<?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">JBM</journal-id><journal-title-group><journal-title>Journal of Biosciences and Medicines</journal-title></journal-title-group><issn pub-type="epub">2327-5081</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jbm.2018.65013</article-id><article-id pub-id-type="publisher-id">JBM-84776</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Splenectomy in Patient with Splendid Cysts
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Vinícius</surname><given-names>Moreira Paladino</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>Thiago</surname><given-names>Sande Miguel</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>Débora</surname><given-names>Trindade Martins</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>Nayrton</surname><given-names>Kalys Cruz dos Anjos</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>Fernando</surname><given-names>Antonio Galvão Pereira Junior</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>Marcia</surname><given-names>Machado Galvão Pereira</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>Carolina</surname><given-names>Galvão Teixeira</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>Vinicius</surname><given-names>Sande Miguel</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>Bruna</surname><given-names>Sande Miguel</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>Daniel</surname><given-names>Almeida da Costa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>The Medical School at the Center of Higher Education of Valen&amp;amp;ccedil;a, Valen&amp;amp;ccedil;a, Brazil</addr-line></aff><aff id="aff2"><addr-line>Suprema Medical School, Juiz de Fora, Brazil</addr-line></aff><aff id="aff3"><addr-line>Universidade Grande Rio Medical School, Rio de Janeiro, Brazil</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>acosttta@icloud.com(DADC)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>21</day><month>05</month><year>2018</year></pub-date><volume>06</volume><issue>05</issue><fpage>120</fpage><lpage>125</lpage><history><date date-type="received"><day>14,</day>	<month>October</month>	<year>2017</year></date><date date-type="rev-recd"><day>21,</day>	<month>May</month>	<year>2018</year>	</date><date date-type="accepted"><day>24,</day>	<month>May</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>
 
 
  Introduction: Splenic cysts are uncommon and usually do not generate signs and symptoms, being diagnosed by incidental findings. Case report: A 35-year-old, female patient attended the Luiz Gioseffi Jannuzzi School Hospital (HELGJ) presenting episodes of vomiting and abdominal pain in the left hypochondrium. She was hospitalized for diagnostic investigation. Computed tomography showed the splenic cyst. The procedure was the surgical approach by laparotomy with splenectomy. Histopathological confirmed the diagnosis. Discussion: Compared to the scarce reports in literature, the case described presented typical epidemiology and clinical features. Conclusions: Given the rarity of this pathology cases, it is essential to report these in order to elucidate the specificities and also to discuss diagnostic and therapeutic methods.
 
</p></abstract><kwd-group><kwd>Splenectomy</kwd><kwd> Splendid Cysts</kwd><kwd> Abdominal Pain</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Non-parasitic splenic cysts are considered uncommon, with relatively few reports in literature. They are mostly incidental findings during imaging or necropsy studies [<xref ref-type="bibr" rid="scirp.84776-ref1">1</xref>] . They can be classified into two groups according to their characteristics and pathological bases. True splenic cysts have a cellular layer and are probably of congenital (mesothelial or dermoid) or neoplastic origin. On the other hand, the false or pseudocysts have a wall of fibrous tissue, almost always calcified, and it is not covered by a cellular layer, and abdominal trauma is its main etiological factor [<xref ref-type="bibr" rid="scirp.84776-ref2">2</xref>] .