scholarly journals Giant renal leiomyoma: a case report and brief review of the literature

2013 ◽  
Vol 3 (5) ◽  
pp. 58 ◽  
Author(s):  
Matei Andreoiu ◽  
Darrel Drachenberg ◽  
Ross MacMahon

We report on a very large renal leiomyoma in a man presentingwith a 1-year history of lower back and flank pain and a rapidlygrowing abdominal mass. Since a cystic renal cell carcinomacould not be ruled out, a postembolization right radical nephrectomywas performed. Diagnosis was confirmed by pathologic andhistologic analysis. Renal leiomyomas are very rare benign tumoursthat are nearly indistinguishable from leiomyosarcoma or renalcell carcinoma preoperatively. This case represents the secondlargest such entity reported and demonstrates the limited abilityof accurate diagnostic determination preoperatively, with pathologicexamination and immune-histochemical staining postnephrectomyrepresenting the only definitive means of diagnosis. A briefreview of the literature and an outline of typical clinical and pathologicfeatures of renal leiomyomas are also presented.

2013 ◽  
Vol 140 (suppl 1) ◽  
pp. A018-A018
Author(s):  
Tsetan Dolkar ◽  
Evgeniya Angelova ◽  
Ramapriya Vidhun ◽  
Dov Bloch

2005 ◽  
Vol 129 (4) ◽  
pp. 523-526 ◽  
Author(s):  
Shveta Mehra ◽  
Moonja Chung-Park

Abstract We report a case of gallbladder paraganglioma that was discovered during nonrelated surgery. Retrospective study disclosed a family history of pheochromocytoma. The occurrence of gallbladder paraganglioma in the presence of family history of endocrine neoplasia supports that gallbladder paraganglioma may indeed occur as a part of the multiple endocrine neoplasm syndrome. Gallbladder paraganglioma is a rare tumor, and so far to our knowledge only 6 cases have been reported in the literature. Three cases were discovered incidentally during cholecystectomy for cholelithiasis, 2 presented with right upper quadrant pain, and 1 manifested with gastrointestinal bleeding. We herein review all reported cases of paraganglioma of gallbladder and biliary system.


2008 ◽  
Vol 132 (10) ◽  
pp. 1672-1674
Author(s):  
Seethalakshmi Viswanathan ◽  
Sangeeta B. Desai ◽  
S. R. Prabhu ◽  
Mahul B. Amin

Abstract We describe an extremely rare occurrence of a squamous differentiation in a sarcomatoid chromophobe renal cell carcinoma in a 45-year-old woman with nodal and lung metastasis at presentation. The tumor on histology showed all 3 components intimately admixed with each other, which to the best of our knowledge is the first such case to be reported in the literature. The renal pelvis was smooth walled and uninvolved. Kidney-specific cadherin was positive in the chromophobe renal cell carcinoma areas and negative in the sarcomatoid and squamous areas.


2003 ◽  
Vol 40 (4) ◽  
pp. 251-255 ◽  
Author(s):  
Carlos Augusto Real Martinez ◽  
Rogério Tadeu Palma ◽  
Jaques Waisberg

BACKGROUND: Retroperitoneal lipoma is an extremely rare neoplasm. AIMS: The authors report a case of giant retroperitoneal lipoma in a 32-year-old white female, with a history of pain and an abdominal mass over a 2-year period. Total abdominal ultrasonography and barium enema showed a large mass located in the retroperitoneal space behind the ascending colon. Laparotomy showed a large encapsulated tumor measuring 20 x 13 x 10 cm and weighing 3.400 g. The histological study revealed a benign neoplasm of fatty cells. CONCLUSION: The patient remains well 17 years after surgery, without recurrentce of the disease.


2015 ◽  
Vol 14 (2) ◽  
pp. 133-138 ◽  
Author(s):  
Issei UEDA ◽  
Takatoshi AOKI ◽  
Hodaka OKI ◽  
Hiroyuki TAKAHASHI ◽  
Yoshiko HAYASHIDA ◽  
...  

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