<?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">OJRad</journal-id><journal-title-group><journal-title>Open Journal of Radiology</journal-title></journal-title-group><issn pub-type="epub">2164-3024</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojrad.2019.91003</article-id><article-id pub-id-type="publisher-id">OJRad-90005</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  Imaging Findings of Children Stroke in Burkina Faso and Etiological Approach
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bénilde</surname><given-names>Marie Ange Tiemtore-Kambou</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>Prosper</surname><given-names>Précieux Sagbohan</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>Dominique</surname><given-names>Bicaba</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>Nina-Astrid</surname><given-names>Nde-Ouedraogo</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Zakari</surname><given-names>Nikiema</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Prosper</surname><given-names>David Lamien</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Adama</surname><given-names>Gnoumou</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Oussé&amp;iuml;ni</surname><given-names>Diallo</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rabiou</surname><given-names>Cisse</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib></contrib-group><aff id="aff5"><addr-line>Yalgado Ouedraogo Teaching Hospital, Ouagadougou, Burkina Faso</addr-line></aff><aff id="aff1"><addr-line>Faculty of Health Sciences, Ouaga 1 Pr Joseph Ki-Zerbo University, Ouagadougou, Burkina Faso</addr-line></aff><aff id="aff3"><addr-line>SanouSouroTeaching Hospital, Bobo-Dioulasso, Burkina Faso</addr-line></aff><aff id="aff2"><addr-line>Bogodogo Teaching Hospital, Ouagadougou, Burkina Faso</addr-line></aff><aff id="aff4"><addr-line>Yati Clinic, Ouagadougou, Burkina Faso</addr-line></aff><pub-date pub-type="epub"><day>04</day><month>01</month><year>2019</year></pub-date><volume>09</volume><issue>01</issue><fpage>20</fpage><lpage>35</lpage><history><date date-type="received"><day>25,</day>	<month>October</month>	<year>2018</year></date><date date-type="rev-recd"><day>15,</day>	<month>January</month>	<year>2019</year>	</date><date date-type="accepted"><day>18,</day>	<month>January</month>	<year>2019</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: Stroke is defined as a sudden onset focal neurological deficit of presumed vascular origin. Although it is essentially adult and elderly condition, stroke can occur in children. Their diagnosis essentially radiological is based on two main imaging modalities namely Computed Tomography (CT) and/or Magnetic Resonance Imaging (MRI). Our study aimed to study radiological features of stroke in children with an etiologic approach in three health facilities of Ouagadougou. 
  Material and Method: We conducted a retrospective study with descriptive focus during 11-year period from January 1
  <sup>st</sup>, 2006 to September 1
  <sup>st</sup>, 2017 among children aged between 02 months and 16 years who underwent brain CT scan and/or MRI; in whom diagnosis of stroke had been established in radiology department of Yalgado Ouedraogo Teaching Hospital (CHU-YO), Schiphra Methodist Medical Center (CM Schipphra) and Saint Camille Hospital of Ouagadougou (HOSCO). 
  Results: 40 cases of pediatric stroke were collected including 23 at HOSCO, 15 at CHU-YO and 03 at CM Schipphra. Mean age was 6.45 years, with extremes of 2 months and 192 months. Unilateral contralateral motor weakness was the most common clinical presentation (32.5%) followed by seizures (17.5%). Ischemic stroke dominated in 82.5% of cases. Sino-venous thrombosis was rare and suspected in only one case. Sylvian artery was mostly affected in ischemic stroke for 56.25% of patients. The main etiologic factors found were hematologic (67.50%) then infectious factors (25%). Sickle cell disease was always incriminated in hematologic factor. Homozygous SS patients were the most numerous (82%).
   Conclusion: Stroke diagnosis in children is based on etiologic investigation, biology with a major role of medical imaging. Sickle cell disease accounts a lot in occurrence of stroke in children in our context.
