<?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">OJOG</journal-id><journal-title-group><journal-title>Open Journal of Obstetrics and Gynecology</journal-title></journal-title-group><issn pub-type="epub">2160-8792</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojog.2021.117079</article-id><article-id pub-id-type="publisher-id">OJOG-110604</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>
 
 
  Endometriosis Diagnosis Correlation of Laparoscopic Visualization and Histopathology Confirmation in Low Resource Setting
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>J.</surname><given-names>Wanyoike Gichuhi</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>Julius</surname><given-names>Ogengo</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>Peter</surname><given-names>Gichangi</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Anatomy, University of Nairobi, Nairobi, Kenya</addr-line></aff><aff id="aff1"><addr-line>Department of Obstetrics &amp;amp; Gynaecology, University of Nairobi, Nairobi, Kenya</addr-line></aff><pub-date pub-type="epub"><day>05</day><month>07</month><year>2021</year></pub-date><volume>11</volume><issue>07</issue><fpage>845</fpage><lpage>852</lpage><history><date date-type="received"><day>8,</day>	<month>June</month>	<year>2021</year></date><date date-type="rev-recd"><day>13,</day>	<month>July</month>	<year>2021</year>	</date><date date-type="accepted"><day>16,</day>	<month>July</month>	<year>2021</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>
 
 
  Background: 
  Endometriosis is enigmatic
   clinical entity which is described as the location of the endometrial tissue external of the uterine cavity. Endometriosis constitutes a serious health issue due to its high affliction of 10% of reproductive women. With limited resources in Africa, it is essential to assess whether diagnosis of endometriosis by laparoscopic visualization can be used as a substitute for histology. <b>Objective: </b>To correlate the diagnosis of endometriosis by laparoscopic visualization and the histological confirmation of the biopsy taken. <b>Methods: </b>
  A<b> </b>
  prospective cross sectional study with a sample size of 443 was undertaken in the diagnosis of endometriosis among Africans in Nairobi, Kenya from March 2019 to March 2021. Women undergoing laparoscopy were screened for endometriosis by visualization and a biopsy was taken for histopathology. Diagnosis of endometriosis by visualization was correlated with histological confirmed endometriosis. <b>Results:</b> Women with a diagnosis of endometriosis through laparoscopic visualization were found to be 77 (17.4%) and 30 (6.8%) had positive histology for endometriosis. Laparoscopic visualization diagnosis had a low positive predictive value of 39%. <b>Conclusion: </b>Laparoscopic visualization diagnosis had a low positive predictive value of 39% and this d
  id
   not correlate with histopathologic diagnosis. It 
  is 
  essential to perform biopsy with histopathology for the confirmation of endometriosis.
 
</p></abstract><kwd-group><kwd>Endometriosis</kwd><kwd> Diagnosis</kwd><kwd> Laparoscopy</kwd><kwd> Africa</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Background</title><p>Endometriosis is a woman’s reproductive ailment, described as presence of endometriotic glands and stroma outside the endometrial cavity, mainly in the pelvic peritoneum, ovary and rectovaginal septum. Endometriosis is a crippling ailment that affects the quality of life and afflicts 6% - 10% of women and its symptomatology encompasses mainly chronic pelvic pain, dysmenorrhoea, dyspareunia and infertility and hence it is one of the most frequent gynaecological ailments [<xref ref-type="bibr" rid="scirp.110604-ref1">1</xref>]. Endometriosis manifests with chronic pelvic pain and infertility, and both have high prevalence of as high as 35% - 50% [<xref ref-type="bibr" rid="scirp.110604-ref2">2</xref>]. In first world countries, there is clear documentation of the diagnosed endometriosis, however, in the developing countries, there are scanty documentations [<xref ref-type="bibr" rid="scirp.110604-ref3">3</xref>]. Endometriosis has been exhaustively investigated in the developed world, however, this is not the case in Africa. The understanding, diagnosis and establishment of the disease burden of endometriosis in Africa are essential for the appropriate management of this disease. There is a conception that African women are hardly inflicted with endometriosis and that is most likely due to poor diagnosis methodology [<xref ref-type="bibr" rid="scirp.110604-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.110604-ref4">4</xref>]. There is scanty literature on Africans on the endometriosis clinical presentation and the prevalence [<xref ref-type="bibr" rid="scirp.110604-ref3">3</xref>]. Diagnosis of endometriosis can only be effectively performed through laparoscopy or laparotomy; limitation of laparoscopic facilities that are essential in diagnosis and treatment in Africa and lack of awareness of the impact of endometriosis may account for low detection and hence prevalence of endometriosis in African [<xref ref-type="bibr" rid="scirp.110604-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.110604-ref5">5</xref>]. The gold standard for the diagnosis of endometriosis is laparoscopic visualization and histological confirmation and this has revolutionized the management of this disease [<xref ref-type="bibr" rid="scirp.110604-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.110604-ref7">7</xref>]. Laparoscopic visualization diagnosis of endometriosis has been documented to have positively predictive value of 45% [<xref ref-type="bibr" rid="scirp.110604-ref8">8</xref>]. Endometriosis can mimic other pathologies such as pelvic infection, endosalpingiosis and cancer in clinical appearance and therefore better laparoscopic optics resolution, recognition of various clinical manifestations of endometriosis and methodological assessment of the pelvic anatomy are imperative [<xref ref-type="bibr" rid="scirp.110604-ref9">9</xref>].