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|Title:||Primary liver leiomyoma: a review of this unusual tumour.|
|Authors:||Perini, Marcos Vinicius;Fink, Michael Anthony;Yeo, David Andrew;Carvalho, Carlos Alberto;Morais, Carlos Floriano;Jones, Robert M;Christophi, Christopher|
|Affiliation:||Department of Surgery, Austin Hospital, The University of Melbourne, Melbourne, Victoria 3084, Australia. email@example.com|
|Citation:||Anz Journal of Surgery 2012; 83(4): 230-3|
|Abstract:||Primary liver leiomyoma (PLL) should be considered in the differential diagnosis of liver lesions. A literature review has been completed and two cases are reported. The first is a 45-year-old white woman complaining of vague abdominal pain. She was initially evaluated with abdominal ultrasonography (US) that revealed a heterogeneous liver mass measuring 18 cm in greatest diameter. The tumour demonstrated hypointensity on T1-weighted and hyperintensity on T2-weighted magnetic resonance imaging. The second case is a 45-year-old Asian male who had undergone kidney transplantation 16 years ago for IgA glomerulonephritis and who developed mild, self-limiting epigastric pain. US showed a 4.3-cm-diameter lesion that was predominantly hypoechoic and was either compressing or arising from segment 2 of the liver. Computed tomography showed a well-circumscribed 4-cm-diameter mass that appeared to be arising from segments 2/3 of the liver and was adjacent to the anterior gastric wall. He underwent an uneventful laparoscopic left lateral sectionectomy and discharged on post-operative day 3. Pathological examination of the resection specimen confirmed the lesion as a PLL in each case. Herein, we report two cases of PLL and review the literature regarding this uncommon disorder.|
|Internal ID Number:||22984931|
|Appears in Collections:||Journal articles|
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