<?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">
    ojog
   </journal-id>
   <journal-title-group>
    <journal-title>
     Open Journal of Obstetrics and Gynecology
    </journal-title>
   </journal-title-group>
   <issn pub-type="epub">
    2160-8792
   </issn>
   <issn publication-format="print">
    2160-8806
   </issn>
   <publisher>
    <publisher-name>
     Scientific Research Publishing
    </publisher-name>
   </publisher>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="doi">
    10.4236/ojog.2025.1511164
   </article-id>
   <article-id pub-id-type="publisher-id">
    ojog-147473
   </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>
    Hyperlactation and Recurrent Postpartum Breast Abscesses Revealing an Unrecognized Prolactinoma: A Case Report and Literature Review
   </title-group>
   <contrib-group>
    <contrib contrib-type="author" xlink:type="simple">
     <name name-style="western">
      <surname>
       Michèle Florence
      </surname>
      <given-names>
       Mendoua
      </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>
       Marcel Gérardin
      </surname>
      <given-names>
       Mbarga
      </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>
       Serge
      </surname>
      <given-names>
       Nyada
      </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>
       Gervais Mounchikpou
      </surname>
      <given-names>
       Ngouhouo
      </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>
       Emile
      </surname>
      <given-names>
       Mboudou
      </given-names>
     </name> 
     <xref ref-type="aff" rid="aff1"> 
      <sup>1</sup>
     </xref>
    </contrib>
   </contrib-group> 
   <aff id="aff1">
    <addr-line>
     aDepartment of Surgery and Specialties, Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon
    </addr-line> 
   </aff> 
   <aff id="aff2">
    <addr-line>
     aDepartment of Radiology, Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon
    </addr-line> 
   </aff> 
   <aff id="aff3">
    <addr-line>
     aDepartment of Gynecology-Obstetrics, Faculty of Medicine and Biomedical Sciences, University of Yaounde I, Yaounde, Cameroon
    </addr-line> 
   </aff> 
   <pub-date pub-type="epub">
    <day>
     03
    </day> 
    <month>
     11
    </month>
    <year>
     2025
    </year>
   </pub-date> 
   <volume>
    15
   </volume> 
   <issue>
    11
   </issue>
   <fpage>
    1957
   </fpage>
   <lpage>
    1963
   </lpage>
   <history>
    <date date-type="received">
     <day>
      15,
     </day>
     <month>
      October
     </month>
     <year>
      2025
     </year>
    </date>
    <date date-type="published">
     <day>
      22,
     </day>
     <month>
      October
     </month>
     <year>
      2025
     </year> 
    </date> 
    <date date-type="accepted">
     <day>
      22,
     </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>
    <b>Introduction</b>
    <b>:</b> Prolactinoma is the most common secreting pituitary tumor. In women of childbearing age, it typically manifests as amenorrhea-galactorrhea. In the postpartum period, its association with pathological hyperlactation is rare but can potentially cause severe breast complications. We report a case of recurrent postpartum breast engorgement and abscesses, complicating hyperlactation induced by an unrecognized prolactinoma. 
    <b>Clinical Observation</b>
    <b>:</b> The patient was a 32-year-old multiparous woman with no notable medical history, who presented 10 days after an uneventful delivery with abundant, painful lactation, associated with frequent and repeated bilateral engorgements. The condition progressed to recurrent breast abscesses, requiring several surgical drainages and repeated antibiotic treatments. Hormonal assays revealed significant hyperprolactinemia at 358 ng/mL. Pituitary MRI showed a 6.8 mm microadenoma compatible with a prolactinoma. Treatment with cabergoline led to a rapid reduction in lactation but also caused alopecia, prompting early discontinuation of treatment. 
    <b>Discussion</b>
    <b>:</b> Hyperlactation related to a prolactinoma is an exceptional postpartum phenomenon. Excess prolactin promotes milk stasis and predisposes individuals to engorgements and subsequent iterative breast infections. Diagnosis is based on hormonal assays and pituitary imaging. Cabergoline remains the treatment of choice, enabling the regulation of lactation and prevention of complications. 
    <b>Conclusion</b>
    <b>:</b> This case illustrates the importance of considering an underlying endocrine disorder in the face of unexplained recurrent postpartum breast abscesses. Screening for hyperprolactinemia should be part of the etiological assessment in any case of persistent pathological hyperlactation after childbirth.
