We report a patient who presented with a urothelial carcinoma recurrence developed nine years after radical cystoprostatectomy, related to Muir-Torre syndrome

Anass Anaye

Bernard Chevaux

Edgardo Pezzetta

Floryn Cherbanyk

Jean-Joseph Boillat

Marc Prod’homme

Case Reports in Urology

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Urothelial Carcinoma Recurrence in an Ileal Neobladder Nine Years after Primary Surgery with Muir-Torre Syndrome

We report a patient who presented with a urothelial carcinoma recurrence developed nine years after radical cystoprostatectomy, related to Muir-Torre syndrome.</jats:p

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Case ReportUrothelial Carcinoma Recurrence in an Ileal Neobladder NineYears after Primary Surgery with Muir-Torre SyndromeFloryn Cherbanyk,1 Marc Prod’homme,1 Edgardo Pezzetta,1Bernard Chevaux,2 Anass Anaye,3 and Jean-Joseph Boillat11Department of Surgery and Urology, Riviera-Chablais Hospital, 1820 Montreux, Switzerland2Department of Oncology, Riviera-Chablais Hospital, 1800 Vevey, Switzerland3Department of Radiology, Riviera-Chablais Hospital, 1820 Montreux, SwitzerlandCorrespondence should be addressed to Floryn Cherbanyk; floryn.cherbanyk@hopitalrivierachablais.chReceived 18 January 2016; Accepted 15 March 2016Academic Editor: Michele GallucciCopyright © 2016 Floryn Cherbanyk et al. This is an open access article distributed under the Creative Commons AttributionLicense, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properlycited.We report a patient who presented with a urothelial carcinoma recurrence developed nine years after radical cystoprostatectomy,related to Muir-Torre syndrome.1. IntroductionIt is well known that most of urothelial carcinomas arepapillary and multifocal and can recur after endoscopicresection. More than 70% of patients develop one or morerecurrence after transurethral resection (TUR) of a primarynoninvasive bladder tumor [1]. In urinary diversion usingisolated gut segment, secondary malignancy as adenocarci-nomas resulting of the irritation of the intestinal mucosa bythe contact with urine is not uncommon, which has beenrarely reported and is a secondary malignancy as urothelialcarcinoma.2. Case PresentationWe present a patient with a urothelial carcinoma recurrencedeveloped nine years after primary surgery.In November 2004, a 66-year-old man had been diag-nosed with a grade II to III urothelial carcinoma becauseof the finding of a unilateral hydronephrosis due to astenosis by a tumor in the left ureter. His laboratory findingswere within normal limits and thoracoabdominal computedtomography did not show evidence of metastatic disease. Aradical cystoprostatectomy with W-shaped ileal neobladderwas performed. The urothelial carcinoma grade III waslocated in the area of the opening of left ureter. There wasalso an in situ carcinoma in the same area and a spreadout in the perivesical tissue. No cancer was detected in theprostatic urethra.TheTNMclassificationwas pT3a pN1 (1/13)cM0, G3, L1, and stage IV. After the surgery, the patientunderwent adjuvant chemotherapy by 3 courses of cisplatinand gemcitabine.In 2006, he underwent a right enlarged hemicolectomybecause of an invasive adenocarcinoma. In 2010, a Muir-Torre syndrome was discovered after a biopsy of sebaceouscysts. The genetic analyses revealed a MSH2 gene mutation(c.293 296dup (p.Val100X) heterozygous duplication). Then,a subtotal colectomy for a local recurrence of the colicadenocarcinoma was performed.Seven years later in 2012, the patient reported haema-turia. A cystoscopic examination with TUR biopsy of theneobladder was performed, showing a malpighian urothelialmetaplasia.In 2014, actually nine years after the ileal neobladdersurgery, he presented with haematuria again. Preliminaryblood results were within normal limits, apart from anaemiaand chronic kidney failure (creatinine clearance 40mL/min).A native abdominal computed tomography was performedand showed a tissular thickening on the anterior and left partsof the neobladder, dimensions 14 × 8mm (Figure 1).Hindawi Publishing CorporationCase Reports in UrologyVolume 2016, Article ID 4762514, 5 pageshttp://dx.doi.org/10.1155/2016/47625142 Case Reports in UrologyFigure 1: Abdominal CT-scan: lesion of the anterior wall of the neobladder.Figure 2: Pelvic US pictures.The radiological assessment was completed by ultra-sonography with intravenous injection of sulphur hexaflu-oride (SonoVue) contrast agent (Figure 2). It showedenhancement of the mass during arterial and portal phases,with a wash-out in late venous phase.The cystoscopic view identified a local tumor, anteriorand on the