 
</p></abstract><kwd-group><kwd>Stroke</kwd><kwd> Children</kwd><kwd> Brain CT/MRI</kwd><kwd> Ouagadougou</kwd><kwd> Burkina Faso</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Stroke is defined by World Health Organization (WHO) as “a clinical syndrome consisting of rapidly developing clinical signs of focal (or global in case of coma) disturbance of cerebral function lasting more than 24 hours or leading to death with no apparent cause other than a vascular origin” [<xref ref-type="bibr" rid="scirp.90005-ref1">1</xref>].</p><p>Although it is mainly adult and elderly disease, stroke can occur at any age notably in children.</p><p>Pediatric stroke is a relatively rare disease with an estimated incidence of 2.5 - 13/100,000/year [<xref ref-type="bibr" rid="scirp.90005-ref2">2</xref>]. Its mortality rate is about 0.6/100,000/year [<xref ref-type="bibr" rid="scirp.90005-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref4">4</xref>]. Child stroke has also serious morbidity and long-term outcome marked by its socio-psychological impact and costs particularly in our precarious context. From hence early diagnosis enabling specific treatment including thrombolysis or embolization is required to minimize occurrence of sequelae.</p><p>Stroke diagnosis in children is based on etiological investigation, laboratory tests and major role of medical imaging. Imaging modalities used in emergency are Computed Tomography (CT) and Magnetic Resonance Imaging (MRI). They help to confirm diagnosis, to determine type of stroke, to search etiology, to guide and participate in treatment, to recognize signs of severity, and to follow up.</p><p>However in our context, a particular cause is Sickle Cell Disease (SCD). Stroke is the most severe complication of SCD. Though Ogeng’o in Kenya noted a pediatric ischemic stroke prevalence of 56.3% compared to 43.7% of hemorrhagic stroke [<xref ref-type="bibr" rid="scirp.90005-ref5">5</xref>]. In Burkina Faso, B&#233;r&#233; [<xref ref-type="bibr" rid="scirp.90005-ref6">6</xref>] noted ischemic CT lesions as cause of cerebral palsy in child with a frequency of 6.7%. No studies have been done on pediatric stroke in our context.</p><p>We propose to study radiological features of stroke in children with an etiological approach.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>We conducted a descriptive retrospective study from January 1<sup>st</sup>, 2006 to September 1<sup>st</sup>, 2017, in radiology departments of Yalgado Ouedraogo Teaching Hospital (CHU-YO), Schiphra Protestant Medical Center and Saint Camille Hospital of Ouagadougou (HOSCO) of Burkina Faso.</p><p>This study concerned children from 02 months to 16 years old who underwent head CT scan and/or MRI in one of the three health facilities previously mentioned and for whom diagnosis of stroke had been established. We have expressly excluded children under two months because of challenge in achieving and obtaining results of a brain CT/MRI scan in our context of those children (sedation requirement) and also predominance of obstetric and perinatal causes.</p><p>For head CT exam, we used GENERAL ELECTRIC HISPEED 08 slices machine at Schiphra Protestant Medical Center, SIEMENS SOMATOM EMOTION 32 slices and 64 slices devices respectively at HOSCO and CHU-YO.</p><p>Complementary brain MRI scan were performed at HOSCO using a SIEMENS MAGNETOM ESSENZA 1.5 Tesla device.</p><p>Images were reported by a senior radiology consultant.</p><p>Useful information was collected via data collection forms. Variables of our study were:</p><p>- Epidemiological: age, sex, educational levels;</p><p>- Clinical: neurological symptoms, general signs;</p><p>- Radiological:</p><p>・ Imaging modalities;</p><p>・ Type of stroke;</p><p>・ Spontaneous hyperdensity (location, volume, intraventricular hemorrhagic flood, subarachnoid hyperdensity, brain herniation);</p><p>・ Hypodense area (localization, vascular territory;</p><p>・ Early CT signs of ischaemic stroke: cortical hypo density with associated parenchymal swelling with resultant gyral effacement (e.g. insular ribbon sign), loss of grey-white matter differentiation, and hypo attenuation of deep nuclei, hyper dense segment of a vessel;</p><p>・ Hyperdensity within a thrombosed sinus;</p><p>- Etiological factors: hematological, infectious, cerebral, cardiac, surgical.</p><p>For patients diagnosed of stroke, data was collected from TDM and/or MRI scans records and patient interviews available.