<?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">
    ojpathology
   </journal-id>
   <journal-title-group>
    <journal-title>
     Open Journal of Pathology
    </journal-title>
   </journal-title-group>
   <issn pub-type="epub">
    2164-6775
   </issn>
   <issn publication-format="print">
    2164-6783
   </issn>
   <publisher>
    <publisher-name>
     Scientific Research Publishing
    </publisher-name>
   </publisher>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="doi">
    10.4236/ojpathology.2026.161002
   </article-id>
   <article-id pub-id-type="publisher-id">
    ojpathology-147278
   </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>
    Primary Squamous Cell Carcinoma of the Breast: A Case Report 
   </title-group>
   <contrib-group>
    <contrib contrib-type="author" xlink:type="simple">
     <name name-style="western">
      <surname>
       Lalaina
      </surname>
      <given-names>
       Nomenjanahary
      </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>
       Zo Irène
      </surname>
      <given-names>
       Raivoherivony
      </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>
       Vahatra Joëlle
      </surname>
      <given-names>
       Razafimahefa
      </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>
       Nantenaina Soa
      </surname>
      <given-names>
       Randrianjafisamindrakotroka
      </given-names>
     </name> 
     <xref ref-type="aff" rid="aff3"> 
      <sup>3</sup>
     </xref>
    </contrib>
   </contrib-group> 
   <aff id="aff1">
    <addr-line>
     aDepartment of Pathology, Joseph Ravoahangy Andrianavalona University Hospital, Antananarivo, Madagascar
    </addr-line> 
   </aff> 
   <aff id="aff2">
    <addr-line>
     aDepartment of Pathology, Andrainjato University Hospital, Fianarantsoa, Madagascar
    </addr-line> 
   </aff> 
   <aff id="aff3">
    <addr-line>
     aDepartment of Pathology, Medical School of Antananarivo, Antananarivo, Madagascar
    </addr-line> 
   </aff> 
   <pub-date pub-type="epub">
    <day>
     14
    </day> 
    <month>
     11
    </month>
    <year>
     2025
    </year>
   </pub-date> 
   <volume>
    16
   </volume> 
   <issue>
    01
   </issue>
   <fpage>
    16
   </fpage>
   <lpage>
    20
   </lpage>
   <history>
    <date date-type="received">
     <day>
      19,
     </day>
     <month>
      September
     </month>
     <year>
      2025
     </year>
    </date>
    <date date-type="published">
     <day>
      15,
     </day>
     <month>
      September
     </month>
     <year>
      2025
     </year> 
    </date> 
    <date date-type="accepted">
     <day>
      15,
     </day>
     <month>
      November
     </month>
     <year>
      2025
     </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>
    Primary squamous cell carcinoma of the breast is rare. We report a case of primary squamous cell carcinoma of the breast. It is a 47-year-old woman. She has an ulcerated, budding mass measuring 11 cm in diameter in the right breast. She underwent a right mastectomy. The diagnosis was non-keratinizing, moderately differentiated squamous cell carcinoma of the breast, stage IIIB invasive. Immunohistochemical testing was negative for estrogen and progesterone receptors but positive for cytokeratin CK 5/6. Diagnosis is histological and it is important to differentiate its primary breast origin from skin tumors or metastases from other organs.
