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1. Mohanty D, Jain BK, Agrawal V, Gupta A: Cystic nephroma: a diagnostic dilemma. Saudi J Kidney Dis Transpl; 2010 May;21(3):518-20
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Cystic nephroma (CN) is a rare benign neoplasm of kidney with excellent prognosis.
  • [MeSH-major] Kidney / pathology. Kidney Neoplasms / diagnosis. Nephroma, Mesoblastic / diagnosis

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  • (PMID = 20427881.001).
  • [ISSN] 1319-2442
  • [Journal-full-title] Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia
  • [ISO-abbreviation] Saudi J Kidney Dis Transpl
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Saudi Arabia
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2. Li L, Yao JL, di Sant'Agnese PA, Bourne PA, Picken MM, Young AN, Shen SS, Huang J: Expression of claudin-7 in benign kidney and kidney tumors. Int J Clin Exp Pathol; 2008;1(1):57-64
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Expression of claudin-7 in benign kidney and kidney tumors.
  • We studied the expression of claudin-7 in benign and neoplastic kidneys by immunohistochemical staining.

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  • (PMID = 18784823.001).
  • [ISSN] 1936-2625
  • [Journal-full-title] International journal of clinical and experimental pathology
  • [ISO-abbreviation] Int J Clin Exp Pathol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2480537
  • [Keywords] NOTNLM ; chromophobe / claudin-7 / clear cell / kidney / neoplasm / oncocytoma / papillary
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3. Mondal SK, Mallick MG, Bandyopadhyay R, Mondal PK: Neurofibroma of kidney: an uncommon neoplasm and diagnostic dilemma with solitary fibrous tumor. J Cancer Res Ther; 2010 Jul-Sep;6(3):388-90
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  • [Title] Neurofibroma of kidney: an uncommon neoplasm and diagnostic dilemma with solitary fibrous tumor.
  • Neurofibroma of kidney is an extremely rare tumor.
  • Here, we report a solitary neurofibroma of right kidney in a 54-year-old woman.
  • Radiological investigations (ultrasonography and computed tomography) detected a solid mass in the upper pole of right kidney and clinicoradiologically renal cell carcinoma was suspected.
  • Microscopically, tumor consisted of benign spindle-shaped cells accompanied by fibrous tissue.
  • [MeSH-major] Kidney Neoplasms / diagnosis. Neurofibroma / diagnosis

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  • (PMID = 21119287.001).
  • [ISSN] 1998-4138
  • [Journal-full-title] Journal of cancer research and therapeutics
  • [ISO-abbreviation] J Cancer Res Ther
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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4. Thyavihally YB, Tongaonkar HB, Desai SB: Benign mixed epithelial stromal tumor of the renal pelvis with exophytic growth: case report. Int Semin Surg Oncol; 2005 Sep 9;2:18
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  • [Title] Benign mixed epithelial stromal tumor of the renal pelvis with exophytic growth: case report.
  • BACKGROUND: Mixed epithelial and stromal tumor (MEST) is a distinctive benign composite neoplasm of the kidney predominantly seen in females mostly in the perimenopausal period.
  • Although these tumors are known to arise from renal pelvis, our case was distinct in that it had no intrapelvic component growing in exophytic fashion.
  • A computed tomography scan of abdomen and pelvis showed a 9 x 7 cm uniformly solid mass with poor contrast enhancement situated in the inferomedial aspect of the left kidney.
  • On exploration, the mass was arising from the inferior and anterior aspect of left renal pelvis, and was attached to it with a narrow pedicle.
  • The mass was excised preserving the kidney.
  • Microscopically, the tumor was composed of large collagenized areas containing bundles of spindle cells and several 'microcysts' lined by cuboidal epithelium suggestive of a benign mixed epithelial stromal tumor.
  • Commonly, it arises from the renal parenchyma and pelvis and nephrectomy is advocated to manage these tumors.
  • CONCLUSION: MEST is a distinctive benign tumor of the kidney that should be distinguished from other renal neoplasms.
  • MEST arising from the renal pelvis and growing exophytically is a rare entity.

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  • (PMID = 16150156.001).
  • [ISSN] 1477-7800
  • [Journal-full-title] International seminars in surgical oncology : ISSO
  • [ISO-abbreviation] Int Semin Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1215508
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5. Richter M, Meyer W, Küster J, Middel P: Exophytic benign mixed epithelial stromal tumour of the kidney: case report of a rare tumour entity. Diagn Pathol; 2010;5:16
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Exophytic benign mixed epithelial stromal tumour of the kidney: case report of a rare tumour entity.
  • BACKGROUND: Mixed epithelial and stromal tumour (MEST) represents a recently described benign composite neoplasm of the kidney, which predominantly affects perimenopausal females.
  • Most tumours are benign, although rare malignant cases have been observed.
  • A CT scan of the abdomen showed a 30-mm-in-diameter uniform mass adjacent to the pelvis of the left kidney.
  • Surgical exploration showed a tumour arising from the lower anterior hilus of the left kidney.
  • The tumour could be excised by preserving the kidney.
  • Commonly, the tumour arises from the renal parenchyma or pelvis.
  • CONCLUSION: MEST represents a distinctive benign tumour entity of the kidney, which affects perimenopausal woman.
  • By imaging studies it is difficult to distinguish between a benign or malignant nature of the tumour.
  • [MeSH-major] Epithelial Cells / pathology. Kidney Neoplasms / pathology. Mixed Tumor, Malignant / pathology. Stromal Cells / pathology

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  • (PMID = 20193076.001).
  • [ISSN] 1746-1596
  • [Journal-full-title] Diagnostic pathology
  • [ISO-abbreviation] Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2842239
  • [General-notes] NLM/ Original DateCompleted: 20100609
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6. Huang KH, Huang CY, Chung SD, Pu YS, Shun CT, Chen J: Malignant epithelioid angiomyolipoma of the kidney. J Formos Med Assoc; 2007 Feb;106(2 Suppl):S51-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Malignant epithelioid angiomyolipoma of the kidney.
  • Angiomyolipoma (AML) is a common benign renal tumor composed of thick-walled blood vessels, smooth muscle, and adipose tissue, but the malignant epithelioid variant is extremely rare.
  • Computed tomography showed a heterogeneously enhanced mass without fat density in the left kidney.

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  • (PMID = 17493897.001).
  • [ISSN] 0929-6646
  • [Journal-full-title] Journal of the Formosan Medical Association = Taiwan yi zhi
  • [ISO-abbreviation] J. Formos. Med. Assoc.
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Singapore
  • [Chemical-registry-number] 0 / Antigens, Neoplasm; 0 / Melanoma-Specific Antigens; 0 / Neoplasm Proteins
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7. Rajalakshmi V, Chandran P, Selvambigai, Ganesh J: Metanephric stromal tumor: a novel pediatric renal neoplasm. Indian J Pathol Microbiol; 2009 Jul-Sep;52(3):389-91
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metanephric stromal tumor: a novel pediatric renal neoplasm.
  • Metanephric stromal tumor of kidney is a novel pediatric benign stromal specific renal neoplasm.
  • This tumor is usually centered in the renal medulla with a characteristic microscopic appearance which differentiates this lesion from congenital mesoblastic nephroma and clear cell sarcoma of the kidney.
  • The differentiation of metanephric stromal tumor from clear cell sarcoma of the kidney will spare the child from the ill effects of adjuvant chemotherapy.
  • [MeSH-major] Kidney Neoplasms / diagnosis. Kidney Neoplasms / pathology. Stromal Cells / pathology

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  • (PMID = 19679970.001).
  • [ISSN] 0974-5130
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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8. Paspulati RM, Bhatt S: Sonography in benign and malignant renal masses. Radiol Clin North Am; 2006 Nov;44(6):787-803
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sonography in benign and malignant renal masses.
  • This article gives an overview of the benign and malignant renal mass lesions and the role of ultrasonography in their characterization.
  • [MeSH-major] Kidney Neoplasms / ultrasonography
  • [MeSH-minor] Diagnosis, Differential. Humans. Neoplasm Metastasis

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  • (PMID = 17147987.001).
  • [ISSN] 0033-8389
  • [Journal-full-title] Radiologic clinics of North America
  • [ISO-abbreviation] Radiol. Clin. North Am.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 132
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9. Bacci G, Ferrari C, Longhi A, Ferrari S, Forni C, Bacchini P, Palmerini E, Briccoli A, Pignotti E, Balladelli A, Picci P: Second malignant neoplasm in patients with osteosarcoma of the extremities treated with adjuvant and neoadjuvant chemotherapy. J Pediatr Hematol Oncol; 2006 Dec;28(12):774-80
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Second malignant neoplasm in patients with osteosarcoma of the extremities treated with adjuvant and neoadjuvant chemotherapy.
  • Twenty-six patients (2.15%) developed a second malignant neoplasm at a median of 7.6 years (1 to 25 y) after primary osteosarcoma treatment.
  • Second neoplasms were leukemia (10), breast (7), lung (2), kidney (2), central nervous system cancer (2), soft tissue (1), parotid (1), and colon (1).
  • The rate of second malignancies observed in the osteosarcoma group was significantly higher than that observed in the control group of 1160 patients with benign tumors treated in the same period at our Institute (2.2% vs. 0.8%, P<0.009).
  • Our study showed that the risk of second neoplasm within 15 years increased and then leveled off and that although secondary solid tumors could be explained as unrelated cases, leukemias seem to be over represented.

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  • (PMID = 17164644.001).
  • [ISSN] 1077-4114
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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10. Chen JH, Yu CY, Pai CY, Chan DC, Chen CJ, Yu JC, Liu YC: Castleman's disease in the left upper retroperitoneal space mimicking an adrenal neoplasm: report of a case and literature review. Jpn J Clin Oncol; 2005 Jun;35(6):353-6
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  • [Title] Castleman's disease in the left upper retroperitoneal space mimicking an adrenal neoplasm: report of a case and literature review.
  • Castleman's disease is a rare disorder characterized by benign proliferation of lymphoid tissue.
  • We report a case of a 51-year-old woman with a Castleman's tumor located superomedial to the upper pole of the left kidney that mimicked an adrenal neoplasm.

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  • (PMID = 15928190.001).
  • [ISSN] 0368-2811
  • [Journal-full-title] Japanese journal of clinical oncology
  • [ISO-abbreviation] Jpn. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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11. Gajanayake I, Priestnall SL, Benigni L, English K, Summers BA, Garden OA: Paraneoplastic hypercalcemia in a dog with benign renal angiomyxoma. J Vet Diagn Invest; 2010 Sep;22(5):775-80
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Paraneoplastic hypercalcemia in a dog with benign renal angiomyxoma.
  • The present report describes a previously unreported renal neoplasm causing paraneoplastic hypercalcemia and highlights the possibility of paraneoplastic hypercalcemia being caused by a benign neoplasm.
  • [MeSH-major] Dog Diseases / diagnosis. Hypercalcemia / veterinary. Kidney Diseases / veterinary. Myxoma / veterinary

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  • (PMID = 20807942.001).
  • [ISSN] 1040-6387
  • [Journal-full-title] Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc
  • [ISO-abbreviation] J. Vet. Diagn. Invest.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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12. Bierer S, Wülfing C, Bode ME, Pühse G, Brinkmann OA, Hertle L: [Bilateral renal angiomyolipomas with a thrombus in the inferior caval vein. Rare growth pattern of a benign tumor]. Urologe A; 2005 Dec;44(12):1469-72
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Bilateral renal angiomyolipomas with a thrombus in the inferior caval vein. Rare growth pattern of a benign tumor].
  • [Transliterated title] Bilaterale renale Angiomyolipome mit Thrombus in der Vena cava inferior. Seltenes Wachstumsverhalten eines benignen Tumors.
  • These are benign tumors, but in rare cases they show a more aggressive growth pattern with invasion into the venous system but without revealing any signs of malignancy.
  • [MeSH-major] Angiomyolipoma / complications. Angiomyolipoma / diagnosis. Kidney Neoplasms / complications. Kidney Neoplasms / diagnosis. Vena Cava, Inferior / pathology. Venous Thrombosis / diagnosis. Venous Thrombosis / etiology
  • [MeSH-minor] Adult. Female. Humans. Neoplasm Invasiveness

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  • (PMID = 16133230.001).
  • [ISSN] 0340-2592
  • [Journal-full-title] Der Urologe. Ausg. A
  • [ISO-abbreviation] Urologe A
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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13. Shannon BA, Cohen RJ, de Bruto H, Davies RJ: The value of preoperative needle core biopsy for diagnosing benign lesions among small, incidentally detected renal masses. J Urol; 2008 Oct;180(4):1257-61; discussion 1261
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The value of preoperative needle core biopsy for diagnosing benign lesions among small, incidentally detected renal masses.
  • PURPOSE: We determined the safety and accuracy of preoperative needle core biopsy for diagnosing benign lesions among small incidental asymptomatic renal masses.
  • Diagnostic biopsies revealed 138 malignant (75%) and 46 benign (25%) lesions.
  • Of these patients 108 (59%) underwent renal surgery, which showed a 100% biopsy accuracy rate for distinguishing malignant from benign lesions and a 98% rate for determining histological tumor type.
  • Followup with radiological imaging was performed for 59 lesions in patients with nondiagnostic biopsies or benign masses and for 16 low grade malignant tumors in elderly patients.
  • CONCLUSIONS: We found that needle core biopsy was a safe and accurate technique for distinguishing between malignant and benign tumors in small asymptomatic incidentally detected renal masses.
  • [MeSH-major] Biopsy, Fine-Needle / methods. Carcinoma, Renal Cell / pathology. Carcinoma, Renal Cell / surgery. Kidney Neoplasms / pathology. Kidney Neoplasms / surgery
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Cohort Studies. Female. Humans. Immunohistochemistry. Incidental Findings. Kidney Diseases / diagnosis. Kidney Diseases / surgery. Male. Middle Aged. Neoplasm Staging. Nephrectomy / methods. Preoperative Care / methods. Prognosis. Retrospective Studies. Sensitivity and Specificity