</p><p>Data analysis was performed on Windows 7 computer using Excel statistical tools for data entry and Epi Info for processing. MRI images were viewed on Radiant Dicom 32-bit viewer software.</p><p>Data collection was managed in anonymity and absolute confidentiality. The study was conducted with authorization of Head of Department in the three health centers.</p></sec><sec id="s3"><title>3. Results</title><p>There were 3482 cerebral CT scans performed between 2006 and 2017 in the three health centers, and 174 brain MRI exams performed between 2013 and 2017 at HOSCO which had established stroke diagnosis.</p><p>A total of 40 children aged from 2 months to 16 years had a diagnosis of stroke on CT and/or MRI, which represents 1.14% of CT scans. Among them, 23 (57.5%) were followed up at HOSCO, 15 (37.5%) at CHU-YO and 03 (5%) at Schiphra Protestant Medical Center.</p><p>Mean age of patients was 77.55 &#177; 57.75 months, or 6.45 years with interval ends of 2 and 192 months. The most represented age group were children over 5 (60 months) counting 55% of all (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>Male sex was dominant in 57.50% of cases (n = 23). Sex ratio was 1.35.</p><p>Distribution of patients by clinical signs was summarized on <xref ref-type="table" rid="table1">Table 1</xref>.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of patients by clinical signs</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Clinical sign</th><th align="center" valign="middle" >Size</th></tr></thead><tr><td align="center" valign="middle" >Coma</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Lethargy</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Mental retardation</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Aphasia</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Headache</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >Seizures</td><td align="center" valign="middle" >7</td></tr><tr><td align="center" valign="middle" >Unilateral contralateral motor weakness</td><td align="center" valign="middle" >13</td></tr><tr><td align="center" valign="middle" >Fever</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >General state worsening during acute sickle cell crisis</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Abnormal ballet movements</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Repeated loss of consciousness</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Psychomotor delay</td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >Amnesia</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Behavioral disorder</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Mixed symptoms</td><td align="center" valign="middle" >5</td></tr></tbody></table></table-wrap><p>Unilateral contralateral motor weakness was the most frequent sign (n = 13) followed by tonic-clonic seizures (n = 7) and psychomotor delay (n = 4).</p><p>All 40 patients underwent brain CT scan. Complementary MRI was performed by 03 patients or 7.5% of cases. <xref ref-type="fig" rid="fig2">Figure 2</xref> shows distribution of TDM examinations by year. The highest rate of performing CT scan was observed in 2015 and 2017.</p><p>Ischemic stroke dominated in 82.5% of cases (n = 33 patients) followed by hemorrhagic stroke in 15% (n = 6). Sino-venous thrombosis was rare suspected in one child (n = 1).</p><p>Three patients (7.5%) CT scans demonstrate area of intracerebral hyperdensity representing hematoma. Two were located in left frontal and left temporal lobes; the third in right parietal lobe. <xref ref-type="fig" rid="fig3">Figure 3</xref> illustrates these hematomas. There was no brain herniation or meningeal irritation associated with these hematomas.</p><p>Subarachnoid hyperdensities were observed in 4 patients. <xref ref-type="fig" rid="fig4">Figure 4</xref> shows a case of subarachnoid hemorrhage.</p><p>34 (85%) patients had one or more intracerebral hypo attenuated including one suspected case of cerebral venous thrombosis. 32.3% of them were found in right hemisphere and 47.1% in left hemisphere. 20.6% cases demonstrated bilateral hemisphere involvement.</p><p>Superficial middle cerebral artery (MCA) was most affected in 10 (31.25%) patients followed by deep MCA in 8 (25%) and border zones ischemic stroke between MCA and ACA concerning 2 cases.</p><p>Figures 5-7 show CT features of these hypodensities.</p><p>Hyperdensity within a cerebral artery was found in two patients.