<?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">
    ojoph
   </journal-id>
   <journal-title-group>
    <journal-title>
     Open Journal of Ophthalmology
    </journal-title>
   </journal-title-group>
   <issn pub-type="epub">
    2165-7408
   </issn>
   <issn publication-format="print">
    2165-7416
   </issn>
   <publisher>
    <publisher-name>
     Scientific Research Publishing
    </publisher-name>
   </publisher>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="doi">
    10.4236/ojoph.2024.143020
   </article-id>
   <article-id pub-id-type="publisher-id">
    ojoph-134251
   </article-id>
   <article-categories>
    <subj-group subj-group-type="heading">
     <subject>
      Articles
     </subject>
    </subj-group>
    <subj-group subj-group-type="Discipline-v2">
     <subject>
      Medicine 
     </subject>
     <subject>
       Healthcare
     </subject>
    </subj-group>
   </article-categories>
   <title-group>
    Bilateral Congenital Upper Eyelid Eversion (Ectropion): A Rare Presentation Responded Well to Conservative Treatment at Temeke Regional Referral Hospital-Tanzania
   </title-group>
   <contrib-group>
    <contrib contrib-type="author" xlink:type="simple">
     <name name-style="western">
      <surname>
       Husna
      </surname>
      <given-names>
       Msangi
      </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>
       Annamary
      </surname>
      <given-names>
       Stanslaus
      </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>
       Hussein
      </surname>
      <given-names>
       Msuma
      </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>
       Salha
      </surname>
      <given-names>
       Omary
      </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>
       Milka
      </surname>
      <given-names>
       Mafwiri
      </given-names>
     </name> 
     <xref ref-type="aff" rid="aff4"> 
      <sup>4</sup>
     </xref>
    </contrib>
   </contrib-group> 
   <aff id="aff1">
    <addr-line>
     aDepartment of Ophthalmology, Temeke Regional Referral Hospital, Dar-es-salaam, Tanzania
    </addr-line> 
   </aff> 
   <aff id="aff2">
    <addr-line>
     aDepartment of Surgery and Urology, Temeke Regional Referral Hospital, Dar-es-salaam, Tanzania
    </addr-line> 
   </aff> 
   <aff id="aff3">
    <addr-line>
     aDepartment of Paediatric and Child Health, Temeke Regional Referral Hospital, Dar-es-salaam, Tanzania
    </addr-line> 
   </aff> 
   <aff id="aff4">
    <addr-line>
     aDepartment of Ophthalmology, Muhimbili University of Health and Allied Sciences, Dar-es-salaam, Tanzania
    </addr-line> 
   </aff> 
   <pub-date pub-type="epub">
    <day>
     07
    </day> 
    <month>
     06
    </month>
    <year>
     2024
    </year>
   </pub-date> 
   <volume>
    14
   </volume> 
   <issue>
    03
   </issue>
   <fpage>
    204
   </fpage>
   <lpage>
    207
   </lpage>
   <history>
    <date date-type="received">
     <day>
      7,
     </day>
     <month>
      April
     </month>
     <year>
      2024
     </year>
    </date>
    <date date-type="published">
     <day>
      25,
     </day>
     <month>
      April
     </month>
     <year>
      2024
     </year> 
    </date> 
    <date date-type="accepted">
     <day>
      25,
     </day>
     <month>
      June
     </month>
     <year>
      2024
     </year> 
    </date>
   </history>
   <permissions>
    <copyright-statement>
     © 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>
    Congenital eversion of the upper eyelids is a rare condition, the exact cause of which remains unknown. It is more frequently associated with Down’s syndrome and black babies. If diagnosed early and treated properly, the condition can be managed without surgery. We report a case of non syndromic congenital bilateral severe upper eyelid eversion in otherwise normal 3 days old neonate of African descent (Tanzanian), born by vaginal delivery. The case was conservatively managed by lubricants, antibiotics and eyelid patching. We report this case because from the best of our knowledge it has never been documented here at our hospital and Tanzania before.
