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 <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" "http://jats.nlm.nih.gov/publishing/1.0/JATS-journalpublishing1.dtd"> <article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="mini-review" dtd-version="1.0" xml:lang="en">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">IJIP</journal-id>
      <journal-title-group>
        <journal-title>International Journal of Infection Prevention</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2690-4837</issn>
      <publisher>
        <publisher-name>Open Access Pub</publisher-name>
        <publisher-loc>United States</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.14302/issn.2690-4837.ijip-19-3145</article-id>
      <article-id pub-id-type="publisher-id">IJIP-19-3145</article-id>
      <article-categories>
        <subj-group>
          <subject>mini-review</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>The Elliptical Aggregates – Idiopathic Granulomatous Mastitis</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Anubha</surname>
            <given-names>Bajaj</given-names>
          </name>
          <xref ref-type="aff" rid="idm1842677092">1</xref>
          <xref ref-type="aff" rid="idm1842676444">*</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1842677092">
        <label>1</label>
        <addr-line>MD. (Pathology) Panjab University, Department of Histopathology, A.B. Diagnostics, A-1, Ring Road, Rajouri Garden, New Delhi, 110027, India</addr-line>
      </aff>
      <aff id="idm1842676444">
        <label>*</label>
        <addr-line>corresponding author </addr-line>
      </aff>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>El-Sabbagh</surname>
            <given-names>AH</given-names>
          </name>
          <xref ref-type="aff" rid="idm1842787420">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1842787420">
        <label>1</label>
        <addr-line>professor of plastic surgery, faculty of medicine, mansoura university, Egypt.</addr-line>
      </aff>
      <author-notes>
        <corresp>
    
    Anubha Bajaj, Pathology, <addr-line>Panjab University, Department of Histopathology, A.B.             Diagnostics, A-1, Ring Road, Rajouri Garden, New Delhi, 110027, India</addr-line>. Email: <email>anubha.bajaj@yahoo.com</email></corresp>
        <fn fn-type="conflict" id="idm1842136116">
          <p>The authors have declared that no competing interests exist.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub" iso-8601-date="2020-01-03">
        <day>03</day>
        <month>01</month>
        <year>2020</year>
      </pub-date>
      <volume>1</volume>
      <issue>1</issue>
      <fpage>25</fpage>
      <lpage>31</lpage>
      <history>
        <date date-type="received">
          <day>24</day>
          <month>12</month>
          <year>2019</year>
        </date>
        <date date-type="accepted">
          <day>31</day>
          <month>12</month>
          <year>2019</year>
        </date>
        <date date-type="online">
          <day>03</day>
          <month>01</month>
          <year>2020</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© </copyright-statement>
        <copyright-year>2020</copyright-year>
        <copyright-holder>Anubha Bajaj</copyright-holder>
        <license xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri xlink:href="http://openaccesspub.org//ijip/article/1235">This article is available from http://openaccesspub.org//ijip/article/1235</self-uri>
      <abstract>
        <p>Idiopathic granulomatous mastitis  was initially scripted in 1972 by Kessler and Wolloch and is cogitated as an infrequent, benign, chronic inflammatory disorder. It commonly implicates females of reproductive age group, especially women who have breast fed in the preceding five to six years. Idiopathic granulomatous mastitis is commonly discerned in Asia and Mediterranean region although true incidence is undetermined. Diverse ethnicities delineate a diverse disease prevalence. Elimination of adjunctive causes of granulomatous inflammation makes idiopathic granulomatous mastitis a diagnosis of exclusion. As per the natural history, idiopathic granulomatous mastitis is designated as a self limiting disorder <xref ref-type="bibr" rid="ridm1842049540">1</xref>.        </p>
      </abstract>
      <kwd-group>
        <kwd>Chronic</kwd>
        <kwd>disease</kwd>
        <kwd>disorder</kwd>
        <kwd>diagnosis</kwd>
      </kwd-group>
      <counts>
        <fig-count count="10"/>
        <table-count count="0"/>
        <page-count count="7"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec id="idm1842535828" sec-type="intro">
      <title>Introduction</title>
      <sec id="idm1842535108">
        <title>Disease Characteristics </title>
