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Hindawi Publishing Corporation Case Reports in Urology Volume 2013, Article ID 789039, 3 pages http://dx.doi.org/10.1155/2013/789039 Case Report A Rare Metastasis to the Bladder Rishi A. Modh, Katherine A. Corbyons, and Lawrence L. Yeung Department of Urology, University of Florida, 1600 SW Archer Road, P.O. Box 100247, Gainesville, FL 32610, USA Correspondence should be addressed to Rishi A. Modh; [email protected]fl.edu Received 21 January 2013; Accepted 13 February 2013 Academic Editors: M. Gallucci, S. Gudjonsson, and F. M. Solivetti Copyright © 2013 Rishi A. Modh et al. is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Primary bladder cancer is the fiſth most common malignancy but secondary malignancies of the bladder are rare. Distinguishing primary adenocarcinomas of the bladder from secondary adenocarcinomas is difficult and relies on immunohistochemical staining. Prostate, colorectal, breast, and lung all can produce metastatic adenocarcinomas to the bladder. Further management of the malignancy varies depending on the source, thus making proper diagnosis critical. We present only the fiſth documented case of metastatic adenocarcinoma of the lung to bladder and performed a review of the literature. 1. Introduction Bladder cancer is the fiſth most commonly diagnosed malig- nancy. An estimated 73 510 individuals will be diagnosed with bladder cancer in 2012. Most bladder cancers are diagnosed at an early stage (non-muscle-invasive), but up to 25% present at more advanced, invasive stages [1]. e majority of primary cancers of the bladder are pure urothelial while squamous cell, small cell, and glandular or adenocarcinoma account for a small percentage. Urothelial carcinomas can have mixed histologic variants including squamous, glandular, sarcomatoid, micropapillary, small cell, and plasmacytoid. Rare histologic subtypes of primary bladder cancers include small cell, sarcomatoid, and pheochromocytoma [2]. Secondary cancers to the bladder are also rare. ey are oſten categorized as direct extension of tumor from surrounding organs, metastasis, and lymphoma/leukemias. e most common sites of spread to the bladder are prostate, colorectal, or cervical sites. Breast, lung, and skin primaries are less common sources. Diagnosis and eventual treatment rely on the patient’s history, the surgical specimen, and immunohistochemical staining. Primary adenocarcinomas of the bladder account for approximately 2% of bladder tumors and usually involve the embryological remnant of the urachus [3, 4]. Differentiating primary adenocarcinomas of the bladder and metastatic adenocarcinoma lesions can be difficult and relies heavily on pathologic evaluation. We present an unusual case of metastatic adenocarcinoma of the lung to the bladder. 2. Case Report An 81-year-old female with a 50-pack-year history of smoking was initially referred to the neurosurgical clinic for leſt carpal tunnel syndrome. She underwent carpal tunnel release but her pain progressed to her leſt shoulder. A chest X- ray revealed a new atypical density in the leſt upper lobe measuring 5 × 2.5 cm. A followup CT and PET scan demon- strated two lung masses suspicious for malignancy and three small nodules in the right lung that were suspicious for metastatic disease. MRI examination revealed a Pancoast tumor extending from the leſt lung apex to the brachial plexus and into the vertebral bodies and neural foramina from C6 through T1. She eventually underwent a CT-guided biopsy that was immunoreactive for TTF-1 and CK7, suggesting adenocarcinoma of the lung as the primary source. Six months aſter completion of chemotherapy, she devel- oped three days of worsening abdominal pain and a deteri- oration in her renal function. A CT scan revealed bilateral hydronephrosis and thickening within the leſt lateral and posterior bladder (Figures 1 and 2). She eventually underwent cystoscopy, transurethral resection of the concerning area, and ureteral stent placement. e bladder mucosa appeared normal on exam with extrinsic compression into the lumen of the bladder. Urine cytology was negative for malignancy and she never developed gross hematuria. e final pathology revealed adenocarcinoma involving the muscularis propria with benign urothelial mucosa with

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Page 1: Case Report A Rare Metastasis to the Bladderdownloads.hindawi.com/journals/criu/2013/789039.pdfProstate, colorectal, breast, and lung all can produce metastatic adenocarcinomas to

Hindawi Publishing CorporationCase Reports in UrologyVolume 2013, Article ID 789039, 3 pageshttp://dx.doi.org/10.1155/2013/789039

Case ReportA Rare Metastasis to the Bladder

Rishi A. Modh, Katherine A. Corbyons, and Lawrence L. Yeung

Department of Urology, University of Florida, 1600 SW Archer Road, P.O. Box 100247, Gainesville, FL 32610, USA

Correspondence should be addressed to Rishi A. Modh; [email protected]

Received 21 January 2013; Accepted 13 February 2013

Academic Editors: M. Gallucci, S. Gudjonsson, and F. M. Solivetti

Copyright © 2013 Rishi A. Modh et al. This is an open access article distributed under the Creative Commons Attribution License,which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Primary bladder cancer is the fifth most common malignancy but secondary malignancies of the bladder are rare. Distinguishingprimary adenocarcinomas of the bladder from secondary adenocarcinomas is difficult and relies on immunohistochemical staining.Prostate, colorectal, breast, and lung all can produce metastatic adenocarcinomas to the bladder. Further management of themalignancy varies depending on the source, thus making proper diagnosis critical. We present only the fifth documented caseof metastatic adenocarcinoma of the lung to bladder and performed a review of the literature.

