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Items 1 to 85 of about 85
1. Wolf JS Jr, Dash A: Failure of percutaneous endoscopic resection of a renal cystic nephroma on longer-term follow-up. J Endourol; 2008 Jul;22(7):1505-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Failure of percutaneous endoscopic resection of a renal cystic nephroma on longer-term follow-up.
  • In 2005 we reported in this journal the treatment of cystic nephroma, a rare but presumed benign renal tumor, with percutaneous resection.
  • Initial follow-up confirmed removal of the intra-pelvic portion of the cystic nephroma and persistence of the unresected intra-parenchymal portion.
  • Laparoscopic radical nephrectomy without adrenalectomy revealed benign cystic nephroma.

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  • (PMID = 18613780.001).
  • [ISSN] 1557-900X
  • [Journal-full-title] Journal of endourology
  • [ISO-abbreviation] J. Endourol.
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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2. Bhat S, Thomas A: Benign multilocular cyst or multilocular cystic nephroma in adults: three case reports. Indian J Surg; 2007 Oct;69(5):209-11

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  • [Title] Benign multilocular cyst or multilocular cystic nephroma in adults: three case reports.
  • Multilocular cystic nephroma is an unusual entity of uncertain etiology that typically arises from the renal parenchyma.
  • Since existing imaging modalities cannot definitely exclude the possibility of multilocular cystic renal cell carcinoma these patients should undergo surgery.

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  • [Cites] Radiology. 1983 Feb;146(2):309-21 [6294736.001]
  • [Cites] Semin Diagn Pathol. 1998 Feb;15(1):2-20 [9503503.001]
  • [Cites] J Magn Reson Imaging. 1996 Jan-Feb;6(1):145-8 [8851419.001]
  • [Cites] Br J Urol. 1981 Feb;53(1):13-7 [7470798.001]
  • (PMID = 23132986.001).
  • [ISSN] 0972-2068
  • [Journal-full-title] The Indian journal of surgery
  • [ISO-abbreviation] Indian J Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3452588
  • [Keywords] NOTNLM ; Cystic Renal cell carcinoma / Cystic Wilm’s tumour / Cystic nephroma / Multilocular cyst / Renal cyst
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3. Omar AM, Khattak AQ, Lee JA: Cystic renal cell carcinoma arising from multilocular cystic nephroma of the same kidney. Int Braz J Urol; 2006 Mar-Apr;32(2):187-9; discussion 189
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  • [Title] Cystic renal cell carcinoma arising from multilocular cystic nephroma of the same kidney.
  • Multilocular cystic nephroma is an uncommon benign entity grouped among the cystic non-genetic diseases.
  • Though multilocular cystic nephroma is usually considered a benign lesion, malignant changes in the cysts should not be overlooked.
  • [MeSH-major] Carcinoma, Renal Cell / pathology. Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology

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  • (PMID = 16650296.001).
  • [ISSN] 1677-5538
  • [Journal-full-title] International braz j urol : official journal of the Brazilian Society of Urology
  • [ISO-abbreviation] Int Braz J Urol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Brazil
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4. Dash A, Wolf JS: Percutaneous treatment of renal cystic nephroma. J Endourol; 2005 Jul-Aug;19(6):724-5
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  • [Title] Percutaneous treatment of renal cystic nephroma.
  • Cystic nephroma is a rare, presumed benign, renal tumor that occurs in both children and adults.
  • We describe treatment of a cystic nephroma that is the first reported, to our knowledge, using endoscopic techniques.

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  • (PMID = 16053364.001).
  • [ISSN] 0892-7790
  • [Journal-full-title] Journal of endourology
  • [ISO-abbreviation] J. Endourol.
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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5. 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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  • [Title] Cystic nephroma: a diagnostic dilemma.
  • Cystic nephroma (CN) is a rare benign neoplasm of kidney with excellent prognosis.
  • An accurate pre-operative diagnosis differentiating CN from other cystic renal malignancies may be impossible by clinical and radiological examination, and histopathological examination provides the final diagnosis.
  • This report describes two adult patients with large multi-locular cystic renal masses on imaging and the diagnosis of CN was clinched post-operatively by the honeycomb appearance of the cut specimen and the finding of multiple, non-communicating fluid filled cysts lined by cuboidal or flattened epithelial cells and absence of blastemal cells on microscopy.
  • [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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6. Baldi A, De Crescenzo V, Giordano DR, Lamberti R, Perna A, Picone C, Lucariello A, Feroce F, Grattacaso S, De Luca A: Cystic nephroma: report of a case and review of the literature. In Vivo; 2007 Sep-Oct;21(5):895-6
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  • [Title] Cystic nephroma: report of a case and review of the literature.
  • Cystic nephroma is a rare benign cystic renal tumor, which has been only recently recognized as an exclusively adult histological entity.
  • We present a case of cystic nephroma, together with clinical, radiological, histopathological and immunohistochemical findings.
  • [MeSH-major] Kidney Diseases, Cystic / pathology

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  • (PMID = 18019431.001).
  • [ISSN] 0258-851X
  • [Journal-full-title] In vivo (Athens, Greece)
  • [ISO-abbreviation] In Vivo
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Greece
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7. Makepeace JC, Sellaturay S, Mushtaq I, Sebire NJ: Benign cystic nephroma. Br J Hosp Med (Lond); 2006 Jan;67(1):45
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  • [Title] Benign cystic nephroma.
  • [MeSH-major] Kidney Diseases, Cystic / pathology

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  • (PMID = 16447413.001).
  • [ISSN] 1750-8460
  • [Journal-full-title] British journal of hospital medicine (London, England : 2005)
  • [ISO-abbreviation] Br J Hosp Med (Lond)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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8. Bjerggaard MM, Barstad B: [Two cases of multilocular cystic nephroma, a rare benign tumor of the kidney]. Ugeskr Laeger; 2005 Nov 14;167(46):4379-80
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  • [Title] [Two cases of multilocular cystic nephroma, a rare benign tumor of the kidney].
  • [Transliterated title] To tilfaelde af multilokulaer cystisk nefrom, en sjaelden benign nyretumor.
  • We present two case reports of multilocular cystic nephroma (MCN).
  • MCN is a rare benign tumor of the kidney that is difficult to differentiate from malignant tumor by diagnostic imaging (ultrasound, CT) and cytology on fine-needle aspiration.
  • [MeSH-major] Kidney Diseases, Cystic / diagnosis. Kidney Neoplasms / diagnosis

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  • (PMID = 16287525.001).
  • [ISSN] 1603-6824
  • [Journal-full-title] Ugeskrift for laeger
  • [ISO-abbreviation] Ugeskr. Laeg.
  • [Language] dan
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Denmark
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9. Subirá Ríos J, Sánchez Zalabardo JM, Elizalde Benito A, Navarro Gíl J, Hijazo Conejos JI, García-Magariño Alonso J, García Calero D, López López JA, Valdivia Uría JG: [Multilocular cystic nephroma. Report of three new cases]. Arch Esp Urol; 2009 Jan-Feb;62(1):62-6
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  • [Title] [Multilocular cystic nephroma. Report of three new cases].
  • [Transliterated title] Nefroma quístico multilocular. Aportación de 3 nuevos casos.
  • OBJECTIVE: To analyze the presentation of multilocular cystic nephroma and its diagnostic-therapy scheme.
  • RESULTS: Multilocular cystic nephroma is a benign lesion, rare that appears both in adult age, generally asymptomatic, and in children, frequently as a palpable mass.
  • CONCLUSIONS: The great variety of clinical presentations, differential diagnosis and places of origin of the cases is demonstrated, being this a reflection of our daily medical practice, in which we cannot reach definitive diagnosis with imaging tests, being the Bosniak's classification very useful for the setting of indication for surgery, which will give definitive diagnosis of multilocular cystic nephroma or what is more important will rule out malignancy.

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  • (PMID = 19400449.001).
  • [ISSN] 0004-0614
  • [Journal-full-title] Archivos españoles de urología
  • [ISO-abbreviation] Arch. Esp. Urol.
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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10. 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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  • [Title] Cystic nephroma in the adult: pathological aspects and therapeutic implications.
  • Cystic nephroma is a benign renal neoplasm.
  • Preoperative diagnosis of Cystic nephroma is difficult to achieve.
  • 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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11. Bahubeshi A, Bal N, Rio Frio T, Hamel N, Pouchet C, Yilmaz A, Bouron-Dal Soglio D, Williams GM, Tischkowitz M, Priest JR, Foulkes WD: Germline DICER1 mutations and familial cystic nephroma. J Med Genet; 2010 Dec;47(12):863-6
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  • [Title] Germline DICER1 mutations and familial cystic nephroma.
  • BACKGROUND: Multilocular cystic nephroma (CN) is a benign kidney tumour and is part of a family of kidney neoplasms including cystic partially differentiated nephroblastoma and Wilms tumour (WT).
  • [MeSH-major] DEAD-box RNA Helicases / genetics. Germ-Line Mutation / genetics. Kidney Diseases, Cystic / complications. Kidney Diseases, Cystic / genetics. Kidney Neoplasms / complications. Kidney Neoplasms / genetics. Ribonuclease III / genetics

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  • (PMID = 21036787.001).
  • [ISSN] 1468-6244
  • [Journal-full-title] Journal of medical genetics
  • [ISO-abbreviation] J. Med. Genet.
  • [Language] eng
  • [Grant] Canada / Canadian Institutes of Health Research / / FRN53888
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] EC 3.1.26.3 / DICER1 protein, human; EC 3.1.26.3 / Ribonuclease III; EC 3.6.4.13 / DEAD-box RNA Helicases
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12. Fujita M, Uehara M, Tei N, Shimizu K, Imazu T, Meguro N, Kiyohara H, Adachi S: [An unusual case of cystic nephroma protruding into the renal pelvis]. Hinyokika Kiyo; 2010 Oct;56(10):577-80
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  • [Title] [An unusual case of cystic nephroma protruding into the renal pelvis].
  • Cystic nephroma is a relatively rare and benign renal lesion of uncertain etiology.
  • Approximately 200 cases have been described, but only a few cases of cystic nephroma with prominent renal pelvis involvement have been reported.
  • Here, we report an unusual case of cystic nephroma that protruded into the renal pelvis.
  • The diagnosis of a malignant or benign lesion was not clear.
  • The characteristics of the resected specimen were consistent with those of cystic nephroma.
  • To our knowledge, this is the fifth case report on cystic nephroma with prominent renal pelvis involvement.
  • [MeSH-major] Kidney Diseases, Cystic / pathology. Kidney Pelvis / pathology