</p><p><xref ref-type="table" rid="table2">Table 2</xref> presents associated CT signs of our patients. Cerebral atrophy was frequently associated in 12 patients.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Others associated CT findings to infarcts</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >CT Findings</th><th align="center" valign="middle" >Number</th></tr></thead><tr><td align="center" valign="middle" >Subarachnoid enhancement</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Calcifications</td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >Brain atrophy</td><td align="center" valign="middle" >12</td></tr><tr><td align="center" valign="middle" >Extra-axial fluid collection</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Brain edema</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Feeding by superficial artery</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Subfalcine mid-line shift</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Ventricular hemorrhage</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Tentorium cerebelli subarachnoid hemorrhage</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Tetraventricular hydrocephalus</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Recurrent infarction</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >25</td></tr></tbody></table></table-wrap><p>Brain MRI was performed in 03 patients (7.5%) and ischemic stroke or sequellae of ischemic stroke had been diagnosed in all cases.</p><p>These MRI features are shown on Figures 8-10.</p><p>Etiological investigation was made in 30 (75%) patients. <xref ref-type="fig" rid="fig1">Figure 1</xref>1 shows distribution of patients by risk factors and etiologies.</p><p>Hematologic factors were dominant (n = 27) followed by infectious factors (n = 8).</p><p>Sickle cell disease was the main hematological factor. Homozygous SS patients were frequently seen in 82% of cases followed by SC heterozygotes (11%) and thalassemic patients (7%).</p><p>Cardiovascular factors observed were tetralogy of Fallot (n = 1), inter-atrial communication (n = 1) and high blood pressure (n = 1).</p><p>Chickenpox was mentioned as history in 06 (15%) patients. Delay between these episodes of varicella and stroke onset could not be clearly determined by parents. Other associated risk factors were mentioned including a case of meningoencephalitis and a case of encephalitis.</p><p>Cerebral factors observed were brain trauma (n = 1), cerebral angioma (n = 1) and AVM (n = 1). <xref ref-type="fig" rid="fig1">Figure 1</xref>2 depicts AVM case.</p><p>We noticed a case of ischemic stroke after cervical vascular tumor surgery in a 16-year-old teenager. Follow-up has been favorable for most patients. We did not register any deaths. Sequellae were observed in 04 patients including one case of limping and three cases of mental retardation.</p></sec><sec id="s4"><title>4. Discussion</title><p>Study on radiological features of stroke in children with etiological approach is a first onset in Burkina Faso. Our study faced some difficulties.</p><p>・ Indeed, it is a relatively rare pathology in children unlike adults.</p><p>・ No studies were conducted on that subject in Burkina Faso.</p><p>・ Stroke diagnosis requires imaging devices, notably CT and MRI, which have recently established in certain health facilities in Ouagadougou. The high cost of these imaging modality prior to onset of free care management of less than 5 years patients has limited size of our sample.</p><p>・ Use of patient’s folders has been difficult due to poor archiving and preservation of CT/MRI images by both parents and Pediatric department.</p><p>Our study has, however, leaded results that raised comments and discussion.</p><p>According to several studies, stroke is less common in children than in adults [<xref ref-type="bibr" rid="scirp.90005-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref9">9</xref>]. We were able to enroll 40 children aged 2 months to 16 years during 11-years period from 2006 to 2017. This number corroborates literature data estimating the annual incidence of child strokes between 1.3 to 13 years for 100,000 children-years [<xref ref-type="bibr" rid="scirp.90005-ref10">10</xref>]. Mean age of our patients was 6.45 years. Sagna, Lengue and Steinlin [<xref ref-type="bibr" rid="scirp.90005-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref11">11</xref>] found younger age groups (less than 5 years). This could be explained by predominance in their study of para-infectious and infectious risk factors whose peak is at preschool years. Male predominance found is consistent with literature data [<xref ref-type="bibr" rid="scirp.90005-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref12">12</xref>]. According to Steinlin and al, for unknown reasons, stroke is twice as likely in boys as in girls [<xref ref-type="bibr" rid="scirp.90005-ref11">11</xref>]. However, literature remains controversial with some studies that find female predominance [<xref ref-type="bibr" rid="scirp.90005-ref13">13</xref>].