   </abstract>
   <kwd-group> 
    <kwd>
     Upper Eyelid Eversion
    </kwd> 
    <kwd>
      Congenital Ectropion
    </kwd> 
    <kwd>
      Conservative Management
    </kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <sec id="s1">
   <title>1. Introduction</title>
   <p>Described for the 1st time in 1896 by Adams as a case of double congenital ectropion, in which the eyelid is completely turned out, with prolapsed conjunctiva and chemosis. Most of the cases described in literature were present at birth, but some cases of late onset have also been reported <xref ref-type="bibr" rid="scirp.134251-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.134251-2">
     [2]
    </xref>.</p>
  </sec><sec id="s2">
   <title>2. Case Presentation</title>
   <p>This is case report of a 3-day-old male baby who was referred to our facility 24 hours after delivery with bilateral eversion of the upper eyelids. The baby was born at term by spontaneous vertex delivery with 3.4 kg and no reported birth trauma. The prenatal history was uneventful.</p>
   <p>On examination: There were out turning of the both eyes (more on the left eye), with chemosis of conjunctiva of both eyes, and no discharge. The rest of anterior segment examination findings were normal (<xref ref-type="fig" rid="fig1">
     Figure 1
    </xref>).</p>
   <p>A diagnosis of bilateral congenital ectropion was reached and possible differentials like Downs syndrome and TORCHES were ruled out. The patient was managed conservatively with pressure dressing by sterile gauze soaked in normal saline. The patient completely resolved with 7 days of treatment with no complications (<xref ref-type="fig" rid="fig2">
     Figure 2
    </xref>). We had a holistic approach of which the treatment team to this rare condition included ophthalmologist, general surgeon and pediatrician.</p>
   <fig id="fig1" position="float">
    <label>Figure 1</label>
    <caption>
     <title>Figure 1. Appearance of the 1-day-old baby with congenital bilateral upper eye lid eversion on admission to our facility</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2020761-rId12.jpeg?20240628042451" />
   </fig>
   <fig id="fig2" position="float">
    <label>Figure 2</label>
    <caption>
     <title>Figure 2. Complete resolution of ectropion after 7 days of conservative therapy.</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2020761-rId13.jpeg?20240628042451" />
   </fig>
  </sec><sec id="s3">
   <title>3. Discussion</title>
   <p>Congenital eversion of upper eyelids is a very rare presentation. The underlying cause of the disease remains largely unknown, yet several possible mechanisms have been postulated. Birth trauma, orbicularis muscle hypotonia, vertical shortening of the anterior eyelid lamella or vertical elongation of the posterior eyelid lamella, lateral elongation of the lid, failure of the orbital septum to fuse with the levator aponeurosis, and absence of an effective lateral canthal ligament have been implied as probable underlying causes <xref ref-type="bibr" rid="scirp.134251-2">
     [2]
    </xref> <xref ref-type="bibr" rid="scirp.134251-3">
     [3]
    </xref> <xref ref-type="bibr" rid="scirp.134251-4">
     [4]
    </xref> <xref ref-type="bibr" rid="scirp.134251-5">
     [5]
    </xref>. Our 3 days neonate had no reported birth trauma and on physical examination did not reveal any skeletal deformity.</p>
   <p>The incidence appears higher in black infants, infants with trisomy 212 and infants born with collodion skin disease <xref ref-type="bibr" rid="scirp.134251-6">
     [6]
    </xref> <xref ref-type="bibr" rid="scirp.134251-7">
     [7]
    </xref>. Moreover most cases are bilateral and present at birth; however, unilateral and late onset have been reported as well <xref ref-type="bibr" rid="scirp.134251-3">
     [3]
    </xref> <xref ref-type="bibr" rid="scirp.134251-5">
     [5]
    </xref>. The index case is of black descent and presented at birth with bilateral disease. In addition he did not have neither clinical nor radiological features of Down’s syndrome no collodion skin disease.</p>
   <p>Generally, conservative management is favoured and surgical options usually become necessary in recalcitrant type. Conservative treatment is mostly supportive and it includes the use of 5% hypertonic saline and lubricant. Documented surgical options include the use of compression sutures, tarsorrhaphy with excision of redundant conjunctiva, subconjunctival injection of hyaluronic acid, fornix sutures, and full thickness skin graft to the upper lid <xref ref-type="bibr" rid="scirp.134251-4">
     [4]
    </xref> <xref ref-type="bibr" rid="scirp.134251-8">
     [8]
    </xref> <xref ref-type="bibr" rid="scirp.134251-9">
     [9]
    </xref>. The present case was treated conservatively with pressure dressing of sterile gauze soaked in normal saline. Complete recovery was achieved within a week of treatment.</p>
  </sec><sec id="s4">
   <title>4. Conclusion</title>
   <p>Despite of the debate on the best mode of treatment of these cases, based on our experience on the management of the index case we still recommend on conservative approach over surgery when patients present early.</p>
  </sec>
 </body><back>
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</article>