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  • (PMID = 21063163.001).
  • [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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13. Chen KT: Cytology of cystic nephroma: a case report. Acta Cytol; 2008 Jan-Feb;52(1):91-3
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  • [Title] Cytology of cystic nephroma: a case report.
  • BACKGROUND: Cystic nephroma is a rare benign multiloculated cystic renal neoplasm that is often confused with multicystic renal cell carcinoma radiographically and cytologically.
  • CASE: A 58-year-old woman was incidentally found to have a multiloculated cystic right renal lesion.
  • Cytologic examination of the fluid aspirated from the lesion was reported as highly suspicious for renal cell carcinoma, but a right nephrectomy revealed a cystic nephroma.
  • CONCLUSION: Cystic nephroma fluid is characterized by the presence of sparse epithelial cells with moderate nuclear atypia.
  • [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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14. Bouhafs A, Cherradi N, Lamaalmi N, Belkacem R, Barahioui M: An unusual case of multilocular cystic nephroma with prominent renal pelvis involvement. Int J Urol; 2006 Apr;13(4):436-8
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  • [Title] An unusual case of multilocular cystic nephroma with prominent renal pelvis involvement.
  • Multilocular cystic nephroma (MCN) is a relatively rare, benign tumor of uncertain etiology.
  • A multilocular cystic lesion was found in the removed specimen, which had a direct tumor extension into the renal pelvis.
  • This growth pattern might be one of the characteristics of this benign renal tumor.
  • [MeSH-major] Kidney Diseases, Cystic / diagnosis. Kidney Neoplasms / diagnosis. Kidney Pelvis

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  • (PMID = 16734866.001).
  • [ISSN] 0919-8172
  • [Journal-full-title] International journal of urology : official journal of the Japanese Urological Association
  • [ISO-abbreviation] Int. J. Urol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
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15. Sambuis C, Albouy B, Riopel C, Gobet F, Grise P, Pfister C: [Multilocular cystic nephroma in an adult: diagnostic and therapeutic strategy]. Prog Urol; 2005 Apr;15(2):315-8
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  • [Title] [Multilocular cystic nephroma in an adult: diagnostic and therapeutic strategy].
  • The authors report two clinical cases of cystic nephroma in adults observed in the department over the last 10 years.
  • Only histological examination can confirm the diagnosis and eliminate multilocular cystic renal carcinoma or necrotic pseudocystic carcinoma.
  • Based on a review of the literature, the authors emphasize recent pathophysiological and immunohistochemical data that could improve the management of this benign disease, in which malignant transformation is also possible.

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  • (PMID = 15999616.001).
  • [ISSN] 1166-7087
  • [Journal-full-title] Progrès en urologie : journal de l'Association française d'urologie et de la Société française d'urologie
  • [ISO-abbreviation] Prog. Urol.
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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16. 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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  • [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).
  • One was composed of a mixture of solid and cystic elements, while the remaining case showed a multicystic cut surface bridged by thick fibrous septa.
  • They were multiloculated cystic in nature.
  • The cystic spaces were separated by thin septa and there was no significant solid or necrotic component.
  • In contrast, the thin-walled cystic spaces in CN were lined by a single layer of epithelium.Immunohistochemical study showed that the epithelial cells were positive for pan-cytokeratin and epithelial membrane antigen.
  • 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
  • [MeSH-minor] Actins / metabolism. Adult. Carcinoma, Renal Cell / pathology. Desmin / metabolism. Diagnosis, Differential. Female. Follow-Up Studies. Humans. Male. Middle Aged. Nephroma, Mesoblastic / pathology. Receptors, Estrogen / metabolism. Retrospective Studies. Vimentin / metabolism

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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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17. Boybeyi O, Karnak I, Orhan D, Ciftci AO, Tanyel FC, Kale G, Senocak ME: Cystic nephroma and localized renal cystic disease in children: diagnostic clues and management. J Pediatr Surg; 2008 Nov;43(11):1985-9
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  • [Title] Cystic nephroma and localized renal cystic disease in children: diagnostic clues and management.
  • BACKGROUND AND PURPOSE: Cystic nephroma (CN) and localized renal cystic disease (LRCD) are rare benign renal entities that can occur in children.
  • The age, sex, family history of renal cystic disease, presenting symptoms, physical examination findings, diagnostic radiologic imaging used, operative findings, details of the surgical procedure, histopathologic features, and outcomes were evaluated.
  • [MeSH-major] Kidney Diseases, Cystic / diagnosis. Kidney Neoplasms / diagnosis. Wilms Tumor / diagnosis

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  • (PMID = 18970929.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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18. Duda-Szymańska J, Kaczmarek J, Papierz W: Cystic nephroma in adults. A report of two cases and review of the literature. Pol J Pathol; 2005;56(2):93-6
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  • [Title] Cystic nephroma in adults. A report of two cases and review of the literature.
  • We present two cases of cystic nephroma in a 55-year old and a 61-year old women.
  • Due to the age of the patients and the location of the lesions, possibility of clear cell carcinoma with cystic changes was considered.
  • However, microscopic examination of postoperative specimens revealed benign nature of the tumors.

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  • (PMID = 16092672.001).
  • [ISSN] 1233-9687
  • [Journal-full-title] Polish journal of pathology : official journal of the Polish Society of Pathologists
  • [ISO-abbreviation] Pol J Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Poland
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19. 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-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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20. Hsiao HL, Wu WJ, Chang MY, Ke HL, Huang CH: Unusual case of multilocular cystic nephroma treated with nephron sparing technique: a case report. Kaohsiung J Med Sci; 2006 Oct;22(10):515-8
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  • [Title] Unusual case of multilocular cystic nephroma treated with nephron sparing technique: a case report.
  • Multilocular cystic nephroma is an unusual entity of uncertain etiology that can affect children and adults equally.
  • This lesion is believed to be part of a spectrum of renal cystic disorders with multilocular cyst and cystic Wilms' tumor representing the two extremes and usually presents with a benign character.
  • After a series of examinations including abdominal ultrasound, computed tomography, and angiography, she underwent partial nephrectomy under the impression of benign lesion.
  • The pathologic examination showed that it was a multilocular cystic nephroma.
  • [MeSH-major] Kidney Diseases, Cystic / surgery. Kidney Neoplasms / surgery

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  • (PMID = 17098684.001).
  • [ISSN] 1607-551X
  • [Journal-full-title] The Kaohsiung journal of medical sciences
  • [ISO-abbreviation] Kaohsiung J. Med. Sci.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China (Republic : 1949- )
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21. Montironi R, Mazzucchelli R, Lopez-Beltran A, Martignoni G, Cheng L, Montorsi F, Scarpelli M: Cystic nephroma and mixed epithelial and stromal tumour of the kidney: opposite ends of the spectrum of the same entity? Eur Urol; 2008 Dec;54(6):1237-46
The Weizmann Institute of Science GeneCards and MalaCards databases. gene/protein/disease-specific - MalaCards for cystic nephroma .

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  • [Title] Cystic nephroma and mixed epithelial and stromal tumour of the kidney: opposite ends of the spectrum of the same entity?
  • OBJECTIVES: The term "renal epithelial and stromal tumour" (REST) was proposed recently to encompass the spectrum of findings observed in cystic nephroma (CN) and mixed epithelial and stromal tumour (MEST) of the kidney.
  • Our aim was to review the broad spectrum of usual and unusual clinical and morphologic findings observed in CN and MEST.
  • RESULTS: CN and MEST have a remarkable similarity in sex predilection, age distribution, and morphologic attributes of both the epithelial and stromal components and immunohistochemical profile, albeit with variation in individual categories, with higher prevalence of stromal-to-epithelial ratio, prominent ovarian-like stroma, smaller cysts, and stromal luteinisation in MEST, and large cysts, thin septa, and low stromal-to-epithelial ratio in CN.
  • Rare and unusual morphologic features, such as endometrioid, cervical, and intestinal differentiation, and luteinised ovarian-like stroma, have been described in MEST.
  • Even though an aggressive behaviour has been reported in very few cases, in general both neoplasms are considered benign and surgical excision is curative.

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  • [CommentIn] Eur Urol. 2008 Dec;54(6):1245-6 [18006142.001]
  • [CommentIn] Eur Urol. 2009 Jul;56(1):e3 [19167806.001]
  • (PMID = 18006141.001).
  • [ISSN] 0302-2838
  • [Journal-full-title] European urology
  • [ISO-abbreviation] Eur. Urol.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Switzerland
  • [Number-of-references] 50
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22. Lane BR, Campbell SC, Remer EM, Fergany AF, Williams SB, Novick AC, Weight CJ, Magi-Galluzzi C, Zhou M: Adult cystic nephroma and mixed epithelial and stromal tumor of the kidney: clinical, radiographic, and pathologic characteristics. Urology; 2008 Jun;71(6):1142-8
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  • [Title] Adult cystic nephroma and mixed epithelial and stromal tumor of the kidney: clinical, radiographic, and pathologic characteristics.
  • OBJECTIVES: Adult cystic nephroma (CN) and mixed epithelial and stromal tumor (MEST) are benign renal tumors readily distinguished from cystic renal cell carcinoma and other malignant variants based on histopathology.
  • Pedunculation of a multiloculated cystic lesion may allow for preoperative suspicion of these lesions in the proper clinical setting.