</p><p>It occurs more in women, during their second, third and fourth life decades [<xref ref-type="bibr" rid="scirp.84776-ref3">3</xref>] . The clinic presents as some asymptomatic or manifesting symptoms such as pain in the left hypochondrium, left hemithorax, epigastrium and/or periumbilical region, resulting from the compression of adjacent viscera. Vomiting, nausea, early satiety, and postprandial fullness may be associated. In emergency cases, such as in the cyst rupture, triggers signs and symptoms of acute abdomen can be presented [<xref ref-type="bibr" rid="scirp.84776-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.84776-ref4">4</xref>] .</p><p>It is usually diagnosed through procedures performed for investigation or therapy of other abdominal conditions, as well as routine physical and radiological examination [<xref ref-type="bibr" rid="scirp.84776-ref2">2</xref>] . The confirmation is made through histopathology, and can be preceded by ultrasound (US) and/or computed tomography (CT), both of the abdomen region, which are performed for possible differential diagnoses [<xref ref-type="bibr" rid="scirp.84776-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.84776-ref5">5</xref>] .</p><p>According to the literature, symptomatic splenic cysts should be treated surgically, with splenectomy being the method of choice. Conservative treatment options, such as percutaneous aspiration or sclerosis, do not result in good long-term control. Several studies have indicated the advantages of surgical treatment by video laparoscopy, however, the gold standard for surgical treatment of splenic cysts remains controversial [<xref ref-type="bibr" rid="scirp.84776-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.84776-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.84776-ref7">7</xref>] .</p><p>This paper’s objective is to report a case of polycystic spleen in women with curative treatment through laparotomy with splenectomy, highlighting the characteristics of this unusual pathology, as well as the diagnostic and therapeutic procedures available.</p></sec><sec id="s2"><title>2. Case Report</title><p>Patient T.H.M.E., 35 years old, female, from the city of Valen&#231;a, State of Rio de Janeiro, attended the Emergency Room (ER) of Luiz Gioseffi Jannuzzi School Hospital (HELGJ) presenting, as a history of the current disease, episodes of vomiting, associated with abdominal pain in the left hypochondrium. Physical examination can detect mass in the Taube space and a large palpable mass in the region.</p><p>The patient was admitted to the Medical Clinic for diagnostic clarification. The US showed the presence of multiple cystic images in the spleen (<xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>). The finding was complemented and confirmed by CT, which described as “Spleen enlarged by the presence of multiple cystic formations, some with perineal calcifications compromising its middle and lower third, measuring about 10.3 &#215; 5.1 cm in the largest cross-sectional diameters”, the images of which are shown below (<xref ref-type="fig" rid="fig3">Figure 3</xref>).</p><p>In view of the condition, the patient underwent laparotomy with splenectomy and removed hyperchromic lesion in umbilical scar (this data was described in the surgical report in this way, what inviabilized deeper details. sorry for not having more clarifications) (<xref ref-type="fig" rid="fig4">Figure 4</xref>). In anatomopathological analysis it was described: “spleen weighing 405 grams, measuring 17 cm, appearing multiloculate</p><p>cysts. Microscopy: multiple cysts coated by cuboid epithelium, with regular nucleus and fibrous wall. As found an injury in umbilical scar, endometrial appearance. Diagnostic conclusion: polycystic spleen and endometriosis”. She was discharged on the fifth postoperative day.</p><p>It should be noted that the patient of the present study was willing to accept the publication of the present report, after explaining its underlying pathology and its relevance. She signed the Free and Informed Consent Form and, thus, proceeded with the present study.</p></sec><sec id="s3"><title>3. Discussion</title><p>In general, the prevalence of splenic cysts is higher among women when compared to men, with the age group between the second and third decades of life, being the most affected [<xref ref-type="bibr" rid="scirp.84776-ref8">8</xref>] . The patient described is female and is 35 years old, which is in agreement with those found in literature. Despite this, this case is relevant in view of the restricted amount of reports described, given their rarity.