14. Yang Y, Nie X, Lu J, Lu XY, Wei YY, Wang H, Han ZH, Chen ZH, Zheng J: [Mixed epithelial and stromal tumor of kidney]. Zhonghua Bing Li Xue Za Zhi; 2006 Jan;35(1):29-31
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Mixed epithelial and stromal tumor of kidney].
  • OBJECTIVE: To study the clinicopathological features and differential diagnoses of mixed epithelial and stromal tumor of the kidney.
  • METHODS: Clinical and pathological characteristics of 4 cases of mixed epithelial and stromal tumor of the kidney were studied.
  • Radiologic studies revealed cystic and solid masses involving the kidney.
  • CONCLUSIONS: Mixed epithelial and stromal tumor of the kidney is a benign neoplasm with distinct histopathological features.
  • [MeSH-major] Kidney Neoplasms / pathology. Neoplasms, Complex and Mixed / pathology. Neoplasms, Glandular and Epithelial / pathology

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  • (PMID = 16608646.001).
  • [ISSN] 0529-5807
  • [Journal-full-title] Zhonghua bing li xue za zhi = Chinese journal of pathology
  • [ISO-abbreviation] Zhonghua Bing Li Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Actins; 0 / Receptors, Estrogen; 0 / Receptors, Progesterone
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15. Moslemi MK: Mixed epithelial and stromal tumor of the kidney or adult mesoblastic nephroma: an update. Urol J; 2010;7(3):141-7
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  • [Title] Mixed epithelial and stromal tumor of the kidney or adult mesoblastic nephroma: an update.
  • PURPOSE: Our aim was to review the spectrum of usual and unusual clinical and morphologic findings observed in mixed epithelial and stromal tumor of the kidney (MEST).
  • RESULTS: Mixed epithelial and stromal tumor is a relatively rare and distinct neoplasm of the kidney that should be distinguished from other renal neoplasms.
  • Although the overall prognosis is favorable, recurrence and malignant transformation of MEST can occur CONCLUSION: It is difficult to distinguish benign or malignant nature on imaging studies.
  • [MeSH-major] Carcinoma, Renal Cell / diagnosis. Kidney Neoplasms / diagnosis. Nephroma, Mesoblastic / diagnosis


16. Coppenrath EM, Mueller-Lisse UG: Multidetector CT of the kidney. Eur Radiol; 2006 Nov;16(11):2603-11
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multidetector CT of the kidney.
  • The technological development of multidetector CT offers new possibilities for better imaging of organic structures that can be used in diagnosis of the kidney.
  • Faster scanning allows studies in different contrast phases, which is helpful for better discrimination of benign or malignant lesions especially in the highly vascularized kidney.
  • Indications for CT investigation of the kidney include urolithiasis, tumor diagnosis and staging, renal trauma, and vascular disease.
  • Even in children, special indications for CT of the kidney remain in polytrauma and tumor staging.
  • Multidetector CT of the kidney has become a very valuable tool in urology, but a careful protocol strategy is mandatory.
  • [MeSH-major] Kidney Diseases / diagnostic imaging. Kidney Diseases / pathology. Tomography, X-Ray Computed
  • [MeSH-minor] Contrast Media / administration & dosage. Humans. Image Processing, Computer-Assisted / methods. Neoplasm Staging. Radiation Dosage

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  • (PMID = 16568265.001).
  • [ISSN] 0938-7994
  • [Journal-full-title] European radiology
  • [ISO-abbreviation] Eur Radiol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Contrast Media
  • [Number-of-references] 57
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17. Ashley RA, Reinberg YE: Familial multilocular cystic nephroma: a variant of a unique renal neoplasm. Urology; 2007 Jul;70(1):179.e9-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Familial multilocular cystic nephroma: a variant of a unique renal neoplasm.
  • Multilocular cystic nephroma (MCN) is a benign renal lesion believed to be unilateral and nonfamilial.
  • [MeSH-major] Kidney Neoplasms / genetics
  • [MeSH-minor] Child, Preschool. Humans. Infant. Kidney Diseases, Cystic / pathology. Male

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  • (PMID = 17656243.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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18. Xiang H, Ding W, Liu F, Ren GP, Wang ZM, Zhu XZ: [Clinicopathologic analysis of mixed epithelial and stromal tumor of kidney and adult cystic nephroma]. Zhonghua Bing Li Xue Za Zhi; 2009 Jul;38(7):436-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Clinicopathologic analysis of mixed epithelial and stromal tumor of kidney and adult cystic nephroma].
  • OBJECTIVE: To study the clinicopathologic features, immunophenotype and differential diagnosis of mixed epithelial and stromal tumor of kidney (MEST) and adult cystic nephroma (CN).
  • CONCLUSIONS: Both MEST and CN are uncommon renal neoplasm.
  • Most of them run a benign clinical course.
  • [MeSH-major] Epithelial Cells / pathology. Kidney Neoplasms / pathology. Neoplasms, Complex and Mixed / pathology. Neoplasms, Cystic, Mucinous, and Serous / pathology. Stromal Cells / pathology

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  • (PMID = 19781188.001).
  • [ISSN] 0529-5807
  • [Journal-full-title] Zhonghua bing li xue za zhi = Chinese journal of pathology
  • [ISO-abbreviation] Zhonghua Bing Li Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / ACTA2 protein, human; 0 / Actins; 0 / Desmin; 0 / Receptors, Estrogen; 0 / Vimentin
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19. Durgun Y, Firat C, Miman MC, Kirimlioglu H: A rare benign laryngeal tumor: angiomyolipoma. J Craniofac Surg; 2010 Nov;21(6):1956-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A rare benign laryngeal tumor: angiomyolipoma.
  • Angiomyolipoma is a mesenchymal neoplasm containing adipose tissue, blood vessels, and smooth muscle fibers.
  • Arising most frequently in the kidney, the tumor may exceptionally be at the head and neck region.

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  • (PMID = 21119467.001).
  • [ISSN] 1536-3732
  • [Journal-full-title] The Journal of craniofacial surgery
  • [ISO-abbreviation] J Craniofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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20. Akhavan A, Cannon GM Jr, Sasatomi E, Franks ME: Synchronous unilateral renal cell carcinoma and Kimura disease of the kidney. Urology; 2006 Sep;68(3):673.e21-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Synchronous unilateral renal cell carcinoma and Kimura disease of the kidney.
  • Kimura disease (KD) is a rare, benign, chronic inflammatory disorder most often found in young Asian males that can simulate a neoplasm.
  • We report a case of renal cell carcinoma and KD within the same kidney.
  • To our knowledge, this is the first reported case of KD involving the kidney confirmed pathologically, as well as the first association of KD with renal cell carcinoma.
  • [MeSH-major] Angiolymphoid Hyperplasia with Eosinophilia / complications. Carcinoma, Renal Cell / complications. Kidney Diseases / complications. Kidney Neoplasms / complications


21. Jadhav MN, Yelikar BR, Patil SB: Epithelioid angiomyolipoma of the kidney: a case report. Indian J Pathol Microbiol; 2007 Apr;50(2):338-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Epithelioid angiomyolipoma of the kidney: a case report.
  • Renal angiomyolipoma is a distinctive benign neoplasm that occurs either sporadically or in patients with tuberous sclerosis complex.
  • Histopathology revealed epithelioid angiomyolipoma of the left kidney with chronic pyelonephritis.
  • [MeSH-major] Angiomyolipoma / pathology. Kidney Neoplasms / pathology
  • [MeSH-minor] Antigens, Neoplasm. Diagnosis, Differential. Female. Humans. Immunohistochemistry. Melanoma-Specific Antigens. Middle Aged. Neoplasm Proteins / metabolism

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  • (PMID = 17883064.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  • [Chemical-registry-number] 0 / Antigens, Neoplasm; 0 / Melanoma-Specific Antigens; 0 / Neoplasm Proteins
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22. Znati K, Chbani L, El Fatemi H, Harmouch T, Kamaoui I, Tazi F, Bennis S, Amarti A: Solitary fibrous tumor of the kidney: a case report and review of the literature. Rev Urol; 2007;9(1):36-40

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Solitary fibrous tumor of the kidney: a case report and review of the literature.
  • A solitary fibrous tumor (SFT) is an unusual spindle cell neoplasm that usually occurs in the pleura but has recently been described in diverse extrapleural sites.
  • Urogenital localization is rare, and only 19 cases of SFT of the kidney have been described.
  • We report a case of a large SFT clinically thought to be renal cell carcinoma arising in the kidney of a 70-year-old man.
  • This tumor is benign in up to 90% of cases.

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  • (PMID = 17396171.001).
  • [ISSN] 1523-6161
  • [Journal-full-title] Reviews in urology
  • [ISO-abbreviation] Rev Urol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC1831532
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23. Dong D, Li H, Yan W, Xu W, Lu L, Zeng Z: The diagnosis and surgical management of juxtaglomerular cell tumor of the kidney. J Hypertens; 2010 Mar;28(3):628-32
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The diagnosis and surgical management of juxtaglomerular cell tumor of the kidney.
  • Juxtaglomerular cell tumor (JCT) of the kidney is a rare benign renal neoplasm.
  • Four cases of JCT of the kidney have been diagnosed and treated surgically in our hospital from January 2005 to August 2008.
  • Pathological examination confirmed the final diagnosis of JCT of the kidney.
  • JCT of the kidney should be kept in mind because they represent a surgically curable cause of secondary hypertension.
  • [MeSH-major] Juxtaglomerular Apparatus / pathology. Kidney Neoplasms / diagnosis. Kidney Neoplasms / surgery

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  • (PMID = 20051908.001).
  • [ISSN] 1473-5598
  • [Journal-full-title] Journal of hypertension
  • [ISO-abbreviation] J. Hypertens.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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24. Ip YT, Yuan JQ, Cheung H, Chan JK: Sporadic hemangioblastoma of the kidney: an underrecognized pseudomalignant tumor? Am J Surg Pathol; 2010 Nov;34(11):1695-700
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sporadic hemangioblastoma of the kidney: an underrecognized pseudomalignant tumor?
  • Hemangioblastoma is a benign tumor that can occur sporadically, or in association with von Hippel-Lindau disease in approximately one-quarter of the cases.
  • This benign neoplasm which can be mistaken for various malignancies such as renal cell carcinoma, epithelioid angiomyolipoma, adrenal cortical carcinoma, and paraganglioma, deserves wider recognition for its occurrence as a primary renal tumor.
  • [MeSH-major] Hemangioblastoma / pathology. Kidney Neoplasms / pathology

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  • [CommentIn] Am J Surg Pathol. 2011 Apr;35(4):623-4 [21378542.001]
  • (PMID = 20924277.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / S100 Proteins; 0 / inhibin-alpha subunit; 57285-09-3 / Inhibins; 68238-35-7 / Keratins; EC 4.2.1.11 / Phosphopyruvate Hydratase
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25. Vujanić GM, Kelsey A, Perlman EJ, Sandstedt B, Beckwith JB: Anaplastic sarcoma of the kidney: a clinicopathologic study of 20 cases of a new entity with polyphenotypic features. Am J Surg Pathol; 2007 Oct;31(10):1459-68
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Anaplastic sarcoma of the kidney: a clinicopathologic study of 20 cases of a new entity with polyphenotypic features.
  • We report 20 cases of a distinct, previously unrecognized renal neoplasm, anaplastic sarcoma of the kidney with polyphenotypic features.
  • Twelve tumors presented in the right kidney, and 5 in the left (laterality was unknown in 3 cases).
  • The tumors involved the pelvi-calyceal system in 5 of the cases.
  • The nodules of cartilage showed both benign and malignant features, often within the same tumor.
  • In the differential diagnosis, anaplastic Wilms tumor, primary renal synovial sarcoma, malignant mesenchymoma, ectomesenchymoma, and mesenchymal chondrosarcomas have been considered but none of these tumors shared the same features as the 20 cases described here which represent a distinct clinicopathologic entity with morphologic features of a polyphenotypic anaplastic sarcoma of the kidney.
  • [MeSH-major] Kidney Neoplasms / pathology. Sarcoma / pathology
  • [MeSH-minor] Adolescent. Adult. Biomarkers, Tumor / analysis. Child. Child, Preschool. Desmin / analysis. Disease-Free Survival. Female. Gene Expression. Humans. Immunoenzyme Techniques. Infant. Male. Neoplasm Recurrence, Local. Neoplasm Staging. Nephrectomy. Oncogene Proteins, Fusion / genetics. Oncogene Proteins, Fusion / metabolism. Phenotype. RNA, Messenger / metabolism. Reverse Transcriptase Polymerase Chain Reaction. Vimentin / analysis

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  • (PMID = 17895746.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Desmin; 0 / Oncogene Proteins, Fusion; 0 / RNA, Messenger; 0 / SYT-SSX fusion protein; 0 / Vimentin
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26. DeWitt J, Gress FG, Levy MJ, Hernandez LV, Eloubeidi MA, Mishra G, Sherman S, Al-Haddad MA, LeBlanc JK: EUS-guided FNA aspiration of kidney masses: a multicenter U.S. experience. Gastrointest Endosc; 2009 Sep;70(3):573-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] EUS-guided FNA aspiration of kidney masses: a multicenter U.S. experience.
  • OBJECTIVE: To describe a multicenter experience with the indications, yield, and complications from attempted EUS-FNA of a kidney mass.
  • PATIENTS: Consecutive subjects undergoing attempted EUS-FNA of a kidney mass.
  • INTERVENTIONS: EUS-FNA of a kidney mass.
  • Kidney masses (median diameter 32 mm; range 11-60 mm) were located in the upper (n = 12) and lower (n = 3) poles of the left (n = 10) and right (n = 5) kidneys, respectively.
  • Results of EUS-FNA (median 3 passes; range 2-4 passes) in 13 (87%) procedures were diagnostic of (n = 7) or highly suspicious for (n = 1) renal cell carcinoma (RCC), atypical cells (n = 2), oncocytoma (n = 1), benign cyst (n = 1), and nondiagnostic (n = 1).
  • [MeSH-major] Biopsy, Fine-Needle / methods. Endosonography / methods. Kidney Neoplasms / pathology. Kidney Neoplasms / ultrasonography
  • [MeSH-minor] Adenoma, Oxyphilic / pathology. Adenoma, Oxyphilic / ultrasonography. Aged. Aged, 80 and over. Carcinoma, Renal Cell / pathology. Carcinoma, Renal Cell / ultrasonography. Cohort Studies. Confidence Intervals. Female. Follow-Up Studies. Hospitals, Teaching. Humans. Immunohistochemistry. Male. Middle Aged. Neoplasm Staging. Probability. Retrospective Studies. Risk Assessment. Sensitivity and Specificity. United States