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  • (PMID = 18313107.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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23. van den Hoek J, de Krijger R, van de Ven K, Lequin M, van den Heuvel-Eibrink MM: Cystic nephroma, cystic partially differentiated nephroblastoma and cystic Wilms' tumor in children: a spectrum with therapeutic dilemmas. Urol Int; 2009;82(1):65-70
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  • [Title] Cystic nephroma, cystic partially differentiated nephroblastoma and cystic Wilms' tumor in children: a spectrum with therapeutic dilemmas.
  • BACKGROUND: Cystic renal tumors are a diagnostic and therapeutic challenge.
  • Cystic nephroma (CN), cystic partially differentiated nephroblastoma (CPDN) and cystic Wilms' tumor (CWT) are a spectrum with CN at the benign end, CWT at the malignant end and CPDN in the intermediate position.
  • CONCLUSIONS: Surgery as first-line therapy should be seriously considered in children who have a cystic renal tumor, but further collaborative studies are needed since the distinction line between CPDN and CWT is not always clear.
  • [MeSH-major] Kidney Diseases, Cystic / surgery. Kidney Neoplasms / surgery. Nephrectomy. Wilms Tumor / surgery

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  • [Copyright] (c) 2009 S. Karger AG, Basel.
  • (PMID = 19172100.001).
  • [ISSN] 1423-0399
  • [Journal-full-title] Urologia internationalis
  • [ISO-abbreviation] Urol. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
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24. Stamatiou K, Polizois K, Kollaitis G, Dahanis S, Zafeiropoulos G, Leventis C, Lambou T: Cystic nephroma: a case report and review of the literature. Cases J; 2008;1(1):267
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  • [Title] Cystic nephroma: a case report and review of the literature.
  • BACKGROUND: The spectrum of cystic renal neoplasms includes both benign and malignant tumors and the order is as follows: benign multilocular cyst, multilocular cystic renal cell cancer and cystic renal cell cancer.
  • Microscopic examination of the resected tissue showed the typical characteristics of a cystic nephroma.
  • CONCLUSION: Cystic nephroma is a relatively rare benign lesion of the kidney.
  • The non-specific clinical findings and the poor contribution of imaging examinations make the preoperative distinction from other cystic renal neoplasias difficult.

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  • [Cites] Semin Diagn Pathol. 1998 Feb;15(1):2-20 [9503503.001]
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  • (PMID = 18947428.001).
  • [ISSN] 1757-1626
  • [Journal-full-title] Cases journal
  • [ISO-abbreviation] Cases J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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25. Yüksel S, Ekim M, Fitöz S, Soygür T, Sertçelik A, Perçinel S, Acar B, Ozçakar ZB, Comba A, Yalçinkaya F: The association of cystic nephroma with pulmonary sequestration: is it a coincidence or not? Pediatr Nephrol; 2006 Jul;21(7):1041-4
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  • [Title] The association of cystic nephroma with pulmonary sequestration: is it a coincidence or not?
  • Cystic nephroma (CN) is a rare, presumably benign, multilocular cystic renal tumor.
  • Pulmonary sequestration (PS) also presents as cystic masses of non-functioning primitive lung tissue.
  • [MeSH-major] Bronchopulmonary Sequestration / complications. Kidney Diseases, Cystic / complications

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  • (PMID = 16773421.001).
  • [ISSN] 0931-041X
  • [Journal-full-title] Pediatric nephrology (Berlin, Germany)
  • [ISO-abbreviation] Pediatr. Nephrol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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26. Kuzgunbay B, Turunc T, Bolat F, Kilinc F: Adult cystic nephroma: a case report and a review of the literature. Urol Oncol; 2009 Jul-Aug;27(4):407-9
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  • [Title] Adult cystic nephroma: a case report and a review of the literature.
  • The histopathological examination is reported as adult cystic nephroma, a rare benign lesion of the kidney.

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  • (PMID = 18555707.001).
  • [ISSN] 1873-2496
  • [Journal-full-title] Urologic oncology
  • [ISO-abbreviation] Urol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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27. Antic T, Perry KT, Harrison K, Zaytsev P, Pins M, Campbell SC, Picken MM: Mixed epithelial and stromal tumor of the kidney and cystic nephroma share overlapping features: reappraisal of 15 lesions. Arch Pathol Lab Med; 2006 Jan;130(1):80-5
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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 and cystic nephroma share overlapping features: reappraisal of 15 lesions.
  • CONTEXT: Cystic nephroma is a rare cystic tumor, which only recently has been recognized as an exclusively adult lesion.
  • Mixed epithelial and stromal tumor of the kidney is also a rare, recently recognized, biphasic tumor composed of tubular and cystic elements embedded in grossly recognizable spindle cell stroma.
  • OBJECTIVES: To compare clinical phenotype, morphology, and immunohistochemistry in mixed epithelial and stromal tumor of the kidney and cystic nephroma in order to explore the relationship between these 2 lesions.
  • DESIGN: Fifteen biphasic lesions (8 mixed epithelial and stromal tumors of the kidney and 7 cystic nephromas) were studied.
  • Cystic nephroma occurred in both sexes; patients were aged 22 to 71 years (mean, 50.4 years), and a history of hormonal therapy was present on occasion.
  • All 15 lesions were benign.
  • Lesions varied by size, the proportion of cystic component, and the amount and cellularity of stroma.
  • In cystic nephroma, focal positivity for hormone receptors was seen in 2 of 7 tumors tested; both positive lesions were from women.
  • The epithelial lining in both mixed epithelial and stromal tumor of the kidney and cystic nephroma lesions was variable with regard to shape, cytoplasmic appearance, and immunophenotype (with focal positivity for CD10, cytokeratin 7, high-molecular-weight keratin, and Ulex europaeus detectable in both lesions).
  • CONCLUSIONS: While mixed epithelial and stromal tumor of the kidney has a strong association with the female sex and hormonal milieu, cystic nephroma can affect both sexes and, on occasion, may also have hormonal associations.
  • [MeSH-major] Kidney Neoplasms / pathology. Nephroma, Mesoblastic / pathology. Stromal Cells / pathology

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  • (PMID = 16390243.001).
  • [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
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Receptors, Estrogen; 0 / Receptors, Progesterone
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28. Jevremovic D, Lager DJ, Lewin M: Cystic nephroma (multilocular cyst) and mixed epithelial and stromal tumor of the kidney: a spectrum of the same entity? Ann Diagn Pathol; 2006 Apr;10(2):77-82
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  • [Title] Cystic nephroma (multilocular cyst) and mixed epithelial and stromal tumor of the kidney: a spectrum of the same entity?
  • The recently described mixed epithelial and stromal tumor (MEST) of the kidney and adult cystic nephroma (CN) (multilocular cyst) are rare benign cystic renal neoplasms that are composed of epithelial and stromal elements.
  • All cases have acted in a benign fashion with no history of recurrence or metastasis.
  • [MeSH-major] Kidney Diseases, Cystic / diagnosis. Kidney Neoplasms / diagnosis. Neoplasms, Complex and Mixed / diagnosis

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  • (PMID = 16546041.001).
  • [ISSN] 1092-9134
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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29. Turbiner J, Amin MB, Humphrey PA, Srigley JR, De Leval L, Radhakrishnan A, Oliva E: Cystic nephroma and mixed epithelial and stromal tumor of kidney: a detailed clinicopathologic analysis of 34 cases and proposal for renal epithelial and stromal tumor (REST) as a unifying term. Am J Surg Pathol; 2007 Apr;31(4):489-500
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cystic nephroma and mixed epithelial and stromal tumor of kidney: a detailed clinicopathologic analysis of 34 cases and proposal for renal epithelial and stromal tumor (REST) as a unifying term.
  • Cystic nephroma (CN) and mixed epithelial and stromal tumor (MEST) are rare benign renal neoplasms that have overlapping clinical and morphologic features, including predominance in middle-aged women, variably cystic architecture, eosinophilic cells, and hobnail cells lining the cysts and ovarian-type stroma.
  • Follow-up in both categories of tumors (mean 3.2 y, median 3 y for CNs and mean 2.5 y, median of 2 y for MESTs) showed no evidence of recurrence or metastases in keeping with their benign nature.
  • This study highlights the remarkable similarity between CN and MEST in sex predilection, age distribution, and morphologic attributes of both the epithelial and stromal components and immunohistochemical profile albeit with variation in individual categories with higher prevalence of stromal to epithelial ratio, prominent ovarian stroma, smaller cysts with phyllodes glands pattern and stromal luteinization being more common in MEST; and large cysts, thin septae and low stromal to epithelial ratio in CN.
  • On the basis of detailed morphologic analysis of this series of CN and MEST, we propose a unifying term of "renal epithelial and stromal tumor" (REST) to encompass the spectrum of findings observed in these tumors at least until new molecular studies can prove or disprove this challenging hypothesis.
  • [MeSH-major] Kidney Neoplasms / classification. Kidney Neoplasms / pathology. Neoplasms, Glandular and Epithelial / classification. Neoplasms, Glandular and Epithelial / pathology. Nephroma, Mesoblastic / classification. Nephroma, Mesoblastic / pathology

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  • (PMID = 17414095.001).
  • [ISSN] 0147-5185
  • [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 / Receptors, Estrogen; 0 / Receptors, Progesterone
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30. Puvaneswary M, Macintosh J, Cassey J: Cystic partially differentiated nephroblastoma. Australas Radiol; 2006 Jun;50(3):255-7
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  • [Title] Cystic partially differentiated nephroblastoma.
  • Cystic partially differentiated nephroblastoma is a relatively rare tumour of the kidney usually affecting infants.
  • Cystic Wilms' tumour and multilocular cystic nephroma should be distinguished from cystic partially differentiated nephroblastoma.
  • Multilocular cystic nephroma is a benign tumour whereas cystic Wilms' tumour is at the malignant end of the range of classification of such tumours.
  • Cystic partially differentiated nephroblastoma may undergo local recurrence but there is no report of metastasis.
  • [MeSH-major] Kidney Diseases, Cystic / radiography. Kidney Neoplasms / radiography. Wilms Tumor / radiography

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  • (PMID = 16732826.001).
  • [ISSN] 0004-8461
  • [Journal-full-title] Australasian radiology
  • [ISO-abbreviation] Australas Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
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31. Argani P: Metanephric neoplasms: the hyperdifferentiated, benign end of the Wilms tumor spectrum? Clin Lab Med; 2005 Jun;25(2):379-92
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metanephric neoplasms: the hyperdifferentiated, benign end of the Wilms tumor spectrum?
  • The relationship of Wilms tumor, MAF with mitoses or combined MA/Wilms tumor lesions, and usual MAF or usual MA may be viewed as analogous to that of neuroblastoma, differentiating neuroblastoma, and ganglioneuroma, in which progressively more mature or differentiated counterparts of malignant embryonal lesions are associated with a greater probability of benign clinical behavior.
  • Such a spectrum already is recognized for cystic ILNR-derived nephroblastic lesions, ranging from cystic Wilms tumor, cystic partially differentiated nephroblastoma, and cystic nephroma.