</p></sec><sec id="s2"><title>2. Objective</title><p>To determine the correlation of endometriosis diagnosis by laparoscopic visualization and histopathology confirmation in indigenous African women.</p></sec><sec id="s3"><title>3. Methods</title><p>This was an analytical cross-selection study with a sample size of 443 patients. The sample size was determined by using the statistical formula of Fisher method. According to studies undertaken in similar settings, the prevalence of endometriosis has been reported to range from 5% - 10%. A conservative estimate of 10% that gives the largest possible sample size will be used for purposes of sample size calculation. The study site was undertaken in 2 purposively selected hospitals across Nairobi city to ensure ownership and varying levels of specialty, that is Kenyatta National Hospital And the Nairobi hospital. The study population was women aged 18 - 49 years undergoing laparoscopic surgery in any of the two participating hospitals and willing to be part of the study. Data was collected using a structured questionnaire and included all case records for patients undergoing laparoscopic surgery. The structured questionnaire was designed by the authors and pretested for validity and reliability. The respondents were informed about the study, its objectives, risks and benefits. The willing participants were requested to provide written consent. The structured questionnaire was completed by the clinician preparing the patient for surgery while completeness and follow-up for any missing information were done by the principle investigator. The patients were reviewed pre-operatively for the history, clinical presentations and investigations. The anatomical location and staging of the endometriosis were documented. The extent of the endometriosis was described using revised America Society for reproductive Medicine (Revised ASM) [<xref ref-type="bibr" rid="scirp.110604-ref7">7</xref>]. Subtle lesion that might represent endometriosis were excised even if endometriosis was not suspected. One to four biopsies were taken from each patient. Histological confirmation of endometriosis was done by staining samples with haematoxylin and eosin. All data obtained from the questionnaire was verified and had double entered into a computer using Microsoft Access database. The data was analyzed using Social SPSS version 22.0. The chi-square and logistic regression were used to determine the predictors of endometriosis among women undergoing laparoscopic surgery (Tables 1-5 and <xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Laparoscopic procedure n = 443</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Surgical Procedure</th><th align="center" valign="middle"  colspan="2"  >Total</th></tr></thead><tr><td align="center" valign="middle" >n</td><td align="center" valign="middle" >%</td></tr><tr><td align="center" valign="middle" >Excision of Endometriotic Tissue</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >6.8</td></tr><tr><td align="center" valign="middle" >Diagnostic Laparoscopy</td><td align="center" valign="middle" >71</td><td align="center" valign="middle" >33.2</td></tr><tr><td align="center" valign="middle" >Adhesionlysis</td><td align="center" valign="middle" >67</td><td align="center" valign="middle" >15.1</td></tr><tr><td align="center" valign="middle" >Ovarian Cystectomy</td><td align="center" valign="middle" >54</td><td align="center" valign="middle" >12.2</td></tr><tr><td align="center" valign="middle" >Oophorectomy</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle" >Myomectomy</td><td align="center" valign="middle" >52</td><td align="center" valign="middle" >11.7</td></tr><tr><td align="center" valign="middle" >Tuboplasty</td><td align="center" valign="middle" >57</td><td align="center" valign="middle" >12.9</td></tr><tr><td align="center" valign="middle" >Salpingectomy</td><td align="center" valign="middle" >20</td><td align="center" valign="middle" >4.5</td></tr><tr><td align="center" valign="middle" >Retrieval of IUD</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >2.0</td></tr><tr><td align="center" valign="middle" >Drainage of Abscess</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >.9</td></tr><tr><td align="center" valign="middle" >Hysterectomy</td><td align="center" valign="middle" >52</td><td align="center" valign="middle" >11.7</td></tr><tr><td align="center" valign="middle" >Appendectomy‎</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle" >Ovarian Drill</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.6</td></tr></tbody></table></table-wrap><p>The main laparoscopic surgeries performed were diagnostic (16%), Adhesionalysis (15.1%), Tuboplasty (18.7%), ovarian cystectomy (12.2%), Myomectomy (11.7%), Hysterectomy (11.7%), excision of endometriosis was 6.8%, Salpingectomy (4.5%), Retrieval of lost IUD (2.0%), appendectomy (1.1%), oophorectomy (1.1%), and ovarian drill (0.6%).