<?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">OJPed</journal-id><journal-title-group><journal-title>Open Journal of Pediatrics</journal-title></journal-title-group><issn pub-type="epub">2160-8741</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojped.2016.61003</article-id><article-id pub-id-type="publisher-id">OJPed-64271</article-id><article-categories><subj-group subj-group-type="heading"><subject>Short Report</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  One Month Ongoing Intussusception: Case Report
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>mrah</surname><given-names>Aydin</given-names></name><xref ref-type="aff" rid="aff1"><sub>1</sub></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>Pediatric Surgery Department, Bahcelievler State Hospital, Istanbul, Turkey</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>dremrahaydin@yahoo.com</email></corresp></author-notes><pub-date pub-type="epub"><day>03</day><month>03</month><year>2016</year></pub-date><volume>06</volume><issue>01</issue><fpage>14</fpage><lpage>16</lpage><history><date date-type="received"><day>29</day>	<month>December</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>5</month>	<year>March</year>	</date><date date-type="accepted"><day>8</day>	<month>March</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>
 
 
  The aim is to present a case operated due to one-month ongoing intussusception and diagnosed as lymphoma. A six years old boy was admitted to our emergency department with complaint of colicky abdominal pain and bilious vomiting for the last month. He was operated due to 3 cm intussusception at ileocecal part. A mass which is about 6 cm in diameter, hard, partly mobile and invaginate the intestine at its posterior aspect was found. Pathology was reported as Burkitt lymphoma. He received two cycles of chemotherapy at post-operative period. He is still event free for the last two years. One must remember that lymphoma can be the lead point in intussusception especially in elderly children.
 
</p></abstract><kwd-group><kwd>Intussusception</kwd><kwd> Burkitt’s Lymphoma</kwd><kwd> Childhood</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Intussusception is defined as invagination of a bowel segment one into another [<xref ref-type="bibr" rid="scirp.64271-ref1">1</xref>] . It is often presented between 3 - 18 months and occurs in 1 - 4 cases per 1000 live births [<xref ref-type="bibr" rid="scirp.64271-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.64271-ref3">3</xref>] . The male to female ratio is 3:2 [<xref ref-type="bibr" rid="scirp.64271-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.64271-ref3">3</xref>] . No underlying pathology can be detected before 2 years of age. However, there is frequently a “lead point” in patients older than 3 years old. Although it’s rare, non-Hodgkin’s lymphoma at terminal ileum and cecum may be the cause of intussusception. We presented a case who had recurrent intussusception for about a month and diagnosed as non-Hodgkin’s lymphoma that located at cecum.</p></sec><sec id="s2"><title>2. Case Report</title><p>Six-year-old male patient was admitted to our emergency department with intermittent colic, abdominal pain and bilious vomiting for a month. All laboratory examinations were normal which had been done in another center. At ultrasonography spontaneously reduced intussusception was diagnosed but no intervention was performed. In the physical examination, vital signs were stable on arrival in the emergency room and there was no external pathology seen on his body. No mass could be palpated but there was tenderness at right upper and lower quadrants of abdomen. All laboratory examinations were normal but mild leukocytosis. Abdominal gas distribution was normal at X-ray. Abdominal ultrasonography was reported as 3 cm intussusception located at with ileocecal. Nasogastric tube and rectal enema was performed for intestinal decompression. Because he had colicky abdominal pain at his follow up operation decision were taken. Pneumatic reduction was performed and no invaginated intestinal segment was seen but a large filling defect was founded at scope. Laparotomy was performed. An exploration was performed with right upper quadrant incision. There was no intussusception but edema and pseudo membrane covered mass at ileocecal region was found. There were lots of lymph nodes around mesenteric region. Approximately 6 cm in diameter, semi-mobile, hard mass found that invaginates the intestine at its posterior aspect (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Ileoascendostomy and lymph node sampling was performed. The control laboratory values