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  • (PMID = 15848742.001).
  • [ISSN] 0272-2712
  • [Journal-full-title] Clinics in laboratory medicine
  • [ISO-abbreviation] Clin. Lab. Med.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 32
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32. Adey GS, Pedrosa I, Rofsky NM, Sanda MG, DeWolf WC: Lower limits of detection using magnetic resonance imaging for solid components in cystic renal neoplasms. Urology; 2008 Jan;71(1):47-51
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  • [Title] Lower limits of detection using magnetic resonance imaging for solid components in cystic renal neoplasms.
  • A group of 21 patients were identified with focal nodular enhancement within cystic renal masses.
  • There were 21 of 159 (13%) patients with complex cystic lesions that displayed focal nodular enhancement, 14 of which (67%) measured 10 mm or larger in size.
  • The single, benign lesion was a cystic nephroma.
  • CONCLUSIONS: The demonstration of solid enhancing nodular components with high-resolution 3D MRI provides excellent positive predictive value for diagnosing neoplastic cystic renal lesions, including a large percentage 10 mm or larger in size.
  • Our experience suggests a 95% likelihood that cystic renal lesions with focal nodular enhancement are malignant.
  • [MeSH-major] Carcinoma, Renal Cell / pathology. Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology

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  • (PMID = 18242363.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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33. Snyder ME, Bach A, Kattan MW, Raj GV, Reuter VE, Russo P: Incidence of benign lesions for clinically localized renal masses smaller than 7 cm in radiological diameter: influence of sex. J Urol; 2006 Dec;176(6 Pt 1):2391-5; discussion 2395-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Incidence of benign lesions for clinically localized renal masses smaller than 7 cm in radiological diameter: influence of sex.
  • PURPOSE: We determined the incidence of benign renal lesions in patients undergoing definitive surgery for localized renal masses 7 cm or less in maximum radiological diameter, and assessed preoperative and clinical parameters associated with benign histology.
  • Logistic regression was done to determine clinical factors associated with benign renal masses, including radiological tumor size, cystic vs solid appearance, patient sex, age, presenting symptoms and race.
  • RESULTS: Of 815 nephrectomies in our data set 134 (16.4%) were associated with benign lesions, including oncocytoma in 87 (10.7%), angiomyolipoma in 17 (2%), simple cysts in 10 (1.2%), metanephric adenoma in 8 (1%), cystic nephroma in 5 (0.6%) and other in 7.
  • On multivariate logistic regression analysis only sex was significantly associated with benign histology with females having an OR of 1.8 (95% CI 1.2 to 2.6, p = 0.002).
  • Tumor size was not independently associated with benign histology (p = 0.13).
  • CONCLUSIONS: A significant number (16.4%) of benign lesions less than 7 cm in radiological diameter were operated on based on suspicious preoperative imaging.
  • Women had almost twice the likelihood of having a benign lesion.

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  • (PMID = 17085108.001).
  • [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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34. Raj GV, Yowell C, Madden JF, Nosnik I, Mouraviev V, Polascik TJ: Malignant cystic nephroma. Can J Urol; 2006 Dec;13(6):3348-50
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  • [Title] Malignant cystic nephroma.
  • AIM: To describe a malignant cystic nephroma in an asymptomatic man.
  • Histopathological analyses of the resected specimen revealed malignant cystic nephroma.
  • [MeSH-major] Kidney Diseases, Cystic / diagnosis. Kidney Neoplasms / diagnosis


35. Bal N, Kayaselçuk F, Polat A, Bolat F, Yilmaz Z, Tuncer I: Familial cystic nephroma in two siblings with pleuropulmonary blastoma. Pathol Oncol Res; 2005;11(1):53-6
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  • [Title] Familial cystic nephroma in two siblings with pleuropulmonary blastoma.
  • Cystic nephroma (CN) and pleuropulmonary blastoma (PPB) are rare tumors.


36. Bouron-Dal Soglio D, Harvey I, Yazbeck S, Rypens F, Oligny LL, Fournet JC: An association of pleuropulmonary blastoma and cystic nephroma: possible genetic association. Pediatr Dev Pathol; 2006 Jan-Feb;9(1):61-4
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  • [Title] An association of pleuropulmonary blastoma and cystic nephroma: possible genetic association.
  • The association of pleuropulmonary blastoma and cystic nephroma is an uncommon entity, with only 4 cases of such an association in the same patient described in English literature.
  • The boy underwent a pulmonary biopsy that showed a pleuropulmonary blastoma and a nephrectomy that showed a cystic nephroma.
  • [MeSH-major] Kidney Neoplasms / genetics. Kidney Neoplasms / pathology. Lung Neoplasms / genetics. Nephroma, Mesoblastic / genetics. Pleural Neoplasms / genetics. Pulmonary Blastoma / genetics

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  • (PMID = 16808637.001).
  • [ISSN] 1093-5266
  • [Journal-full-title] Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
  • [ISO-abbreviation] Pediatr. Dev. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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37. Deeg KH, Gerdemann C, Weingärtner K, Seitz G: Sonographic diagnosis of an unusual case of multilocular cystic nephroma mimicking polycystic kidney disease. Ultraschall Med; 2008 Dec;29 Suppl 5:264-7
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  • [Title] Sonographic diagnosis of an unusual case of multilocular cystic nephroma mimicking polycystic kidney disease.
  • The following is a report of the unusual case of a multilocular cystic nephroma in an 8-year-old boy who was transferred to our unit with a palpable abdominal tumor.
  • The histologic diagnosis was cystic nephroma.
  • [MeSH-major] Kidney Neoplasms / surgery. Kidney Neoplasms / ultrasonography. Nephroma, Mesoblastic / surgery. Nephroma, Mesoblastic / ultrasonography

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  • (PMID = 19034827.001).
  • [ISSN] 1438-8782
  • [Journal-full-title] Ultraschall in der Medizin (Stuttgart, Germany : 1980)
  • [ISO-abbreviation] Ultraschall Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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38. Agarwal AK, Das S, Agarwal A, Ghosh D, Chaterjee N, Pal MS: Pleuropulmonary blastema with cystic nephroma - A rare presentation and surgical dilemma. Indian J Pediatr; 2008 Dec;75(12):1266-8
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  • [Title] Pleuropulmonary blastema with cystic nephroma - A rare presentation and surgical dilemma.
  • Pleuropulmonary balstema with cystic nephroma is a rare dual pathology of pediatric age group.

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  • (PMID = 19057859.001).
  • [ISSN] 0973-7693
  • [Journal-full-title] Indian journal of pediatrics
  • [ISO-abbreviation] Indian J Pediatr
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  • [Chemical-registry-number] Pleuropulmonary blastoma
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39. Luithle T, Szavay P, Furtwängler R, Graf N, Fuchs J, SIOP/GPOH Study Group: Treatment of cystic nephroma and cystic partially differentiated nephroblastoma--a report from the SIOP/GPOH study group. J Urol; 2007 Jan;177(1):294-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Treatment of cystic nephroma and cystic partially differentiated nephroblastoma--a report from the SIOP/GPOH study group.
  • PURPOSE: Cystic partially differentiated nephroblastoma is a rare variant of Wilms tumor, and might be confused with cystic nephroma.
  • To confirm diagnosis of cystic nephroma/partially differentiated nephroblastoma, all patients underwent review by the Reference Pathology Center of SIOP/GPOH.
  • RESULTS: A total of 14 patients with diagnoses of cystic nephroma (7) and cystic partially differentiated nephroblastoma (7) were identified.
  • CONCLUSIONS: In cystic renal tumors radiological findings should always be reviewed by the reference radiologist of the treatment protocol study group.
  • Irrespective of the chosen therapy, outcome of cystic nephroma and cystic partially differentiated nephroblastoma is favorable.
  • Even in large international trials the number of patients with cystic nephroma or cystic partially differentiated nephroblastoma is too small for statistical analysis.

