

    Vancouver: Copy

    Nott James, Khan Asad, Madhotra Ravi, MacFaul George, ROSTAMI KAMRAN. An unusual diagnosis for persistent diarrhoea and vomiting (CLINICAL QUIZ). GASTROENTEROLOGY AND HEPATOLOGY FROM BED TO BENCH[Internet]. 2017;10(1):73-74. Available from: https://sid.ir/paper/324836/en

    IEEE: Copy

    James Nott, Asad Khan, Ravi Madhotra, George MacFaul, and KAMRAN ROSTAMI, “An unusual diagnosis for persistent diarrhoea and vomiting (CLINICAL QUIZ),” GASTROENTEROLOGY AND HEPATOLOGY FROM BED TO BENCH, vol. 10, no. 1, pp. 73–74, 2017, [Online]. Available: https://sid.ir/paper/324836/en

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