</p><p>Clinical presentation of stroke in our sample is predominantly marked by deficient hemi-corporeal motor. This sign was also found in some studies where hemiplegia prevalence could reach 70% to 80% [<xref ref-type="bibr" rid="scirp.90005-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref12">12</xref>]. This hemiplegia was followed closely by seizures in our series as well as in some literature data [<xref ref-type="bibr" rid="scirp.90005-ref14">14</xref>]. Non-focal deficient symptoms likely headache (7.5%), disturbances of consciousness (12.5%), psychomotor retardation (12.5%) were also identified as clinical presentation of child stroke [<xref ref-type="bibr" rid="scirp.90005-ref15">15</xref>].</p><p>Brain CT scan had been performed in 18, 75% of patients in 2015 and 2017. This peak in 2017 could be explained by success of free care to children under 05 in our health policy.</p><p>In opposite, brain MRI scan performing is very low (7.5%) as it is not free despite the fact that it is the gold standard in stroke diagnosis. Among the three health facilities of our cohort, only HOSCO which is a private center is fitted with a 1.5 tesla MRI machine and the cost of brain MRI scan is 100,000 XOF. Despite its weak performing in our study, contribution of MRI is undeniable.</p><p>Predominance of ischemic stroke (82.5%) compared to other types of stroke, particularly hemorrhagic stroke (15%), corroborates results of a US study [<xref ref-type="bibr" rid="scirp.90005-ref16">16</xref>] based on follow-up of 4000 patients during 10 years which found that ischemic stroke occurs mainly before 20 with high-level risk between 1 and 9 years while hemorrhagic stroke is mostly seen after 20.</p><p>Ischemia was located firstly in sylvian artery territory (56.25%) as found by Sagna [<xref ref-type="bibr" rid="scirp.90005-ref9">9</xref>] , Ogeng’o [<xref ref-type="bibr" rid="scirp.90005-ref5">5</xref>] , Tohodj&#232;d&#233; [<xref ref-type="bibr" rid="scirp.90005-ref12">12</xref>] and Ndiaye [<xref ref-type="bibr" rid="scirp.90005-ref7">7</xref>]. This topographic distribution is related to a particular architecture of vascular tree for brain. In fact, MCA is the widest and most direct branch of the endings of internal carotid artery; therefore it leads to receive the most emboli [<xref ref-type="bibr" rid="scirp.90005-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref20">20</xref>].</p><p>Cerebral atrophy was the most associated CT sign in our sample (30%). For some authors, it could be a risk marker for ischemic stroke or intracranial hemorrhage and could explain cognitive disorders seen with some patients [<xref ref-type="bibr" rid="scirp.90005-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref21">21</xref>].</p><p>In our study main etiologies involved in stroke were hematological factors (67.50%) followed by infectious factors (25%) and cerebral factors (20%). Some African studies found similar results [<xref ref-type="bibr" rid="scirp.90005-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref12">12</xref>] with hematologic factors ranked first. The main etiological and hematological factor found was homozygous SS of sickle cell disease (82%). This important source of cerebral infarction in children [<xref ref-type="bibr" rid="scirp.90005-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref23">23</xref>] , is commonly seen in sub-Saharan African population. From our study, we noted that sickle-cell child developed stroke around 6.8 years. This data could help in stroke prevention. In fact, sickle cell disease increases risk of cerebral infarction by 200 to 400 [<xref ref-type="bibr" rid="scirp.90005-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref15">15</xref>]. Therefore stroke is one of the most serious complications of sickle cell disease which requires adequate management including early detection for better monitoring to avoid subsequent complications such as cerebral vasculopathy. Chung in China [<xref ref-type="bibr" rid="scirp.90005-ref24">24</xref>] didn’t find any case of sickle cell disease in his cohort; this difference could be related to the high prevalence of sickle cell disease in Africa and particularly in its black population. Sickle cell disease is also known to increase the risk of stroke recurrence. Elsewhere a study based on Chinese children recorded rather central nervous system infections, Moyamoya disease and head trauma as main causes of pediatric stroke [<xref ref-type="bibr" rid="scirp.90005-ref25">25</xref>].