   </abstract>
   <kwd-group> 
    <kwd>
     Breast Cancer
    </kwd> 
    <kwd>
      Cytokeratin
    </kwd> 
    <kwd>
      Estrogen Receptor
    </kwd> 
    <kwd>
      Progesterone Receptor
    </kwd> 
    <kwd>
      Squamous Cell Carcinoma
    </kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <sec id="s1">
   <title>1. Introduction</title>
   <p>Breast cancer is the most common gynecological cancer. The most common histological type is non-specific carcinoma, followed by lobular carcinoma. Primary Squamous Cell Carcinoma of the breast (PSCC) is very rare, accounting for 0.1% to 2% of invasive carcinoma. Few cases have been reported in the literature to date <xref ref-type="bibr" rid="scirp.147278-1">
     [1]
    </xref>. It is important to differentiate its primary breast origin from skin tumors or metastases from other organs such as the esophagus, cervix, or anus.</p>
   <p>We report a case of primary squamous cell carcinoma of the breast in order to differentiate its epidemiological and histopathological features.</p>
  </sec><sec id="s2">
   <title>2. Observation</title>
   <p>The patient was a 47-year-old woman. She has two children and came to Joseph Ravoahangy Andrianavalona (JRA) University Hospital for a tumor in her right breast. The disease apparently began with a small breast nodule on the right side, without a skin lesion, which gradually increased in size and became increasingly painful. Due to a lack of financial resources, she had not consulted a doctor. Twenty-four months later, the lump had become ulcerated and very large, interfering with the patient’s daily activities. She therefore came for a consultation at the oncology department of the JRA University Hospital.</p>
   <p>The medical history revealed no personal or family history of breast cancer.</p>
   <p>Physical examination revealed an ulcerated, budding mass of the breast on the right side, measuring 11 cm in diameter, with lymphadenopathy. The contralateral breast was normal. The rest of the examination was normal.</p>
   <p>Imaging did not reveal any other tumor locations.</p>
   <p>The patient underwent breast fine needle aspiration, but the smears consisted mainly of inflammatory cells such as neutrophils, macrophages, and lymphocytes, against a dirty background, with no neoplastic cells, suggesting a suppurative mastitis lesion.</p>
   <p>Despite the result of fine needle aspiration, the clinical appearance (<xref ref-type="fig" rid="fig1">
     Figure 1
    </xref>) prompted the oncologist to treat the mass as a malignant lesion. After two courses of chemotherapy, the patient underwent a mastectomy with lymph node dissection.</p>
   <fig id="fig1" position="float">
    <label>Figure 1</label>
    <caption>
     <title>Source: Department of Pathology, JRA University Hospital.<xref ref-type="bibr" rid="scirp.147278-"></xref>Figure 1. Mastectomy with axillary lymph node dissection. Ulcerated lesion with necrotic-hemorrhagic changes on cut.</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1940455-rId13.jpeg?20251118025326" />
   </fig>
   <p>On macroscopic examination, the mastectomy specimen measured 17 × 13 × 4 cm and contained an ulcerated, budding mass measuring 11 cm, with heterogeneous white sections with necrotic and hemorrhagic changes (<xref ref-type="fig" rid="fig1">
     Figure 1
    </xref>). The lymph node dissection specimen measured 8 × 7 × 3 cm, with 39 lymph nodes ranging from 0.5 to 2 cm in diameter.</p>
   <p>Histological examination revealed that the mass corresponded to a carcinomatous proliferation consisting of cells with moderate cytonuclear atypia. They were organized in clusters or rows, with squamous differentiation without keratinization. The stroma was necrotic and inflammatory. No other histological type was observed. There was no evidence of Paget’s disease of the nipple, endovascular carcinomatous, or perineural invasion. Only one of the lymph nodes showed metastasis, without capsular rupture.</p>
   <p>The diagnosis was non-keratinizing, moderately differentiated squamous cell carcinoma of the breast, pT4bN1aM0, stage IIIB.</p>
   <p>Immunohistochemical testing was negative for estrogen and progesterone receptors but positive for cytokeratin CK 5/6.</p>
  </sec><sec id="s3">
   <title>3. Discussion</title>
   <p>Squamous cell carcinoma is one of the most common histological types of cancer that develops in an organ or system covered with squamous epithelium, such as the skin, cervix, vagina, esophagus, and anus. Its primary location in the breast is rare, with a frequency of 0.1% to 2% among invasive breast carcinomas <xref ref-type="bibr" rid="scirp.147278-1">
     [1]
    </xref>.</p>
