<?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.2016.61006</article-id><article-id pub-id-type="publisher-id">OJPed-64276</article-id><article-categories><subj-group subj-group-type="heading"><subject>Review</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Neonatal Necrotizing Fasciitis after Circumcision: A Case Report and Review of Literature
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>da</surname><given-names>L. Rivera Cruz</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>Zasha</surname><given-names>F. Vázquez Colón</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>Hector</surname><given-names>Quintero</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>Cesar</surname><given-names>Carballo Cuello</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>Victor</surname><given-names>N. Ortiz Justiniano</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Pediatric Surgery Department, Puerto Rico Children’s Hospital, Bayamón, Puerto Rico</addr-line></aff><aff id="aff2"><addr-line>Universidad Central del Caribe School of Medicine, Bayamón, Puerto Rico</addr-line></aff><aff id="aff1"><addr-line>Puerto Rico Children’s Hospital, Bayamón, Puerto Rico</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>paponoel2@gmail.com(VNOJ)</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>29</fpage><lpage>33</lpage><history><date date-type="received"><day>7</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>
 
 
  Background: Necrotizing fasciitis is a soft tissue infection that occurs predominantly in adults. Although rare, only 70 cases have been reported in neonates. This entity, most commonly caused by multiple organisms is often fatal, with 50% mortality. The combination of a low incidence and high mortality in this subgroup strengthens the need for early diagnosis, prompt recognition and immediate surgical treatment in order to improve survival. Aim: The aim of this case report is to bring awareness of a clinical condition that relies mostly on physical examination and where early diagnosis and immediate surgical treatment are needed in order to improve survival. Case presentation: We report the case of an 8-day-old boy presenting neonatal necrotizing fasciitis after circumcision. Patient presented with lower back erythema and areas of fluctuation. He was started on antibiotic therapy and 24 hours after admission, he was taken to the operating room for multiple fasciotomies, debridement and cleansing of affected areas. Findings were consistent with necrotizing fasciitis. After surgical intervention, local care was given until complete healing was achieved, approximately one month after admission. Conclusion: The surgeon must be attentive for the possible occurrence of this lethal infection that may develop post operatively after clean or clean-contaminated procedures. Preparation for treating these patients immediately with adequate fluid resuscitation, appropriate antibiotics and aggressive surgical debridement of non-viable tissue will provide the maximal potential for recovery. These prompt measures will offer the best chance for survival and eventually decrease the 50% mortality rate associated to the neonatal population.
 
</p></abstract><kwd-group><kwd>Cellulitis</kwd><kwd> Abscess</kwd><kwd> Subcutaneous</kwd><kwd> Erythema</kwd><kwd> Penrose</kwd><kwd> Debridement</kwd><kwd> Granulation</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Necrotizing Fasciitis (NF) is a rare and life threatening subcutaneous tissue infection. In the neonatal population, it occurs most commonly as a complication of surgical procedures such as circumcisions, or infections such as omphalitis and balanitis [<xref ref-type="bibr" rid="scirp.64276-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.64276-ref2">2</xref>] . NF is characterized by a widespread fascial necrosis with separation and infarction of the overlying skin and subcutaneous tissue [<xref ref-type="bibr" rid="scirp.64276-ref3">3</xref>] . The affected area may be erythematous, swollen, warm, shiny and painful [<xref ref-type="bibr" rid="scirp.64276-ref4">4</xref>] . Infants and neonates who develop this disease are characteristically healthy, unlike the adult population in which diabetes and immunosuppression serve as predisposing risk factors [<xref ref-type="bibr" rid="scirp.64276-ref5">5</xref>] . In adults, most cases arise in the extremities, while in neonates lesions predominantly occur in the abdominal wall and trunk area, predisposing for a mortality of nearly 50% [<xref ref-type="bibr" rid="scirp.64276-ref6">6</xref>] . The combination of a low incidence and high mortality in this subgroup strengthens the need for early diagnosis, prompt recognition and immediate surgical treatment in order to improve survival [<xref ref-type="bibr" rid="scirp.64276-ref7">7</xref>] . We present the case of an 8-day-old infant who developed necrotizing fasciitis after a circumcision.