        <p>Essentially an uncommon condition of obscure origin, granulomatous mastitis simulates an abscess or carcinoma breast on radiography. As radiographic features are inconclusive, definitive diagnosis is usually obtained with a  core tissue biopsy and histological analysis. Repetitive tissue sampling is required to exclude a metamorphosis into carcinoma breast. Associated aetiological factors such as various  infections, duct ectasia  or a distinctive autoimmune mechanism may not be discovered. </p>
        <p>Granulomatous mastitis frequently emerges in the third or fourth decade of life with a demonstrable age range betwixt 11 years to 83 years.  Reoccurrence is observed in a significant percentage of instances and varies betwixt 5% to 50%.  An infectious aetiology of granulomatous mastitis requires elimination as corticosteroids are contraindicated in infectious aetiologies <xref ref-type="bibr" rid="ridm1842051628">2</xref><xref ref-type="bibr" rid="ridm1842156524">3</xref>.                 </p>
      </sec>
      <sec id="idm1842534388">
        <title>Disease Pathogenesis </title>
        <p>Mechanism of inflammation in idiopathic granulomatous mastitis  is comprised of  an injurious  deterioration of ductal epithelium followed by metamorphosis and luminal secretions within the lobular connective tissue. Localized inflammation within the connective tissue accompanied by migration of macrophages and lymphocytes within the inflamed region evokes a focal, granulomatous inflammatory response.  However, pre-emptive factor  triggering the inflammation remains elusive.</p>
        <p>Trigger factors indicated are constituted by  pregnancy, lactation, autoimmune disorders, hyperprolactinaemia and tobacco consumption.  Enhanced severity and duration of disease can be cogitated in inflammation arising within the puerperal period <xref ref-type="bibr" rid="ridm1842051628">2</xref><xref ref-type="bibr" rid="ridm1842156524">3</xref>.    </p>
        <p>Of obscure aetiology, factors such as hormonal imbalance, autoimmunity,  undetermined microbiological agents, smoking contraceptive pills, lactation, hyperprolactinaemia, infection with Corynebacterium  and  antitrypsin deficiency are  implicated in the genesis of granulomatous mastitis. Certain aetiological factors may be undiscernible with the employment of current diagnostic modalities <xref ref-type="bibr" rid="ridm1842156524">3</xref>. </p>
      </sec>
      <sec id="idm1842532948">
        <title>Clinical Elucidation  </title>
        <p>Majority of subjects (90%) depict a unilateral lesion appearing as a palpable mass or an abscess situated in the upper segment of  breast. The tender, erythematous, inflamed mass detectable within the breast parenchyma enlarges gradually and can be   associated with pain and lymphadenopathy. Emergence of a hard, irregular nodule in the breast parenchyma can recapitulate carcinoma breast. Nipple and cutaneous retraction as well as nipple discharge can be discerned. Enunciated mass in the breast parenchyma or nodule can depict a sequential breast abscess which can drain spontaneously. Comprehensive  breast parenchyma may be incriminated barring the nipple. Multiple fistulae or  sinus tracts can be exemplified in advanced              disease <xref ref-type="bibr" rid="ridm1842156524">3</xref><xref ref-type="bibr" rid="ridm1841901372">4</xref>.            </p>
      </sec>
      <sec id="idm1842533884">
        <title>Histological Elucidation  </title>
        <p>On gross examination, a firm to hard, mildly  nodular mass is delineated.</p>
        <p>Core needle  biopsy of idiopathic granulomatous mastitis enunciates multiple aggregates of                         non- caseating epitheloid cell granulomas within and encompassing breast lobules, constituted of              epitheloid histiocytes, lymphocytes, neutrophils and multinucleated giant cells. Granulomatous inflammation is predominantly lobulo-centric. The inflammation is preponderantly composed of lymphocytes, plasma cells, epitheloid histiocytes, multinucleated giant cells                  and neutrophils. Neutrophils can configure micro-abscesses and encompass vacant micro-cystic cavities, morphological features which are in common with cystic neutrophilic granulomatous mastitis. Non specific lobulitis along with a  lymphoid and plasma cell infiltrate accompanies the granulomatous inflammation. Necrosis is usually absent. Neutrophilic micro-abscesses can be accompanied by fistula formation <xref ref-type="bibr" rid="ridm1841901372">4</xref><xref ref-type="bibr" rid="ridm1841898420">5</xref>.</p>
        <p>Multinucleated giant cells are detected in an estimated three fourths (78.5%) instances.  Plasma cells are discernible in around half (53.9%) of the subjects and usually appear at the margins of cystic vacuoles with centric accumulation of neutrophils within the granulomas.  </p>