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  • (PMID = 19560139.001).
  • [ISSN] 1097-6779
  • [Journal-full-title] Gastrointestinal endoscopy
  • [ISO-abbreviation] Gastrointest. Endosc.
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] United States
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27. Engholm G, Hakulinen T, Gislum M, Tryggvadóttir L, Klint A, Bray F, Storm HH: Trends in the survival of patients diagnosed with kidney or urinary bladder cancer in the Nordic countries 1964-2003 followed up to the end of 2006. Acta Oncol; 2010 Jun;49(5):655-64
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Trends in the survival of patients diagnosed with kidney or urinary bladder cancer in the Nordic countries 1964-2003 followed up to the end of 2006.
  • BACKGROUND: Previous studies have shown systematic differences between the Nordic Countries in population-based relative survival following a kidney or urinary bladder cancer diagnosis.
  • RESULTS: The survival following bladder cancer was higher than for kidney cancer and highest for men.
  • Survival increased over the years in all countries, more for kidney cancer than bladder cancer.
  • For Danish kidney cancer patients, the rate of increase over all the years has been lower than in the other countries, especially among women, resulting in a survival in Denmark some 10-20% points lower than elsewhere in 1999-2003.
  • CONCLUSION: The increasing 5-year relative survival in all the Nordic countries for both kidney and bladder cancer are promising, but for kidney cancer a higher percentage detected coincidentally during an imaging investigation for other diseases could play a role.
  • Denmark had the lowest survival, despite their known practice of including benign conditions with invasive bladder cancers.
  • The lower Danish survival after kidney and bladder cancer in the first year after diagnosis could be due to later diagnosis on average, a higher co-morbidity from smoking-related diseases, and perhaps, less adequate cancer treatment and management in Denmark.
  • [MeSH-major] Kidney Neoplasms / mortality. Urinary Bladder Neoplasms / mortality
  • [MeSH-minor] Adult. Age Distribution. Aged. Aged, 80 and over. Denmark / epidemiology. Female. Finland / epidemiology. Follow-Up Studies. Humans. Iceland / epidemiology. Incidence. Male. Mass Screening. Middle Aged. Mortality / trends. Neoplasm Staging. Norway / epidemiology. Registries. Risk Factors. Survival Analysis. Survival Rate / trends. Sweden / epidemiology

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  • (PMID = 20156116.001).
  • [ISSN] 1651-226X
  • [Journal-full-title] Acta oncologica (Stockholm, Sweden)
  • [ISO-abbreviation] Acta Oncol
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
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28. Kwon JE, Kang JH, Kwon GY: Mixed epithelial and stromal tumor of the kidney: a case report. J Korean Med Sci; 2007 Feb;22(1):159-62
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Mixed epithelial and stromal tumor of the kidney: a case report.
  • The descriptive term "mixed epithelial and stromal tumor of the kidney" was recently proposed for a group of renal tumors characterized histologically by a mixture of stromal and epithelial proliferation.
  • It is a rare benign neoplasm of the kidney which has been reported under various names such as adult type mesoblastic nephroma or others.
  • [MeSH-major] Kidney Neoplasms / pathology. Neoplasms, Glandular and Epithelial / pathology

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  • [Cites] Pathol Res Pract. 2000;196(2):135-9 [10707372.001]
  • [Cites] Histopathology. 1999 Jul;35(1):65-73 [10383716.001]
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  • (PMID = 17297273.001).
  • [ISSN] 1011-8934
  • [Journal-full-title] Journal of Korean medical science
  • [ISO-abbreviation] J. Korean Med. Sci.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2693557
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29. Obulareddy SJ, Xin J, Truskinovsky AM, Anderson JK, Franklin MJ, Dudek AZ: Metanephric adenoma of the kidney: an unusual diagnostic challenge. Rare Tumors; 2010;2(2):e38
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metanephric adenoma of the kidney: an unusual diagnostic challenge.
  • Although metanephric adenoma (MA) is a rare, benign neoplasm of epithelial cells, it is often difficult to distinguish this entity from other malignant neoplasms preoperatively.

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  • (PMID = 21139840.001).
  • [ISSN] 2036-3613
  • [Journal-full-title] Rare tumors
  • [ISO-abbreviation] Rare Tumors
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
  • [Other-IDs] NLM/ PMC2994510
  • [Keywords] NOTNLM ; Wilm’s tumor / differential diagnosis. / metanephric adenoma / papillary renal cell carcinoma
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30. Bosco M, Galliano D, La Saponara F, Pacchioni D, Bussolati G: Cytologic features of metanephric adenoma of the kidney during pregnancy: a case report. Acta Cytol; 2007 May-Jun;51(3):468-72
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cytologic features of metanephric adenoma of the kidney during pregnancy: a case report.
  • BACKGROUND: Metanephric adenoma (MA) is a relatively rare neoplasm derived from metanephric blastema and composed of well-differentiated epithelial nephroblastic cells.
  • In view of its invariably benign clinical outcome, a preoperative diagnosis of this tumor could be of critical importance.
  • Transabdominal ultrasound examination disclosed a mass in her left kidney.
  • [MeSH-major] Adenoma / pathology. Kidney Neoplasms / pathology. Pregnancy Complications, Neoplastic / pathology

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  • (PMID = 17536558.001).
  • [ISSN] 0001-5547
  • [Journal-full-title] Acta cytologica
  • [ISO-abbreviation] Acta Cytol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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31. Al-Ahmadie HA, Yilmaz A, Olgac S, Reuter VE: Glomus tumor of the kidney: a report of 3 cases involving renal parenchyma and review of the literature. Am J Surg Pathol; 2007 Apr;31(4):585-91
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Glomus tumor of the kidney: a report of 3 cases involving renal parenchyma and review of the literature.
  • Glomus tumor is a rare mesenchymal neoplasm affecting the subcutaneous tissue of the distal extremities in the majority of cases.
  • We report 3 cases of the glomus tumor family in the kidney, a solid glomus tumor, a glomangioma, and a glomangiomyoma.
  • To date, all 3 tumors have followed a benign course without evidence of recurrence or metastasis.
  • This report expands the spectrum of mesenchymal tumors of the kidney.
  • [MeSH-major] Glomus Tumor / pathology. Kidney Neoplasms / pathology

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  • (PMID = 17414106.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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32. Antonelli A, Zani D, Dotti P, Tralce L, Simeone C, Cunico SC: Use of the appendix as ureteral substitute in a patient with a single kidney affected by relapsing upper urinary tract carcinoma. ScientificWorldJournal; 2005 Apr 5;5:276-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Use of the appendix as ureteral substitute in a patient with a single kidney affected by relapsing upper urinary tract carcinoma.
  • The treatment of upper urinary tract transitional cell carcinoma (UT-TCC) in single-kidney patients requires the radical removal of cancer, but also, when feasible, the preservation of the continuity of the urinary tract by various surgical techniques.
  • In the literature, the cecal appendix has rarely been used as a ureteral substitute, moreover in benign pathological conditions, showing encouraging early results.
  • The positive functional and oncological outcomes obtained after a lengthy follow-up in a single-kidney patient with UT-TCC treated by ureteral resection and appendix interposition confirm the viability of this surgical option.
  • [MeSH-major] Appendix / transplantation. Carcinoma, Transitional Cell / surgery. Neoplasm Recurrence, Local / surgery. Ureter / surgery. Ureteral Neoplasms / surgery

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  • (PMID = 15962193.001).
  • [ISSN] 1537-744X
  • [Journal-full-title] TheScientificWorldJournal
  • [ISO-abbreviation] ScientificWorldJournal
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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33. Ma L, Kowalski D, Javed K, Hui P: Atypical angiomyolipoma of kidney in a patient with tuberous sclerosis: a case report with p53 gene mutation analysis. Arch Pathol Lab Med; 2005 May;129(5):676-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Atypical angiomyolipoma of kidney in a patient with tuberous sclerosis: a case report with p53 gene mutation analysis.
  • Angiomyolipoma (AML) is the most common benign mesenchymal tumor of the kidney.
  • [MeSH-major] Angiomyolipoma / pathology. Genes, p53. Kidney Neoplasms / pathology. Mutation. Tuberous Sclerosis / pathology
  • [MeSH-minor] Adult. Biomarkers, Tumor / analysis. Cytoplasm / ultrastructure. DNA Mutational Analysis. DNA, Neoplasm / genetics. Female. Humans. Immunohistochemistry. Intercellular Junctions / ultrastructure. Nephrectomy. Polymerase Chain Reaction. Polymorphism, Single-Stranded Conformational. Treatment Outcome

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  • (PMID = 15859641.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / DNA, Neoplasm
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34. Park SE, Park NS, Chun JM, Park NW, Yang YJ, Yun GW, Lee HJ, Yun HJ, Jo DY, Song KS, Kim S: A case of recurrent solid pseudopapillary tumor of the pancreas with involvement of the spleen and kidney. Cancer Res Treat; 2006 Apr;38(2):118-20

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of recurrent solid pseudopapillary tumor of the pancreas with involvement of the spleen and kidney.
  • Most SPTPs are considered to be benign and only rarely metastasize.
  • We report here on a 27-year old woman with recurrent SPTP with involvement of both the spleen and left kidney at the time of the initial diagnosis, and with aggressive behavior.
  • She underwent exploratory laparotomy with distal pancreatectomy, left nephrectomy and splenectomy, and was diagnosed with SPTP with invasion to both the spleen and left kidney.

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  • (PMID = 19771270.001).
  • [ISSN] 1598-2998
  • [Journal-full-title] Cancer research and treatment : official journal of Korean Cancer Association
  • [ISO-abbreviation] Cancer Res Treat
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2741664
  • [Keywords] NOTNLM ; Neoplasm metastasis / Pancreas / Solid pseudopapillary tumor
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35. Gassler N, Haferkamp A, Flechtenmacher C, Hohenfellner M, Schirmacher P, Autschbach F: [Renal oncocytoma with metastasis from breast carcinoma: a contribution to the differential diagnosis of tumourous lesions of the kidney]. Pathologe; 2006 May;27(3):217-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Renal oncocytoma with metastasis from breast carcinoma: a contribution to the differential diagnosis of tumourous lesions of the kidney].
  • [Transliterated title] Onkozytom der Niere mit Metastase eines Mammakarzinoms : Differenzialdiagnose tumoröser Läsionen der Niere.
  • In conclusion, metastasis of breast carcinoma to a benign renal tumour is very rare.
  • [MeSH-major] Adenoma, Oxyphilic / secondary. Breast Neoplasms / pathology. Kidney Neoplasms / secondary. Neoplasm Metastasis

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  • [Cites] Int J Surg Pathol. 2003 Apr;11(2):127-35 [12754635.001]
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  • (PMID = 16642392.001).
  • [ISSN] 0172-8113
  • [Journal-full-title] Der Pathologe
  • [ISO-abbreviation] Pathologe
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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36. Kim HJ, Kim CH, Choi YJ, Ayala AG, Amirikachi M, Ro JY: Juxtaglomerular cell tumor of kidney with CD34 and CD117 immunoreactivity: report of 5 cases. Arch Pathol Lab Med; 2006 May;130(5):707-11
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juxtaglomerular cell tumor of kidney with CD34 and CD117 immunoreactivity: report of 5 cases.
  • CONTEXT: Juxtaglomerular cell tumor is a rare renal neoplasm.
  • Renin immunohistochemistry and electron microscopic documentation of rhomboid crystals are the primary methods of diagnosing this benign tumor.
  • [MeSH-major] Adenocarcinoma / pathology. Antigens, CD34 / analysis. Juxtaglomerular Apparatus / pathology. Kidney Neoplasms / pathology. Proto-Oncogene Proteins c-kit / analysis

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  • (PMID = 16683889.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD34; 0 / Biomarkers, Tumor; EC 2.7.10.1 / Proto-Oncogene Proteins c-kit
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37. Fine SW, McCarthy DM, Chan TY, Epstein JI, Argani P: Malignant solitary fibrous tumor of the kidney: report of a case and comprehensive review of the literature. Arch Pathol Lab Med; 2006 Jun;130(6):857-61
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Malignant solitary fibrous tumor of the kidney: report of a case and comprehensive review of the literature.
  • Approximately 10% of the neoplasm consisted of haphazardly arranged spindle cells admixed with dense collagenous bands, which is typical of benign SFT.
  • Immunohistochemically, we observed CD34 labeling in the benign SFT component with loss of expression in the sarcomatous component, focal labeling for Bcl-2 protein in both areas, and absence of labeling for cytokeratin, renal cell carcinoma marker, S100 protein, CD117, and muscle markers in both areas.
  • To our knowledge, this is the first reported case of malignant renal SFT, likely representing transformation from a histologically documented benign SFT component.
  • [MeSH-major] Fibrosarcoma / pathology. Kidney / pathology. Kidney Neoplasms / pathology

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  • (PMID = 16740040.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD34; 0 / Biomarkers, Tumor; 0 / Proto-Oncogene Proteins c-bcl-2
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38. Rotman S, Déruaz C, Venetz JP, Chaubert P, Benhattar J, Meuwly JY, Jichlinski P, Guillou L, Moll S, Pascual M, Lemoine R: De novo concurrent papillary renal cell carcinoma and angiomyolipoma in a kidney allograft: evidence of donor origin. Hum Pathol; 2006 Apr;37(4):481-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] De novo concurrent papillary renal cell carcinoma and angiomyolipoma in a kidney allograft: evidence of donor origin.
  • In the general population, renal cell carcinoma (RCC) is a relatively common neoplasm; however, the papillary RCC subtype is infrequent and represents only 10 to 15% of all RCC.
  • Angiomyolipoma is a well-known common benign tumor.
  • In transplant recipients, RCC can develop in native kidneys, but its occurrence "de novo" in the renal allograft is very rare with an estimated incidence of less than 0.5%.
  • Microsatellite analysis of the allograft, as compared with the recipient peripheral blood leukocytes, demonstrated that the 2 tumors (1 malignant and 1 benign) were of donor origin.
  • To our knowledge, this is the first report of de novo concurrent papillary RCC and angiomyolipoma in a renal allograft.
  • [MeSH-major] Angiomyolipoma / etiology. Carcinoma, Renal Cell / etiology. Kidney Neoplasms / etiology. Kidney Transplantation / adverse effects. Tissue Donors