   <p>Primary squamous cell carcinoma of the breast affects women aged 31 to 83, with a peak at 55 years old <xref ref-type="bibr" rid="scirp.147278-2">
     [2]
    </xref>. Our patient was 47 years old at the time of diagnosis.</p>
   <p>The etiopathogenesis remains controversial. It has been suggested that it is an extreme form of squamous metaplasia developed on adenocarcinoma <xref ref-type="bibr" rid="scirp.147278-3">
     [3]
    </xref>. This hypothesis is the most widely accepted by authors, as the squamous cell carcinomas, they reported were consecutive to benign lesions likely to cause squamous metaplasia, such as inflammation, breast abscesses, or breast implants, or to radiotherapy sessions <xref ref-type="bibr" rid="scirp.147278-4">
     [4]
    </xref>-<xref ref-type="bibr" rid="scirp.147278-9">
     [9]
    </xref>. In our case, no similar history was reported by the patient.</p>
   <p>The diagnosis of primary squamous cell carcinoma of the breast is made after ruling out a cutaneous origin, breast metastasis from a distant carcinoma, and a significant glandular component within the tumor <xref ref-type="bibr" rid="scirp.147278-5">
     [5]
    </xref> <xref ref-type="bibr" rid="scirp.147278-10">
     [10]
    </xref>. Our case was purely squamous cell carcinoma and there was no distant primary cancer, such as skin, cervix or vagina. The skin involvement was considered to be local extension at an advanced stage, as according to the history of the disease, the nodule, at first, was developed on the breast parenchyma without a skin lesion.</p>
   <p>The clinical manifestation of our case was a clinically advanced breast mass (skin ulceration with budding lesion, with a lymphadenopathy). The clinical and radiological appearance of these tumors is not specific <xref ref-type="bibr" rid="scirp.147278-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.147278-11">
     [11]
    </xref>.</p>
   <p>In our case, the fine needle aspiration was only inflammatory, without tumor cells identified. The absence of tumor cells observed in this case could be due to the large inflammatory and necrotic appearance of the lesion and the samples did not show any neoplastic proliferation. But usually, this test helps the diagnosis, as in the cases of Zein Ahmed <xref ref-type="bibr" rid="scirp.147278-1">
     [1]
    </xref> and Gupta R. K. <xref ref-type="bibr" rid="scirp.147278-12">
     [12]
    </xref>. However, sometimes the fine needle aspiration is negative, as in our case, or leads to an inaccurate diagnosis, as in the case of Flikweert E. R. <xref ref-type="bibr" rid="scirp.147278-11">
     [11]
    </xref>, where adenocarcinoma based on the fine needle aspiration was made. Histological examination provides the final diagnosis. It shows malignant squamous cells, cohesive, organized in clusters or rows, or in layers, with or without keratinization <xref ref-type="bibr" rid="scirp.147278-13">
     [13]
    </xref> <xref ref-type="bibr" rid="scirp.147278-14">
     [14]
    </xref>.</p>
   <p>Squamous cell carcinoma is not lymphophilic. More than 70% of reported cases were free of lymph node metastasis <xref ref-type="bibr" rid="scirp.147278-15">
     [15]
    </xref>. In our case, however, one of the 39 lymph nodes was metastatic. Zein Ahmed <xref ref-type="bibr" rid="scirp.147278-1">
     [1]
    </xref> reported three positive lymph nodes in his case.</p>
   <p>Unlike adenocarcinoma, squamous cell carcinoma of the breast lacks hormone receptors. If hormone receptor testing is positive, a glandular component that has gone unnoticed must be sought. This is a very aggressive tumor, with negative hormone receptors and refractory to treatment, with a poor prognosis. The prognosis appears to be comparable to that of undifferentiated carcinomas. <xref ref-type="bibr" rid="scirp.147278-1">
     [1]
    </xref> It was a malignant tumor with a low survival rate. Marital status, age, surgical procedure, tumor size, and several positive lymph nodes were independent predictors of patient survival. Researchers believed that breast squamous cell carcinoma was highly invasive and worse than the prognosis of typical triple-negative breast cancer <xref ref-type="bibr" rid="scirp.147278-16">
     [16]
    </xref>.</p>
  </sec><sec id="s4">
   <title>4. Conclusion</title>
   <p>Primary squamous cell carcinoma of the breast is rare. The clinical and radiological appearance is nonspecific, and fine needle aspirations are sometimes negative. Diagnosis is histological, but metastatic origin or extension of cutaneous squamous cell carcinoma must always be ruled out before confirming the primary nature of the breast tumor.</p>
  </sec>
 </body><back>
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</article>