   </abstract>
   <kwd-group> 
    <kwd>
     Prolactinoma
    </kwd> 
    <kwd>
      Hyperlactation
    </kwd> 
    <kwd>
      Breast Abscess
    </kwd> 
    <kwd>
      Postpartum
    </kwd> 
    <kwd>
      Hyperprolactinemia
    </kwd> 
    <kwd>
      Cabergoline
    </kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <sec id="s1">
   <title>1. Introduction</title>
   <p>Prolactinoma is the most common secreting pituitary tumor, accounting for nearly 40% of pituitary adenomas <xref ref-type="bibr" rid="scirp.147473-1">
     [1]
    </xref>. It primarily manifests in women of childbearing age through hyperprolactinemia, which is responsible for amenorrhea, galactorrhea, or infertility <xref ref-type="bibr" rid="scirp.147473-2">
     [2]
    </xref> <xref ref-type="bibr" rid="scirp.147473-3">
     [3]
    </xref>. During pregnancy and the postpartum period, prolactin plays a major physiological role in lactogenesis and the maintenance of lactation <xref ref-type="bibr" rid="scirp.147473-4">
     [4]
    </xref>. However, in cases of active prolactinoma, milk production can become excessive and pathological, leading to unusual local complications. Postpartum hyperlactation (or “oversupply syndrome”) is an often underestimated condition, defined by milk production significantly exceeding the infant’s needs. Hyperlactation, defined as a daily milk production exceeding 1.5 liters (approximately &gt;1500 mL/day) or persistent milk leakage beyond normal physiologic levels, was used as the diagnostic criterion in this study. Clinically, hyperlactation (also called galactorrhea due to overproduction) is generally considered when: milk output &gt;1.5 L/day in established lactation, or engorgement and leakage causing discomfort not attributable to normal early postpartum physiology <xref ref-type="bibr" rid="scirp.147473-5">
     [5]
    </xref> <xref ref-type="bibr" rid="scirp.147473-6">
     [6]
    </xref>. It promotes milk stasis, painful engorgements, and eventually bacterial superinfection, which can progress to recurrent mastitis or breast abscesses <xref ref-type="bibr" rid="scirp.147473-7">
     [7]
    </xref> <xref ref-type="bibr" rid="scirp.147473-8">
     [8]
    </xref>. Endocrine causes of this condition remain exceptional in the literature, with only a few cases of prolactinomas leading to pathological hyperlactation having been described <xref ref-type="bibr" rid="scirp.147473-9">
     [9]
    </xref>-<xref ref-type="bibr" rid="scirp.147473-11">
     [11]
    </xref>. Cabergoline, a dopaminergic agonist, is the standard treatment for prolactinomas, allowing for rapid normalization of prolactin levels and tumor regression <xref ref-type="bibr" rid="scirp.147473-12">
     [12]
    </xref>. However, its use in the postpartum period should be cautious due to its inhibitory effect on lactation and potential long-term side effects <xref ref-type="bibr" rid="scirp.147473-13">
     [13]
    </xref> <xref ref-type="bibr" rid="scirp.147473-14">
     [14]
    </xref>. We report here a rare case of recurrent postpartum breast engorgements and abscesses complicating hyperlactation due to an unrecognized prolactinoma, to draw attention to this little-known endocrine cause of pathological hyperlactation and recurrent breast infections.</p>
  </sec><sec id="s2">
   <title>2. Case Presentation</title>
   <p>We report the case of a 34-year-old patient, G2P2002, with no notable medical history. Her first delivery was at term and complication-free, followed by normal exclusive breastfeeding for six months. During her second pregnancy, her milk production started late, on the third day postpartum. Ten days postpartum, the patient noted excessive milk production, significantly greater than what she experienced during her first pregnancy. This hyperlactation caused repeated breast engorgement despite attempts to manually express milk using “traditional methods,” and resulted in cracked nipples. Breastfeeding became painful and uncomfortable for both the mother (breast tension, pain) and the newborn, who was hindered by an overly abundant milk flow that made suction difficult.</p>
