<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJU</journal-id><journal-title-group><journal-title>Open Journal of Urology</journal-title></journal-title-group><issn pub-type="epub">2160-5440</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oju.2016.611028</article-id><article-id pub-id-type="publisher-id">OJU-72070</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  A Case Report: Metastasis of Clear Cell Ovarian Cancer in Morrison’s Pouch as Differential Diagnosis to Exophytic Kidney Tumor
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Stine</surname><given-names>Lohmann</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Anna</surname><given-names>Krarup Keller</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Urology, Aarhus University Hospital, Aarhus, Denmark</addr-line></aff><aff id="aff1"><addr-line>Department of Urology, Regional Hospital West, Holstebro, Denmark</addr-line></aff><pub-date pub-type="epub"><day>17</day><month>11</month><year>2016</year></pub-date><volume>06</volume><issue>11</issue><fpage>173</fpage><lpage>177</lpage><history><date date-type="received"><day>September</day>	<month>10,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>November</month>	<year>14,</year>	</date><date date-type="accepted"><day>November</day>	<month>17,</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  A 62-year-old woman with a history of curatively treated mucinous ovarian cancer, presented with dyspnea, anorexia and right-upper-quadrant pain at consultation with her general practitioner. A CT scan revealed several lymph node metastases in lungs and abdomen as well as a tumor in Morrison’s pouch and biopsy revealed renal cell carcinoma. Therefore, she was referred to Department of Urology. The multidisciplinary team could not immediately reject that there could be an exophytic tumor in the right kidney but discrepancy between histology and imaging, led to several biopsies including laparoscopic procedure. Re-examination of the primary ovarian cancer showed that one percent was classified as clear cell carcinoma. The final diagnose was metastatic clear cell ovarian carcinoma. The patient was terminal and suffered of cachexia and pleural effusion. The patient deceased four months after first consultation.
 
</p></abstract><kwd-group><kwd>Ovarian Cancer</kwd><kwd> Clear Cell Adenocarcinoma</kwd><kwd> Renal Cell Cancer</kwd><kwd> Immunohistochemistry</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Incidence of new ovarian cancer in Europe in 2012 is estimated to 65,538 [<xref ref-type="bibr" rid="scirp.72070-ref1">1</xref>] and for kidney cancer 43,435 (women) [<xref ref-type="bibr" rid="scirp.72070-ref2">2</xref>] . There is variation in the incidence rate across the continent with a higher incidence of ovary cancer in northern European countries, with Denmark having the second highest in the world [<xref ref-type="bibr" rid="scirp.72070-ref3">3</xref>] .</p><p>Ovarian cancer often has no symptoms at the early stages, so the disease is generally advanced when it is diagnosed and therefore it has a poor prognosis [<xref ref-type="bibr" rid="scirp.72070-ref4">4</xref>] . Symptoms can be abdominal pain, urinary symptoms, constipation and abdominal swelling with weight loss. Furthermore, these patients have a lower rate of survival relative to many other cancer disease sites. An estimated 70% - 75% of patients will experience a recurrence [<xref ref-type="bibr" rid="scirp.72070-ref5">5</xref>] with a median time to recurrence of 18 - 24 months [<xref ref-type="bibr" rid="scirp.72070-ref6">6</xref>] .</p><p>The most common type of kidney cancer is clear cell renal carcinoma [<xref ref-type="bibr" rid="scirp.72070-ref7">7</xref>] which accounts for 75% - 90% of all cases. Clear cell adenocarcinoma of the ovary is less common, about 3% - 10% [<xref ref-type="bibr" rid="scirp.72070-ref8">8</xref>] . It classifies as a so-called Type 1, like mucinous carcinomas, which are slow growing tumors and often diagnosed in lowest stadium I, despite of the frequently large size. Clear cell carcinoma of the ovary is per definition highly malignant and has a worse prognosis compared to other cell types [<xref ref-type="bibr" rid="scirp.72070-ref9">9</xref>] .</p><p>Here we report on a patient with metastatic clear cell ovarian cancer years after intended curative treatment.</p></sec><sec id="s2"><title>2. Patient Presentation</title><p>A 62 years old woman, with a history of ovarian cancer, was referred from the local Diagnostic Center with renal cell carcinoma, histological verified.</p><p>The patient was diagnosed with left-sided ovary cancer and classified as 1A mucinous adenocarcinoma in 2012. At this time serum Ca-125 was 17. The patient underwent curative surgery with hysterectomy, bilateral salpingo-oophorectomy and omentectomy. The removed lymph nodes were without metastases and therefore no adjuvant chemotherapy was given. Subsequent controls were without relapse the following years.</p><p>The patient had in spring 2016 consulted her general practitioner (GP) because of dyspnea the last two months, newly anorexia and weight loss and upper right abdominal pain with radiation to the back. This was just four months after the last control at the department of gynaecology. The GP ordered x-ray of the lungs and ultrasound of abdomen. Because of a tumor suspect process, the radiologist added a CT thorax and abdomen and found several suspicious lymph nodes in both lungs and abdomen. More importantly, the scan detected a large tumor in Morrison’s pouch (see <xref ref-type="fig" rid="fig1">Figure 1</xref>). Serum CA-125 was normal. Several biopsies failed and did not deliver sufficient material for histological analysis and a CT-guided biopsy revealed renal cell carcinoma.