1. Introduction

Bladder cancer is the fifth most commonly diagnosed malig-nancy. An estimated 73 510 individuals will be diagnosedwithbladder cancer in 2012.Most bladder cancers are diagnosed atan early stage (non-muscle-invasive), but up to 25% presentatmore advanced, invasive stages [1].Themajority of primarycancers of the bladder are pure urothelial while squamouscell, small cell, and glandular or adenocarcinoma accountfor a small percentage. Urothelial carcinomas can havemixed histologic variants including squamous, glandular,sarcomatoid, micropapillary, small cell, and plasmacytoid.Rare histologic subtypes of primary bladder cancers includesmall cell, sarcomatoid, and pheochromocytoma [2].

Secondary cancers to the bladder are also rare. Theyare often categorized as direct extension of tumor fromsurrounding organs, metastasis, and lymphoma/leukemias.The most common sites of spread to the bladder are prostate,colorectal, or cervical sites. Breast, lung, and skin primariesare less common sources. Diagnosis and eventual treatmentrely on the patient’s history, the surgical specimen, andimmunohistochemical staining. Primary adenocarcinomasof the bladder account for approximately 2% of bladdertumors and usually involve the embryological remnant ofthe urachus [3, 4]. Differentiating primary adenocarcinomasof the bladder and metastatic adenocarcinoma lesions canbe difficult and relies heavily on pathologic evaluation. Wepresent an unusual case of metastatic adenocarcinoma of thelung to the bladder.

2. Case Report

An81-year-old femalewith a 50-pack-year history of smokingwas initially referred to the neurosurgical clinic for leftcarpal tunnel syndrome. She underwent carpal tunnel releasebut her pain progressed to her left shoulder. A chest X-ray revealed a new atypical density in the left upper lobemeasuring 5 × 2.5 cm. A followup CT and PET scan demon-strated two lung masses suspicious for malignancy and threesmall nodules in the right lung that were suspicious formetastatic disease. MRI examination revealed a Pancoasttumor extending from the left lung apex to the brachial plexusand into the vertebral bodies and neural foramina from C6through T1. She eventually underwent a CT-guided biopsythat was immunoreactive for TTF-1 and CK7, suggestingadenocarcinoma of the lung as the primary source.

Six months after completion of chemotherapy, she devel-oped three days of worsening abdominal pain and a deteri-oration in her renal function. A CT scan revealed bilateralhydronephrosis and thickening within the left lateral andposterior bladder (Figures 1 and 2). She eventually underwentcystoscopy, transurethral resection of the concerning area,and ureteral stent placement. The bladder mucosa appearednormal on exam with extrinsic compression into the lumenof the bladder. Urine cytology was negative for malignancyand she never developed gross hematuria.

The final pathology revealed adenocarcinoma involvingthe muscularis propria with benign urothelial mucosa with

Page 2: Case Report A Rare Metastasis to the Bladderdownloads.hindawi.com/journals/criu/2013/789039.pdfProstate, colorectal, breast, and lung all can produce metastatic adenocarcinomas to

2 Case Reports in Urology

Figure 1: Abdominal and Pelvic CT showing a thickened posteriorand left lateral wall.

Figure 2: Abdominal andPelvic CT showing bilateral hydronephro-sis.

reactive changes. Immunophenotypically, this wasmost com-patible with a lung primary. The tumor was immunoreactivefor CK7 and Napsin A, partially immunoreactive for p53,and nonreactive for CK20, TTF-1, Surfactant B, and estrogenreceptor (ER).

3. Discussion

In order to differentiate metastatic adenocarcinoma of lungfrom primary adenocarcinoma of the bladder, immuno-histochemical studies are required. The original diagnosisof adenocarcinoma of the lung was dependent on TTF-1positivity. However, in our case, TTF-1 was negative whileNapsin A and CK7 were positive. A previous case reportwas able to distinguish a patient’s new primary adeno-carcinoma of bladder with previously diagnosed primaryadenocarcinoma of the lung. In this case, the patient’s bladderspecimen was negative for Napsin A and TTF-1 but waspositive for more bladder-specific stains including GATA3and S100P [5]. Napsin A has been shown to be a reliablemarker to distinguish adenocarcinoma of the lung fromprimary adenocarcinoma of the bladder. It is more sensitiveand specific for primary adenocarcinoma of the lung thanTTF-1 [6]. These immunohistochemical stains, along withthe pathologic specimen predominately involving the outerlayers of the bladder muscle while sparing the mucosa,

provide strong evidence of metastatic spread of a primaryadenocarcinoma of the lung.