39. Sokolova IA, Hes O, Michal M, Matsko DE: [Small-cell variant of renal oncocytoma]. Arkh Patol; 2007 Sep-Oct;69(5):34-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Renal oncocytoma is a distinct benign tumor accounting for approximately 3-5% of all renal tumors.
  • This neoplasm is easily recognizable in its classic form: there are polygonal cells with abundant granular eosinophilic cytoplasm filled with mitochondria.
  • [MeSH-major] Adenoma, Oxyphilic / pathology. Carcinoma, Small Cell / pathology. Cytoplasm / pathology. Kidney Neoplasms / pathology. Mitochondria / pathology
  • [MeSH-minor] Aged. Female. Humans. Neoplasm Metastasis

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  • (PMID = 18074818.001).
  • [ISSN] 0004-1955
  • [Journal-full-title] Arkhiv patologii
  • [ISO-abbreviation] Arkh. Patol.
  • [Language] rus
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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40. Mongha R, Bansal P, Dutta A, Das RK, Kundu AK: Wunderlich's syndrome with hepatic angiomyolipoma in tuberous sclerosis. Indian J Cancer; 2008 Apr-Jun;45(2):64-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Nephron preserving approach was tried but the right kidney could not be salvaged.
  • Hepatic Angiomyolipoma is a benign mesenchymal neoplasm of the liver which is rarely reported in literature.
  • [MeSH-major] Angiomyolipoma / complications. Hemorrhage / etiology. Kidney Diseases / etiology. Kidney Neoplasms / complications. Liver Neoplasms / complications. Tuberous Sclerosis / complications


41. Derouiche A, Ouni A, Kourda N, Hentati H, Ben Slama MR, Chebil M: Cystic nephroma in the adult: pathological aspects and therapeutic implications. Pathologica; 2007 Dec;99(6):446-9
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  • Cystic nephroma is a benign renal neoplasm.
  • The differential diagnoses of Cystic nephroma are recently described mixed epithelial and stromal tumours of the kidney and cystic renal cell carcinoma.
  • The Authors report three cases of Cystic nephroma and illustrate the clinical, radiological and histological features of this renal neoplasm.
  • [MeSH-major] Diagnostic Errors. Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology

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  • (PMID = 18416340.001).
  • [ISSN] 0031-2983
  • [Journal-full-title] Pathologica
  • [ISO-abbreviation] Pathologica
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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42. Jalpota Y, Tewari V, Madan R: Recurrent nephrogenic adenoma of urinary bladder in a renal allograft recipient--a case report. Indian J Pathol Microbiol; 2006 Apr;49(2):261-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Nephrogenic adenoma is a rare benign tumour-like lesion within the urothelial mucosa of the urinary tract.
  • Clinically it mimics bladder neoplasm.
  • Though it attains an extensive spread in bladder mucosa and has a high tendency to recur, the clinical course is benign.
  • [MeSH-major] Adenoma / pathology. Kidney Neoplasms. Neoplasm Recurrence, Local / pathology. Urinary Bladder Neoplasms / pathology

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  • (PMID = 16933732.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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43. Guglielminetti D, Guerra E, Minguzzi MT, Zanzi F, Poddie DB: [Retractile mesenteritis: case report]. G Chir; 2009 Jan-Feb;30(1-2):30-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The mesenteritis is a benign disease and sometimes it is related to urogenital neoplasm.
  • [MeSH-minor] Adenocarcinoma / complications. Adenocarcinoma / therapy. Adenocarcinoma, Clear Cell / surgery. Anti-Inflammatory Agents / therapeutic use. Antimetabolites, Antineoplastic / therapeutic use. Combined Modality Therapy. Diagnosis, Differential. Fluorouracil / therapeutic use. Humans. Intestinal Obstruction / etiology. Intestinal Obstruction / surgery. Kidney Neoplasms / surgery. Male. Methylprednisolone / therapeutic use. Middle Aged. Neoadjuvant Therapy. Neoplasms, Multiple Primary / therapy. Panniculitis / diagnosis. Panniculitis / etiology. Panniculitis / therapy. Parenteral Nutrition. Rectal Neoplasms / complications. Rectal Neoplasms / therapy

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  • (PMID = 19272229.001).
  • [ISSN] 0391-9005
  • [Journal-full-title] Il Giornale di chirurgia
  • [ISO-abbreviation] G Chir
  • [Language] ita
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents; 0 / Antimetabolites, Antineoplastic; U3P01618RT / Fluorouracil; X4W7ZR7023 / Methylprednisolone
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44. El Jack AK, Tomaszewski JE, Haller DG, Siegelman ES: Metastatic PEComa arising from renal angiomyolipoma: MRI findings. J Magn Reson Imaging; 2007 Jul;26(1):159-61
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  • The perivascular epithelioid cell tumor (PEComa) is a neoplasm composed primarily of HMB-45-positive epithelioid cells with a perivascular distribution.
  • Both benign and malignant PEComas have been reported in diverse anatomic locations.
  • [MeSH-major] Angiomyolipoma / diagnosis. Angiomyolipoma / pathology. Epithelioid Cells / pathology. Kidney Neoplasms / pathology. Liver Neoplasms / diagnosis. Liver Neoplasms / secondary. Magnetic Resonance Imaging / methods

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  • [Copyright] Copyright 2007 Wiley-Liss, Inc.
  • (PMID = 17659554.001).
  • [ISSN] 1053-1807
  • [Journal-full-title] Journal of magnetic resonance imaging : JMRI
  • [ISO-abbreviation] J Magn Reson Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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45. Ritchie R, Thiruchelvam N, Adamson A: Laparoscopic deroofing of a renal cyst: the hidden invasion. Surg Laparosc Endosc Percutan Tech; 2007 Aug;17(4):358-60
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  • Cysts of the kidney usually originate from the renal parenchyma after tubule obstruction; rarely pyelocalyceal cysts occur, originating from transitional urothelium.
  • Neoplasia is a rare but possible complication.
  • A 45-year-old man was found to have a cyst related to the right kidney.
  • No communication within the renal pelvis was detected however histology revealed transitional cell carcinoma.
  • This case should serve as a warning to clinicians that seemingly benign cysts of the kidney may harbor underlying neoplasia.
  • [MeSH-major] Carcinoma, Transitional Cell / complications. Kidney Diseases, Cystic / complications. Kidney Diseases, Cystic / surgery. Kidney Neoplasms / complications
  • [MeSH-minor] Humans. Laparoscopy. Male. Middle Aged. Neoplasm Invasiveness. Tomography, X-Ray Computed

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  • (PMID = 17710070.001).
  • [ISSN] 1530-4515
  • [Journal-full-title] Surgical laparoscopy, endoscopy & percutaneous techniques
  • [ISO-abbreviation] Surg Laparosc Endosc Percutan Tech
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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46. Tabibi A, Parvin M, Abdi H, Bashtar R, Zamani N, Abadpour B: Correlation between size of renal cell carcinoma and its grade, stage, and histological subtype. Urol J; 2007;4(1):10-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • INTRODUCTION: The aim of this study was to determine the correlation between histological subtype, size, grade, and stage of the kidney tumors and to investigate whether a correlation exists between the size of the kidney tumor and its behavior.
  • MATERIALS AND METHODS: Between 1996 and 2004, we had 212 patients with radical or partial nephrectomy due to a kidney tumor at Shaheed Labbafinejad Medical Center.
  • RESULTS: Of 212 pathologic blocks, 17 (8%) were benign and 195 (92%) were malignant masses including 179 renal cell carcinoma (RCC) tumors.
  • Malignant tumors were slightly greater compared with the benign ones (P=.10).
  • Significant relations between the size of the kidney tumor and the nuclear grade (P=.007), clinical symptoms (P=.02), and extracapsular extension (P<.001) were observed.
  • [MeSH-major] Carcinoma, Renal Cell / pathology. Kidney Neoplasms / pathology. Tumor Burden
  • [MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Carcinoma, Squamous Cell / secondary. Carcinoma, Squamous Cell / surgery. Carcinoma, Transitional Cell / pathology. Carcinoma, Transitional Cell / surgery. Child. Child, Preschool. Female. Humans. Male. Middle Aged. Neoplasm Staging. Nephrectomy. Sarcoma / pathology. Sarcoma / surgery. Wilms Tumor / pathology. Wilms Tumor / surgery

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  • (PMID = 17514604.001).
  • [ISSN] 1735-1308
  • [Journal-full-title] Urology journal
  • [ISO-abbreviation] Urol J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Iran
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47. Ficarra V, Secco S, Fracalanza S, Novara G, Gidaro S, Cindolo L, Schips L: Expanding indication for elective nephron-sparing surgery in renal cell carcinoma. Arch Ital Urol Androl; 2009 Jun;81(2):86-90
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Nephron-sparing surgery is the reference standard for the management of a small renal masses, especially in patients with a solitary kidney or bilateral renal tumors.
  • The rationale for elective partial nephrectomy is based on the risk of developing kidney failure and the significant percentage of benign lesions on final histopathologic examination.
  • Recent studies have demonstrated comparable survival and recurrence rates with partial and radical nephrectomy for renal tumors of 4 cm or less, and it is well demonstrated that radical nephrectomy is a significant risk factor for the development of chronic kidney disease.
  • The purpose of this paper was to underline the evolution of, and expanding indications for, a nephron-sparing approach also for renal masses between 4 and 7 centimeters and a normal contralateral kidney, presuming a careful and sensible patient selection.

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  • (PMID = 19760862.001).
  • [ISSN] 1124-3562
  • [Journal-full-title] Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica
  • [ISO-abbreviation] Arch Ital Urol Androl
  • [Language] ENG
  • [Publication-type] Journal Article; Review
  • [Publication-country] Italy
  • [Number-of-references] 28
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48. Colović R, Grubor N, Radak V, Micev M, Stojković M, Colović N: [Aggressive intraabdominal fibromatosis]. Vojnosanit Pregl; 2006 Sep;63(9):839-42
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Intraabdominal or mesenteric fibromatosis is a rare benign nonmetastatic neoplasm that appears as a sporadic lesion or in patients with familiar polyposis.
  • CASE REPORT: We presented a 22-year-old woman in whom an aggressive intraabdominal fibromatosis had appeared during the first pregnancy as a well circumscribed ovoid tumor, involving the terminal ileum, the caecum, the ascending colon, the right kidney, the ureter, and the right common iliac artery.
  • [MeSH-major] Fibromatosis, Abdominal / pathology. Fibromatosis, Aggressive / pathology. Neoplasm Recurrence, Local. Pregnancy Complications, Neoplastic / pathology

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  • (PMID = 17039898.001).
  • [ISSN] 0042-8450
  • [Journal-full-title] Vojnosanitetski pregled
  • [ISO-abbreviation] Vojnosanit Pregl
  • [Language] srp
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Serbia and Montenegro
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49. Lee EY: CT imaging of mass-like renal lesions in children. Pediatr Radiol; 2007 Sep;37(9):896-907
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Mass-like renal lesions in children occur in a diverse spectrum of conditions including benign and malignant neoplasm, infection, infarction, lymphatic malformation, and traumatic injury.
  • [MeSH-major] Infarction / diagnostic imaging. Kidney / blood supply. Kidney / diagnostic imaging. Kidney Neoplasms / diagnostic imaging. Nephritis / diagnostic imaging. Tomography, X-Ray Computed / methods

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  • [Cites] J Laparoendosc Adv Surg Tech A. 2006 Feb;16(1):74-6 [16494555.001]
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  • (PMID = 17639370.001).
  • [ISSN] 0301-0449
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] Germany
  • [Number-of-references] 18
  •  go-up   go-down


50. Khayyata S, Grignon DJ, Aulicino MR, Al-Abbadi MA: Metanephric adenoma vs. Wilms' tumor: a report of 2 cases with diagnosis by fine needle aspiration and cytologic comparisons. Acta Cytol; 2007 May-Jun;51(3):464-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Metanephric adenoma (MA) is a rare benign renal neoplasm that can occur at any age, whereas, Wilms' tumor (WT) is the most common malignant renal neoplasm in children and is occasionally seen in adults.
  • [MeSH-major] Adenoma / diagnosis. Adenoma / pathology. Kidney Neoplasms / diagnosis. Kidney Neoplasms / pathology. Wilms Tumor / diagnosis. Wilms Tumor / pathology
  • [MeSH-minor] Adult. Biopsy, Fine-Needle. Cell Nucleolus / pathology. Cell Nucleus Shape. Diagnosis, Differential. Female. Humans. Kidney / pathology. Kidney / surgery. Male. Nephrectomy


51. Karasavvidou F, Barbanis S, Gravas S, Ioannou M, Oeconomou A, Pappa D, Melekos MD, Koukoulis G: Primary renal epithelioid hemangioendothelioma. Onkologie; 2009 Apr;32(4):203-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Epithelioid hemangioendothelioma (EH) is a rare vascular neoplasm with an unpredictable malignant potential that has been described mainly in soft tissue, liver, and lung.
  • Abdominal ultrasound and computed tomography scan revealed a solitary mass of 4.0 x 3.2 cm in the outer surface of the right kidney.
  • CONCLUSIONS: Although EH may have a histologically benign appearance and can be treated using a nephron-sparing approach, this neoplasm is potentially malignant urging the need for a long-term follow-up in these patients.
  • [MeSH-major] Abdominal Pain / etiology. Hemangioendothelioma, Epithelioid / complications. Hemangioendothelioma, Epithelioid / diagnosis. Kidney Neoplasms / complications. Kidney Neoplasms / diagnosis

