<?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">OJPathology</journal-id><journal-title-group><journal-title>Open Journal of Pathology</journal-title></journal-title-group><issn pub-type="epub">2164-6775</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojpathology.2019.91001</article-id><article-id pub-id-type="publisher-id">OJPathology-89179</article-id><article-categories><subj-group subj-group-type="heading"><subject>Case Report</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 of Struma Ovarii Diagnosed by Cytology during Laparoscopic Surgery
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kenji</surname><given-names>Niwa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Motoki</surname><given-names>Takenaka</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tsuneo</surname><given-names>Ishihara</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>Sakae</surname><given-names>Mori</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Keigo</surname><given-names>Kuwabara</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Saki</surname><given-names>Murase</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yoshio</surname><given-names>Yamaguchi</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Takuji</surname><given-names>Tanaka</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Obstetrics &amp;amp; Gynecology, Gifu University School of Medicine, Gifu City, Japan</addr-line></aff><aff id="aff4"><addr-line>Department of Diagnostic Pathology &amp;amp; Research Center of Diagnostic Pathology, Gifu Municipal Hospital, Gifu City, Japan</addr-line></aff><aff id="aff3"><addr-line>Section of Laboratory Medicine, Gujo City Hospital, Gujo City, Japan</addr-line></aff><aff id="aff1"><addr-line>Department of Obstetrics &amp;amp; Gynecology, Gujo City Hospital, Gujo City, Japan</addr-line></aff><pub-date pub-type="epub"><day>17</day><month>12</month><year>2018</year></pub-date><volume>09</volume><issue>01</issue><fpage>1</fpage><lpage>9</lpage><history><date date-type="received"><day>16,</day>	<month>October</month>	<year>2018</year></date><date date-type="rev-recd"><day>14,</day>	<month>December</month>	<year>2018</year>	</date><date date-type="accepted"><day>17,</day>	<month>December</month>	<year>2018</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>
 
 
  We report a case of pure struma ovarii tumor diagnosed by cytology during laparoscopic surgery. The patient was a 34-year-old Japanese woman, gravida 1, para 1, who had the left adnexal mass, and was pre-operatively diagnosed as left ovarian endometriotic cyst or mature cystic teratoma by magnetic resonance imaging findings. She underwent laparoscopy, and the content of the left ovarian cystic tumor was found to be yellow gelatinous material, suggesting mature cystic teratoma. The imprint cytology of the tumor showed benign glandular pattern, suggesting struma ovarii. Histopathological findings led us to the diagnosis of pure struma ovarii with positive reactions for thyroglobulin and thyroid transcription factor-1. No metastases or disseminated lesions were detected. The patient has no recurrent signs 7 months after the operation.
 
</p></abstract><kwd-group><kwd>Struma Ovarii</kwd><kwd> Cytology</kwd><kwd> Immunocytochemistry</kwd><kwd> Immunohistochemistry</kwd><kwd> Thyroglobulin</kwd><kwd> Thyroid Transcription Factor-1</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Struma ovarii is a rare type of ovarian tumor that has been reported to represent 0.5% - 1.0% of all ovarian tumors [<xref ref-type="bibr" rid="scirp.89179-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref3">3</xref>] . This tumor is the most common type of monodermal teratoma and comprises approximate 3.0% of all ovarian teratomas [<xref ref-type="bibr" rid="scirp.89179-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref5">5</xref>] . It is defined as histologically characterized by the presence of thyroid-like glands at least 50%. Malignant transformation of the struma ovarii, which is associated with BRAF mutations and RET/PTC rearrangements [<xref ref-type="bibr" rid="scirp.89179-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref7">7</xref>] , as seen in papillary thyroid carcinoma of the eutopic thyroid, rarely occurs and its rate is reported to vary, ranging from 5% - 10% [<xref ref-type="bibr" rid="scirp.89179-ref8">8</xref>] . Struma ovarii is predominantly found in women between the ages of 40 and 60 years [<xref ref-type="bibr" rid="scirp.89179-ref9">9</xref>] . While magnetic resonance imaging (MRI) analysis has