To our knowledge, only four prior cases of primaryadenocarcinoma of the lung with metastatic spread to thebladder have been identified in the literature. The firstdescribed casewas a single patient in Spain, where the authorsdescribed an intact urothelium at endoscopic resection withthe tumor affecting the lamina propria and containing thesame immunologic characteristics of the patient’s previousadenocarcinoma of the lung [7].

The next case was seen in a review of 282 secondarylesions of the bladder. In this review, secondary lesions repre-sented on 2.3% of all bladder tumors and the majority werefrom colorectal or genitourinary primaries. Eight of thesewere identified as primary lung and only one was deemed asadenocarcinoma of lung [8].

In Japan, a case of adenocarcinoma of the lungwithmeta-stasis was made after the bladder biopsy specimen was posi-tive for TTF-1, and CK7 and negative for CK20. Interestinglythis case also noted normal appearing bladder mucosa andprimary involvement of the bladder muscularis [9].

Finally, a group in France described a patient with ade-nocarcinoma of the lung who presented with hematuria. Thebiopsy specimen again was positive for CK-7 and TTF-1without any expression of CK-20 [10].

While rare, metastatic adenocarcinoma of the lung isimportant to distinguish from primary adenocarcinomasof the bladder, especially when cystoscopic examinationof the bladder does not correlate with diagnostic imagingfindings. This diagnosis relies on pathologic evaluation andimmunohistochemical staining. Distinguishing between thetwo entities is critical to propermanagement of the respectivemalignancy.

References

[1] N. Howlader, A. M. Noone, M. Krapcho et al., Eds., SEERCancer Statistics Review, 1975–2009 (Vintage 2009 Populations),National Cancer Institute, Bethesda, Md, USA.

[2] M. J.Wasco, S. Daignault, Y. Zhang et al., “Urothelial carcinomawith divergent histologic differentiation (Mixed HistologicFeatures) predicts the presence of locally advanced bladdercancer when detected at transurethral resection,” Urology, vol.70, no. 1, pp. 69–74, 2007.

[3] V. Velcheti and R. Govindan, “Metastatic cancer involvingbladder: a review,”The Canadian Journal of Urology, vol. 14, no.1, pp. 3443–3448, 2007.

[4] M. J.Wasco, S. Daignault, Y. Zhang et al., “Urothelial carcinomawith divergent histologic differentiation (Mixed HistologicFeatures) predicts the presence of locally advanced bladdercancer when detected at transurethral resection,” Urology, vol.70, no. 1, pp. 69–74, 2007.

[5] M. R. Raspollini, C. E. Comin, A. Crisci, and M. Chilosi,“The use of placental S100 (S100P), CATA3 and napsin a inthe differential diagnosis of primary adenocarcinoma of thebladder and bladder metastasis from adenocarcinoma of thelung,” Pathologica, vol. 102, no. 1, pp. 33–35, 2010.

[6] B. M. Turner, P. T. Cagle, I. M. Sainz et al., “A new markerfor lung adenocarcinoma, is complementary andmore sensitiveand specific than thyroid transcription factor 1 in the differential

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Case Reports in Urology 3

diagnosis of primary pulmonary carcinoma: evaluation of 1674cases by tissue microarray,” Archives of Pathology & LaboratoryMedicine, vol. 136, no. 2, pp. 163–171, 2012.

[7] A. Martın-Marquina Aspiunza, F. Dıez-Caballero Alonso, F. I.Rodrıguez-Rubio Cortadellas et al., “Bladder metastasis of lungadenocarcinoma,” Actas Urologicas Espanolas, vol. 21, no. 4, pp.406–408, 1997.

[8] A. W. Bates and S. I. Baithun, “Secondary neoplasms of thebladder are histological mimics of nontransitional cell primarytumours: clinicopathological and histological features of 282cases,” Histopathology, vol. 36, no. 1, pp. 32–40, 2000.

[9] H. Shirakawa, N. Kozakai, M. Sawafuji, H. Sugiura, and S. Hara,“Urinary bladder metastasis originating from lung adenocarci-noma: a case definitively diagnosed by immunohistochemistry,”Journal of Urology, vol. 9, no. 2, pp. 530–532, 2012.

[10] L. Sakhri, B. Mennecier, D. Jacqmin et al., “Atypical metastaticsite of lung adenocarcinoma,” Revue de Pneumologie Clinique,vol. 67, no. 6, pp. 375–379, 2011.

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