<?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">CRCM</journal-id><journal-title-group><journal-title>Case Reports in Clinical Medicine</journal-title></journal-title-group><issn pub-type="epub">2325-7075</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/crcm.2021.102005</article-id><article-id pub-id-type="publisher-id">CRCM-107312</article-id><article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  A Case Report of an Invasive Scalp Actinomycosis
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Youssouf</surname><given-names>Sogoba</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>Jean</surname><given-names>Paul Dembele</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>Boubacar</surname><given-names>Sogoba</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>Moussa</surname><given-names>Diallo</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>Seybou</surname><given-names>Hassane Diallo</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>Oumar</surname><given-names>Coulibaly</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>Quenum</surname><given-names>Kisito</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>Oumar</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>Drissa</surname><given-names>Kanikomo</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>Youssoufa</surname><given-names>Maiga</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Infectious Diseases, H&amp;amp;ocirc;pital du Point G, Bamako, Mali</addr-line></aff><aff id="aff3"><addr-line>Department of Neurologie, H&amp;amp;ocirc;pital Gabriel Touré, Bamako, Mali</addr-line></aff><aff id="aff5"><addr-line>Department of Neurosurgery, University Hospital of Parakou, Parakou, Benin</addr-line></aff><aff id="aff4"><addr-line>Department of Neurosurgery, H&amp;amp;ocirc;pital du Mali, Bamako, Mali</addr-line></aff><aff id="aff1"><addr-line>Department of Neurosurgery, H&amp;amp;ocirc;pital Gabriel Touré, Bamako, Mali</addr-line></aff><pub-date pub-type="epub"><day>20</day><month>02</month><year>2021</year></pub-date><volume>10</volume><issue>02</issue><fpage>34</fpage><lpage>38</lpage><history><date date-type="received"><day>16,</day>	<month>January</month>	<year>2021</year></date><date date-type="rev-recd"><day>21,</day>	<month>February</month>	<year>2021</year>	</date><date date-type="accepted"><day>24,</day>	<month>February</month>	<year>2021</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: Actinomycosis is a bacterial infection characterized by a chronic, suppurative and granulomatous process. The causative organism was identified in 1891 as 
  <em>Actinomycosis israelii</em>. The disease is usually caused by the introduction of the bacteria through minor wound. Actinomycosis was classified by Cope into 3 different forms: cervicofacial (50%), pulmonothoracic (30%) and abdominopelvic (20%). Actinomycosis is an insidious disease but occasionally the clinical course can be more aggressive, involving underline tissue and organs. Involvement of scalp by actinomycosis is rare causing diagnostic dilemma and could be mistaken for different pathologies, such as tuberculosis or carcinoma. The most common clinical findings are local tumefaction with abscesses and sinuses draining pus that contains the granule of the causative organism. CT scan and MRI are aspecific for diagnosis, but they can help in defining the localization and the extension of the lesion. The certain diagnostic is based on cytology and/or biopsy. 
  Case: A 24 year-old-man was admitted to our neurosurgical department with a 16-month history of multiple scalp ulcerated lesions and swelling of the head. He was complaining of headache. Physical examination revealed multiple scalp subcutaneous nodules and ulcerated lesions with swelling of the head. Our examination of the oral cavity revealed a poor oral hygiene condition with multiple caries. The CT scan revealed multiple scalp subcutaneous masses with chronic inflammatory changes of the skull. Routine laboratory test was normal. Surgical biopsy was performed and the histological result was compatible with actinomycosis. After histological confirmation, parenteral Penicillin 20 million units daily were given for 4 weeks. Clinical improvement was observed after completing a 4-week regimen of intravenous antibiotics. 
  Conclusion: Involvement of scalp by actinomycosis could be mistaken for different pathologies, such as tuberculosis or carcinoma. This emphasizes the importance of biopsy for histological confirmation of the disease.