been reported to be useful for the differential diagnosis [<xref ref-type="bibr" rid="scirp.89179-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref12">12</xref>] , the preoperative differential diagnosis between the struma ovarii and other malignant tumor is difficult due to the morphological similarities. In fact, only a few reports concerning cytological diagnosis of struma ovarii have been reported [<xref ref-type="bibr" rid="scirp.89179-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref14">14</xref>] , although immunocytochemistry might be a valuable tool for accurate diagnosis of the struma ovarii [<xref ref-type="bibr" rid="scirp.89179-ref14">14</xref>] . We present here a rare case of struma ovarii in a 34-year-old woman, and the imprint cytology during the laparoscopic surgery was useful for the diagnosis of the neoplasm. Immunocytochemical and immunohistochemical examinations of thyroglobulin were useful to confirm the above diagnosis.</p></sec><sec id="s2"><title>2. Case Report</title><p>A 34-year-old Japanese woman, gravida 1 para 1 with normal menstruation cycle, was referred to the Department of Obstetrics &amp; Gynecology, Gujo City Hospital, because of the left adnexal mass and secondary infertility introduced from a fertility clinic. Her sociodemographic and clinical characteristic of the patient was summarized in <xref ref-type="table" rid="table1">Table 1</xref>. Her medical history included her left ovarian cystectomy under a laparoscope at 32-year-old in other hospital in other prefecture. However, the patient and her family did not know the detailed information. Other diseases including thyroid tumor were not reported. Hyperthyroidism could not be detected. Magnetic resonance imaging (MRI) in our hospital revealed the left ovarian tumor containing cystic and solid parts, measuring 6.8 &#215; 5.2 &#215; 7.0 cm. The cystic part showed variable signal intensity on the T2-weighed MRI scan (<xref ref-type="fig" rid="fig1">Figure 1</xref>(A)) and slightly high on T1-weighted (<xref ref-type="fig" rid="fig1">Figure 1</xref>(B)), suggesting the content being bleeding or gelatinous (highly viscous) and colloidal material. MRI examination did not detect enlarged lymph nodes, ascites and disseminated lesions in the peritoneum. Pelvic ultrasonography (USG) showed right polycystic ovary (<xref ref-type="fig" rid="fig2">Figure 2</xref>(A)) and left ovarian cystic tumor with papillary protrusions (<xref ref-type="fig" rid="fig2">Figure 2</xref>(B)) before operation. Clinical laboratory data, including tumor markers (CA125, 7.2 U/ml; CA19-9, 8.6 U/ml) showed within normal limitations. Based on the above findings, our working diagnosis was left ovarian endometriotic cyst or mature cystic teratoma.</p><p>Under the working diagnosis, the patient underwent laparoscopy one month after her first visit. She received laparoscopic left oophorectomy (<xref ref-type="fig" rid="fig3">Figure 3</xref>) and the tumor dropped into the ENDOPUCH&#174;(Ethicon, TX) without rupture. Her right ovarian drilling was also performed for trigger ovulation in this patient with polycystic ovary syndrome, suggested by the pelvic USG before surgery (<xref ref-type="fig" rid="fig2">Figure 2</xref>(A)). Electrocautery or a laser is used to destroy parts of the ovaries. The content of the cystic tumor was yellowish gelatinous fluid with approximate 150 ml, suggesting a mature cystic teratoma. There was no peritoneal fluid (ascites). On the imprint cytology of the tumor, the tumor cells showed glandular pattern. The tumor was thus suggested to be struma ovarii arising from a mature cystic teratoma (<xref ref-type="fig" rid="fig4">Figure 4</xref>(A)), and immunocytochemistry performed after the operation revealed that the tumor cells were positive for thyroglobulin (<xref ref-type="fig" rid="fig4">Figure 4</xref>(B)). The patient made uneventful recovery, and was discharged on the post-operative third day. Pelvic USG revealed that the number of right ovarian follicles decreased (<xref ref-type="fig" rid="fig2">Figure 2</xref>(C)) and left ovarian tumor disappeared in her left adnexal lesion (<xref ref-type="fig" rid="fig2">Figure 2</xref>(D)).</p><p>The left ovarian mass having cystic and solid parts (<xref ref-type="fig" rid="fig5">Figure 5</xref>) was fixed in 4% buffered formalin, routinely processed, and embedded in paraffin for histological and immunohistochemical examinations. After which 3 - 4 μm-thick sections were stained with hematoxylin and eosin (H &amp; E) for pathological diagnosis. In addition, immunohistochemistry using DAKO monoclonal antibodies, such as thyroglobulin (1:200 dilution, DAKO), thyroid transcription factor (TTF)-1 (1:200 dilution), inhibin (1:50 dilution) and calretinin (1:2000 dilution) was performed.