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  • (PMID = 17162067.001).
  • [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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40. Lenz MP, Warmann SW, Scheel-Walter HG, Schäfer J, Wehrmann M, Hacker HW, Fuchs J: A complicated case of bilateral cystic nephroma in a 16-month-old boy. Pediatr Surg Int; 2005 Dec;21(12):1011-4
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  • [Title] A complicated case of bilateral cystic nephroma in a 16-month-old boy.
  • We describe a case of a progressive bilateral cystic nephroma (BCN) in a child undergoing a multistaged surgical procedure.
  • [MeSH-major] Kidney Diseases, Cystic / surgery. Kidney Neoplasms / surgery

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  • (PMID = 16273373.001).
  • [ISSN] 0179-0358
  • [Journal-full-title] Pediatric surgery international
  • [ISO-abbreviation] Pediatr. Surg. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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41. Zhou M, Kort E, Hoekstra P, Westphal M, Magi-Galluzzi C, Sercia L, Lane B, Rini B, Bukowski R, Teh BT: Adult cystic nephroma and mixed epithelial and stromal tumor of the kidney are the same disease entity: molecular and histologic evidence. Am J Surg Pathol; 2009 Jan;33(1):72-80
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult cystic nephroma and mixed epithelial and stromal tumor of the kidney are the same disease entity: molecular and histologic evidence.
  • Adult cystic nephroma (CN) and mixed epithelial and stromal tumor of the kidney (MEST) are considered as separate entities in the 2004 World Health Organization classification of renal neoplasms.
  • Histologic examination of 26 CN and 13 MEST focused on the cystic septal thickness, cyst-to-stroma ratio, stromal cellularity and composition, types of epithelial cells lining cysts and glands, and estrogen and progesterone receptors expression.
  • This study provides the most convincing molecular evidence that CN and MEST represent different parts of the morphologic spectrum of the same disease.
  • [MeSH-major] Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology. Neoplasms, Complex and Mixed / pathology. Neoplasms, Glandular and Epithelial / pathology

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  • [CommentIn] Am J Surg Pathol. 2010 Jan;34(1):126-7; author reply 127 [20035151.001]
  • (PMID = 18971776.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Receptors, Estrogen; 0 / Receptors, Progesterone
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42. Shaheen IS, Fitzpatrick M, Brownlee K, Bhuskute N, Elliott M, Powis M, Ahmad N, Tyerman K: Bilateral progressive cystic nephroma in a 9-month-old male infant requiring renal replacement therapy. Pediatr Nephrol; 2010 Sep;25(9):1755-8
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  • [Title] Bilateral progressive cystic nephroma in a 9-month-old male infant requiring renal replacement therapy.
  • We report the case of a 3-year-old boy who presented at 9 months of age with abdominal distension and was found to have a triad of bilateral cystic nephroma, pleuropulmonary blastoma (PPB) and juvenile intestinal polyps.
  • [MeSH-major] Kidney Neoplasms / therapy. Neoplasms, Cystic, Mucinous, and Serous / therapy. Renal Replacement Therapy

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  • (PMID = 20414683.001).
  • [ISSN] 1432-198X
  • [Journal-full-title] Pediatric nephrology (Berlin, Germany)
  • [ISO-abbreviation] Pediatr. Nephrol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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43. Hora M, Hes O, Michal M, Boudová L, Chudácek Z, Kreuzberg B, Klecka J: Extensively cystic renal neoplasms in adults (Bosniak classification II or III)--possible "common" histological diagnoses: multilocular cystic renal cell carcinoma, cystic nephroma, and mixed epithelial and stromal tumor of the kidney. Int Urol Nephrol; 2005;37(4):743-50
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Extensively cystic renal neoplasms in adults (Bosniak classification II or III)--possible "common" histological diagnoses: multilocular cystic renal cell carcinoma, cystic nephroma, and mixed epithelial and stromal tumor of the kidney.
  • OBJECTIVE(S): To give an algorithm for resolution of extensively cystic renal neoplasms, preoperatively classified in the Bosniak classification as a category II and III.
  • Extensively cystic tumours were found in 10 cases.
  • Extensively cystic tumours were defined as multicystic tumours without any solid nodules visible neither on CT, nor grossly in the specimen at operation (the Bosniak classification type II or III).
  • RESULTS: Seven multilocular cystic renal cell carcinomas, three mixed epithelial and stromal tumour of the kidney and one cystic nephroma were diagnosed on histology.
  • CONCLUSION(S): Extensively cystic renal tumours classified as the Bosniak type II or III correspond histologically to the entities mentioned above (multilocular cystic renal cell carcinoma, cystic nephroma, mixed epithelial and stromal tumour of the kidney).
  • In such cases, the nephron sparing surgery is indicated, whenever technically feasible, as almost all extensively cystic renal tumours have a good prognosis.

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  • (PMID = 16362592.001).
  • [ISSN] 0301-1623
  • [Journal-full-title] International urology and nephrology
  • [ISO-abbreviation] Int Urol Nephrol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Hungary
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44. Chu LC, Hruban RH, Horton KM, Fishman EK: Mixed epithelial and stromal tumor of the kidney: radiologic-pathologic correlation. Radiographics; 2010 Oct;30(6):1541-51
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Mixed epithelial and stromal tumor (MEST) of the kidney is a rare, typically benign lesion that occurs predominantly in perimenopausal women.
  • At computed tomography (CT), it typically manifests as a multiloculated cystic renal mass with a variable proportion of solid and cystic components and containing internal septa that demonstrate heterogeneous and delayed contrast material enhancement.
  • MEST may mimic a variety of benign and malignant renal lesions, such as adult cystic nephroma, complex renal cyst, and cystic renal cell carcinoma.

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  • [Copyright] © RSNA, 2010.
  • (PMID = 21071374.001).
  • [ISSN] 1527-1323
  • [Journal-full-title] Radiographics : a review publication of the Radiological Society of North America, Inc
  • [ISO-abbreviation] Radiographics
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
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45. Boman F, Hill DA, Williams GM, Chauvenet A, Fournet JC, Soglio DB, Messinger Y, Priest JR: Familial association of pleuropulmonary blastoma with cystic nephroma and other renal tumors: a report from the International Pleuropulmonary Blastoma Registry. J Pediatr; 2006 Dec;149(6):850-854
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Familial association of pleuropulmonary blastoma with cystic nephroma and other renal tumors: a report from the International Pleuropulmonary Blastoma Registry.
  • OBJECTIVE: To characterize the association of pleuropulmonary blastoma (PPB) with cystic nephroma (CN) and other renal tumors.
  • Two children with PPB and bilateral renal cystic tumors also had intussusceptions because of small bowel juvenile polyps.


46. 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.
  • It is a rare benign neoplasm of the kidney which has been reported under various names such as adult type mesoblastic nephroma or others.
  • We report a case of mixed epithelial and stromal tumor in a 47 yr old female patient presenting as a partly cystic and partly solid renal mass.
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Middle Aged. Nephroma, Mesoblastic / pathology

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  • [Cites] Pathol Res Pract. 2000;196(2):135-9 [10707372.001]
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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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47. Sukov WR, Cheville JC, Lager DJ, Lewin JR, Sebo TJ, Lewin M: Malignant mixed epithelial and stromal tumor of the kidney with rhabdoid features: report of a case including immunohistochemical, molecular genetic studies and comparison to morphologically similar renal tumors. Hum Pathol; 2007 Sep;38(9):1432-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Mixed epithelial stromal tumor of the kidney (MEST)/adult cystic nephroma (CN) is a lesion characterized by epithelial lined tubular or cystic structures interspersed within a variably prominent, distinctive spindle-cell stroma.
  • Although typically benign, cases with malignant features have been reported.
  • Histologically, the tumor displayed multiple tubules and variably sized cystic structures lined by benign epithelium with an intervening malignant-appearing spindle-cell stroma.

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  • (PMID = 17707262.001).
  • [ISSN] 0046-8177
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Comparative Study; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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48. Priest JR, Williams GM, Hill DA, Dehner LP, Jaffé A: Pulmonary cysts in early childhood and the risk of malignancy. Pediatr Pulmonol; 2009 Jan;44(1):14-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The earliest manifestation of PPB is a malignant lung cyst in young children, clinically and radiographically indistinguishable from benign congenital lung cysts.
  • Histopathologic examination differentiates cystic PPB from the benign cystic variants.
  • Surgical excision of cystic PPB (with or without chemotherapy) cures approximately 85-90% of children.
  • If not excised, cystic PPB evolves to cystic/solid or solid high-grade sarcoma (cure rate 45-60%) by age 2-6 years.
  • Numerous reports of "malignancy in a congenital lung cyst" are now understood as the characteristic progression of cystic PPB.
  • Detailed family history may reveal the hallmarks of PPB in the patient or young relatives: a unique constellation of diseases including lung cysts, cystic nephroma, childhood cancers, stromal sex-chord ovarian tumors, seminomas or dysgerminomas, intestinal polyps, thyroid hyperplasias, and hamartomas.
  • These diagnoses predict that a lung cyst is more likely PPB than a benign congenital cyst.

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  • [Copyright] Copyright 2008 Wiley-Liss, Inc.
  • [CommentIn] Pediatr Pulmonol. 2010 Jan;45(1):103; author reply 104 [19960525.001]
  • (PMID = 19061226.001).
  • [ISSN] 1099-0496
  • [Journal-full-title] Pediatric pulmonology
  • [ISO-abbreviation] Pediatr. Pulmonol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Number-of-references] 94
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49. Sibony M, Vieillefond A: [Non clear cell renal cell carcinoma. 2008 update in renal tumor pathology]. Ann Pathol; 2008 Oct;28(5):381-401
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The group of oncocytomas/chromophobe renal cell carcinomas can be considered as a spectrum from benign (oncocytoma) to malignant neoplasm (chromophobe renal cell carcinoma).
  • Angiomyolipoma is usually a benign mesenchymatous neoplasm, that can be sporadic or familial (tuberous sclerosis).
  • Renal epithelial and stromal tumors (REST) is a new concept gathering two benign mixed mesenchymal and epithelial tumors: cystic nephroma and mixed epithelial and stromal tumors (MEST).