</p><p>As for symptomatology, the majority of patients are asymptomatic, but there may be, at rest or physical examination, pain may be present in the left hypochondrium, left hemithorax, epigastrium and/or periumbilical region [<xref ref-type="bibr" rid="scirp.84776-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.84776-ref10">10</xref>] . And several times, associated with gastrointestinal symptoms, such as early satiety, postprandial fullness, nausea and vomiting [<xref ref-type="bibr" rid="scirp.84776-ref11">11</xref>] . In this case, it was reported as a history of the current disease, episodes of vomiting and abdominal pain in the left hypochondrium region. Physical examination can detect mass in the Traube space and a large palpable mass in the region. Although many pathologies present similar clinical manifestations, the hypothesis that patients were already evolving with splenic cysts, although previously asymptomatic, is strongly considered since the results of US and CT showed multiple nodules in the spleen [<xref ref-type="bibr" rid="scirp.84776-ref5">5</xref>] .</p><p>Currently, the US and CT are the most requested complementary and indicated by the theoretical basis exams. The latter method is the most sensitive allowing the identification of septa, more frequent in true cysts, and/or calcifications, which would indicate a false cyst [<xref ref-type="bibr" rid="scirp.84776-ref12">12</xref>] . Therefore, there is one more fact that contributes in favor of treating splenic cysts in the case reported above.</p><p>Therapy with a surgical approach through laparotomy with splenectomy is the most indicated [<xref ref-type="bibr" rid="scirp.84776-ref13">13</xref>] , although currently, for asymptomatic cases and presenting cysts smaller than two centimeters, which do not show calcifications or increased internal or collateral circulation, expectant management is accepted [<xref ref-type="bibr" rid="scirp.84776-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.84776-ref15">15</xref>] .</p><p>Recent case studies indicate the advantages of video laparoscopy approach (VL) for performing the cyst crackling. This procedure has the purpose of allowing free drainage in the peritoneal cavity so that the fluid is reabsorbed. Another factor that favors this indication is that the splenic tissue is not altered, and there is only the resection of the cyst dome. One point questioned in the VL approach is the high recurrence rate, but with epiploonuse this concern has decreased [<xref ref-type="bibr" rid="scirp.84776-ref6">6</xref>] .</p></sec><sec id="s4"><title>4. Conclusions</title><p>After literature review and the report, the reduced number of cases of splenic cyst described in literature was evidenced.</p><p>In summary, the diagnosis is made due to incidental findings during investigations of various pathologies involving the gastrointestinal tract and/or abdominal region. The patient usually presents himself asymptomatic, but in some cases gastrointestinal symptoms may be present. Therapy is a matter of discussion, but laparotomy is still considered in the gold standard. Only in asymptomatic patients with specific cyst characteristics, expectant management can be accepted.</p></sec><sec id="s5"><title>Cite this paper</title><p>Paladino, V.M., Miguel, T.S., Martins, D.T., dos Anjos, N.K.C., Junior, F.A.G.P., Pereira, M.M.G., Teixeira, C.G., Miguel, V.S., Miguel, B.S. and da Costa, D.A. (2018) Splenectomy in Patient with Splendid Cysts. Journal of Biosciences and Medicines, 6, 120-125. https://doi.org/10.4236/jbm.2018.65013</p></sec></body><back><ref-list><title>References</title><ref id="scirp.84776-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ingle, S.B., Hinge, C.R. and Patrike, S. (2014) Epithelial Cysts of the Spleen: A Minireview. World Journal of Gastroenterology, 20, 13899.https://doi.org/10.3748/wjg.v20.i38.13899</mixed-citation></ref><ref id="scirp.84776-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Alvarez, G.C., Silveira, M.L.D., Costa, E.M.D., Pagliarin, F.V. and Costa, I. (2000) Cisto epidermóide de bao em criana. Arquivos de Gastroenterologia, 37, 69-77. https://doi.org/10.1590/S0004-28032000000100013</mixed-citation></ref><ref id="scirp.84776-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Alves, J.G., Estevam, D.L., Santos, J.L.D. and Genn, C.M.S. (1991) Cisto esplênico. Jornal Brasileiro de Medicina, 61, 48-50.