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  • [Copyright] Copyright 2009 S. Karger AG, Basel.
  • (PMID = 19372717.001).
  • [ISSN] 1423-0240
  • [Journal-full-title] Onkologie
  • [ISO-abbreviation] Onkologie
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
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52. Minervini A, Serni S, Giubilei G, Lanzi F, Vittori G, Lapini A, Carini M: Multiple ipsilateral renal tumors: retrospective analysis of surgical and oncological results of tumor enucleation vs radical nephrectomy. Eur J Surg Oncol; 2009 May;35(5):521-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • RESULTS: All patients who had NSS had tumors confined within the kidney, as did 82% of patients treated with RN.
  • The sole presence of concomitant accompanying benign histology to the primary RCC was diagnosed in 20% of patients.
  • Two patients recurred locally after NSS, elsewhere in the kidney, resulting in a crude ipsilateral recurrence rate of 17%.
  • CONCLUSIONS: For patients with multiple ipsilateral renal tumors, 20% of the satellite lesions are benign and 6% develop a contralateral metachronous recurrence.
  • [MeSH-major] Carcinoma, Renal Cell / surgery. Kidney Neoplasms / surgery. Neoplasms, Multiple Primary / surgery. Nephrectomy / methods
  • [MeSH-minor] Aged. Disease Progression. Female. Humans. Male. Middle Aged. Neoplasm Staging. Prognosis. Retrospective Studies. Risk. Survival Analysis. Treatment Outcome

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  • (PMID = 18640001.001).
  • [ISSN] 1532-2157
  • [Journal-full-title] European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
  • [ISO-abbreviation] Eur J Surg Oncol
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] England
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53. Cao Y, Paner GP, Perry KT, Flanigan RC, Campbell SC, Picken MM: Renal neoplasms in younger adults: analysis of 112 tumors from a single institution according to the new 2004 World Health Organization classification and 2002 American Joint Committee on Cancer Staging System. Arch Pathol Lab Med; 2005 Apr;129(4):487-91
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  • The number of oncocytomas was also significantly lower in younger adults than in older adults (2% vs 11%, P < .001), and this presumably age-related benign neoplasm was not identified in patients younger than 40 years in this study.
  • Younger female adults tended to have more benign miscellaneous neoplasms than did their male counterparts (64% vs 36%, P < .001).
  • Malignant and benign renal neoplasms tend to have a contrasting sex distribution in younger adults.
  • [MeSH-major] Carcinoma, Renal Cell / pathology. Kidney Neoplasms / pathology
  • [MeSH-minor] Adult. Age Distribution. Female. Humans. Male. Neoplasm Staging. Sex Distribution

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  • (PMID = 15794671.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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54. Matsushima M, Asakura H, Sakamoto H, Horinaga M, Nakahira Y, Yanaihara H: Leiomyoma of the bladder presenting as acute urinary retention in a female patient: urodynamic analysis of lower urinary tract symptom; a case report. BMC Urol; 2010;10:13
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  • Benign mesenchymal tumors are rare.
  • Leiomyoma of the bladder is the most common benign neoplasm.

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  • (PMID = 20684762.001).
  • [ISSN] 1471-2490
  • [Journal-full-title] BMC urology
  • [ISO-abbreviation] BMC Urol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2924335
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55. Lane BR, Tiong HY, Campbell SC, Fergany AF, Weight CJ, Larson BT, Novick AC, Flechner SM: Management of the adrenal gland during partial nephrectomy. J Urol; 2009 Jun;181(6):2430-6; discussion 2436-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Pathological analysis revealed direct invasion of the adrenal gland by renal cell carcinoma (1), renal cell carcinoma metastasis (2), other adrenal neoplasms (3) or benign tissue (42, 87%).
  • The rarity of metachronous adrenal metastasis and the lack of an observable benefit to concomitant adrenalectomy support adrenal preservation during partial nephrectomy except as previously outlined.
  • [MeSH-major] Adrenal Gland Neoplasms / surgery. Adrenalectomy. Carcinoma, Renal Cell / surgery. Kidney Neoplasms / surgery. Nephrectomy / methods
  • [MeSH-minor] Adrenal Glands. Aged. Female. Humans. Male. Middle Aged. Neoplasm Invasiveness

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  • (PMID = 19371896.001).
  • [ISSN] 1527-3792
  • [Journal-full-title] The Journal of urology
  • [ISO-abbreviation] J. Urol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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56. Klatte T, Patard JJ, de Martino M, Bensalah K, Verhoest G, de la Taille A, Abbou CC, Allhoff EP, Carrieri G, Riggs SB, Kabbinavar FF, Belldegrun AS, Pantuck AJ: Tumor size does not predict risk of metastatic disease or prognosis of small renal cell carcinomas. J Urol; 2008 May;179(5):1719-26
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • RESULTS: Of the tumors 88% were renal cell carcinoma and 12% were benign.
  • Tumor size alone is not sufficient to distinguish renal cell carcinoma with benign behavior from aggressive small renal cell carcinoma.
  • [MeSH-major] Carcinoma, Renal Cell / pathology. Kidney Neoplasms / pathology
  • [MeSH-minor] Female. Humans. Male. Middle Aged. Neoplasm Recurrence, Local. Nephrectomy. Prognosis. Survival Rate

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  • [CommentIn] Eur Urol. 2009 Mar;55(3):751-2 [19650211.001]
  • [CommentIn] J Urol. 2008 May;179(5):1657 [18343448.001]
  • (PMID = 18343437.001).
  • [ISSN] 1527-3792
  • [Journal-full-title] The Journal of urology
  • [ISO-abbreviation] J. Urol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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57. Terada N, Arai Y, Kinukawa N, Terai A: The 10-year natural history of simple renal cysts. Urology; 2008 Jan;71(1):7-11; discussion 11-2
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  • The rate of size increase of the neoplasm-bearing cysts was similar to that of the other benign renal cysts in the same age category.
  • There seems to be no specific pattern observed in the neoplasm-bearing renal cysts.
  • [MeSH-major] Kidney Diseases, Cystic / pathology

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  • (PMID = 18242354.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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58. Tan GC, Shiran MS, Swaminathan M, Phang KS, Rohaizak M: Large retrosternal parathyroid carcinoma with primary hyperparathyroidism. Asian J Surg; 2007 Oct;30(4):286-9
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  • Clinical indicators favouring parathyroid carcinoma over benign disease include markedly raised serum calcium levels, PTH and alkaline phosphatase.
  • A palpable neck mass with both kidney and skeletal manifestations also give a high index of suspicion of parathyroid carcinoma.

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  • (PMID = 17962134.001).
  • [ISSN] 1015-9584
  • [Journal-full-title] Asian journal of surgery
  • [ISO-abbreviation] Asian J Surg
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
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59. Hornsby CD, Cohen C, Amin MB, Picken MM, Lawson D, Yin-Goen Q, Young AN: Claudin-7 immunohistochemistry in renal tumors: a candidate marker for chromophobe renal cell carcinoma identified by gene expression profiling. Arch Pathol Lab Med; 2007 Oct;131(10):1541-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • This differential diagnosis is important because chromophobe RCC is malignant, whereas oncocytoma is benign.
  • [MeSH-major] Biomarkers, Tumor / metabolism. Carcinoma, Renal Cell / metabolism. Gene Expression. Gene Expression Profiling / methods. Kidney Neoplasms / metabolism. Membrane Proteins / metabolism
  • [MeSH-minor] Adenoma, Oxyphilic / diagnosis. Claudins. Diagnosis, Differential. Immunohistochemistry. RNA, Messenger / metabolism. RNA, Neoplasm / analysis

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  • (PMID = 17922590.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / 1 U54 CA119338-02
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Validation Studies
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / CLDN7 protein, human; 0 / Claudins; 0 / Membrane Proteins; 0 / RNA, Messenger; 0 / RNA, Neoplasm
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60. Li G, Cuilleron M, Cottier M, Gentil-Perret A, Lambert C, Genin C, Tostain J: The use of MN/CA9 gene expression in identifying malignant solid renal tumors. Eur Urol; 2006 Feb;49(2):401-5
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  • RESULTS: There were 28 RCCs (19 clear cell carcinomas, 7 papillary carcinomas and 2 chromophobe carcinomas) and 7 benign tumors proved by postoperative pathology.
  • [MeSH-major] Antigens, Neoplasm / analysis. Biomarkers, Tumor / analysis. Carbonic Anhydrases / analysis. Kidney Neoplasms / chemistry. Kidney Neoplasms / pathology
  • [MeSH-minor] Adenocarcinoma, Clear Cell / chemistry. Adenocarcinoma, Clear Cell / pathology. Biopsy. Carcinoma, Papillary / chemistry. Carcinoma, Papillary / pathology. Carcinoma, Renal Cell / chemistry. Carcinoma, Renal Cell / pathology. Cytological Techniques. False Positive Reactions. Female. Gene Expression Regulation, Neoplastic. Genetic Predisposition to Disease. Humans. Male. Middle Aged. Pilot Projects. RNA, Neoplasm / analysis. Reverse Transcriptase Polymerase Chain Reaction. Sensitivity and Specificity

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  • (PMID = 16387417.001).
  • [ISSN] 0302-2838
  • [Journal-full-title] European urology
  • [ISO-abbreviation] Eur. Urol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 0 / Antigens, Neoplasm; 0 / Biomarkers, Tumor; 0 / RNA, Neoplasm; EC 4.2.1.1 / CA9 protein, human; EC 4.2.1.1 / Carbonic Anhydrases
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61. Paner GP, Turk TM, Clark JI, Lindgren V, Picken MM: Passive seeding in metanephric adenoma: a review of pseudometastatic lesions in perinephric lymph nodes. Arch Pathol Lab Med; 2005 Oct;129(10):1317-21
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  • However, rarely, inconsequential passive transport of benign neoplastic cells to the lymph node can occur and may cause confusion as to the nature of the neoplasm (ie, malignant vs benign).
  • [MeSH-major] Adenoma / pathology. Kidney Neoplasms / pathology. Lymph Nodes / pathology. Neoplasm Seeding
  • [MeSH-minor] Adult. Biomarkers, Tumor / analysis. Carcinoma, Renal Cell / diagnosis. Carcinoma, Renal Cell / secondary. Cytogenetic Analysis. Diagnosis, Differential. Female. Humans. Kidney / pathology. Neoplasm Metastasis / diagnosis. Pregnancy. Wilms Tumor / diagnosis

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  • (PMID = 16196523.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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62. Shao L, Manalang M, Cooley L: Juxtaglomerular cell tumor in an 8-year-old girl. Pediatr Blood Cancer; 2008 Feb;50(2):406-9
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  • Juxtaglomerular cell tumor (JGCT) is an extremely rare renal neoplasm in the pediatric population.
  • It is considered a benign tumor arising from the juxtaglomerular apparatus of the kidney.
  • We report a case of JGCT in an 8-year-old female who presented with severe hypertension, elevated serum renin level, and a well circumscribed tumor in the right kidney.
  • [MeSH-major] Juxtaglomerular Apparatus / pathology. Kidney Neoplasms / pathology

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  • [Copyright] (c) 2007 Wiley-Liss, Inc.
  • (PMID = 16972237.001).
  • [ISSN] 1545-5017
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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63. Montanari E, Del Nero A, Bernardini P, Mangiarotti B, Confalonieri S, Grisotto M, Cordima G: Percutaneous therapy of low stage and grade urothelial neoplasia: long-term follow up. Arch Ital Urol Androl; 2005 Dec;77(4):211-4
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  • [Title] Percutaneous therapy of low stage and grade urothelial neoplasia: long-term follow up.
  • With the advent of sophisticated techniques for the endo-urologic management of many benign urologic diseases of the upper tract, there has been growing enthusiasm for the application of these same techniques in the management of upper tract TCC, which is also supported by recent advances in the development of small calibre telescopes with improved optics and the development of small calibre adjunctive instruments and laser fibers.
  • 4 pts (5 renal units: 4 T1G2 and 1 TaG1) underwent percutaneous resection for a tumor in a solitary kidney (2 cases), one case for bilateral neoplasm, and in the other case the lesion was unilateral with chronic renal failure.

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  • (PMID = 16444935.001).
  • [ISSN] 1124-3562
  • [Journal-full-title] Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica
  • [ISO-abbreviation] Arch Ital Urol Androl
  • [Language] ENG
  • [Publication-type] Journal Article
  • [Publication-country] Italy
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64. Russo P: Open partial nephrectomy: an essential operation with an expanding role. Curr Opin Urol; 2007 Sep;17(5):309-15
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  • RECENT FINDINGS: Renal tumors are a family of neoplasms ranging from the benign oncocytoma, to the indolent papillary and chromophobe carcinomas, to the more potentially malignant clear cell carcinomas that account for 54% of the lesions resected, but 90% of those that metastasize.
  • Twenty-six percent of patients prior to operation already have stage 3 chronic kidney disease with an estimated glomerular filtration rate of less than 60 ml/min/1.73 m.
  • Chronic kidney disease is an independent risk factor for the development of cardiovascular disease, hospitalization and death.
  • SUMMARY: Partial nephrectomy is an essential surgical approach to the small kidney tumor and provides equivalent local tumor control while preventing the new onset or worsening of chronic kidney disease.
  • [MeSH-major] Kidney Cortex / surgery. Kidney Neoplasms / surgery. Nephrectomy / methods. Renal Insufficiency, Chronic / prevention & control
  • [MeSH-minor] Cardiovascular Diseases / etiology. Cardiovascular Diseases / prevention & control. Glomerular Filtration Rate. Humans. Neoplasm Staging. Patient Selection. Risk Assessment. Risk Factors. Treatment Outcome

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  • (PMID = 17762622.001).
  • [ISSN] 0963-0643
  • [Journal-full-title] Current opinion in urology
  • [ISO-abbreviation] Curr Opin Urol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 48
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65. Kyle CC, Wingo MS, Carey RI, Leveillee RJ, Bird VG: Diagnostic yield of renal biopsy immediately prior to laparoscopic radiofrequency ablation: a multicenter study. J Endourol; 2008 Oct;22(10):2291-3
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  • Renal biopsies were performed in each patient during transperitoneal laparoscopy after mobilization of the kidney and prior to RFA.
  • Final pathology revealed renal cell carcinoma in 95, oncocytic neoplasm in 26, and angiomyolipoma in 9.8 patients were considered to have nondiagnostic biopsies.
  • In this group, final pathology revealed benign cysts in 3, inconclusive specimens in 3, fibrosis in 1, and normal tissue in 1.