</p><p>Diagnosing renal cell carcinoma was a bit surprising, but the multidisciplinary team could not immediately reject, that there could be an exophytic tumor in the right kidney. Needing better histological material led to a laparoscopic excision of some of the tumor in Morrison’s pouch. This time it showed adenocarcinoma but could not be differentiated furthermore.</p><p>At this time, the patient was hospitalized at Department of Urology because of progressive dyspnea and significant edema of the lower limbs. A CT scan of the lungs showed pleural effusion and the patient underwent bilateral tube thoracostomy, which improved respiration. Cytology demonstrated a few days later malignant cells. Additionally, CA-125 had risen to 223 during the four months that had passed since first consultation at the patients GP.</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> CT scan of right kidney and tumor in Morrison’s pouch</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-5000361x2.png"/></fig><p>Pathological diagnosis was uncertain and material was therefore sent to Aarhus University Hospital for a second opinion. Here, the pathologists went through the patients previous tissue samples; the ovarian cancer from 2012 consisted of 1% clear cell ovarian carcinoma. Followed by immunohistochemically staining of the present tissue from Morrison’s pouch confirmed that the latter was metastasis from the clear cell ovarian cancer.</p><p>The patient never received any additional treatment. The patient stayed hospitalized several weeks because of the difficult management of the pleural effusion. Furthermore, there was provided prophylactic antibiotics to avoid pneumonia, although blood sample showed normal infection level. Furthermore, the patient suffered of severe cachexia and transferred to hospice and died three weeks later. The final pathological diagnosis came but just one day ante mortem.</p></sec><sec id="s3"><title>3. Discussion</title><p>This patient had difficult diagnostic challenges for several reasons. First, the tumor had close relation to the right kidney. From the CT scan the kidney appeared to be well defined and without irregularities but as mentioned it is difficult to contradict histological analysis. Second, the morphology for clear cell renal cell carcinoma is not unique and makes it challenging to distinguish between other clear cell variants.</p><p>By immunohistochemically staining, renal cell carcinoma is positive for CD10 and renal cell carcinoma monoclonal antibody (RCCma), while being negative for Ca-125. Nevertheless it has been suggested, that PAX2 and PAX8 are more stable markers. Unfortunately, they are both also positive regarding clear cell from the ovary [<xref ref-type="bibr" rid="scirp.72070-ref10">10</xref>] . This patient was amongst others negative for estrogen, Ca-125, CD10 and PAX8.</p><p>Renal cell carcinoma metastasize locally to vena renalis et cava and perirenal as well as hematogenous dissemination to liver, lungs and bone [<xref ref-type="bibr" rid="scirp.72070-ref7">7</xref>] . By hematogenous dissemination, the cells go through several steps of both intra- and extravasation before it can metastasize to other organs. The biology of ovarian carcinoma differs from that of hematogenously metastasizing tumors because ovarian cancer cells primarily disseminate within the peritoneal cavity-the peritoneum and omentum, but occasionally there can be lymphogenous involvement-primarily paraaortic [<xref ref-type="bibr" rid="scirp.72070-ref11">11</xref>] .</p><p>Regarding survival of type 1 ovarian cancer, mucinous cancers have a better prognosis compared to clear cell [<xref ref-type="bibr" rid="scirp.72070-ref3">3</xref>] . Never the less it has not been possible to reduce mortality in clear cell stadium IA-IB by giving adjuvant chemotherapy and it is therefore not recommended in Denmark [<xref ref-type="bibr" rid="scirp.72070-ref3">3</xref>] . Overall, diagnosed ovarian cancer often reveals an advanced stage with metastasis and is therefore associated with high mortality. Dissemination is believed to involve less steps, because only a single cell or a group of cancer cells will have to release from the primary tumor. The transportation of cells is passive mechanism by movement of the peritoneal fluid, which gives multiple possibilities of sites for metastasis [<xref ref-type="bibr" rid="scirp.72070-ref11">11</xref>] .</p><p>Immunohistochemical staining are our reliable way to make histological diagnoses, but in this case, the patient’s primary histology was reassessed for clarification.</p></sec><sec id="s4"><title>4. Conclusion</title><p>In conclusion, metastasis of previous cancer is of great importance in differential diagnosis. One should consider it a likely diagnosis even though primary cancer was of lower TNM and completed curative treatment.</p></sec><sec id="s5"><title>Cite this paper</title><p>Lohmann, S. and Keller, A.K. (2016) A Case Report: Metastasis of Clear Cell Ovarian Cancer in Morrison’s Pouch as Differential Diagnosis to Exo- phytic Kidney Tumor. Open Journal of Uro- logy, 6, 173-177. http://dx.doi.org/10.4236/oju.2016.611028</p></sec></body><back><ref-list><title>References</title><ref id="scirp.72070-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ovary, EUCAN Cancer Factsheets.  