   <p>During the first month of breastfeeding, the patient noticed a decrease in the infant’s appetite and the appearance of white deposits on the tongue and oral mucosa (thrush). The diagnosis of neonatal oral candidiasis was made during a pediatric consultation and treated effectively, with the complete disappearance of lesions. Three months postpartum, the patient experienced sharp pain in her right breast. Despite hot water massages, relief was temporary. The breast was tense, heavy, warm, and painful, with a sensation of electric shocks. After breastfeeding, it became engorged again in less than 20 minutes, necessitating frequent use of a breast pump for decongestion. The overproduction of milk caused the infant to choke during feedings. Repeated use of the breast pump, without significant improvement, led to chronic breast overdistension, causing intense inflammation, fever, and persistent pain. The patient sought emergency care due to purulent discharge from the right breast, despite the healing of the nipple cracks.</p>
   <p>Upon admission, she had a fever of 39˚C, distended and asymmetrical breasts, painful on palpation, with erythematous areas and purulent discharge on expression. Given the excessive milk production and recurring engorgements, a serum prolactin level was requested, revealing hyperprolactinemia at 358 ng/mL. The patient was referred for an endocrinology consultation. Pituitary MRI revealed a pituitary microadenoma (<xref ref-type="fig" rid="fig1">
     Figure 1
    </xref> &amp; <xref ref-type="fig" rid="fig2">
     Figure 2
    </xref>).</p>
   <p>The management involved the immediate suppression of lactation and cessation of breastfeeding. Treatment with cabergoline 0.5 mg per week for two months was initiated, along with surgical drainage of the abscesses, local care (washing with saline solution, betadine dressing twice daily). Abcess fluid cultures were performed and revealed the presence of Staphylococcus aureus. The antibiotic susceptibility testing showed resistance to amoxicillin-clavulanic acid and sensitivity to lincomycin and clindamycin. Treatment was initiated with lincomycin at a dosage of 500 mg every 12 hours for a duration of 10 days.</p>
   <fig id="fig1" position="float">
    <label>Figure 1</label>
    <caption>
     <title>
      <xref ref-type="bibr" rid="scirp.147473-"></xref>Figure 1. MRI: Sagittal section of a round hypodense formation on T2, measuring 6.8 mm along its major axis, deforming the sellar diaphragm.</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1433808-rId13.jpeg?20251125114632" />
   </fig>
   <fig id="fig2" position="float">
    <label>Figure 2</label>
    <caption>
     <title>
      <xref ref-type="bibr" rid="scirp.147473-"></xref>Figure 2. MRI: Coronal section of a round hypodense formation on T2.</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1433808-rId14.jpeg?20251125114632" />
   </fig>
   <p>The evolution was favorable: milk secretion gradually decreased, the breast suppuration disappeared, and the signs of infection regressed. However, the patient subsequently experienced diffuse alopecia (<xref ref-type="fig" rid="fig3">
     Figure 3
    </xref>), prompting the early discontinuation of cabergoline after one month of treatment and she was referred for a dermatological evaluation.</p>
   <fig id="fig3" position="float">
    <label>Figure 3</label>
    <caption>
     <title><p class="imgGroupCss_v"><img class=" imgMarkCss lazy" data-original="https://html.scirp.org/file/1433808-rId16.jpeg?20251125114632" /></p><p class="imgGroupCss_v"><img class=" imgMarkCss lazy" data-original="https://html.scirp.org/file/1433808-rId17.jpeg?20251125114632" /></p><xref ref-type="bibr" rid="scirp.147473-"></xref>Figure 3. Onset of progressive alopecia.</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1433808-rId15.jpeg?20251125114632" />
   </fig>
  </sec><sec id="s3">
   <title>3. Discussion</title>
   <p>The reported case illustrates a rare form of postpartum hyperlactation secondary to a prolactinoma, complicated by iterative engorgements and breast abscesses. This presentation is exceptional: the literature reports fewer than ten similar cases described in the past twenty years <xref ref-type="bibr" rid="scirp.147473-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.147473-2">
     [2]
    </xref>.</p>
   <sec id="s3_1">
    <title>3.1. Hyperprolactinemia and Pathological Hyperlactation</title>
    <p>In a normal postpartum period, prolactin reaches physiological peaks between 100 and 250 ng/mL during milk production and then gradually decreases after the sixth week <xref ref-type="bibr" rid="scirp.147473-3">
      [3]
     </xref>. In our observation, the value of 358 ng/mL was significantly higher than these thresholds, confirming the pathological nature. Authors, notably Alebna et al. (2022) in Ghana, have described severe hyperlactation linked to undiagnosed prolactinomas, responsible for recurrent mastitis with prolactin levels ranging from 300 to 600 ng/mL, comparable to our patient <xref ref-type="bibr" rid="scirp.147473-9">
      [9]