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  • (PMID = 18937593.001).
  • [ISSN] 1557-900X
  • [Journal-full-title] Journal of endourology
  • [ISO-abbreviation] J. Endourol.
  • [Language] ENG
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] United States
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66. Wang FM, Liu HQ, Liu SR, Tang SP, Yang L, Feng GS: SHP-2 promoting migration and metastasis of MCF-7 with loss of E-cadherin, dephosphorylation of FAK and secretion of MMP-9 induced by IL-1beta in vivo and in vitro. Breast Cancer Res Treat; 2005 Jan;89(1):5-14
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  • The loss of E-cadherin-mediated adhesion and the increase of MMP-9-induced migration had been shown to play an important role in the transition of epithelial tumors from a benign to an invasive state.
  • When injected into the abdominal cavity of nude mice, SHP-2-GFP-transfected cells metastasized widely to the lung, kidney, but MCF-7 with SHP-2C > S-GFP was not observed in the these organs.
  • [MeSH-major] Breast Neoplasms / physiopathology. Cadherins / metabolism. Cell Movement. Focal Adhesions / chemistry. Matrix Metalloproteinase 9 / secretion. Neoplasm Metastasis / physiopathology. Protein Tyrosine Phosphatases / metabolism. Protein-Tyrosine Kinases / chemistry

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  • (PMID = 15666191.001).
  • [ISSN] 0167-6806
  • [Journal-full-title] Breast cancer research and treatment
  • [ISO-abbreviation] Breast Cancer Res. Treat.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Cadherins; 0 / Interleukin-1; 0 / Intracellular Signaling Peptides and Proteins; EC 2.7.10.1 / Protein-Tyrosine Kinases; EC 2.7.10.2 / Focal Adhesion Kinase 1; EC 2.7.10.2 / Focal Adhesion Protein-Tyrosine Kinases; EC 2.7.10.2 / Ptk2 protein, mouse; EC 3.1.3.48 / Protein Tyrosine Phosphatase, Non-Receptor Type 11; EC 3.1.3.48 / Protein Tyrosine Phosphatases; EC 3.1.3.48 / Ptpn11 protein, mouse; EC 3.4.24.35 / Matrix Metalloproteinase 9
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67. Knezević V, Poljak M, Bradamante Z, Serman D, Levak-Svajger B, Svajger A: Yolk sac carcinoma derived from the rat epiblast as a renal isograft. Coll Antropol; 2005 Jun;29(1):189-97
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  • From the rest of the cylinder the 4 cell layers were isolated and transplanted separately under the kidney capsule of isogenic adult males.
  • After 4 weeks the hypoblast was resorbed, the extraembryonic ectoderm gave rise to hemorrhagic cysts and trophoblastic giant cells, the extraembryonic (visceral yolk sac) endoderm formed benign cystic PYS/VYS tumors, and the epiblast developed into a benign teratoma.
  • It destroyed the teratoma and the recipient's kidney, metastasized to peritoneum and other sites, and caused abundant ascites containing clustered tumor cells.
  • [MeSH-major] Carcinoma / pathology. Carcinoma / veterinary. Endodermal Sinus Tumor / pathology. Endodermal Sinus Tumor / veterinary. Kidney Neoplasms / pathology. Kidney Neoplasms / veterinary. Teratoma / pathology. Teratoma / veterinary
  • [MeSH-minor] Animals. Ascites. Ectoderm. Embryo, Mammalian. Female. Kidney / pathology. Male. Neoplasm Metastasis. Neoplasms, Experimental. Rats. Transplants

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  • (PMID = 16117321.001).
  • [ISSN] 0350-6134
  • [Journal-full-title] Collegium antropologicum
  • [ISO-abbreviation] Coll Antropol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Croatia
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68. Valette F, Querellou S, Oudoux A, Carlier T, Dupas B, Chatal JF, Couturier O: Comparison of positron emission tomography and lymphangiography in the diagnosis of infradiaphragmatic Hodgkin's disease. Acta Radiol; 2007 Feb;48(1):59-63
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  • In two of the 24 negative patients, PET showed additional lesions in the spleen and one celiac lymph node (one patient), and in the right kidney and the right iliac crest (one patient).
  • In the other, PET was falsely positive (PET done within 24 hours after a negative LAG), which was confirmed by biopsy (benign inflammatory, probably due to LAG medium).
  • [MeSH-major] Hodgkin Disease / diagnosis. Neoplasm Staging / methods. Positron-Emission Tomography / methods
  • [MeSH-minor] Adolescent. Adult. Diaphragm / radiography. Diaphragm / radionuclide imaging. Female. Fluorodeoxyglucose F18. Humans. Kidney / radionuclide imaging. Lymph Nodes / radionuclide imaging. Lymphography / methods. Male. Middle Aged. Radiopharmaceuticals. Reproducibility of Results. Retrospective Studies. Spleen / radionuclide imaging

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  • (PMID = 17325926.001).
  • [ISSN] 0284-1851
  • [Journal-full-title] Acta radiologica (Stockholm, Sweden : 1987)
  • [ISO-abbreviation] Acta Radiol
  • [Language] eng
  • [Publication-type] Comparative Study; Evaluation Studies; Journal Article
  • [Publication-country] Sweden
  • [Chemical-registry-number] 0 / Radiopharmaceuticals; 0Z5B2CJX4D / Fluorodeoxyglucose F18
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69. Reichelt O, Gajda M, Chyhrai A, Wunderlich H, Junker K, Schubert J: Ultrasound-guided biopsy of homogenous solid renal masses. Eur Urol; 2007 Nov;52(5):1421-6
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  • By applying these results to 30 patients of study 2 (18 men, 12 women; aged 63+/-7.7 yr, tumor size 29+/-11.3mm) who met these sonographic criteria on preoperative transabdominal ultrasound, we bioptically diagnosed 8 (26.7%) benign tumors; 25 of 30 (83.3%) patients were accurately diagnosed.
  • CONCLUSIONS: Kidney tumors that appear noncystic and homogenous on preoperative ultrasound are more likely to be of benign origin.
  • However, experienced and dedicated histopathologic evaluation remains crucial to observe patients with clearly benign biopsy results.
  • [MeSH-major] Biopsy / methods. Kidney Neoplasms / pathology. Ultrasonography, Doppler / methods
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Diagnosis, Differential. Female. Humans. Male. Middle Aged. Neoplasm Staging / methods. Nephrectomy / methods. Prospective Studies. Reproducibility of Results

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  • [CommentIn] Eur Urol. 2007 Nov;52(5):1426-7 [17306923.001]
  • (PMID = 17306920.001).
  • [ISSN] 0302-2838
  • [Journal-full-title] European urology
  • [ISO-abbreviation] Eur. Urol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Switzerland
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70. Burger M, Denzinger S, Filbeck T, Hartmann A, Rössler W, Hammerschmied C: A metachronous, atypical, multifocal renal oncocytoma with a concomitant renal cell carcinoma of the contralateral side and bilateral multifocal oncocytomas: two case reports and review of literature. ScientificWorldJournal; 2005 Jul 20;5:545-9
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  • Oncocytomas are benign renal tumours that rarely appear bilateral or multifocal or with coexisting RCC.
  • The first case was a 63 years old patient presenting with a history of nephrectomy for a pT1 G1 pN0 R0 papillary RCC 4 years prior to presentation, showed two tumours of a singular kidney.
  • [MeSH-major] Adenoma, Oxyphilic / pathology. Carcinoma, Renal Cell / pathology. Kidney Neoplasms / pathology. Neoplasms, Second Primary / pathology
  • [MeSH-minor] Chromosome Deletion. Chromosomes, Human, Pair 1 / ultrastructure. Chromosomes, Human, Pair 10 / ultrastructure. DNA, Neoplasm / genetics. Diagnosis, Differential. Follow-Up Studies. Humans. Incidental Findings. Middle Aged. Nephrectomy / methods. Nucleic Acid Hybridization. Remission Induction

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  • (PMID = 16075151.001).
  • [ISSN] 1537-744X
  • [Journal-full-title] TheScientificWorldJournal
  • [ISO-abbreviation] ScientificWorldJournal
  • [Language] eng
  • [Publication-type] Case Reports; Comparative Study; Journal Article; Review
  • [Publication-country] England
  • [Chemical-registry-number] 0 / DNA, Neoplasm
  • [Number-of-references] 12
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71. Marino G, Pedalino M, Di Primio OG, Piras D, Vella R, Verces E, Carbonatto P: [Wunderlich syndrome. Clinical and therapeutic aspects of a long-term experience]. Urologia; 2010 Jul-Sep;77(3):193-7
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  • This syndrome may occur in patients with benign or malignant neoplasm of the kidney, arterial venous fistulae, immunovasculitis and other phlogosis of the kidney.
  • MATERIALS AND METHODS: We present 19 cases of acute spontaneous hemoretroperitoneum or Wunderlich's syndrome diagnosed from 1996 to 2009, related to the following conditions: 7 renal carcinomas, 4 angiomyolipomas, 2 adrenal hemorrhages, 1 bleeding polycystic kidney, 2 hemorrhagic renal cysts and three cases of immunovasculitis.
  • CONCLUSIONS: The spontaneous hemoretroperitoneum is a rare syndrome associated with acute kidney disease often unknown to the patient and only in selected cases with small hematoma; it is possible to perform arteriography with selective embolization of branches avoiding renal access surgery.
  • [MeSH-major] Hemoperitoneum / diagnosis. Hemoperitoneum / therapy. Kidney Diseases / diagnosis. Kidney Diseases / therapy

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  • (PMID = 20931549.001).
  • [ISSN] 0391-5603
  • [Journal-full-title] Urologia
  • [ISO-abbreviation] Urologia
  • [Language] ita
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Italy
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72. Bahrami A, Truong LD, Shen SS, Krishnan B: Synchronous renal and adrenal masses: an analysis of 80 cases. Ann Diagn Pathol; 2009 Feb;13(1):9-15
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  • The renal masses included 76 RCCs, 3 oncocytomas, and 1 malignant pheochromocytoma of adrenal gland involving the kidney.
  • Although the gross pathologic impression of adrenal masses in the presence of RCC was metastasis, on histologic examination, 56% of them were found to be benign lesions (mostly adrenal adenoma/hyperplasia), whereas malignant involvement from RCC was seen in 43%.
  • The benign and malignant nature of the adrenal lesions in the context of RCC could not be discriminated based on the size of adrenal mass.
  • [MeSH-major] Adrenal Gland Neoplasms / pathology. Adrenal Glands / pathology. Carcinoma, Renal Cell / pathology. Kidney / pathology. Kidney Neoplasms / pathology
  • [MeSH-minor] Adenoma, Oxyphilic / pathology. Adenoma, Oxyphilic / surgery. Adrenalectomy. Adult. Aged. Diagnosis, Differential. Female. Humans. Male. Middle Aged. Neoplasm Staging. Nephrectomy. Pheochromocytoma / pathology. Pheochromocytoma / surgery. Retrospective Studies

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  • (PMID = 19118776.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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73. Stojanović M, Goldner B: [Incidental finding of malignant renal cystic tumour diagnosed sonographically]. Srp Arh Celok Lek; 2008 Mar-Apr;136(3-4):166-9
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  • Cystic neoplasm results from haemorrhage, necrosis and colliquation of a solid tumour or tumour occurring within the wall of a cyst.
  • CASE OUTLINE: The authors present a 59-year-old woman with a sonographic finding of a simple cyst in the upper pole of the right kidney revealed during gynaecological ultrasonography.
  • Contrast CT scan would be performed to examine the "suspicious" lesion because it clearly shows if a cystic lesion is benign or malignant.
  • [MeSH-major] Cystadenocarcinoma / ultrasonography. Kidney Neoplasms / ultrasonography

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  • (PMID = 18720753.001).
  • [ISSN] 0370-8179
  • [Journal-full-title] Srpski arhiv za celokupno lekarstvo
  • [ISO-abbreviation] Srp Arh Celok Lek
  • [Language] srp
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Serbia
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74. Lee MG, Huh JS, Chung SK, Lee JH, Byun DS, Ryu BK, Kang MJ, Chae KS, Lee SJ, Lee CH, Kim JI, Chang SG, Chi SG: Promoter CpG hypermethylation and downregulation of XAF1 expression in human urogenital malignancies: implication for attenuated p53 response to apoptotic stresses. Oncogene; 2006 Sep 21;25(42):5807-22
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  • To explore the XAF1's candidacy for a suppressor in urogenital tumorigenesis, we investigated the XAF1 status in a series of cancer cell lines and primary tumors derived from the bladder, kidney and prostate.
  • Expression of XAF1 transcript was undetectable or extremely low in 60% (3/5) of bladder, 66% (10/15) of kidney, and 100% (3/3) prostate cancer cell lines.
  • Abnormal reduction of XAF1 was also found in 33% (18/55) of primary bladder and 40% (8/20) of primary kidney tumors, and showed a correlation with advanced stage and high grade of bladder tumor.
  • Hypermethylation at 14 CpG sites in the 5' proximal region of the XAF1 promoter was highly prevalent in cancers versus adjacent normal or benign tissues and tightly associated with reduced gene expression.
  • [MeSH-major] DNA Methylation. Dinucleoside Phosphates / genetics. Neoplasm Proteins / genetics. Promoter Regions, Genetic. Tumor Suppressor Protein p53 / genetics. Urogenital Neoplasms / genetics
  • [MeSH-minor] Gene Expression Regulation, Enzymologic. Gene Expression Regulation, Neoplastic. Humans. Intracellular Signaling Peptides and Proteins. Kidney Neoplasms / enzymology. Kidney Neoplasms / genetics. Male. Prostatic Neoplasms / enzymology. Prostatic Neoplasms / genetics. Reverse Transcriptase Polymerase Chain Reaction. Urinary Bladder Neoplasms / enzymology. Urinary Bladder Neoplasms / genetics

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  • (PMID = 16909101.001).
  • [ISSN] 0950-9232
  • [Journal-full-title] Oncogene
  • [ISO-abbreviation] Oncogene
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Dinucleoside Phosphates; 0 / Intracellular Signaling Peptides and Proteins; 0 / Neoplasm Proteins; 0 / Tumor Suppressor Protein p53; 0 / XAF1 protein, human; 2382-65-2 / cytidylyl-3'-5'-guanosine
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75. Bektas S, Okulu E, Kayigil O, Ertoy Baydar D: Inflammatory myofibroblastic tumor of the perirenal soft tissue misdiagnosed as renal cell carcinoma. Pathol Res Pract; 2007;203(6):461-5
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  • Inflammatory myofibroblastic tumor (IMT) of the kidney or perirenal soft tissue is a rare benign lesion that can mimic a malignant renal neoplasm.
  • [MeSH-major] Carcinoma, Renal Cell / diagnosis. Diagnostic Errors. Fibroblasts / pathology. Inflammation / pathology. Kidney Neoplasms / diagnosis. Muscle Cells / pathology. Soft Tissue Neoplasms / diagnosis


76. Thompson RH, Kurta JM, Kaag M, Tickoo SK, Kundu S, Katz D, Nogueira L, Reuter VE, Russo P: Tumor size is associated with malignant potential in renal cell carcinoma cases. J Urol; 2009 May;181(5):2033-6
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  • MATERIALS AND METHODS: We identified 2,675 patients treated surgically at our institution for renal cell carcinoma or a benign tumor between 1989 and 2007.
  • Histological subtype and tumor size were obtained from our kidney cancer database and logistic regression analysis was performed.
  • RESULTS: Of the 2,675 tumors 311 (12%) were benign and 2,364 (88%) were renal cell carcinoma.
  • The incidence of benign tumors decreased from 38% for tumors less than 1 cm to 7% for tumors 7 cm or greater.