        <p>Special stains such as Gomori-Methanamine Silver (GMS) and Periodic acid Schiff’s (PAS) stain for fungal spores or mycelia  are usually non reactive.  Acid fast bacilli or Mycobacterial species are usually not detected on Zeihl Neelsen stain. Gram’s stain is mandated for discovering gram positive bacilli. Fungal and mycobacterial cultures usually do not reveal any results. Axillary and internal mammary lymphadenopathy is observed <xref ref-type="bibr" rid="ridm1841901372">4</xref><xref ref-type="bibr" rid="ridm1841898420">5</xref>. </p>
        <p>Fine needle aspiration can demonstrate a cellular exudate indicative of an abscess  with an intense inflammatory infiltrate preponderantly composed of neutrophils. Ductal epithelial cells may be                      absent. Cytological examination delineates abundant and accumulated epitheloid histiocytes, neutrophils, lymphocytes with a variable degree of  granuloma formation and an absence of necrosis <xref ref-type="bibr" rid="ridm1841898420">5</xref>.</p>
        <p><xref ref-type="fig" rid="idm1842426540">Figure</xref>, <xref ref-type="fig" rid="idm1842423228">Figure 2</xref>, <xref ref-type="fig" rid="idm1842423516">Figure 3</xref>, <xref ref-type="fig" rid="idm1842420204">Figure 4</xref>, <xref ref-type="fig" rid="idm1842420996">Figure 5</xref>, <xref ref-type="fig" rid="idm1842418908">Figure 6</xref>, <xref ref-type="fig" rid="idm1842411972">Figure 7</xref>, <xref ref-type="fig" rid="idm1842412188">Figure 8</xref>, <xref ref-type="fig" rid="idm1842408732">Figure 9</xref>, <xref ref-type="fig" rid="idm1842408372">Figure 10</xref>.</p>
        <fig id="idm1842426540">
          <label>Figure 1.</label>
          <caption>
            <title> Granulomatous  mastitis with the configuration of epitheloid cell granuloma and a lymphoid and plasma cell infiltrate9.</title>
          </caption>
          <graphic xlink:href="images/image1.jpg" mime-subtype="jpg"/>
        </fig>
        <fig id="idm1842423228">
          <label>Figure 2.</label>
          <caption>
            <title> Granulomatous mastitis with articulated epitheloid cell granuloma, lymphocytic, plasma cell and                   neutrophilic infiltration10.</title>
          </caption>
          <graphic xlink:href="images/image2.jpg" mime-subtype="jpg"/>
        </fig>
        <fig id="idm1842423516">
          <label>Figure 3.</label>
          <caption>
            <title> Granulomatous mastitis with               scattered langhans and foreign body giant cells, epitheloid cell granuloma and lymphoid ingress11.</title>
          </caption>
          <graphic xlink:href="images/image3.jpg" mime-subtype="jpg"/>
        </fig>
        <fig id="idm1842420204">
          <label>Figure 4.</label>
          <caption>
            <title> Granulomatous  mastitis with                epitheloid cell granuloma, langhans and              foreign body giant cells with lymphocytic              rimming12. </title>
          </caption>
          <graphic xlink:href="images/image4.jpg" mime-subtype="jpg"/>
        </fig>
        <fig id="idm1842420996">
          <label>Figure 5.</label>
          <caption>
            <title> Granulomatous mastitis  with disseminated epitheloid cell granuloma, langhans giant cells,               lymphocytic and plasma cell dispersal13.</title>
          </caption>
          <graphic xlink:href="images/image5.jpg" mime-subtype="jpg"/>
        </fig>
        <fig id="idm1842418908">
          <label>Figure 6.</label>
          <caption>
            <title> Granulomatous  mastitis with numerous epitheloid cell              granuloma, foreign body giant cells and a peripheral rimming with              lymphocytes14.</title>
          </caption>
          <graphic xlink:href="images/image6.png" mime-subtype="png"/>
        </fig>
        <fig id="idm1842411972">
          <label>Figure 7.</label>
          <caption>
            <title> Granulomatous mastitis with scattered epitheloid cells,            neutrophilic exudate and aggregates of epithelod cells15. </title>
          </caption>
          <graphic xlink:href="images/image7.png" mime-subtype="png"/>
        </fig>
        <fig id="idm1842412188">
          <label>Figure 8.</label>
          <caption>
            <title> Granulomatous mastitis with              disseminated epitheloid cells admixed with neutrophils, lymphocytes and plasma cells 16.</title>
          </caption>
          <graphic xlink:href="images/image8.png" mime-subtype="png"/>
        </fig>
        <fig id="idm1842408732">
          <label>Figure 9.</label>
          <caption>
            <title> Granulomatous mastitis with circumscribed epitheloid cell granuloma, foreign body giant cells and a perimeter of lymphocytes 17.</title>
          </caption>
          <graphic xlink:href="images/image9.png" mime-subtype="png"/>
        </fig>
        <fig id="idm1842408372">
          <label>Figure 10.</label>
          <caption>
            <title> Granulomatous mastitis with a ductal circumscription of epitheloid cells, plasma cells, lymphocytes and neutrophils 18.</title>
          </caption>