</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Histological findings on laparoscopic biopsies (n = 443)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >n</th><th align="center" valign="middle" >%</th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Adenomyosis</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >1.8</td></tr><tr><td align="center" valign="middle" >Appendicitis</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle" >Cervical dysplasia</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.2</td></tr><tr><td align="center" valign="middle" >Clinical endometriosis but histologically no endometriosis</td><td align="center" valign="middle" >24</td><td align="center" valign="middle" >5.4</td></tr><tr><td align="center" valign="middle" >Confirmed histological endometriosis</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >6.8</td></tr><tr><td align="center" valign="middle" >Ectopic pregnancy</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >Endometrial hyperplasia</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.2</td></tr><tr><td align="center" valign="middle" >Fallopian tubes</td><td align="center" valign="middle" >23</td><td align="center" valign="middle" >5.2</td></tr><tr><td align="center" valign="middle" >Myoma</td><td align="center" valign="middle" >88</td><td align="center" valign="middle" >19.9</td></tr><tr><td align="center" valign="middle" >No pathology</td><td align="center" valign="middle" >196</td><td align="center" valign="middle" >44.2</td></tr><tr><td align="center" valign="middle" >Ovarian cyst</td><td align="center" valign="middle" >45</td><td align="center" valign="middle" >10.2</td></tr><tr><td align="center" valign="middle" >Ovarian malignancy</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >Teratoma</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1.1</td></tr></tbody></table></table-wrap><p>The prevalence of histological confirmed endometriosis was 6.8%, however the most common pathology was myoma (19.9%) and 44.2% of women had no pathology detected histologically.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Signs of Endometriosis (n = 30)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Signs of Endometriosis</th><th align="center" valign="middle" >n</th><th align="center" valign="middle" >%</th></tr></thead><tr><td align="center" valign="middle" >Puckered blue-black</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >20.0</td></tr><tr><td align="center" valign="middle" >Powder-burned appearance</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >33.3</td></tr><tr><td align="center" valign="middle" >Subtle (Popular, Glandular, vesicular)</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >10.0</td></tr><tr><td align="center" valign="middle" >Haemorrhagic (Red vesicular or Flame-like)</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >26.7</td></tr><tr><td align="center" valign="middle" >Fibrotic lesions (White to black pigmented).</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >30.0</td></tr><tr><td align="center" valign="middle" >Chocolate cyst/endometrioma.</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >26.7</td></tr><tr><td align="center" valign="middle" >Deep Infiltrating Endometriosis</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >26.7</td></tr><tr><td align="center" valign="middle" >Extra pelvic</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >6.7</td></tr></tbody></table></table-wrap><p>The most common form of presentation in superficial endometriosis was powder-burned appearance (33%) followed by fibrotic lesions (White to black pigmented), (30%), puckered blue-black (20%), subtle (10%) whilst endometrioma and deep infiltrating endometriosis accounted for 26.7% with extra pelvic endometriosis being 2%.</p><table-wrap-group id="4"><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Anatomical site of Endometriosis (n = 30)</title></caption><table-wrap id="4_1"><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >n</th><th align="center" valign="middle" >%</th></tr></thead><tr><td align="center" valign="middle" >Anatomic site of endometriosis</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Anterior uterine</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >6.7</td></tr><tr><td align="center" valign="middle" >Extra pelvic site</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >3.3</td></tr><tr><td align="center" valign="middle" >Gut</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >3.3</td></tr></tbody></table></table-wrap><table-wrap id="4_2"><table><tbody><thead><tr><th align="center" valign="middle" >Bilateral ovaries</th><th align="center" valign="middle" >2</th><th align="center" valign="middle" >6.7</th></tr></thead><tr><td align="center" valign="middle" >Posterior uterine</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >6.7</td></tr><tr><td align="center" valign="middle" >Pouch of Douglas</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >30.0</td></tr><tr><td align="center" valign="middle" >Utero-sacral ligaments</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >20.0</td></tr><tr><td align="center" valign="middle" >Unilateral ovary</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >23.3</td></tr></tbody></table></table-wrap></table-wrap-group><p>The endometriosis implants’ sites were on the Pouch of Douglas (30%), Unilateral ovaries (23.3%), uterosacral (20%), posterior uterus (6.7%), Bilateral ovaries (6.7%), Anterior uterus (6.7%), Gut (3.3%) and extra pelvic site (3.3%).