</mixed-citation></ref><ref id="scirp.84776-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Schlittler, L.A. and Dallagasperina, V.W. (2010) Cistos esplênicos nao-parasitários. Revista do Colegio Brasileiro de Cirurgioes, 37, 442-446. https://doi.org/10.1590/S0100-69912010000600011</mixed-citation></ref><ref id="scirp.84776-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Rabushka, L.S., Kawashima, A. and Fishman, E.K. (1994) Imaging of the Spleen: CT with Supplemental MR Examination. Radiographics, 14, 307-332.https://doi.org/10.1148/radiographics.14.2.8190956</mixed-citation></ref><ref id="scirp.84776-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Pitombo, M.B., Leal, P.R.F. and Albuquerque, R.M.D. (2000) Abordagem videolaparoscópica de cisto esplênico nao parasitário. Revista do Colegio Brasileiro de Cirurgioes, 27, 350-351. https://doi.org/10.1590/S0100-69912000000500013</mixed-citation></ref><ref id="scirp.84776-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Guerra, M.R.V., Ribeiro, M.A., Nam, M.F., Casale, A.L.V., Martins, C.P.B., Morais, C.E.L.D., et al. (2012) Cisto esplênico nao parasitário—tratamento por laparoscopia. Diagnóstico &amp; Tratamento, 17, 51-55.</mixed-citation></ref><ref id="scirp.84776-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Kang, S.I. and Jeon, S.Y. (2013) Primary Non-Parasitic Splenic Cyst: A Case Report. Korean Journal of Hepato-Biliary-Pancreatic Surgery, 17, 139-141.https://doi.org/10.14701/kjhbps.2013.17.3.139</mixed-citation></ref><ref id="scirp.84776-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Rana, A.P.S., Kaur, M., Singh, P., Malhotra, S. and Kuka, A.S. (2014) Splenic Epidermoid Cyst—A Rare Entity. Journal of Clinical and Diagnostic Research, 8, 175.https://doi.org/10.7860/JCDR/2014/6901.4050</mixed-citation></ref><ref id="scirp.84776-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Cianci, P., Tartaglia, N., Altamura, A., Fersini, A., Vovola, F., Sanguedolce, F., et al. (2016) A Recurrent Epidermoid Cyst of the Spleen: Report of a Case and Literature Review. World Journal of Surgical Oncology, 14, 98. https://doi.org/10.1186/s12957-016-0857-x</mixed-citation></ref><ref id="scirp.84776-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Baier, A., Abreu, P., de Campos, M., Casani, J., Ferreira, L. and Dummer, C. (2017) Pseudocisto esplênico nao parasítico: um relato de caso. Clinical &amp; Biomedical Research, 37, No. 2. https://doi.org/10.4322/2357-9730.71786</mixed-citation></ref><ref id="scirp.84776-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Torresa, B.M., Garcíab, M.M., Antac, M.á.Z., Munoz-Najard, A.J.G. and Dovaoe, J.C.T. (2017) Giant Splenic Cyst in a Teenage Girl. Case Report. Revista Chilena de Pediatria, 88, 388-392.</mixed-citation></ref><ref id="scirp.84776-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Palermo, M., Blanco, L., Acquafresca, P., Menendez, J. and Garcia, R. (2015) Reduce Port Laparoscopic Splenectomy For Giant Epitelial Cyst. Arquivos Brasileiros de Cirurgia Digestiva, 28, 282-285. https://doi.org/10.1590/s0102-6720201500040016</mixed-citation></ref><ref id="scirp.84776-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Kenney, C.D., Hoeger, Y.E., Yetasook, A.K., Linn, J.G., Denham, E.W., Carbray, J. and Ujiki, M.B. (2014) Management of Non-Parasitic Splenic Cysts: Does Size Really Matter? Journal of Gastrointestinal Surgery, 18, 1658-1663. https://doi.org/10.1007/s11605-014-2545-x</mixed-citation></ref><ref id="scirp.84776-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Navarini, D., Aita, L.N., Fleck, F.P.D.A., Madalosso, C.A.S., Moraes Junior, I.D.S. and Fornari, F. (2010) Cisto Epidermóide de Bao em paciente previamente hígido. Revista HCPA. Porto Alegre, 30, 192.</mixed-citation></ref></ref-list></back></article>