</p><p>Cardiac embolism is thought to account for 3.7% to 33.3% of ischemic stroke [<xref ref-type="bibr" rid="scirp.90005-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref20">20</xref>]. In our patient group, we mainly found congenital heart diseases such as tetralogy of Fallot and atrial septal defect, unlikely to SALIH’s study in Saudi Arabia where it was acquired rheumatic heart disease [<xref ref-type="bibr" rid="scirp.90005-ref26">26</xref>]. Acquired rheumatic heart disease is a common post-streptococcal complication. Is their rarity in our study due to good management of group A post-streptococcal disorders in children?</p><p>Cerebral risk-factors have also been found in literature [<xref ref-type="bibr" rid="scirp.90005-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref14">14</xref>]. According to B&#233;jot [<xref ref-type="bibr" rid="scirp.90005-ref14">14</xref>] , main cause of intracranial hemorrhage in children is arteriovenous malformation (AVM) rather than high blood pressure that is observed in adult. They account for between 14% and 57% of all brain bleeding causes depending on studies and annual risk of cerebral hemorrhage in children with AVM is about 3%. Angioma, which has been poorly screened before arrival of MRI, could however represent up to 25% of cases of cerebral hemorrhage [<xref ref-type="bibr" rid="scirp.90005-ref14">14</xref>].</p><p>We did not notice any deaths in our series. Lengue [<xref ref-type="bibr" rid="scirp.90005-ref8">8</xref>] reported a mortality rate of 0.92% that was the lowest of 4% to 28% [<xref ref-type="bibr" rid="scirp.90005-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.90005-ref27">27</xref>]. However, this absence of death is subject to the 10 patients who could not be reached during interview because of wrong number in CT and MRI report registers.</p><p>In our cohort, 04 patients had long-term sequellae such as lameness and mental retardation. Ndiaye [<xref ref-type="bibr" rid="scirp.90005-ref7">7</xref>] and Tohodj&#232;d&#233; [<xref ref-type="bibr" rid="scirp.90005-ref2">2</xref>] obtained similar results. These stroke sequellae are current in literature [<xref ref-type="bibr" rid="scirp.90005-ref14">14</xref>]. The observed sequellae are numerous and could increase socio-economic impact of this pathology especially in our countries with limited resources and affect severely prognosis of these children.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Pediatric stroke is predominantly ischemic with sickle-cell disease as main cause. CT is first-line imaging modality and contributes a lot in stroke diagnosis in our context. However, MRI which is the gold standard imaging modality in this investigation is poorly used in Burkina Faso. Etiological predominance of sickle cell disease suggests implementation of adequate prevention measures to control this pathology. In addition, the prevention of stroke recurrence with hematologic etiology is based on establishment of blood transfusion program aimed at lowering S Hemoglobin level and decreasing cerebral arteries velocity on transcranial Doppler scan. This technique is not yet implemented in our context. Future prospective studies on the contribution of this transfusion program to the secondary prevention of stroke in sickle cell patients are therefore necessary.</p><p>Further prospective study on contribution of this blood transfusion program in stroke prevention of sickle cell’s patients is therefore needed.</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>Tiemtore-Kambou, B.M.A., Sagbohan, P.P., Bicaba, D., Nde-Ouedraogo, N.-A., Nikiema, Z., Lamien, P.D., Gnoumou, A., Diallo, O. and Cisse, R. (2019) Imaging Findings of Children Stroke in Burkina Faso and Etiological Approach. 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