</p></sec><sec id="s2"><title>2. Case Report</title><p>Case of an 8-day-old baby boy had undergone circumcision at two days of age and was doing well until one day prior to admission when he developed fever. He was taken to the Emergency Room at another institution and on physical examination was found with lower back erythema consistent with cellulitis. He was transferred to our institution due to suspicion of abscess formation and for pediatric surgery evaluation. On physical examination he was found irritable, afebrile, with some areas of mild fluctuation and induration in the left buttock. A lumbosacral and buttock sonogram was performed and results came negative for abscess. Laboratory values revealed leukopenia at 3 &#215; 10<sup>9</sup>/L (3000 cells/μL) and a significantly elevated C-Reactive Protein (CRP) at 25 mg/dl (238.1 nmol/L). Broad-spectrum antibiotic therapy was started with Vancomycin and Gentamicin, along with intravenous fluid (IVF) hydration and bowel rest. After 24 hours of admission he was found irritable, with unchanged cellulitis and persistent lower back fluctuation. He was taken to the operating room for multiple fasciotomies, debridement and cleansing of affected areas. On gross examination there was grayish fascia with scattered necrosis and multiple areas of abscesses, consistent with necrotizing fasciitis and abscesses. Penrose drains were left in place to keep the wounds open (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Daily bedside debridement was performed and on postoperative day five, he was taken to the operating room for Penrose drains removal. Wound cultures were positive for Staphylococcus aureus and Citrobacter freundi susceptible to Vancomycin and Meropenem; antibiotics were tailored accordingly. Local care was performed on a daily basis with hydrogel wound dressing and subsequently with antimicrobial silver dressing until an adequate wound bed of granulation tissue was present.</p><p>Epithelialization and contraction were achieved by use of topical silver nitrate. Complete healing was reached approximately one month after admission (<xref ref-type="fig" rid="fig2">Figure 2</xref>). The patient was discharged home and followed up closely in the outpatient clinics.</p></sec><sec id="s3"><title>3. Discussion</title><p>In 1871, a confederate army surgeon, Joseph Jones was credited for describing NF infections as hospital gangrene [<xref ref-type="bibr" rid="scirp.64276-ref8">8</xref>] . Wilson was the first to describe this condition as necrotizing fasciitis in 1952. He stated the typical clinical presentation of NF that is tachycardia, fever and local infection leading to necrosis of the subcutaneous and superficial tissues [<xref ref-type="bibr" rid="scirp.64276-ref9">9</xref>] . This pathology most commonly occurs in adults, mainly affecting the extremities, contrary to neonates where it is considered rare and mostly involves the abdomen, low back and perineal area. In the neonatal population, it is usually associated with one of several underlying conditions such as omphalitis, mastitis, balanitis, necrotizing enterolocolitis, immunodeficiency, bullous impetigo, surgical wound infection, or trauma [<xref ref-type="bibr" rid="scirp.64276-ref10">10</xref>] -[<xref ref-type="bibr" rid="scirp.64276-ref14">14</xref>] . Our patient presented with NF a few days after circumcision, an unusual finding scarcely reported in the literature.</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Extensive erythema evident after debridement and placement of Penrose drains along with sloughed off skin and some devitalized tissue. Arrow direction is caudalad</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/6-1330470x7.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Complete wound healing approximately 3 months after admission</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/6-1330470x8.png"/></fig><p>An estimated one in three males worldwide is circumcised for religious, cultural or medical reasons [<xref ref-type="bibr" rid="scirp.64276-ref15">15</xref>] . In a large meta-analysis of prospective and retrospective series, Weiss et al. reported the median frequency of any adverse event of 1.5% [<xref ref-type="bibr" rid="scirp.64276-ref16">16</xref>] . Most commonly, adverse events include bleeding and infection. In rare cases, urethrocutaneous fistula, meatal stenosis, scabs, glanular amputation or necrosis, and necrotizing fasciitis, among others, have been documented.