were within normal limits in the post-operative period. No additional pathology was detected in the thoracic and abdominal pelvic CT. At 5<sup>th</sup> post-operative day nasogastric tube was taken and he started enteral feeding. He was discharged at 7<sup>th</sup> post-operative day. Pathology was reported as Burkitt’s lymphoma and reactive hyperplasia at lymph nodes. Immunohistochemical examinations were as CD20 (+), CD10 focal (+), CD3-reactive T lymphocytes (+), Pax5 (+), dt (−), EBV (−), CD21 (−) CD23 (−), MUM-1 (−), bcl-6 (−), bcl-2 (−) and Ki-67 proliferative index was determined as 90%. Scintigraphy of whole body scan was normal. Chemotherapy was performed for two cycles. He has been well and free of disease for the last two years.</p></sec><sec id="s3"><title>3. Discussion</title><p>Intussusception is the second most common childhood abdominal emergency [<xref ref-type="bibr" rid="scirp.64271-ref1">1</xref>] . Only in 1.5% - 12% of cases underlying pathology can be found [<xref ref-type="bibr" rid="scirp.64271-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.64271-ref5">5</xref>] . These are Meckel’s diverticulum, polyps, duplication, mesenteric cyst, intestinal hemorrhage and lymphoma [<xref ref-type="bibr" rid="scirp.64271-ref6">6</xref>] . Although it’s rare, lymphoma because of its malignant nature is the most noticeable one and is “lead point” 6.5% of intussusceptions [<xref ref-type="bibr" rid="scirp.64271-ref5">5</xref>] . Navarone et al. stated that accompanied by weight loss and long term complaints were the tips for gastrointestinal lymphoma [<xref ref-type="bibr" rid="scirp.64271-ref7">7</xref>] . In our case it was all for a month but he didn’t lose any weight.</p><p>Burkitt’s lymphoma constitutes about 40% - 50% of non-Hodgkin’s lymphoma in childhood [<xref ref-type="bibr" rid="scirp.64271-ref8">8</xref>] . Patients often present with abdominal mass. Also abdominal pain, vomiting or sign and symptoms of intestinal obstruction due to mass effect or intussusception can be observed [<xref ref-type="bibr" rid="scirp.64271-ref9">9</xref>] . It’s mostly seen age between 5 - 15 years [<xref ref-type="bibr" rid="scirp.64271-ref10">10</xref>] . Our patient was 6 years old and had abdominal pain and vomiting for about a month. Many ultrasonographies were performed and all reported spontaneously improved intussusception. His physical examination was consistent with acute abdomen. Pneumatic reduction was performed according to these findings. Even no intussusception was seen at pneumatic reduction because his clinical findings were consisted with intussusception he was operated.</p><p>10% of non-Hodgkin’s lymphoma cases are limited to the gastrointestinal tract [<xref ref-type="bibr" rid="scirp.64271-ref11">11</xref>] . Philips et al. stated that intestinal lymphoma may be associated with ulcerative colitis, chronic antigenic stimulation or Epstein-Barr virus in immune suppressed patients [<xref ref-type="bibr" rid="scirp.64271-ref12">12</xref>] . However, none of these factors was observed in our case.</p><p>Role of surgery in the treatment of Burkitt lymphoma is controversial. Burkitt’s lymphoma originated from B lymphocytes serves very good response to combination chemotherapy. It was rapidly responsive and has prolonged remission [<xref ref-type="bibr" rid="scirp.64271-ref13">13</xref>] . But there are many opposing papers in the literature. Margrath et al. suggested removal</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title>Per operative view of the mass</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/3-1330476x6.png"/></fig><p>of more than 90% of the mass prior to chemotherapy at their Uganda based studies [<xref ref-type="bibr" rid="scirp.64271-ref14">14</xref>] . Our case was operated due to consisted acute abdomen findings at physical examination. Extensive resection was performed for preserving tumor free margins and lymph node sampling was performed for staging.</p></sec><sec id="s4"><title>4. Conclusion</title><p>Treatment of intussusception should be individualized according to age and intestinal segment. Malignancy should be remembered especially later in childhood as a cause of intussusception and surgical treatment should always be kept in mind.</p></sec><sec id="s5"><title>Cite this paper</title><p>EmrahAydin, (2016) One Month Ongoing Intussusception: Case Report. Open Journal of Pediatrics,06,14-16. doi: 10.4236/ojped.2016.61003</p></sec></body><back><ref-list><title>References</title><ref id="scirp.64271-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Byrne, A.T., Geoghegan, T., Govender, P., et al. (2005) The Imaging of Intussusception. Clinical Radiology, 60, 39-46.  