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  • (PMID = 19286217.001).
  • [ISSN] 1527-3792
  • [Journal-full-title] The Journal of urology
  • [ISO-abbreviation] J. Urol.
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / T32 CA082088; None / None / / T32 CA082088-09; United States / NCI NIH HHS / CA / T32 CA082088-09; United States / NCI NIH HHS / CA / T32-CA82088
  • [Publication-type] Comparative Study; Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS131623; NLM/ PMC2734327
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77. Chen KT: Cytology of cystic nephroma: a case report. Acta Cytol; 2008 Jan-Feb;52(1):91-3
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  • BACKGROUND: Cystic nephroma is a rare benign multiloculated cystic renal neoplasm that is often confused with multicystic renal cell carcinoma radiographically and cytologically.
  • [MeSH-major] Kidney Diseases, Cystic / diagnosis. Kidney Neoplasms / diagnosis

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  • [CommentIn] Acta Cytol. 2010 Mar-Apr;54(2):233-4 [20391987.001]
  • (PMID = 18323282.001).
  • [ISSN] 0001-5547
  • [Journal-full-title] Acta cytologica
  • [ISO-abbreviation] Acta Cytol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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78. Dhingra S, Nada R, Rayat CS, Joshi K: Unusual eosinophilic variant of chromophobe cell renal carcinoma--an ultrastructural diagnosis. Indian J Pathol Microbiol; 2005 Apr;48(2):255-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • EVCCRC is a potentially malignant neoplasm whereas renal oncocytoma is totally benign.
  • [MeSH-major] Carcinoma, Renal Cell / diagnosis. Carcinoma, Renal Cell / ultrastructure. Eosinophils / pathology. Kidney Neoplasms / diagnosis. Kidney Neoplasms / ultrastructure

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  • (PMID = 16758688.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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79. Lane BR, Babineau D, Kattan MW, Novick AC, Gill IS, Zhou M, Weight CJ, Campbell SC: A preoperative prognostic nomogram for solid enhancing renal tumors 7 cm or less amenable to partial nephrectomy. J Urol; 2007 Aug;178(2):429-34
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We present novel nomograms that predict the likelihood of benign, likely indolent or potentially aggressive pathological findings based only on readily identifiable preoperative factors.
  • Using retrospectively collected data on all 862 patients who underwent partial nephrectomy for a single, solid, enhancing, clinical T1 (7 cm or less) tumor between 1999 and 2005 tumors were classified as benign or malignant.
  • The likelihood of benign, likely indolent or potentially aggressive pathological findings was modeled using multivariable logistic regression models based on age, gender, radiographic tumor size, symptoms at presentation and smoking history.
  • RESULTS: Of 862 small renal masses 20% were benign and 80% were malignant but only 30% of cancers (24% of small renal masses) were potentially aggressive.
  • Factors that were most strongly associated with the likelihood of benign pathology were age, gender, tumor size and smoking history.
  • A nomogram constructed to predict benign histology proved to be relatively accurate and discriminating (bootstrap corrected concordance index 0.644) and calibrated.
  • Small renal masses in older men and younger women were more likely to be benign.
  • CONCLUSIONS: Clinical factors provide substantial predictive ability to predict benign vs malignant pathology for small renal masses amenable to partial nephrectomy.
  • Although most of these small renal masses are benign or indolent, our ability to predict potentially aggressive cancer in this population remains limited.
  • [MeSH-major] Carcinoma, Renal Cell / surgery. Kidney Neoplasms / surgery. Nephrectomy / methods. Nomograms
  • [MeSH-minor] Adult. Age Factors. Aged. Aged, 80 and over. Female. Humans. Likelihood Functions. Male. Middle Aged. Multivariate Analysis. Neoplasm Staging. Precancerous Conditions / pathology. Precancerous Conditions / surgery. Prognosis. Registries. Retrospective Studies. Sex Factors. Treatment Outcome

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  • (PMID = 17561141.001).
  • [ISSN] 0022-5347
  • [Journal-full-title] The Journal of urology
  • [ISO-abbreviation] J. Urol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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80. Nisman B, Yutkin V, Nechushtan H, Gofrit ON, Peretz T, Gronowitz S, Pode D: Circulating tumor M2 pyruvate kinase and thymidine kinase 1 are potential predictors for disease recurrence in renal cell carcinoma after nephrectomy. Urology; 2010 Aug;76(2):513.e1-6
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  • RESULTS: Significantly higher levels of TuM2-PK and TK1 were found in 116 patients with RCC compared with 20 healthy participants (P < .001 and P = .03), but not compared with 27 patients with benign kidney tumors (P = .13 and P = .72).
  • [MeSH-major] Biomarkers, Tumor / blood. Carcinoma, Renal Cell / blood. Carcinoma, Renal Cell / surgery. Kidney Neoplasms / blood. Kidney Neoplasms / surgery. Neoplasm Recurrence, Local / blood. Neoplasm Recurrence, Local / diagnosis. Nephrectomy. Pyruvate Kinase / blood. Thymidine Kinase / blood

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  • [Copyright] Copyright 2010 Elsevier Inc. All rights reserved.
  • (PMID = 20573390.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; EC 2.7.1.21 / Thymidine Kinase; EC 2.7.1.21 / thymidine kinase 1; EC 2.7.1.40 / Pyruvate Kinase
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81. Lokken RP, Gervais DA, Arellano RS, Tuncali K, Morrison PR, Tatli S, Mueller PR, Silverman SG: Inflammatory nodules mimic applicator track seeding after percutaneous ablation of renal tumors. AJR Am J Roentgenol; 2007 Oct;189(4):845-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • OBJECTIVE: The objective of our study was to report the occurrence of benign inflammatory nodules that develop in or near applicator tracks after percutaneous radiofrequency ablation and cryoablation of renal tumors.
  • CONCLUSION: Benign inflammatory nodules occur rarely after percutaneous ablation of renal tumors and may mimic tumor seeding of the applicator track.
  • [MeSH-major] Kidney Neoplasms / diagnosis. Kidney Neoplasms / surgery. Neoplasm Seeding. Nephrectomy / adverse effects. Nephritis / diagnosis. Nephritis / etiology

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  • (PMID = 17885054.001).
  • [ISSN] 1546-3141
  • [Journal-full-title] AJR. American journal of roentgenology
  • [ISO-abbreviation] AJR Am J Roentgenol
  • [Language] eng
  • [Grant] United States / NCRR NIH HHS / RR / U41RR019703
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] United States
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82. Pertia A, Nikoleishvili D, Trsintsadze O, Gogokhia N, Managadze L, Chkhotua A: Loss of p27(Kip1) CDKI is a predictor of poor recurrence-free and cancer-specific survival in patients with renal cancer. Int Urol Nephrol; 2007;39(2):381-7
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The importance of cyclin-dependent kinase inhibitors (CDKI) in benign and malignant urological diseases is a subject of intense ongoing investigation.
  • The goal of the current study was to analyze the expression of p27((Kip1))CDKI in benign and malignant renal cells and assess their possible association with different clinical parameters.
  • Expression of p27((Kip1)) is significantly decreased in RCC as compared with normal kidney tissue.
  • [MeSH-major] Intracellular Signaling Peptides and Proteins / genetics. Kidney Neoplasms / genetics. Neoplasm Recurrence, Local / genetics

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  • [Cites] Int J Cancer. 2002 Dec 20;102(6):601-7 [12448001.001]
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  • (PMID = 17310312.001).
  • [ISSN] 0301-1623
  • [Journal-full-title] International urology and nephrology
  • [ISO-abbreviation] Int Urol Nephrol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / CDKN1B protein, human; 0 / Intracellular Signaling Peptides and Proteins; 147604-94-2 / Cyclin-Dependent Kinase Inhibitor p27
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83. Chaplin A, Conrad DM, Tatlidil C, Jollimore J, Walsh N, Covert A, Pasternak S: Primary cutaneous PEComa. Am J Dermatopathol; 2010 May;32(3):310-2
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • They constitute a spectrum of lesions in different organs including angiomyolipoma of the kidney and liver, sugar tumor of the lung, lymphangiomatosis, and lymphangiomyoma.
  • Follow-up data is limited but they appear to behave in a benign fashion.
  • We report an additional case with the goal of alerting dermatopathologists to this distinctive unusual neoplasm.
  • [MeSH-minor] Antigens, Neoplasm / analysis. Biomarkers, Tumor / analysis. Biopsy. Desmin / analysis. Female. Humans. Leg. Melanoma-Specific Antigens. Microphthalmia-Associated Transcription Factor / analysis. Middle Aged. Neoplasm Proteins / analysis. Treatment Outcome

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  • (PMID = 20139753.001).
  • [ISSN] 1533-0311
  • [Journal-full-title] The American Journal of dermatopathology
  • [ISO-abbreviation] Am J Dermatopathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, Neoplasm; 0 / Biomarkers, Tumor; 0 / Desmin; 0 / MITF protein, human; 0 / Melanoma-Specific Antigens; 0 / Microphthalmia-Associated Transcription Factor; 0 / Neoplasm Proteins
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84. Kaposztas Z, Etheridge WB, Kahan BD: Case report: successful treatment of posttransplant lymphoproliferative disorder and quiescence of dermatomyositis with rituximab and sirolimus. Transplant Proc; 2008 Jun;40(5):1744-6
The Lens. Cited by Patents in .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A 65-year-old Caucasian woman received a primary en bloc kidney transplant from a deceased 2-year-old donor.
  • After a benign course for 9 months and after an increase in MMF from 2 to 3 g daily, she presented with pneumonia owing to Candida albicans, which was responsive to antibiotics, as was the PTLD.
  • The immunosuppressive regimen was converted to sirolimus (SRL) and rituximab, with over 90% necrosis of the neoplasm at 1 month.
  • [MeSH-major] Antibodies, Monoclonal / therapeutic use. Dermatomyositis / drug therapy. Immunosuppressive Agents / adverse effects. Kidney Transplantation / adverse effects. Lymphoproliferative Disorders / drug therapy. Postoperative Complications / drug therapy. Sirolimus / therapeutic use
  • [MeSH-minor] Aged. Antibodies, Monoclonal, Murine-Derived. Appendectomy. Child, Preschool. Female. Humans. Kidney Function Tests. Ovariectomy. Rituximab

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  • (PMID = 18589184.001).
  • [ISSN] 0041-1345
  • [Journal-full-title] Transplantation proceedings
  • [ISO-abbreviation] Transplant. Proc.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Murine-Derived; 0 / Immunosuppressive Agents; 4F4X42SYQ6 / Rituximab; W36ZG6FT64 / Sirolimus
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85. Pancholi V, Munjal K, Jain M, Munjal S, Agrawal R, Nandedkar S: Preoperative diagnosis of renal angiomyolipoma with fine needle aspiration cytology: a report of 3 cases. Acta Cytol; 2006 Jul-Aug;50(4):466-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Angiomyolipoma is a rare benign neoplasm, commonly involving the kidney.
  • [MeSH-major] Angiomyolipoma / diagnosis. Kidney / pathology. Kidney Neoplasms / diagnosis

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  • (PMID = 16901016.001).
  • [ISSN] 0001-5547
  • [Journal-full-title] Acta cytologica
  • [ISO-abbreviation] Acta Cytol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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86. Brandal P, Busund LT, Heim S: Chromosome abnormalities in juxtaglomerular cell tumors. Cancer; 2005 Aug 1;104(3):504-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Juxtaglomerular cell tumors (JGCT; also known as reninomas) are considered benign tumors of the kidney, although there have been reports of both malignant behavior and a JGCT-related death.
  • The IP-FISH results were in accordance with the karyotypic findings for the first tumor, whereas Tumor 2 was found to be diploid for most investigated chromosomes, except for trisomy for chromosomes 4 and 10 and monosomy for chromosomes 9 and X.
  • [MeSH-major] Chromosome Aberrations. Juxtaglomerular Apparatus / pathology. Kidney Neoplasms / genetics
  • [MeSH-minor] Adult. Child. Chromosomes, Human, Pair 10 / genetics. Chromosomes, Human, Pair 11 / genetics. Chromosomes, Human, Pair 9 / genetics. Chromosomes, Human, X / genetics. DNA, Neoplasm / analysis. Female. Humans. In Situ Hybridization, Fluorescence. Interphase. Karyotyping. Nucleic Acid Hybridization