</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Histological confirmed endometriosis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >NO</th><th align="center" valign="middle" >%</th></tr></thead><tr><td align="center" valign="middle" >Confirmed histological endometriosis</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >6.8%</td></tr><tr><td align="center" valign="middle" >Clinical endometriosis by visualization</td><td align="center" valign="middle" >77</td><td align="center" valign="middle" >17.4%</td></tr></tbody></table></table-wrap><p>Endometriosis clinical diagnosed by visualization was 77 (17.4%) and out of this 30 (6.8%) were histologically confirmed.</p></sec><sec id="s4"><title>4. Discussion</title><p>The mean age of the women in the study was 33 years and there was no statistical difference between the women with endometriosis and those without.</p><p>Endometriosis clinically diagnosed by visualization was 77 (17.4%) and out of this only 30 (6.8%) were histologically confirmed as endometriosis. Laparoscopic visualization diagnosis had a low positive predictive value of 39%. This was lower than other studies study that found laparoscopic visualization diagnosis of endometriosis to have positive predictive value of 45% and 63.8% [<xref ref-type="bibr" rid="scirp.110604-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.110604-ref10">10</xref>].</p><p>The prevalence of endometriosis has been speculated to be as high as 10% in the women of reproductive age, however, the findings in this study showed a lower prevalence [<xref ref-type="bibr" rid="scirp.110604-ref5">5</xref>]. This study was not consisted with a Nigerian study in Ibadan where the prevalence of endometriosis with only laparoscopic visualization and no histological examination was found to be 48.8% [<xref ref-type="bibr" rid="scirp.110604-ref11">11</xref>]. This study showed the prevalence of endometriosis with laparoscopic visualization to be 17.4%. This study was not consisted with Chapmans laparoscopic studies in African American women, where he found prevalence of histologically confirmed endometriosis to be 21% in women who had had pelvic inflammatory disease [<xref ref-type="bibr" rid="scirp.110604-ref12">12</xref>].</p><p>The main laparoscopic surgery performed were diagnostic (33.2%), Adhesionalysis (15.1%), Tuboplasty (18.7%), Ovarian cystectomy (12.2%), Myomectomy (11.7%), Hysterectomy (11.7%), excision of endometriosis (6.8%, Salpingectomy (4.5%), Retrieval of lost IUD (2.0%), appendectomy (1.1%), oophorectomy (1.1%), and ovarian drill (0.6%).</p><p>The sites of the endometriosis implants were on the Pouch of Douglas (30%), Unilateral ovaries (23.3%), uterosacral (20%), posterior uterus (6.7%), Bilateral ovaries (6.7%), Anterior uterus (6.7%), Gut (3.3%) and extra pelvic site (3.3%). This was consisted with a study by Wanyonyi et al. [<xref ref-type="bibr" rid="scirp.110604-ref10">10</xref>] who found most endometriotic positive biopsies biopsies were found in the ovary and posterior cul-de-sac [<xref ref-type="bibr" rid="scirp.110604-ref10">10</xref>].</p><p>The majority of the histological confirmed endometriosis were superficial endometriosis (43%), with ovarian and deep infiltrating endometrioma each having (27%) and extra pelvic endometriosis having (2%). The most common form of presentation of superficial endometriosis was powder-burned appearance (33%) followed by fibrotic lesions (30%), puckered blue-black (20%) and subtle (10%).</p><p>The overall histopathology findings were confirmed histological endometriosis (6.8%), myoma (19.9%), ovarian cyst (10.2%), fallopian tubes (5.2%)., adenomyosis (1.8%), teratoma (1.1%,) appendicitis (1.1%), ectopic pregnancy (0.9%), ovarian malignancy (0.9%), endometrial hyperplasia (0.2%), cervical dysplasia (0.2%) and no pathology (44.2%). Laparoscopic visualization of endometriosis among Africans in low resource setting does not correlate with histopathologic diagnosis due to presence of multiple pathologies which may be diagnosed as endometriosis by clinical appearance. It is essential to perform biopsy with histopathology for confirmation of endometriosis.</p></sec><sec id="s5"><title>5. Conclusion</title><p>The endometriosis diagnosed by laparoscopic visualization was 17.4% and the histological confirmed endometriosis was 6.8%. Laparoscopic visualization diagnosis had a low positive predictive value of 39% and did not correlate with histopathologic diagnosis due to presence of multiple lesions which may mimic endometriosis on laparoscopic visualization. For definitive diagnosis of endometriosis performance of biopsy with histopathological confirmation is imperative.</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>Cite this paper</title><p>Gichuhi, J.W., Ogengo, J. and Gichangi, P. (2021) Endometriosis Diagnosis Correlation of Laparoscopic Visualization and Histopathology Confirmation in Low Resource Setting. Open Journal of Obstetrics and Gynecology, 11, 845-852. https://doi.org/10.4236/ojog.2021.117079</p></sec></body><back><ref-list><title>References</title><ref id="scirp.110604-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Burney, R.O. and Giudice, L.C. (2012) Pathogenesis and Pathophysiology of Endometriosis. Fertility and Sterility, 98, 511-519.  
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