http://dx.doi.org/10.1016/j.crad.2004.07.007</mixed-citation></ref><ref id="scirp.64271-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">DiFiore, J.W. (1999) Intussusception. Seminars in Pediatric Surgery, 8, 214-220.  
http://dx.doi.org/10.1016/S1055-8586(99)70029-6</mixed-citation></ref><ref id="scirp.64271-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Simpson, T., Ivey, J. and Borkowski, S. (2004) Pediatric Management Problems. Intussusception. Pediatric Nursing, 30, 326-327.</mixed-citation></ref><ref id="scirp.64271-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Ong, N.T. and Beasley, S.W. (1990) The Lead Point in Intussusception. Journal of Pediatric Surgery, 25, 640-643.  
http://dx.doi.org/10.1016/0022-3468(90)90353-B</mixed-citation></ref><ref id="scirp.64271-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Blakelock, R.T. and Beasley, S.W. (1998) The Clinical Implications of Non-Idiopathic Intussusception. Pediatric Surgery International, 14, 163-167. http://dx.doi.org/10.1007/s003830050475</mixed-citation></ref><ref id="scirp.64271-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Sorantin, E. and Lindbichler, F. (2004) Management of Intussusception. European Radiology, 14, 146-154.  
http://dx.doi.org/10.1007/s00330-003-2033-2</mixed-citation></ref><ref id="scirp.64271-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Navarro, O., Dugougeat, F., Kornecki, A., et al. (2000) The Impact of Imaging in the Management of Intussusception Owing to Pathologic Lead Points in Children. A Review of 43 Cases. Pediatric Radiology, 30, 594-603.  
http://dx.doi.org/10.1007/s002470000261</mixed-citation></ref><ref id="scirp.64271-ref8"><label>8</label><mixed-citation publication-type="book" xlink:type="simple">Perkins, S.L. and Morris, S.W. (2007) Biology and Pathology pf Pediatric NHL. In: Weinsten, H.J., Hudson, M.M. and Link, M.P., Eds., Pediatric Lymphomas (Pediatric Oncology), Springer, New York, 101-106.  
http://dx.doi.org/10.1007/978-3-540-68753-5_6</mixed-citation></ref><ref id="scirp.64271-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Sandlund, J.T., Downing, J.R. and Crist, W.M. (1996) Non-Hodgkin’s Lymphoma in Childhood. The New England Journal of Medicine, 334, 1238-1248. http://dx.doi.org/10.1056/NEJM199605093341906</mixed-citation></ref><ref id="scirp.64271-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Bethel, C.A., Bhattacharyya, N. and Hutchinson, C. (1997) Alimentary Tract Malignancies in Children. Journal of Pediatric Surgery, 32, 1004-1009. http://dx.doi.org/10.1016/S0022-3468(97)90387-0</mixed-citation></ref><ref id="scirp.64271-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Herrmann, R., Panahon, A.M., Barcos, M.P., et al. (1980) Gastrointestinal Involvement in Non-Hodgkin’s Lymphoma. Cancer, 46, 215-222. http://dx.doi.org/10.1002/1097-0142(19800701)46:1&lt;215::AID-CNCR2820460136&gt;3.0.CO;2-6</mixed-citation></ref><ref id="scirp.64271-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Philips, D.L., Keefe, E.B., Benner, K.G., et al. (1989) Colonic Lymphoma in the Transplant Patient. Digestive Diseases and Sciences, 34, 150-154. http://dx.doi.org/10.1007/BF01536173</mixed-citation></ref><ref id="scirp.64271-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Wang, S.M., Huang, F.C., Wu, C.H., et al. (2010) Ileocecal Burkitt’s Lymphoma Presenting as Ileocolic Intussusception with Appendiceal Invagination and Acute Appendicitis. Journal of the Formosan Medical Association, 109, 476- 479. http://dx.doi.org/10.1016/S0929-6646(10)60080-0</mixed-citation></ref><ref id="scirp.64271-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Magrath, I.T., Janus, C. and Dwards, B. (1984) An Effective Therapy for Both Undifferentiated (Including Burkitt’s) Lymphomas and Lymphoblastic Lymphomas in Children and Young Adults. Blood, 63, 1102-1111.</mixed-citation></ref></ref-list></back></article>