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  • (PMID = 19068393.001).
  • [ISSN] 0242-6498
  • [Journal-full-title] Annales de pathologie
  • [ISO-abbreviation] Ann Pathol
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 84
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50. Nur S, Badr R, Sandoval C, Brudniki A, Yeh A: Syndromic presentation of a pleuropulmonary blastoma associated with congenital cystic adenomatoid malformation. A case report. J Pediatr Surg; 2007 Oct;42(10):1772-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Syndromic presentation of a pleuropulmonary blastoma associated with congenital cystic adenomatoid malformation. A case report.
  • Pleuropulmonary blastoma (PPB) is a rare malignant mesenchymal pediatric tumor with a well-recognized association with congenital cystic adenomatoid malformation (CCAM).
  • Recently, it has been described in a patient with CCAM, multiple jejunal polyps, and cystic nephroma.
  • [MeSH-major] Cystic Adenomatoid Malformation of Lung, Congenital / complications. Lung Neoplasms / pathology. Mesenchymoma / pathology. Peutz-Jeghers Syndrome / pathology. Respiration Disorders / etiology

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  • (PMID = 17923214.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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51. Sangoi AR, Higgins JP: Bilateral mixed epithelial stromal tumor in an end-stage renal disease patient: the first case report. Hum Pathol; 2008 Jan;39(1):142-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Although first intimated in the 1970s, mixed epithelial stromal tumor has been recognized as a diagnostic entity for less than 10 years, with an identity that has been challenged by overlap between other cystic renal neoplasms, most notably with cystic nephroma.
  • We describe the presentation and pertinent radiologic, histologic, and immunophenotypic findings of these neoplasms with a review of the current debate regarding mixed epithelial stromal tumor and cystic nephroma taxonomy.

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  • (PMID = 18070633.001).
  • [ISSN] 0046-8177
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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52. Bindhu J, Imtiaz A, Kumar RV, Thejaswini MD: Cystic variant of favorable-histology Wilms' tumor presenting with osteolytic metastasis to the ribs. J Postgrad Med; 2010 Jan-Mar;56(1):28-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cystic variant of favorable-histology Wilms' tumor presenting with osteolytic metastasis to the ribs.
  • Cystic neoplasms of the kidney presenting in childhood always present a therapeutic dilemma.
  • Low-risk renal tumors of childhood cover a wide spectrum: cystic nephroma, cystic partially differentiated nephroblastoma and cystic Wilms' tumor.
  • The present case presented such a therapeutic dilemma and was finally diagnosed as a cystic variant of favorable-histology Wilms' tumor with osteolytic metastasis to the ribs.

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  • (PMID = 20393247.001).
  • [ISSN] 0972-2823
  • [Journal-full-title] Journal of postgraduate medicine
  • [ISO-abbreviation] J Postgrad Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  • [Chemical-registry-number] 0 / Antineoplastic Agents
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53. Weibl P, Lutter I, Breza J, Pechan J, Blazko M, Gajdosova T, Pindak D: Cystic renal cell carcinoma--rare clinical finding. Radiographic variations of tumor/cyst appearance and further diagnostic work-up. Bratisl Lek Listy; 2006;107(3):96-100
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  • [Title] Cystic renal cell carcinoma--rare clinical finding. Radiographic variations of tumor/cyst appearance and further diagnostic work-up.
  • OBJECTIVES: To review the cases of cystic renal cell carcinoma and multilocular cystic nephroma, point out the radiographic variations and define further diagnostic work-up.
  • MATERIALS AND METHODS: Between 2003 and 2005 5 patients with suspected cystic renal cell carcinoma were treated surgically (1 pt underwent radical nephrectomy, 1 pt laparoscopic cyst decortication, 3 pts ablation), 2 patients with multilocular cystic nephroma underwent ultrasound guided biopsy.
  • RESULTS: Histopathologic examination confirmed cystic renal cell carcinoma (CRCC) T1aNOM0 Fuhrman grade 1 in 3 cases, T1bN0M0 Fuhrman grade 2 in one case.
  • Biopsy in 2 patients with multilocular cystic nephroma did not confirm the presence of malignant cells.
  • The mean tumor size was 4.2 cm (range 3.7 to 5.5) for CRCC and 4.7 cm (range 4 to 4.5 cm) for multilocular cystic nephroma.
  • Small cystic renal cell carcinomas up to 4 cm in diameter have usually favourable pathology and prognosis, which offers the minimally invasive nephron-sparing treatment options such as excision, ablation or partial nephrectomy (Fig. 9, Ref. 18).

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  • (PMID = 16796133.001).
  • [ISSN] 0006-9248
  • [Journal-full-title] Bratislavské lekárske listy
  • [ISO-abbreviation] Bratisl Lek Listy
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Slovakia
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54. Wootton-Gorges SL, Thomas KB, Harned RK, Wu SR, Stein-Wexler R, Strain JD: Giant cystic abdominal masses in children. Pediatr Radiol; 2005 Dec;35(12):1277-88
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Giant cystic abdominal masses in children.
  • In this pictorial essay the common and uncommon causes of large cystic and cyst-like abdominal masses in children are reviewed.
  • We discuss and illustrate the following: mesenchymal hamartoma, choledochal cyst, hydrops of the gallbladder, congenital splenic cyst, pancreatic pseudocyst, pancreatic cystadenoma, hydronephrosis, multicystic dysplastic kidney, multilocular cystic nephroma, adrenal hemorrhage, mesenteric and omental cysts, gastrointestinal duplication cyst, meconium pseudocyst, ovarian cysts and cystic neoplasms, hematocolpos, urachal cysts, appendiceal abscess, abdominal and sacrococcygeal teratoma, and CSF pseudocyst.

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  • (PMID = 16151789.001).
  • [ISSN] 0301-0449
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 29
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55. Agnihotri S, Jeebun N, Ramputty P: Multicystic nephroma: a rare entity. J Nephrol; 2009 May-Jun;22(3):411-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multicystic nephroma: a rare entity.
  • Multicystic nephroma is a rare renal pathology, which is characterized usually by a unilateral renal mass with multiple thin-walled cysts divided by septa.
  • We report the case of a boy aged 2 years, who was diagnosed in utero with an abdominal cystic lesion during routine antenatal ultrasonography examination.
  • The patient underwent a nephrectomy, and diagnosis of cystic nephroma was confirmed by histology.

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  • (PMID = 19557719.001).
  • [ISSN] 1121-8428
  • [Journal-full-title] Journal of nephrology
  • [ISO-abbreviation] J. Nephrol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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56. Cross SF, Arbuckle S, Priest JR, Marshall G, Charles A, Dalla Pozza L: Familial pleuropulmonary blastoma in Australia. Pediatr Blood Cancer; 2010 Dec 15;55(7):1417-9
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  • Each had a family history of childhood tumors which collectively included PPB, infant lung cyst, cystic nephroma, medullo-epithelioma and a Sertoli-Leydig ovarian tumor.

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  • (PMID = 20981696.001).
  • [ISSN] 1545-5017
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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57. Bisceglia M, Ragazzi M, Galliani CA, Lastilla G, Rosai J: TTF-1 expression in nephroblastoma. Am J Surg Pathol; 2009 Mar;33(3):454-61
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  • The unexpected observation of nuclear immunoreactivity for thyroid transcription factor-1 (TTF-1) associated with an apparent lack of nuclear immunoreactivity for Wilms tumor-1 protein (WT1) in the pulmonary metastasis of a morphologically typical case of nephroblastoma affecting a 6.5-year-old male prompted us to examine the expression of these 2 markers (and CD56) in a series of 48 nephroblastomas, 5 adult metanephric adenomas, and 1 pediatric cystic nephroma.
  • The single cystic nephroma was TTF-1-negative, WT1-negative, and CD56-positive.

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  • (PMID = 19011567.001).
  • [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 / Antigens, CD56; 0 / Biomarkers, Tumor; 0 / Nuclear Proteins; 0 / Transcription Factors; 0 / WT1 Proteins; 0 / thyroid nuclear factor 1
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58. Gupta R, Dhingra K, Singh S, Nigam S, Jain S: Multicystic nephroma: a case report. Acta Cytol; 2007 Jul-Aug;51(4):651-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multicystic nephroma: a case report.
  • BACKGROUND: Cystic nephroma is an uncommon pediatric renal neoplasm.
  • It needs to be differentiated from cystic partially differentiated nephroblastoma and from other renal neoplasms showing extensive cystic change.
  • CASE: A 7-month-old female with a left-sided abdominal lump was diagnosed as having cystic Wilms' tumor on computed tomography.
  • However, histopathologic examination showed it to be a multicystic nephroma.
  • CONCLUSION: This case highlights 1 extreme and unexpected cytologic appearance of cystic nephroma; it may result in misdiagnosis.

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  • (PMID = 17718146.001).
  • [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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59. Taskinen S, Lohi J, Kivisaari R, Fagerholm R, Rintala R, Taskinen M: Segmental cystic kidney tumours in children. Scand J Urol Nephrol; 2009;43(6):476-81
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Segmental cystic kidney tumours in children.
  • OBJECTIVE: Segmental cystic tumours in the kidney are extremely rare in children.
  • MATERIAL AND METHODS: The operative database from 1993 to 2008 of the Hospital for Children and Adolescents, University of Helsinki, was evaluated for segmental cystic renal tumours without any solid component.
  • All patients underwent kidney-preserving surgery with resection of the cystic tumour.
  • Two patients had neoplasias: one cystic nephroma and one cystic partially differentiated nephroblastoma.
  • Both of these patients had associated or predisposing disease (type I cystic pleuropulmonary blastoma of the lung and mulibrey nanism, respectively).
  • Two patients had a non-neoplastic tumour; localized cystic disease of the kidney and segmental adult type autosomal dominant polycystic kidney disease.
  • Neoplastic cystic tumours had a fibrous capsule in preoperative magnetic resonance imaging and also in operation, unlike non-neoplastic lesions.
  • CONCLUSIONS: Preoperative and perioperative diagnosis is difficult in cases of segmental cystic kidney tumours in a child.
  • [MeSH-major] Kidney / pathology. Kidney Diseases, Cystic / diagnosis. Kidney Diseases, Cystic / pathology

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  • (PMID = 19968582.001).
  • [ISSN] 1651-2065
  • [Journal-full-title] Scandinavian journal of urology and nephrology
  • [ISO-abbreviation] Scand. J. Urol. Nephrol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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60. Azoulay S, Vieillefond A, Paraf F, Pasquier D, Cussenot O, Callard P, Sibony M: Tubulocystic carcinoma of the kidney: a new entity among renal tumors. Virchows Arch; 2007 Nov;451(5):905-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Tubulocystic carcinoma is a distinctive kidney tumor, with noteworthy macroscopic and microscopic characteristics, which can be distinguished from other cystic kidney tumors, including cystic nephroma, multilocular cystic renal cell carcinoma and some solid tumors with extensive cystic changes.
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Humans. Immunohistochemistry. Kidney Diseases, Cystic / pathology. Male. Middle Aged

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  • (PMID = 17786473.001).
  • [ISSN] 0945-6317
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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61. Singh S, Gupta R, Nigam S, Khurana N, Aggarwal SK, Chaturvedi KU, Mandal AK: Clinico-pathological profile of 22 cases of cystic renal dysplasia. Indian J Pathol Microbiol; 2007 Jan;50(1):6-10
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  • [Title] Clinico-pathological profile of 22 cases of cystic renal dysplasia.
  • We studied 22 cases of cystic renal dysplasia diagnosed over a period often years to identify the spectrum of morphological changes in dysplastic kidney, with special emphasis on mesenchymal changes.
  • As cystic renal dysplasia is not a hereditary disease, it must be differentiated from polycystic kidney disease.
  • Other differential diagnoses are cystic nephroma and cystic partially differentiated nephroblastoma.
  • Histopathological examination is the final diagnostic tool since radiological features alone may not be sufficient to exclude other cystic renal lesions.