</p><p>Necrotizing soft tissue infections occurs when bacteria infect the superficial fascia. It can be caused by two bacteriological entities, type 1 which is polymicrobial and type 2 by group A beta hemolytic Streptococcal species. Type 1 is a mixed infection caused by aerobic and anaerobic bacteria and is highly correlated to risk factors such as diabetes, vascular disease, immune compromise, and recent surgery, such as circumcision in neonates. Type 2 occurs primarily among healthy individuals with recent skin injury, laceration or surgery [<xref ref-type="bibr" rid="scirp.64276-ref17">17</xref>] . There are limited cases reported of NF in the neonatal population, most are type 1 (polymicrobial) or type 2 with group A Streptococcus in combination with Staphylococcus aureus. Wound cultures of our patient were positive for Staphylococcus aureus and Citrobacter species, thus it can be categorized as type 1.</p><p>This pathology is thought to occur because bacteria secrete pyogenic exotoxins that stimulate inflammatory cytokine production by the host, producing a cascade of cytodestructive events such as shock, tissue destruction and possible organ failure [<xref ref-type="bibr" rid="scirp.64276-ref16">16</xref>] . Microvascular thrombosis leads to fat and fascial necrosis, causing a greater systemic inflammatory response that may lead to disfiguring wounds or potential multiorgan failure [<xref ref-type="bibr" rid="scirp.64276-ref18">18</xref>] .</p><p>Early in the disease, skin changes are variable as well as laboratory findings, for which timely diagnosis is based on a high index of suspicion. Clinical clues for diagnosis are: pain out of proportion to the clinical appearance of the affected skin, marked soft tissue edema, rapid symptom progression, and signs of systemic toxicity. Diagnosis of NF is mainly clinical, supported by advanced symptoms and sometimes crepitus.</p><p>Although laboratory studies are an important aspect in the workup for NF, the diagnosis is established definitively by surgical exploration. Radiographic studies, such as soft tissue plain films, or computed tomography (CT) scans, can be useful to assess muscle involvement, but it is not reliable for evaluation of the fascia. It is important to emphasize that surgical intervention should not be delayed while waiting for laboratories or other diagnostic studies. None of these diagnostic studies have shown to be effective in the diagnosis of NF. It relies mostly on high index of clinical suspicion, as we have previously stated [<xref ref-type="bibr" rid="scirp.64276-ref18">18</xref>] .</p><p>The gold-standard management of NF is surgical. It should consist of extensive fascial and soft tissue debridement along with hemodynamic support and antibiotic therapy. In our case, patient showed significant improvement after surgical debridement was done and treatment with intravenous antibiotics was started. Early intervention upon his worsening course allowed for his positive outcome.</p></sec><sec id="s4"><title>4. Conclusion</title><p>The surgeon must be attentive for the possible occurrence of this lethal infection that may develop post operatively after clean or clean-contaminated procedures. Preparation for treating these patients immediately with adequate fluid resuscitation, appropriate antibiotics and aggressive surgical debridement of non-viable tissue will provide the maximal potential for recovery. These prompt measures will offer the best chance for survival and eventually decrease the 50% mortality rate associated to the neonatal population [<xref ref-type="bibr" rid="scirp.64276-ref19">19</xref>] .</p></sec><sec id="s5"><title>Cite this paper</title><p>Ada L. RiveraCruz,Zasha F. V&#225;zquezCol&#243;n,HectorQuintero,Cesar CarballoCuello,Victor N. OrtizJustiniano,11, (2016) Neonatal Necrotizing Fasciitis after Circumcision: A Case Report and Review of Literature. Open Journal of Pediatrics,06,29-33. doi: 10.4236/ojped.2016.61006</p></sec><sec id="s6"><title>Abbreviations</title><p>Necrotizing fasciitis (NF), C-reactive protein (CRP), intravenous fluids (IVF), computed tomography (CT)</p></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.64276-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Hsieh, W., Yang, P., Chao, H. and Lai, J. 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