          <graphic xlink:href="images/image10.jpg" mime-subtype="jpg"/>
        </fig>
      </sec>
      <sec id="idm1842481540">
        <title>Differential Diagnosis </title>
        <p>Idiopathic granulomatous mastitis requires a segregation from diseases such as peri-ductal mastitis or carcinoma breast. </p>
        <p>An infective aetiology such as fungal or mycobacterial infection, autoimmune conditions  delineated as sarcoidosis with distribution of                         non-caseating granulomas, devoid of a lobular distribution and Wegener’s granulomatosis with polyangiitis demonstrating necrotizing vasculitis require distinction. </p>
        <p>Despite a varied differential diagnosis,  granulomatous mastitis is predominantly an idiopathic disorder<xref ref-type="bibr" rid="ridm1842051628">2</xref><xref ref-type="bibr" rid="ridm1842156524">3</xref>. Possible association of Corynebacterium infection with granulomatous mastitis can be observed and is designated as cystic neutrophilic granulomatous mastitis. Aforesaid condition typically displays lipo- granulomas comprised of clear, vacuolated  spaces with a peripheral  rimming of neutrophils along with a circumscription of granulomatous inflammation <xref ref-type="bibr" rid="ridm1842051628">2</xref><xref ref-type="bibr" rid="ridm1842156524">3</xref>. </p>
        <p>A distinctive histological attribute of granulomatous inflammation admixed with acute inflammation and concurrent cystic spaces indicates a probable accumulation with exceptional, gram                positive bacilli within the clear, vacuolated spaces. Microbiological analysis for isolation of Corynebacterium, particularly Corynebacterium kroppenstedtii is necessitated in concurrence with aforesaid morphological aspects to arrive at a cogent diagnosis. Corynebacterium is a gram positive bacillus which appears as a constituent of skin microbiota.                             Thus, a possible source can be on account of                bacterial colonization, infection or contamination. Corynebacterium kroppenstedtii can be isolated in around two fifths (40%) instances of definitive granulomatous lobar mastitis <xref ref-type="bibr" rid="ridm1841946860">6</xref><xref ref-type="bibr" rid="ridm1841944268">7</xref>.</p>
        <p>Granulomatous mastitis necessitates a demarcation from Squamous  Metaplasia of Lacteriferous ducts (SMOLD), a condition which demonstrates  epithelium lined lacteriferous ducts with concurrent squamous metaplasia, essentially occurs in the nipple and delineates a singular sinus tract at the edge of the aerola. Multinucleated giant cells  can be associated with keratinous debris. The condition can be incited by tobacco intake <xref ref-type="bibr" rid="ridm1842051628">2</xref><xref ref-type="bibr" rid="ridm1842156524">3</xref>.</p>
      </sec>
      <sec id="idm1842487948">
        <title>Investigative Assay </title>
        <p>Ultrasonography depicts cutaneous thickening, cutaneous retraction and a persistent,  poorly circumscribed, hypoechoic mass of varying diameter. The mass is initially subdermal  and multiple,                   deep-seated masses may be cogitated, occasionally extraneous to the breast tissue. Lymphadenopathy may or may not be detectable.  Ultrasonography is beneficial in discerning infectious conditions such as effusions, inflammation of mammary parenchyma and fatty tissues, abscess formation along with the  emergence of a fistulous tract <xref ref-type="bibr" rid="ridm1841946860">6</xref><xref ref-type="bibr" rid="ridm1841944268">7</xref>.</p>
        <p>Magnetic resonance imaging (MRI) depicts a  heterogeneous admixture of fibrous and glandular tissue along with several, tiny, fluid-filled cavities rimmed            with inflammatory cells and granulomas within the breast tissue, a few of which progress to fistula formation <xref ref-type="bibr" rid="ridm1841946860">6</xref><xref ref-type="bibr" rid="ridm1841944268">7</xref>.</p>
        <p>Magnetic resonance imaging can depict                     a gradually evolving mass or a non-specific, heterogeneous enhancement or a clustered augmentation with ring formation within the breast tissue.  Adjunctive findings on magnetic resonance imaging are defined as cutaneous thickening and retraction along with retraction of the nipple.                                                                                                Mammography delineates an enhanced echogenicity, focal asymmetry of the nodule disassociated with nodular distortion and micro-calcifications along  with infrequent, well-defined mammary nodules.                                Doppler studies exemplify an amplification of nodular vascularization.  Levels of certain cytokines such as interleukin 33(IL-33)  are enhanced in idiopathic granulomatous mastitis with a sensitivity of  93.7% and specificity of  96%, values which are beneficial in segregating granulomatous mastitis from carcinoma breast <xref ref-type="bibr" rid="ridm1842051628">2</xref><xref ref-type="bibr" rid="ridm1842156524">3</xref>.</p>