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  • (PMID = 17474245.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
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62. Moch H: [Cystic renal neoplasms. New entities and molecular findings]. Pathologe; 2010 Oct;31 Suppl 2:239-43
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Cystic renal neoplasms. New entities and molecular findings].
  • Established renal tumors with dominant cysts include cystic nephroma, mixed epithelial and stromal tumor, synovial sarcoma and multilocular cystic renal cancer (WHO classification 2004).
  • Multilocular cystic renal cell carcinoma is composed almost exclusively of cysts and is regarded as a specific subtype of clear cell renal cancer.

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  • (PMID = 20652265.001).
  • [ISSN] 1432-1963
  • [Journal-full-title] Der Pathologe
  • [ISO-abbreviation] Pathologe
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; 0 / TFE3 protein, human; EC 6.3.2.19 / VHL protein, human; EC 6.3.2.19 / Von Hippel-Lindau Tumor Suppressor Protein
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63. Sahni VA, Mortele KJ, Glickman J, Silverman SG: Mixed epithelial and stromal tumour of the kidney: imaging features. BJU Int; 2010 Apr;105(7):932-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Specific imaging features analysed included lesion size, location, enhancement and cystic composition.
  • RESULTS: All mixed epithelial and stromal tumours appeared as well-marginated, multi-septate cystic masses with a nodular component.
  • CONCLUSION: Mixed epithelial and stromal tumours of the kidney have a diverse radiographic appearance, indistinguishable from multilocular cystic nephroma and cystic renal cell carcinoma.

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  • (PMID = 19818075.001).
  • [ISSN] 1464-410X
  • [Journal-full-title] BJU international
  • [ISO-abbreviation] BJU Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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64. Tienari J, Lehtonen S, Lehtonen E: CD2-associated protein in human urogenital system and in adult kidney tumours. Virchows Arch; 2005 Apr;446(4):394-401
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  • The epithelium lining the cysts in multilocular cystic RCCs (n=3) and in cystic nephroma (n=1) was strongly positive.

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  • (PMID = 15785926.001).
  • [ISSN] 0945-6317
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Adaptor Proteins, Signal Transducing; 0 / Biomarkers, Tumor; 0 / CD2-associated protein; 0 / Cytoskeletal Proteins; 0 / Proteins
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65. Mai KT, Elkeilani A, Veinot JP: Mixed epithelial and stromal tumour (MEST) of the kidney: report of 14 cases with male and PEComatous variants and proposed histopathogenesis. Pathology; 2007 Apr;39(2):235-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • METHODS AND RESULTS: Fourteen MEST were originally diagnosed as cystic nephroma which represents an incidence of 1.6% of renal neoplasms in adults.
  • [MeSH-minor] Adult. Aged. Angiomyolipoma / pathology. Diagnosis, Differential. Female. Humans. Immunohistochemistry. Kidney Diseases, Cystic / pathology. Male. Middle Aged. Receptors, Estrogen / metabolism. Receptors, Progesterone / metabolism. Sex Factors

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  • (PMID = 17454754.001).
  • [ISSN] 0031-3025
  • [Journal-full-title] Pathology
  • [ISO-abbreviation] Pathology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Receptors, Estrogen; 0 / Receptors, Progesterone
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66. Iczkowski KA, Gapin TB, Wajsman Z: Small lymphocytic lymphoma involving an enlarging complex renal cyst. Arch Pathol Lab Med; 2005 Jan;129(1):111-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Computed tomographic scan disclosed diffuse mesenteric and retroperitoneal adenopathy consistent with chronic lymphocytic leukemia, as well as a 4.5-cm complex cystic right renal mass, which 17 months later enlarged to 6.2 cm.
  • The mass resembled multiloculated cystic nephroma.
  • [MeSH-major] Kidney Diseases, Cystic / complications. Kidney Neoplasms / complications. Leukemia, Lymphocytic, Chronic, B-Cell / complications

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  • (PMID = 15628890.001).
  • [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
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67. Tickoo SK, Gopalan A, Tu JJ, Harik LR, Al-Ahmadie HA, Fine SW, Olgac S, Reuter VE: Estrogen and progesterone-receptor-positive stroma as a non-tumorous proliferation in kidneys: a possible metaplastic response to obstruction. Mod Pathol; 2008 Jan;21(1):60-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The presence of estrogen and progesterone-receptor-positive stroma is well known in renal mixed epithelial and stromal tumor, cystic nephroma, and angiomyolipoma with epithelial cysts.
  • In six cases, the nephrectomies were performed for a non-functional kidney, and in three for tumors (one each of chromophobe, clear cell, and acquired cystic disease-associated renal cell carcinoma).
  • In one it was present at the periphery of an acquired cystic disease-associated renal cell carcinoma, as well as around non-tumorous cysts.

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  • (PMID = 17873894.001).
  • [ISSN] 0893-3952
  • [Journal-full-title] Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
  • [ISO-abbreviation] Mod. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Receptors, Estrogen; 0 / Receptors, Progesterone
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68. Bisceglia M, Galliani CA, Senger C, Stallone C, Sessa A: Renal cystic diseases: a review. Adv Anat Pathol; 2006 Jan;13(1):26-56
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Renal cystic diseases: a review.
  • This review aims to assist in the categorization of inherited, developmental, and acquired cystic disease of the kidney as well as to provide a pertinent, up-to-date bibliography.
  • The conditions included are autosomal-dominant polycystic kidney disease, autosomal-recessive polycystic kidney disease, unilateral renal cystic disease (localized cystic disease), renal simple cysts, multicystic dysplastic kidney, pluricystic kidney of the multiple malformation syndromes, juvenile nephronophthisis and medullary cystic disease, medullary sponge kidney, primary glomerulocystic kidney disease, and glomerulocystic kidney associated with several systemic disorders mainly of genetic or chromosomal etiology, cystic kidney in tuberous sclerosis, and in von Hippel-Lindau syndrome, cystic nephroma, cystic variant of congenital mesoblastic nephroma, mixed epithelial stromal tumor of the kidney, renal lymphangioma, pyelocalyceal cyst, peripylic cyst and perinephric pseudocyst, acquired renal cystic disease of long-term dialysis, and cystic renal cell carcinoma and sarcoma.
  • [MeSH-major] Kidney Diseases, Cystic / classification. Kidney Diseases, Cystic / pathology

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  • (PMID = 16462154.001).
  • [ISSN] 1072-4109
  • [Journal-full-title] Advances in anatomic pathology
  • [ISO-abbreviation] Adv Anat Pathol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 240
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69. Han XN, Peng LR, Liu GH, Wang J: [Multiphasic spiral CT scanning features in 100 patients with small renal cell carcinoma]. Zhonghua Zhong Liu Za Zhi; 2007 May;29(5):382-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Clear cell renal cell carcinoma exhibited rich blood supply and inhomogeneous density due to hemorrhage, necrosis or cystic degeneration.
  • Multilocular clear cell renal cell carcinoma presented as a multilocular cystic mass with thin wall and septa, instead of an expansile nodule.
  • CONCLUSION: Commonly encountered subtypes of the small renal cell carcinoma exhibit their own specific features in multiphasic spiral CT, which may be helpful in differential diagnosis, but each subtype should be differentiated from the renal oncocytoma, cystic nephroma, complex renal cyst, renal angiomyolipoma with minimal fat and renal infiltrating urothelial carcinoma.

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  • (PMID = 17892138.001).
  • [ISSN] 0253-3766
  • [Journal-full-title] Zhonghua zhong liu za zhi [Chinese journal of oncology]
  • [ISO-abbreviation] Zhonghua Zhong Liu Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
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70. Sanz Mayayo E, García Navas R, Rodríguez-Patrón Rodríguez R, Arias Fúnez F, Lennie Zuccarino A, Mayayo Dehesa T: [Ultrasonography for the study of small renal masses]. Arch Esp Urol; 2006 May;59(4):333-42
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We analyze its contribution to the differential diagnosis of the cystic pathology, to the definition of solid masses, to the detection and characterization of small size masses, and to the definition of the vascular patterns of various tumors.
  • RESULTS: Ultrasonography offers a diagnostic safety of 98% in cystic masses, being able to detect them from 0.5 cm diameter in favourable conditions.
  • The differential diagnosis of multiloculated masses, multivesicular hydatid cyst, multiloculated cystic nephroma, and multiloculated cystic carcinoma still poses great difficulty, the same way it happens with other radiological tests.