left part of the neobladder. We performed a TURcomplete resection of this lesion.The histologic analysis revealed a high grade papillaryurothelial carcinoma with a malpighian differentiation. Thistumor invaded the muscularis propria of the ileal neobladder(Figure 3).According to a multidisciplinary oncologic meeting, weproposed to the patient neoadjuvant chemotherapy followedby another TUR or a partial resection of the neobladder.Nevertheless, after discharge from the hospital, he presentedwith a seizure. A cerebral magnetic resonance imaging(Figure 4) revealed a right frontal cerebral mass, suspectedas a metastatic lesion, confirmed by the biopsy-excisionperformed by craniotomy in the Neurosurgery Department.A postoperative cerebral MRI revealed a residual tumor.Therefore, a stereotaxic radiotherapy of the residual tumorand resection cavity was performed. The following cerebralMRI did not show any sign of residual tumor.Then, the patient began chemotherapy with carboplatinand gemcitabine, for the recurrence of the neobladderurothelial carcinoma. The chemotherapy was stopped afterthe first course because of the occurrence of a central bilateralpulmonary embolism.After that a cystoscopic examination was proposed tohim (Figure 5), showing a necrotic tumor of the anteriorwall of the neobladder, without infiltration of the openingof ureters. An anterior neobladder resection was performedimmediately (Figure 6). The final histopathologic exami-nation revealed the same high grade papillary urothelialcarcinoma with malpighian differentiation, and the surgicaloncological margins were free of tumor.On the conclusion of multidisciplinary oncologic meet-ing, it was proposed to the patient to perform a clinicalfollow-up, urine cytology, and an abdominal CT-scan afterthree months.3. DiscussionWe report the case of a patient with a high grade urothelialcarcinoma in an ileal neobladder nine years after radicalcystoprostatectomy.Secondary malignancy occurrence is well described inthe literature, regarding ureterosigmoidostomy, cystoplasty,and intestinal conduit. The most likely presentation is ade-nocarcinoma [7]. Some cases of secondary adenocarcinomadeveloping in a replaced bowel segment of urinary diversionshave been reported. Secondary adenocarcinoma developed20 years after surgery in about 0.5% of those in whom anileal segment was used [8]. In our knowledge, only 6 cases,including ours, are published in the literature [2–6] (Table 1).Some studies demonstrated that urothelial carcinomas haveCase Reports in Urology 3Figure 3: Histologic cross sections showed a high grade papillary urothelial carcinoma with muscularis propria invasion.Figure 4: Cerebral MRI: right frontal lesion.Figure 5: Preoperative cystoscopic views; we can note the necrotic aspect of the tumor on the anterior wall.the ability to seed and implant, even onnonurothelial surfaces[1].The Muir-Torre syndrome is a rare condition, withapproximately 200 cases reported [9]. It is an autosomal dom-inant inherited cancer susceptibility syndrome considered tobe a subset of the Lynch syndrome, also known as hereditarynonpolyposis colorectal cancer (HNPCC) syndrome [10],observed with a frequency range from 1% to 9% of HNPCCpatients [11]. Its diagnosis requires one or more criteriaas colorectal adenocarcinomas associated with sebaceousadenomas and/or carcinomas and genitourinary cancers.And it is confirmed by genetic analysis: the determinationof the primary DNA sequence of MMR genes (MLH1,MLH2, and MSH6). Molecular genetic studies have reportedmicrosatellite instability in the majority of samples fromsebaceous and internal tumors [9–11]. According to Grignon4 Case Reports in Urology(a) (b)Figure 6: Intraoperative view (a) and resection specimen (b).Table 1: Cases of carcinoma recurrence in an ileal neobladder.Investigator Age (years) Sex Recurrence (years) HistologyMoore et al. [2] 62 Male 1 Papillary urothelial carcinomaIde et al. [3] 73 Male 11 Urothelial carcinoma in situMoeen [4] 59 Female 1.5 High grade invasive transitional cell carcinomaSa´nchez et al. [5] Unknown Unknown Unknown UnknownBarba Abad et al. [6] 71 Male 8 High grade transitional cell carcinomaBarba Abad et al. [6] 57 Male 2 Urothelial carcinomaPresent case 66 Male 9 Papillary urothelial carcinomaet al., gastrointestinal tract tumors are the most frequentvisceral malignancies, and urinary tract carcinomas countfor 10% of the cases [12]. In this case, the patient presentedwith sebaceous cysts, gastrointestinal cancers, and urologicneoplasia. The Muir-Torre syndrome may have a causalrole in the development of the ileal neobladder carcinomarecurrence.4. ConclusionIn summary, urinary