Biomedical subjects
Publications and source records attributed to S Merran.
We report the use of a specific handle we designed for interventional procedures guided by fluoro-CT. This handle, easy to use and low cost, improves the procedures reducing dramatically the procedure time.
Renal sinus pathology can be classified into 3 groups: intrinsic lesions that arise from the anatomical components of the sinus (fatty tissue, collecting system, arteries and veins, lymphatic vessels, and nerves); extrinsic lesions that develop within the renal sinus from the renal parenchyma; secondary lesions including metastases and retroperitoneal tumors with renal sinus involvement. The diagnosis of renal sinus disorders often relies on a multimodality approach including IVU, doppler-ultrasonography, and CT. The wide variety of renal sinus diseases that may origin either from the renal parenchyma or the retroperitoneum, and the numerous pitfalls mostly due to anatomic variations, may prevent from making a right etiological diagnosis in numerous cases.
The purpose of this study is to provide an updated pathologic-radiologic classification of cystic renal tumors and to assess imaging diagnostic capabilities. Eighty seven cases of cystic renal tumors explored with multimodality imaging (ultrasonography, CT, MRI, arteriography) and with histopathologic correlation are reported. The most common cystic carcinomas were multilocular cystic renal cell carcinoma (33%) and the pseudocystic necrotic carcinoma (31%), which usually belong to category IV. Less common cystic carcinomas were unilocular cystic renal cell carcinoma (6%) and renal cyst wall carcinoma (6%). The association of thin septa and large locules are suggestive findings for multilocular cystic nephroma, but such criteria are not specific enough to recognize benign multilocular cystic nephroma and to exclude multilocular cystic renal cell carcinoma. Since carcinomatous degeneration may occur within the wall of such tumors, especially in von Hippel Lindau disease, surgery is still required. The results of our study corroborate the Bosniak classification of cystic renal masses: no tumors belonged to the category I or II, all cystic masses which belonged to the category IV were malignant tumors, category III included benign and malignant tumors.
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We report a case of Castleman's disease in a 65-year-old female, revealed by a renal tumor associated with inter-aortico-cava adenopathies and renal chromophobe cell carcinoma. This observation points to the difficulties in differentiating local Castleman's disease, which may be cured by surgical excision, from multicentric disease associated with a dysimmune syndrome of uncertain prognosis. The association of multicentric Castleman's disease with a carcinoma has rarely been described. It could be the emergence of a neoplasia in a context of dysimmunity or Castleman's disease might be related to the production of interleukin 6 by a renal carcinoma.
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