</p><p>Histopathologically, the tumor consisted of normo- and macro-follicular thyroid tissue (<xref ref-type="fig" rid="fig6">Figure 6</xref>(A) and <xref ref-type="fig" rid="fig6">Figure 6</xref>(B)). Other components derived from germ layers except for thyroid tissue were also found. No atypical and/or immature cells were also recognized. Immunohistochemistry showed that glandular cells were positive for thyroglobulin (<xref ref-type="fig" rid="fig6">Figure 6</xref>(C)) and TTF-1 (<xref ref-type="fig" rid="fig6">Figure 6</xref>(D)), while they were negative for inhibing nor calretinin. Our final diagnosis was a pure stroma ovarii in the left ovary. The patient has no recurrent signs 7 months after the operation.</p></sec><sec id="s3"><title>3. Discussion</title><p>In the present case, the imprint cytology and immunecytochemical and immunohistochemical examinations for thyroglobulin and TTF-1 were useful for the diagnosis of the pure struma ovarii, as reported by Wei et al. [<xref ref-type="bibr" rid="scirp.89179-ref15">15</xref>] . Although the detailed pathological information on her ovarian cystectomy, which was done before two years ago, could not be known and the possibility of the mature cystic teratoma exists. Our case was diagnosed as pure struma ovarii at the operation. Only a few cases concerning cytology of struma ovarii have been reported [<xref ref-type="bibr" rid="scirp.89179-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref14">14</xref>] : their cytologic findings included the presence of typically colloid with mosaic pattern, follicles, follicular cells alone and/or sheets of follicular cells [<xref ref-type="bibr" rid="scirp.89179-ref14">14</xref>] . However, these findings are rare [<xref ref-type="bibr" rid="scirp.89179-ref14">14</xref>] , as found in our case. On the other hand, immunocytochemistry was reported to be valuable tool for accurate diagnosis for the struma ovarii [<xref ref-type="bibr" rid="scirp.89179-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref14">14</xref>] .</p><p>Most cases of struma ovarii were asymptomatic, as is the present case [<xref ref-type="bibr" rid="scirp.89179-ref3">3</xref>] . When there is struma ovarii larger than normal thyroid, the patient rarely has hyperthyroidism: thyroid hyperfunction is noted in 5% - 8% of cases [<xref ref-type="bibr" rid="scirp.89179-ref1">1</xref>] . Struma ovarii is defined as histologically characterized by the presence of thyroid-like glands at least 50%, whereas pure struma ovarii has been reported in half number of all struma ovarii [<xref ref-type="bibr" rid="scirp.89179-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref2">2</xref>] . Struma ovarii is predominantly found in women between the ages of 40 and 60 years [<xref ref-type="bibr" rid="scirp.89179-ref9">9</xref>] . The patient was 34 year-old and younger than predominant age distribution (<xref ref-type="table" rid="table1">Table 1</xref>).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Sociodemographic and clinical characteristics of struma ovarii</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Struma ovarii</th><th align="center" valign="middle" >Present case</th></tr></thead><tr><td align="center" valign="middle" >Definition</td><td align="center" valign="middle" >-A mature teratoma composed either exclusively or predominantly of thyroid tissue</td><td align="center" valign="middle" >-Only thyroid tissue is present in the lt. ovarian tumor</td></tr><tr><td align="center" valign="middle" >Epidemiology</td><td align="center" valign="middle"  colspan="2"  >-The most common type of monodermal teratoma</td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >-Reproductive years (mainly 40 - 60 years old)</td><td align="center" valign="middle" >-34 years old</td></tr><tr><td align="center" valign="middle" >Clinical manifestations</td><td align="center" valign="middle" >-Usually present with pain and/or a pelvic mass -Ascites (up to 1/3 of patients) -Rarely hyperthyroidism</td><td align="center" valign="middle" >-Secondary infertility -Polycystic ovary syndrome (rt ovary) -No ascites and hyperthyroidism</td></tr><tr><td align="center" valign="middle" >Macroscopic findings (Tumor size)</td><td align="center" valign="middle" >-Usually unilateral and solid (&lt;10 cm)</td><td align="center" valign="middle" >-Lt. ovary occupied