        <p>Nevertheless, aforesaid non – specific imaging features can be recapitulated by carcinoma breast. Thus, a cogent, non invasive diagnostic modality to differentiate granulomatous mastitis from carcinoma breast remains to be established. </p>
        <p>Core needle biopsy is a sensitive technique (94.5%) to detect granulomatous mastitis whereas a fine needle aspiration is efficacious in around  39% instances. Also, fine needle aspiration  may be inadequate in demarcating idiopathic granulomatous mastitis from adjunctive granulomatous diseases of the breast <xref ref-type="bibr" rid="ridm1841944268">7</xref><xref ref-type="bibr" rid="ridm1841866492">8</xref>.</p>
      </sec>
      <sec id="idm1842486940">
        <title>Therapeutic Options </title>
        <p>A consensus for optimal therapeutic modality for managing idiopathic granulomatous mastitis remains elusive. Granulomatous mastitis can be treated                   with various modalities such as systemic therapy composed of  oral and topical corticosteroids,                 immune-suppressants or surgical excision. Therapeutic intervention is mandated for symptomatic palliation.  Untreated granulomatous mastitis can spontaneously  resolve in roughly  one to two years.                          Granulomatous mastitis can be treated  medically with antibiotics, systemic steroids as with prednisone or  mycophenolate, non steroidal anti inflammatory drugs(NSAIDs), immunosuppressive agents such as methotrexate or azathioprine <xref ref-type="bibr" rid="ridm1841944268">7</xref><xref ref-type="bibr" rid="ridm1841866492">8</xref>. </p>
        <p>Surgical extermination of granulomatous inflammation followed by placement of a surgical drain within the wound with concomitant administration of steroids are a preferred approach.  Also, antibiotics following a wide surgical eradication of the nodule with a broad margin of the healthy tissue or a mastectomy  with subsequent  immune suppression can be adopted. Alternatively, a surgical excision with a wide perimeter of uninvolved tissue with concurrent antibiotic administration can be adopted. Localized excision with a broad perimeter of normal tissue is employed in around three fifths (59%) of subjects and usually the wound heals within a minimal period.  Drainage of associated breast abscess is also employed. Localized surgical  eradication of the nodule can be accompanied by complications such as infection of the surgical site, wound disruption, disease reoccurrence  and delayed wound healing <xref ref-type="bibr" rid="ridm1841944268">7</xref><xref ref-type="bibr" rid="ridm1841866492">8</xref>. </p>
        <p>Median healing time is cogitated at around 84 days whereas median time for emergence of reoccurrence is at an estimated 280 days. Incriminated elderly populations depicting associated comorbid conditions usually demonstrate a delayed healing.                                                       Delayed healing is enunciated in an estimated 10% to 50% instances. Surgical intervention depicts wound complications in  nearly half (52%) the subjects and  relapse of granulomatous mastitis following surgical excision is observed in approximately 13.3%              individuals <xref ref-type="bibr" rid="ridm1841944268">7</xref><xref ref-type="bibr" rid="ridm1841866492">8</xref>. </p>
        <p>Therapy with steroids can be contemplated as the preferential treatment for idiopathic granulomatous mastitis. Adoption of steroids for treating granulomatous mastitis is efficacious and granulomas can be resolved in the absence of a surgical option. Primary therapy                  with steroids is beneficial although the treatment                  may extend up to six months. Essentially a conservative form of management, administration of corticosteroids delineates a superior response in an estimated three fourths(77.8%) subjects. Steroids can wither the lesion when administered  pre-operatively or  post- operatively in persistent masses.</p>
        <p>Immune-suppressive agents such as methotrexate or azathioprine can be adopted in treating reoccurrences of inflammation or in subjects demonstrating deleterious outcomes of prednisone <xref ref-type="bibr" rid="ridm1841944268">7</xref><xref ref-type="bibr" rid="ridm1841866492">8</xref>. Granulomatous mastitis depicts elevated proportion of relapse in  an estimated half (50%) the instances on account of adoption of suboptimal therapeutic modalities. </p>
        <p>Average period of recovery of granulomas usually exceeds  &gt;one  year. Chronic and reoccurring forms of disease can emerge due to adoption of various therapeutic measures <xref ref-type="bibr" rid="ridm1841944268">7</xref><xref ref-type="bibr" rid="ridm1841866492">8</xref>. </p>
      </sec>
    </sec>
  </body>
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