 
</p></abstract><kwd-group><kwd>Actinomycosis</kwd><kwd> Bacterial Infection</kwd><kwd> Computed Tomography</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Actinomycosis is a bacterial infection characterized by a chronic, suppurative and granulomatous process [<xref ref-type="bibr" rid="scirp.107312-ref1">1</xref>]. The causative organism was identified in 1891 as Actinomycosisisraelii [<xref ref-type="bibr" rid="scirp.107312-ref2">2</xref>]. The disease is usually caused by the introduction of the bacteria through minor wound. Actinomycosis was classified by Cope into 3 different forms: cervicofacial (50%), pulmonothoracic (30%) and abdominopelvic (20%) [<xref ref-type="bibr" rid="scirp.107312-ref3">3</xref>]. It is an insidious disease but occasionally the clinical course can be more aggressive, involving underline tissue and organs. Involvement of scalp by actinomycosis is rare causing diagnostic dilemma and could be mistaken for different pathologies, such as tuberculosis or carcinoma [<xref ref-type="bibr" rid="scirp.107312-ref4">4</xref>]. The most common clinical findings are local tumefaction with abscesses and sinuses draining pus that contains the granule of the causative organism. CT scan and MRI are aspecific for diagnosis, but they can help in defining the localization and the extension of the lesion [<xref ref-type="bibr" rid="scirp.107312-ref5">5</xref>]. The certain diagnostic is based on cytology and/or biopsy [<xref ref-type="bibr" rid="scirp.107312-ref6">6</xref>]. In this paper, the authors report a rare case of an invasive scalp actinomycosis that was successfully treated with prolonged intravenous and oral antibiotics.</p></sec><sec id="s2"><title>2. Case Report</title><p>A 24-year-old-man was admitted to our neurosurgical department with a 16-month history of multiple scalp ulcerated lesions and swelling of the head. The patient had a history of headache but no fever. On admission, his body temperature was 37.5˚C, blood pressure 110/70 mmHg, heart rate 65 b.p.m. The consciousness was correct with a Glasgow Coma Scale 15 and no evidence of focal neurological deficit. Physical examination revealed multiple scalp subcutaneous nodules and ulcerated lesions with swelling of the head (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Our examination of the oral cavity revealed a poor oral hygiene condition with multiple caries. The CT scan (<xref ref-type="fig" rid="fig2">Figure 2</xref>) revealed multiple scalp subcutaneous masses with chronic inflammatory changes of the skull. Routine laboratory test was normal particularly white blood cell count, C-reactive protein level, Intradermo-reaction with tuberculin and HIV test. Surgical biopsy was performed and the histological result was compatible with actinomycosis. After histological confirmation, parenteral Penicillin 20 million units daily were given for 4 weeks. Clinical improvement was observed after completing a 4-week regimen of intravenous</p><p>antibiotics. The patient was referred to the dentist and oral amoxicillin was given for an additional treatment.</p></sec><sec id="s3"><title>3. Discussion</title><p>We described a rare case involving a 24-year-old man who developed an invasive scalp actinomycosis. The first description of actinomycosis dates back to 1878 [<xref ref-type="bibr" rid="scirp.107312-ref7">7</xref>]. The causative agent is an anaerobic, Gram-positive bacterium often found as a saprophytic germ in the oral cavity and the gastrointestinal tract. This emphasizes the importance to investigate if the patient has any risk factors to suspect actinomycosis such as poor oral hygiene or immunosuppression [<xref ref-type="bibr" rid="scirp.107312-ref8">8</xref>]. In our case, HIV test was negative but the patient had a poor oral hygiene. Actinomyces is particularly known for its ability to cross tissue planes leading to involvement of contiguous tissue and distant organs [<xref ref-type="bibr" rid="scirp.107312-ref9">9</xref>]. More than 30 species of Actinomyces have been described and the most implicated in human actinomycosis are: Actinomycesisraelii,Actinomyces naeslundii,Actinomyces viscosus,Actinomyces odontolyticus andActinomyces meyeri. The disease usually progresses chronically [<xref ref-type="bibr" rid="scirp.107312-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.107312-ref11">11</xref>]. Actinomycosis is rare and has been sporadically reported in the literature. The most common forms are cervicofacial in 50%, thoracic in 30% and abdominal in 20%. Cranial involvement of actinomycosis is rare and occurs in less than 4% of cases [<xref ref-type="bibr" rid="scirp.107312-ref12">12</xref>]. Involvement of scalp by actinomycosis may cause diagnosis dilemma and could be mistaken for different pathologies, such as tuberculosis or carcinoma [<xref ref-type="bibr" rid="scirp.107312-ref4">4</xref>]. Cases of scalp actinomycosis have been sporadically reported in the literature [<xref ref-type="bibr" rid="scirp.107312-ref10">10</xref>] - [<xref ref-type="bibr" rid="scirp.107312-ref16">16</xref>]. Very often, the disease is localized on a part of the scalp. In our case, actinomycosis was more aggressive involving the entire scalp. The certain diagnosis is based on cytology and/or biopsy [<xref ref-type="bibr" rid="scirp.107312-ref6">6</xref>]. In our case, surgical excision was performed to remove as much as possible the granuloma and to allow histopathological examination. The main therapeutic treatment is administration of antibiotics. Actinomyces is extremely sensitive to penicillin G. Other antibiotics like Erythromycin and tetracycline can be used in patients allergic to penicillin [<xref ref-type="bibr" rid="scirp.107312-ref17">17</xref>]. In the literature, successful treatment was also achieved by using other antibiotics like streptomycine [<xref ref-type="bibr" rid="scirp.107312-ref13">13</xref>], cotrimoxazole [<xref ref-type="bibr" rid="scirp.107312-ref14">14</xref>] and itraconazole [<xref ref-type="bibr" rid="scirp.107312-ref10">10</xref>]. The antibiotic must be administered in high dose over prolonged period because of the tendency of the disease to recur [<xref ref-type="bibr" rid="scirp.107312-ref18">18</xref>]. We used parenteral Penicillin 20 million units daily during 4 weeks followed by oral amoxicillin for additional treatment.</p></sec><sec id="s4"><title>4. Conclusion</title><p>Involvement of scalp by actinomycosis could be mistaken for different pathologies, such as tuberculosis or carcinoma. This emphasizes the importance of biopsy for histological confirmation of the disease.</p></sec><sec id="s5"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>Sogoba, Y., Dembele, J.P., Sogoba, B., Diallo, M., Diallo, S.H., Coulibaly, O., Kisito, Q., Diallo, O., Kanikomo, D. and Maiga, Y. (2021) A Case Report of an Invasive Scalp Actinomycosis. 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