by cystic and solid tumor tissues (7 cm)</td></tr><tr><td align="center" valign="middle" >Serum CA125 level</td><td align="center" valign="middle" >-High level of CA125 is suggestive of malignancy</td><td align="center" valign="middle" >-Within normal limits (7.2 U/ml)</td></tr><tr><td align="center" valign="middle" >Histopathology</td><td align="center" valign="middle" >-Mature thyroid tissue is present predominantly (over 50%) in mature ovarian teratoma</td><td align="center" valign="middle" >-Thyroid tissue is present exclusively in lt. ovarian cystic tumor with papillary projection</td></tr><tr><td align="center" valign="middle" >Malignant transformation</td><td align="center" valign="middle" >-About 5% -Mostly papillary carcinoma with BRAF mutations and RET/PTC rearrangements</td><td align="center" valign="middle" >-None</td></tr><tr><td align="center" valign="middle" >Prognosis &amp; follow-up time</td><td align="center" valign="middle" >-Most cases of typical struma ovarii are benign. -The outcome of histologically and biologically malignant thyroid type tumors in struma is favourable</td><td align="center" valign="middle" >-Well, 7 months after the operation</td></tr></tbody></table></table-wrap><p>Before operation, MRI findings are reported to be useful for the differential diagnosis for the struma ovarii [<xref ref-type="bibr" rid="scirp.89179-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref12">12</xref>] . MRI findings show multilocular cysts with solid components of variable signal density within the loculi. Signal intensity is slightly high on T1-weighted image and very low on T2-weighted image. These findings may suggest presence of hemorrhage or gelatinous (highly viscous) colloidal material of the content [<xref ref-type="bibr" rid="scirp.89179-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref12">12</xref>] .</p><p>As described in previous reports, the key management of struma ovarii is surgical removal [<xref ref-type="bibr" rid="scirp.89179-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref5">5</xref>] . Fertility-conserving surgery in most cases could be performed in the cases of their stated desire or potential for fertility. Laparoscopic removal of large ovarian cysts has been well-established and technically feasible for struma ovarii [<xref ref-type="bibr" rid="scirp.89179-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.89179-ref17">17</xref>] . As struma ovarii is often diagnosed post-operatively, there is concern that the removal of potentially malignant ovarian struma ovarii via laparoscopy may not determine the accurate stage, and increase the possible port site metastasis and spillage of tumor cells into the abdominal cavity. Therefore, we considered that taking out of the ovarian cystic tumor with struma ovarii without rupture must be important, and imprint cytology was useful for diagnosis struma ovarii.</p></sec><sec id="s4"><title>4. Conclusion</title><p>A case of pure struma ovarii tumor diagnosed by cytology during a laparoscopic surgery was reported. The patient was a 34-year-old Japanese woman underwent a laparoscopic left oophorectomy under a preoperative diagnosis of endometriotic cyst or mature cystic teratoma in the left ovary. The content of the left ovarian cystic tumor was yellow gelatinous, suggesting a presence of mature cystic teratoma. The imprint cytology of the tumor showed benign glandular pattern, like as a struma ovarii. Histopathological findings led to the diagnosis of pure struma ovarii with a strong positive reaction for thyroglobulin and TTF-1. No other metastases or disseminated lesions were detected. The patient has no recurrent signs 7 months after her operation.</p></sec><sec id="s5"><title>Acknowledgements</title><p>We thank the editor and reviewers for the constructive comments, which helped us to improve the manuscript. This case report was approved by the patient verbal consent.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Authors’ Contributions</title></sec><sec id="s8"><title>Cite this paper</title><p>Niwa, K., Takenaka, M., Ishihara, T., Mori, S., Kuwabara, K., Murase, S., Yamaguchi, Y. and Tanaka, T. (2019) A Case of Struma Ovarii Diagnosed by Cytology during Laparoscopic Surgery. Open Journal of Pathology, 9, 1-9. https://doi.org/10.4236/ojpathology.2019.91001</p></sec></body><back><ref-list><title>References</title><ref id="scirp.89179-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Roth, L.M. and Talerman, A. (2007) The Enigma of Struma Ovarii. 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