diversions using isolated gut segmentsbear risk of malignancy. In long-term follow-up not onlyadenomas and adenocarcinomas but transitional cell andpapillary urothelial carcinomas may develop in the neoblad-der. Recurrence in the neobladder should be considered inpatients with haematuria who underwent radical cystectomyandorthotopic ileal neobladder.No guidelines exist regardingthe management of urothelial carcinoma recurrence. So,these patients need an expert multidisciplinary team deci-sion.Competing InterestsThe authors declare no competing interests.References[1] M. Herawi, J. T. Leppert, G. V. Thomas, J. B. De Kernion,and J. I. Epstein, “Implants of noninvasive papillary urothelialcarcinoma in peritoneum and ileocolonic neobladder: supportfor ‘seed and soil’ hypothesis of bladder recurrence,” Urology,vol. 67, no. 4, pp. 746–750, 2006.[2] C. D. Moore, K. A. Iczkowski, K. M. Blue, and C. B. Algood,“Urothelial carcinoma recurrence in ileal orthotopic neoblad-der: urethrectomy and creation of ileal conduit,” Urology, vol.69, no. 1, pp. 184.e11–184.e13, 2007.[3] H. Ide, E. Kikuchi, K. Shinoda, M. Mukai, and M. Murai,“Carcinoma in situ developing in an ileal neobladder,” Urology,vol. 69, no. 3, pp. 576.e9–576.e11, 2007.[4] A.Moeen, “Recurrence of isolated transitional cell carcinoma inan orthotopic ileal neobladder: a case report,”African Journal ofUrology, vol. 21, no. 4, pp. 214–216, 2015.[5] Z.D. Sa´nchez, F. J. Lo´pez, G. T. Arocena, P. G. Sanz, B. J. Zudaire,and P. J. Ber´ıan, “Recurrent urothelial tumor in orthotopicneobladder,” Actas Urologicas Espanolas, vol. 25, no. 8, pp. 600–602, 2001.[6] J. F. Barba Abad, E. Tolosa Eizaguirre, A. Rinco´n Mayans, and J.Berian Polo, “Tumor relapse in orthotopic bladder replacement.A report of two cases and literature review,” Actas UrologicasEspanolas, vol. 34, no. 3, pp. 295–297, 2010.Case Reports in Urology 5[7] O. Cakmak, H. Tarhan, O. Celik, U. Kucuk, and Y. O. Ilbey,“Transitional cell carcinoma in orthotopic ileal neobladder,”Case Reports in Urology, vol. 2014, Article ID 218615, 3 pages,2014.[8] J. Hadzˇi-Djokic´, T. Pejcˇic´, V. Andrejevic´, and L. Djurasˇic´,“Transitional cell carcinoma in orthotopic ileal neobladder 12years after radical cystectomy,” Vojnosanitetski Pregled, vol. 70,no. 11, pp. 1062–1064, 2013.[9] F. Bhaijee and A. S. Brown, “Muir-Torre syndrome,” Archives ofPathology& LaboratoryMedicine, vol. 138, no. 12, pp. 1685–1689,2014.[10] G. L. Baiocchi, E. Chiocchi, W. Vermi et al., “The Muir-Torresyndrome: a typical case of misdiagnosis and consequent wors-ened prognosis,” International Journal of Colorectal Disease, vol.30, no. 3, pp. 431–432, 2015.[11] J. Sˇvec, L. Schwarzova´, B. Janosˇ´ıkova´ et al., “Synchronous gastricand sebaceous cancers, a rare manifestation of MLH1-relatedMuir-Torre syndrome,” International Journal of Clinical andExperimental Pathology, vol. 7, no. 8, pp. 5196–5202, 2014.[12] D. J. Grignon, D. T. Shum, andO. Bruckschwaiger, “Transitionalcell carcinoma in the Muir-Torre syndrome,” The Journal ofUrology, vol. 138, no. 2, pp. 406–408, 1987.Submit your manuscripts athttp://www.hindawi.comStem CellsInternationalHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014MEDIATORSINFLAMMATIONofHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Behavioural NeurologyEndocrinologyInternational Journal ofHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Disease MarkersHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014BioMed Research InternationalOncologyJournal ofHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Oxidative Medicine and Cellular LongevityHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014PPAR ResearchThe Scientific World JournalHindawi Publishing Corporation http://www.hindawi.com Volume 2014Immunology ResearchHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Journal ofObesityJournal ofHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014 Computational and  Mathematical Methods in MedicineOphthalmologyJournal ofHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Diabetes ResearchJournal ofHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Research and TreatmentAIDSHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Gastroenterology Research and PracticeHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014Parkinson’s DiseaseEvidence-Based Complementary and Alternative MedicineVolume 2014Hindawi Publishing Corporationhttp://www.hindawi.com

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Urothelial Carcinoma Recurrence in an Ileal Neobladder Nine Years after Primary Surgery with Muir-Torre Syndrome

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