http://eco.iarc.fr/eucan/CancerOne.aspx?Cancer=27&amp;Gender=2#block-map-f</mixed-citation></ref><ref id="scirp.72070-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Kidney, EUCAN Cancer Factsheets.  
http://eco.iarc.fr/eucan/CancerOne.aspx?Cancer=27&amp;Gender=2</mixed-citation></ref><ref id="scirp.72070-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">DGCG (2016) Clinical Guideline for Visitation, Diagnostik, Treatment and Control of Epithelian Ovary-, Tuba- and Primary Peritoneal Cancer including Borderline Tumors. Udgave.</mixed-citation></ref><ref id="scirp.72070-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Jacobs, I.J., Menon, U., Ryan, A., Gentry-Maharaj, A., Burnell, M., Kalsi, J.K., et al. (2016) Ovarian Cancer Screening and Mortality in the UK. Lancet, 387, 945-956. 
https:/doi.org/10.1016/S0140-6736(15)01224-6</mixed-citation></ref><ref id="scirp.72070-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Ozga, M., Aghajanian, C., Myers-Virtue, S., McDonnell, G., Jhanwar, S., Hichenberg, S., et al. (2015) A Systematic Review of Ovarian Cancer and Fear of Recurrence. Palliative &amp; Supportive Care, 13, 1771-1780. https:/doi.org/10.1017/S1478951515000127</mixed-citation></ref><ref id="scirp.72070-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Ushijima, K. (2010) Treatment for Recurrent Ovarian Cancer—At First Relapse. Journal of Oncology, 2010, Article ID: 497429. https:/doi.org/10.1155/2010/497429</mixed-citation></ref><ref id="scirp.72070-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Ljungberg, B., Cowan, N.C., Hanbury, D.C., et al. (2010) EAU Guidelines on Renal Cell Carcinoma: The 2010 Update. European Urology, 58, 398-406. 
https:/doi.org/10.1016/j.eururo.2010.06.032</mixed-citation></ref><ref id="scirp.72070-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Sugiyama, T., Kamura, T., Kigawa, J., Terakawa, N., Kikuchi, Y., Kita, T., Suzuki, M., Sato, I. and Taguchi, K. (2000) Clinical Characteristics of Clear Cell Carcinoma. A Distinct Histologic Type with Poor Prognosis and Resistance to Platinum Based. Cancer, 88, 2584-2589. 
https:/doi.org/10.1002/1097-0142(20000601)88:11&lt;2584::AID-CNCR22&gt;3.0.CO;2-5</mixed-citation></ref><ref id="scirp.72070-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Heintz, A.P., Odicino, F., Maisonneuve, P., et al. (2006) FIGO 26th Annual Report on the Results of Treatment in Gynecological Cancer. International Journal of Gynecology &amp; Obstetrics, 95, S161-S192. https:/doi.org/10.1016/S0020-7292(06)60033-7</mixed-citation></ref><ref id="scirp.72070-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Mentrikoski, M.J., Wendroth, S.M. and Wick, M.R. (2014) Immunohistochemical Distinction of Renal Cell Carcinoma from Other Carcinomas with Clear-Cell Histomorphology: Utility of CD10 and CA-125 in Addition to PAX-2, PAX-8, RCCma, and Adipophilin. Applied Immunohistochemistry &amp; Molecular Morphology, 22, 635-641. 
https:/doi.org/10.1097/PAI.0000000000000004</mixed-citation></ref><ref id="scirp.72070-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Lengyel, E. (2010) Ovarian Cancer Development and Metastasis. American Journal of Pathology, 177, 1053-1064. https:/doi.org/10.2353/ajpath.2010.100105</mixed-citation></ref></ref-list></back></article>