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  • (PMID = 16800131.001).
  • [ISSN] 0004-0614
  • [Journal-full-title] Archivos españoles de urología
  • [ISO-abbreviation] Arch. Esp. Urol.
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 41
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71. Sarin YK, Sengar M: Cystic nephroma. Indian Pediatr; 2005 Jan;42(1):84-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cystic nephroma.
  • [MeSH-major] Kidney Diseases, Cystic / diagnosis. Nephrectomy. Retroperitoneal Neoplasms / diagnosis

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  • (PMID = 15695874.001).
  • [ISSN] 0019-6061
  • [Journal-full-title] Indian pediatrics
  • [ISO-abbreviation] Indian Pediatr
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] India
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72. Bahílo Mateu MP, Budía Alba A, Boronat Tormo F, Jiménez-Cruz FJ: [Multilocular cystic nephroma]. Actas Urol Esp; 2010 Nov;34(10):921-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Multilocular cystic nephroma].
  • [Transliterated title] Nefroma multilocular quístico.

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  • (PMID = 21159301.001).
  • [ISSN] 1699-7980
  • [Journal-full-title] Actas urologicas españolas
  • [ISO-abbreviation] Actas Urol Esp
  • [Language] spa
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Spain
  • [Chemical-registry-number] Clear-cell metastatic renal cell carcinoma
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73. Gursev, Sarda D, Joshi P, Ahmad A, Kothari P: Cystic nephroma in childhood. Afr J Paediatr Surg; 2009 Jan-Jun;6(1):69-70
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cystic nephroma in childhood.
  • [MeSH-major] Kidney Neoplasms / pathology. Kidney Neoplasms / surgery. Nephroma, Mesoblastic / pathology. Nephroma, Mesoblastic / surgery

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  • (PMID = 19661676.001).
  • [ISSN] 0974-5998
  • [Journal-full-title] African journal of paediatric surgery : AJPS
  • [ISO-abbreviation] Afr J Paediatr Surg
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Nigeria
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74. Ben Slama S, Farah F, Goucha A, Ismail O, Ben Slama MR, Zermani R, Ayed M, El Mezni F, Ben Jilani S: [Multilocular cystic nephroma in adults]. Tunis Med; 2008 Jun;86(6):623-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Multilocular cystic nephroma in adults].

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  • (PMID = 19216471.001).
  • [ISSN] 0041-4131
  • [Journal-full-title] La Tunisie médicale
  • [ISO-abbreviation] Tunis Med
  • [Language] fre
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Tunisia
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75. Patnayak R, Reddy MK, Subramanian S, Ravisankar G: Multilocular cystic nephroma of the kidney. Indian J Pathol Microbiol; 2008 Oct-Dec;51(4):563-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multilocular cystic nephroma of the kidney.
  • [MeSH-major] Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology

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  • (PMID = 19008600.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] India
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76. Silver IM, Boag AH, Soboleski DA: Best cases from the AFIP: Multilocular cystic renal tumor: cystic nephroma. Radiographics; 2008 Jul-Aug;28(4):1221-5; discussion 1225-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Best cases from the AFIP: Multilocular cystic renal tumor: cystic nephroma.
  • [MeSH-major] Kidney Diseases, Cystic / radiography. Kidney Neoplasms / radiography. Nephroma, Mesoblastic / radiography

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  • (PMID = 18635639.001).
  • [ISSN] 1527-1323
  • [Journal-full-title] Radiographics : a review publication of the Radiological Society of North America, Inc
  • [ISO-abbreviation] Radiographics
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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77. Abrol N, Gupta N, Arava S, Ray R: Cystic nephroma masquerading as hydatid cyst of the kidney. Indian J Pathol Microbiol; 2010 Oct-Dec;53(4):877-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cystic nephroma masquerading as hydatid cyst of the kidney.
  • [MeSH-major] Echinococcosis / pathology. Kidney / pathology. Kidney Neoplasms / diagnosis. Kidney Neoplasms / pathology. Nephroma, Mesoblastic / diagnosis. Nephroma, Mesoblastic / pathology

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  • (PMID = 21045463.001).
  • [ISSN] 0974-5130
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] India
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78. Stamatiou KN, Sofras F: Multilocular cystic nephroma and multicystic clear cell carcinoma: two faces of the Roman god Janus? Int J Surg Pathol; 2009 Apr;17(2):170-1
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multilocular cystic nephroma and multicystic clear cell carcinoma: two faces of the Roman god Janus?
  • [MeSH-major] Carcinoma, Renal Cell / pathology. Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology. Precancerous Conditions / pathology

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  • (PMID = 18611925.001).
  • [ISSN] 1066-8969
  • [Journal-full-title] International journal of surgical pathology
  • [ISO-abbreviation] Int. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] United States
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79. Mukhopadhyay S, Valente AL, de la Roza G: Corpora albicantia-like bodies in cystic nephroma: yet another similarity to mixed epithelial stromal tumor of kidney. Int J Surg Pathol; 2005 Apr;13(2):233
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Corpora albicantia-like bodies in cystic nephroma: yet another similarity to mixed epithelial stromal tumor of kidney.
  • [MeSH-major] Kidney Neoplasms / pathology. Nephroma, Mesoblastic / pathology

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  • [CommentOn] Int J Surg Pathol. 2004 Jul;12(3):298 [15306946.001]
  • (PMID = 15864392.001).
  • [ISSN] 1066-8969
  • [Journal-full-title] International journal of surgical pathology
  • [ISO-abbreviation] Int. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Comment; Letter
  • [Publication-country] United States
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80. Blanco Parra MA, Suárez Peñaranda JM, Pérez Fentes DA, Puñal Pereira A: [Cystic nephroma. Case report and overview of recent literature]. Actas Urol Esp; 2010 Mar;34(3):301-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Cystic nephroma. Case report and overview of recent literature].
  • [Transliterated title] Nefroma multilocular quístico. Nuevo caso y revisión de la literatura médica reciente.
  • [MeSH-major] Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology

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  • (PMID = 20416255.001).
  • [ISSN] 1699-7980
  • [Journal-full-title] Actas urologicas españolas
  • [ISO-abbreviation] Actas Urol Esp
  • [Language] spa
  • [Publication-type] Case Reports; Letter; Review
  • [Publication-country] Spain
  • [Number-of-references] 8
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81. Michal M, Hes O, Kuroda N, Kazakov DV, Petersson F, Hora M, Daum O: What is a cystic nephroma? Am J Surg Pathol; 2010 Jan;34(1):126-7; author reply 127
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] What is a cystic nephroma?
  • [MeSH-major] Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology. Neoplasms, Complex and Mixed / pathology. Nephroma, Mesoblastic / pathology

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  • [CommentOn] Am J Surg Pathol. 2009 Jan;33(1):72-80 [18971776.001]
  • (PMID = 20035151.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Comment; Letter
  • [Publication-country] United States
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82. Al-Abbadi MA, Grignon DJ: Cystic nephroma: a fine needle aspiration diagnostic pitfall. Acta Cytol; 2010 Mar-Apr;54(2):233-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cystic nephroma: a fine needle aspiration diagnostic pitfall.
  • [MeSH-major] Kidney Diseases, Cystic / diagnosis. Nephroma, Mesoblastic / diagnosis

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  • [CommentOn] Acta Cytol. 2008 Jan-Feb;52(1):91-3 [18323282.001]
  • (PMID = 20391987.001).
  • [ISSN] 0001-5547
  • [Journal-full-title] Acta cytologica
  • [ISO-abbreviation] Acta Cytol.
  • [Language] eng
  • [Publication-type] Case Reports; Comment; Letter
  • [Publication-country] United States
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83. Cheng L, Yang YP, Zhang SB, Zhu YL, Zhang JM: [Cystic nephroma and mixed epithelial stromal tumor of kidney: evolution of terminology, controversies, pathologic features and differential diagnosis]. Zhonghua Bing Li Xue Za Zhi; 2008 Oct;37(10):707-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Cystic nephroma and mixed epithelial stromal tumor of kidney: evolution of terminology, controversies, pathologic features and differential diagnosis].
  • [MeSH-major] Kidney Neoplasms / diagnosis. Kidney Neoplasms / pathology. Nephroma, Mesoblastic / diagnosis. Nephroma, Mesoblastic / pathology

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  • (PMID = 19094493.001).
  • [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] Lectures
  • [Publication-country] China
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84. Algaba F: Editorial comment on: cystic nephroma and mixed epithelial and stromal tumour of the kidney: opposite ends of the spectrum of the same entity? Eur Urol; 2008 Dec;54(6):1245-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Editorial comment on: cystic nephroma and mixed epithelial and stromal tumour of the kidney: opposite ends of the spectrum of the same entity?

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  • [CommentOn] Eur Urol. 2008 Dec;54(6):1237-46 [18006141.001]
  • (PMID = 18006142.001).
  • [ISSN] 0302-2838
  • [Journal-full-title] European urology
  • [ISO-abbreviation] Eur. Urol.
  • [Language] eng
  • [Publication-type] Comment; Editorial
  • [Publication-country] Switzerland
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85. Hora M, Michal M, Hes O: Re: Rodolfo Montironi, Roberta Mazzuccelli, Antonio Lopez-Beltran, et al. Cystic nephroma and mixed epithelial and stromal tumour of the kidney: opposite ends of the spectrum of the same entity? Eur Urol 2008;54:1237-46. Eur Urol; 2009 Jul;56(1):e3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Re: Rodolfo Montironi, Roberta Mazzuccelli, Antonio Lopez-Beltran, et al. Cystic nephroma and mixed epithelial and stromal tumour of the kidney: opposite ends of the spectrum of the same entity? Eur Urol 2008;54:1237-46.
  • [MeSH-major] Carcinoma / pathology. Kidney Diseases, Cystic / pathology. Kidney Neoplasms / pathology. Kidney Neoplasms / surgery

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  • [CommentOn] Eur Urol. 2008 Dec;54(6):1237-46 [18006141.001]
  • (PMID = 19167806.001).
  • [ISSN] 1873-7560
  • [Journal-full-title] European urology
  • [ISO-abbreviation] Eur. Urol.
  • [Language] eng
  • [Publication-type] Comment; Letter; Research Support, Non-U.S. Gov't
  • [Publication-country] Switzerland
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