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  • [Copyright] (c) 2005 American Cancer Society.
  • (PMID = 15968688.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Comparative Study; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA, Neoplasm
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87. Azizi B, Whelan T, Morse M: Renal tumors and the risk of malignancy based on size. Can J Urol; 2009 Dec;16(6):4921-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Of the 180 masses, 20 (11%) were benign and 160 (89%) were malignant lesions.
  • We recommend more aggressive therapies for masses larger than 4 cm and parenchymal sparing procedures for masses smaller than 4 cm as large proportion of these are benign.
  • [MeSH-major] Carcinoma, Renal Cell / epidemiology. Kidney Neoplasms / epidemiology. Neoplasm Staging / methods

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  • (PMID = 20003669.001).
  • [ISSN] 1195-9479
  • [Journal-full-title] The Canadian journal of urology
  • [ISO-abbreviation] Can J Urol
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] Canada
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88. Volpe A, Jewett MA: Current role, techniques and outcomes of percutaneous biopsy of renal tumors. Expert Rev Anticancer Ther; 2009 Jun;9(6):773-83
MedlinePlus Health Information. consumer health - Kidney Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • However, many small masses are benign tumors or low-grade renal cell carcinomas (RCCs).
  • [MeSH-major] Biopsy, Needle / methods. Carcinoma, Renal Cell / pathology. Kidney Neoplasms / pathology
  • [MeSH-minor] Humans. Needles. Neoplasm Metastasis / pathology. Specimen Handling / standards

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  • (PMID = 19496714.001).
  • [ISSN] 1744-8328
  • [Journal-full-title] Expert review of anticancer therapy
  • [ISO-abbreviation] Expert Rev Anticancer Ther
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 89
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89. Yoshino T, Yoneda K: Laparoscopic resection of a retroperitoneal ancient schwannoma: a case report and review of the literature. Anticancer Res; 2008 Sep-Oct;28(5B):2889-91
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  • Schwannomas are benign tumors that arise from neural sheath Schwann cells.
  • Solitary benign schwannomas are generally located in the head and neck, often along the cranial nerves, and are a particularly rare neoplasm among tumors of the retroperitoneal space.
  • A 67-year-old man undergoing a general health check was incidentally found to have a mass beside the left kidney.
  • Computed tomography (CT) revealed a cystic adrenal mass located cephalad to the left kidney.
  • The pathological diagnosis was retroperitoneal benign schwannoma consisting of mixture of a Antoni-A and -B type cells.

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  • (PMID = 19031930.001).
  • [ISSN] 0250-7005
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
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90. Suzuki T, Ueda Y, Shincho M, Mitsui Y, Higuchi Y, Maruyama T, Kondoh N, Nojima M, Yamamoto S, Hirota S, Shima H: [Myolipoma arising from the renal capsule: a case report]. Hinyokika Kiyo; 2008 May;54(5):349-52
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Computed tomorraphy and magnetic resonance imaging showed that the tumor was mixed with muscle and fat tissue, faintly enhanced, and located at the lower portion of the left kidney.
  • Myolipoma is a rare benign neoplasm in the soft tissue of retroperitoneum and abdominal cavity.
  • Since it is difficult to distinguish myolipoma from other benign and malignant tumors with fat tissue only by imaging studies, a surgical approach should be considered.
  • [MeSH-major] Kidney Neoplasms / diagnosis. Lipoma / diagnosis

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  • (PMID = 18546859.001).
  • [ISSN] 0018-1994
  • [Journal-full-title] Hinyokika kiyo. Acta urologica Japonica
  • [ISO-abbreviation] Hinyokika Kiyo
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
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91. Volpe A, Terrone C, Scarpa RM: The current role of percutaneous needle biopsies of renal tumours. Arch Ital Urol Androl; 2009 Jun;81(2):107-12
MedlinePlus Health Information. consumer health - Kidney Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Incidental SRMs are frequently detected in elderly patients and have a very heterogeneous biological behaviour At surgery up to one third have benign histologies and most of those that are malignant are low grade RCCs.
  • Pretreatment percutaneous biopsy can significantly decrease the number of unnecessary surgeries for benign disease and assist the urologist in clinical decision making, especially for elderly and unfit patients who are possible candidates for active surveillance and/or minimally invasive ablative therapies.

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  • (PMID = 19760866.001).
  • [ISSN] 1124-3562
  • [Journal-full-title] Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica
  • [ISO-abbreviation] Arch Ital Urol Androl
  • [Language] ENG
  • [Publication-type] Journal Article; Review
  • [Publication-country] Italy
  • [Number-of-references] 57
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92. Blick C, Ravindranath N, Muneer A, Jones A: Bilateral renal angiomyolipomas with invasion of the renal vein: a case report. ScientificWorldJournal; 2008;8:145-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • An angiomyolipoma (AML) is usually a benign, rare, and, more commonly, a unilateral renal tumour.
  • [MeSH-major] Angiomyolipoma / pathology. Kidney Neoplasms / pathology. Renal Veins / pathology
  • [MeSH-minor] Female. Humans. Middle Aged. Neoplasm Invasiveness. Tomography, X-Ray Computed

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  • (PMID = 18264631.001).
  • [ISSN] 1537-744X
  • [Journal-full-title] TheScientificWorldJournal
  • [ISO-abbreviation] ScientificWorldJournal
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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93. Pacchioni D, Volante M, Casetta G, Sapino A, Marchiò C, Bussolati G: Myxoid renal tumor with myoepithelial differentiation mimicking a salivary gland pleomorphic adenoma: description of a case. Am J Surg Pathol; 2007 Apr;31(4):632-6
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  • We herein report an unusual case of a low-grade myxoid renal epithelial neoplasm, with peculiar and previously unreported morphologic and immunohistochemical features.
  • The tumor proved benign at follow-up.
  • [MeSH-major] Kidney Neoplasms / pathology. Myoepithelioma / pathology. Neoplasms, Glandular and Epithelial / pathology

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  • (PMID = 17414112.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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94. Lam JS, Pantuck AJ, Belldegrun AS, Figlin RA: G250: a carbonic anhydrase IX monoclonal antibody. Curr Oncol Rep; 2005 Mar;7(2):109-15
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  • Furthermore, previous immunobiochemical studies of malignant and benign renal tissues revealed that CA IX was also highly expressed in RCC.
  • [MeSH-major] Antibodies, Monoclonal / therapeutic use. Carcinoma, Renal Cell / immunology. Kidney Neoplasms / immunology
  • [MeSH-minor] Animals. Antigens, Neoplasm / immunology. Carbonic Anhydrase IX. Carbonic Anhydrases / immunology. Clinical Trials as Topic. Humans. Mice. Radioimmunotherapy. Recombinant Fusion Proteins / therapeutic use

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  • (PMID = 15717944.001).
  • [ISSN] 1523-3790
  • [Journal-full-title] Current oncology reports
  • [ISO-abbreviation] Curr Oncol Rep
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Antigens, Neoplasm; 0 / G250 monoclonal antibody; 0 / Recombinant Fusion Proteins; EC 4.2.1.1 / CA9 protein, human; EC 4.2.1.1 / Carbonic Anhydrase IX; EC 4.2.1.1 / Carbonic Anhydrases
  • [Number-of-references] 50
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95. Hour TC, Kuo YZ, Liu GY, Kang WY, Huang CY, Tsai YC, Wu WJ, Huang SP, Pu YS: Downregulation of ABCD1 in human renal cell carcinoma. Int J Biol Markers; 2009 Jul-Sep;24(3):171-8
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  • Renal cell carcinoma (RCC) is the most common malignant tumor of the kidney.
  • ABCD1 expression was also downregulated in four renal cancer cell lines compared to immortalized benign renal tubular cells.
  • [MeSH-minor] Cell Line, Tumor. Female. Humans. Immunohistochemistry. Kidney Neoplasms / genetics. Kidney Neoplasms / pathology. Kidney Tubules / pathology. Male. Neoplasm Staging. Polymerase Chain Reaction. RNA, Messenger / genetics. Reverse Transcriptase Polymerase Chain Reaction

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  • (PMID = 19787628.001).
  • [ISSN] 0393-6155
  • [Journal-full-title] The International journal of biological markers
  • [ISO-abbreviation] Int. J. Biol. Markers
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / ABCD1 protein, human; 0 / RNA, Messenger
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96. Kubacka M, Pośpiech L, Jaworska M, Markowska-Woyciechowska A: [A case of bilateral oncocytomas of the submandibular gland and synchronous renal oncocytomas]. Otolaryngol Pol; 2005;59(6):903-5
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  • Oncocytoma is a rare benign neoplasm observed in numerous of organs.
  • [MeSH-major] Adenoma, Oxyphilic / complications. Kidney Neoplasms / complications. Neoplasms, Multiple Primary. Submandibular Gland Neoplasms / complications

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  • (PMID = 16521462.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
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97. Siddiqui TS, Tariq A, Rehman B, Siddiqui TS, Asim A: Accuracy of multiphase helical tomography in detection and characterisation of suspected renal masses using histopathological findings as gold standard. J Ayub Med Coll Abbottabad; 2010 Jul-Sep;22(3):170-3
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  • If it is found and treated early, the chances of survival from kidney cancer are high.
  • One malignant lesion was not identified and 3 malignant lesions falsely appeared benign in the corticomedullary phase.
  • All lesions were detected in the nephrographic phase and only 1 malignant lesion falsely appeared benign.
  • CONCLUSION: Enhancement of renal neoplasm is time dependent and is better in nephrographic phase.
  • [MeSH-major] Kidney Neoplasms / radiography. Tomography, Spiral Computed / methods

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  • (PMID = 22338448.001).
  • [ISSN] 1025-9589
  • [Journal-full-title] Journal of Ayub Medical College, Abbottabad : JAMC
  • [ISO-abbreviation] J Ayub Med Coll Abbottabad
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] Pakistan
  • [Chemical-registry-number] 0 / Contrast Media
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98. Kalinka A, Gerlach A, Arlart IP, Günes N, Hauser TK, Würstlin S, Bosse A: [Characterization and staging of renal tumors: significance of MRI diagnostics]. Rofo; 2006 Mar;178(3):298-305
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  • [Transliterated title] Charakterisierung und Staging von Nierentumoren: Bedeutung der MRT-Diagnostik.
  • In 29 cases we found lesions bilaterally, in 17 patients only in one kidney, and in four cases we found multifocal renal tumors unilaterally (n = 3) or bilaterally (n = 1).
  • 3/43 lesions were initially reported as being suspected of malignancy but were proven during follow-up or histologically to be benign.
  • [MeSH-major] Carcinoma, Renal Cell / diagnosis. Carcinoma, Renal Cell / pathology. Carcinoma, Transitional Cell / diagnosis. Carcinoma, Transitional Cell / pathology. Kidney Neoplasms / diagnosis. Kidney Neoplasms / pathology. Magnetic Resonance Imaging / methods
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Diagnosis, Differential. Female. Humans. Kidney / pathology. Kidney Diseases, Cystic / diagnosis. Kidney Diseases, Cystic / pathology. Male. Middle Aged. Neoplasm Staging. Retrospective Studies. Tomography, X-Ray Computed

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  • (PMID = 16508837.001).
  • [ISSN] 1438-9029
  • [Journal-full-title] RöFo : Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin
  • [ISO-abbreviation] Rofo
  • [Language] ger
  • [Publication-type] Comparative Study; English Abstract; Journal Article
  • [Publication-country] Germany
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99. Glassman D, Chawla SN, Waldman I, Johannes J, Byrne DS, Trabulsi EJ, Gomella LG: Correlation of pathology with tumor size of renal masses. Can J Urol; 2007 Aug;14(4):3616-20
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  • However, some of these lesions prove to be benign and did not truly warrant extirpation.
  • Overall, 24% of masses were determined to be benign and 76% were malignant.
  • Two hundred thirty masses were smaller than 4 cm and 72 (31.3%) of these were benign.
  • There were 166 lesions between 4 cm and 7 cm with an 18% benign rate.
  • Only eight of these were benign (12.5%).
  • Chi square testing revealed the 31.3% benign rate of the < 4 cm group to be significantly different than the benign rates of the other groups.
  • CONCLUSIONS: The preponderance of renal lesions removed for benign pathology occurs when lesion size is small, typically less than 4 cm.
  • [MeSH-major] Carcinoma, Transitional Cell / pathology. Kidney Neoplasms / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Male. Middle Aged. Neoplasm Staging. Nephrectomy. Retrospective Studies

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  • (PMID = 17784981.001).
  • [ISSN] 1195-9479
  • [Journal-full-title] The Canadian journal of urology
  • [ISO-abbreviation] Can J Urol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Canada
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100. Montgomery E, Epstein JI: Anastomosing hemangioma of the genitourinary tract: a lesion mimicking angiosarcoma. Am J Surg Pathol; 2009 Sep;33(9):1364-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: We describe 6 cases of a poorly recognized vascular neoplasm that can simulate angiosarcoma.
  • RESULTS: There were 6 tumors from 4 men (66%) and 2 women, ranging in age from 49 to 75 years (median, 59.5) involving the kidney and renal hilum (4, 66%) and testis (2).
  • Most kidney (3/4, 75%) tumors showed minor extensions into adjacent adipose tissue.
  • CONCLUSIONS: Anastomosing hemangioma of the genitourinary tract is a rare neoplasm displaying some overlapping features of both sinusoidal hemangioma and hobnail hemangioma of soft tissue and skin.
  • However, in our opinion, it is a unique neoplasm with a proclivity for the kidney.
  • Its anastomosing appearance can lead to concern for angiosarcoma but, despite small numbers and limited follow-up in our series, evidence to date supports that the lesion is benign.
  • [MeSH-minor] Aged. Antigens, CD31 / analysis. Antigens, CD34 / analysis. Biomarkers, Tumor / analysis. Diagnosis, Differential. Factor VIII / analysis. Female. Humans. Kidney Neoplasms / chemistry. Kidney Neoplasms / pathology. Male. Middle Aged. Prospective Studies. Testicular Neoplasms / chemistry. Testicular Neoplasms / pathology. Treatment Outcome

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  • (PMID = 19606014.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Antigens, CD34; 0 / Biomarkers, Tumor; 0 / F8 protein, human; 9001-27-8 / Factor VIII
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