     </xref>. Excessive lactogenic stimulation induces overproduction of milk surpassing the infant’s needs, leading to ductal stasis and chronic inflammation of the breast parenchyma; this mechanism is now well-documented in recent reviews by the Academy of Breastfeeding Medicine <xref ref-type="bibr" rid="scirp.147473-7">
      [7]
     </xref>.</p>
   </sec>
   <sec id="s3_2">
    <title>3.2. Breast Abscesses and Infectious Recurrences</title>
    <p>Postpartum abscesses complicate about 3% to 5% of mastitis cases according to Ding et al. (2024) <xref ref-type="bibr" rid="scirp.147473-8">
      [8]
     </xref>. Recurrent forms, as observed here, are favored by milk stasis but also by repeated manipulation with breast pumps and complete breast expression, which sustain overproduction <xref ref-type="bibr" rid="scirp.147473-5">
      [5]
     </xref> <xref ref-type="bibr" rid="scirp.147473-6">
      [6]
     </xref> <xref ref-type="bibr" rid="scirp.147473-8">
      [8]
     </xref>. Several authors have reported multiple bilateral abscesses in patients with active prolactinomas, confirming the amplifying role of hyperprolactinemia on the infectious dynamics <xref ref-type="bibr" rid="scirp.147473-4">
      [4]
     </xref> <xref ref-type="bibr" rid="scirp.147473-9">
      [9]
     </xref>.</p>
   </sec>
   <sec id="s3_3">
    <title>3.3. Diagnostic Exploration: Importance of Assays and MRI</title>
    <p>In our case, blood assays were crucial in identifying the endocrine origin of the disorder. The Endocrine Society recommends considering pituitary MRI once prolactin levels exceed 100 ng/mL in the absence of known stimulation. The detection of a microadenoma on MRI, as here, is typical: 80% of female prolactinomas measure &lt;10 mm. Similar cases of prolactinomas discovered after a breast infection episode have been reported by Rojbi et al. (2015) and more recently by Gordon et al. (2024), confirming the value of endocrine assessment in recurrent abscess forms <xref ref-type="bibr" rid="scirp.147473-10">
      [10]
     </xref> <xref ref-type="bibr" rid="scirp.147473-11">
      [11]
     </xref>.</p>
   </sec>
   <sec id="s3_4">
    <title>3.4. Management: Balancing Endocrine Control and Breast Treatment</title>
    <p>Therapeutic management requires a dual approach:</p>
    <p>On the breast management side, the latest ABM 2022 recommendations suggest:</p>
    <p>-partial breast emptying for comfort,</p>
    <p>-ultrasound-guided drainage of abscesses,</p>
    <p>-and prevention of overstimulation <xref ref-type="bibr" rid="scirp.147473-5">
      [5]
     </xref>.</p>
    <p>These principles were successfully applied in our case.</p>
    <p>On the endocrine side, cabergoline remains the gold standard for prolactinoma treatment <xref ref-type="bibr" rid="scirp.147473-10">
      [10]
     </xref> <xref ref-type="bibr" rid="scirp.147473-11">
      [11]
     </xref>. Its efficacy in rapidly reducing prolactin levels and tumor size is well-documented, even in the postpartum period <xref ref-type="bibr" rid="scirp.147473-13">
      [13]
     </xref>. However, it inhibits lactation, requiring a shared decision-making process. In the cases reported by Alebna et al. (2022) and Gordon et al. (2024), cabergoline also led to the resolution of hyperlactation and the prevention of recurrent abscesses, as observed in our case <xref ref-type="bibr" rid="scirp.147473-9">
      [9]
     </xref> <xref ref-type="bibr" rid="scirp.147473-11">
      [11]
     </xref>.</p>
   </sec>
   <sec id="s3_5">
    <title>3.5. Side Effects and Follow-Up</title>
    <p>The diffuse alopecia observed in our patient has been described in the literature as a rare but reversible side effect of cabergoline <xref ref-type="bibr" rid="scirp.147473-14">
      [14]
     </xref>. In the series by Yang et al. (2020), the incidence of cutaneous and vasomotor effects remained below 1% <xref ref-type="bibr" rid="scirp.147473-15">
      [15]
     </xref>. Early discontinuation of the treatment led to rapid improvement while maintaining controlled prolactin levels.</p>
   </sec>
   <sec id="s3_6">
    <title>3.6. Strengths and Clinical Lessons</title>
    <p>This observation is among the few reported African cases; it illustrates:</p>
    <p>1) The necessity of considering an endocrine cause in cases of unexplained or recurrent hyperlactation;</p>
    <p>2) The importance of systematic prolactin assays before any repeated breast surgery;</p>
    <p>3) The effectiveness of cabergoline in breaking the vicious cycle of hyperlactation and infection.</p>
   </sec>
  </sec><sec id="s4">
   <title>4. Conclusion</title>
   <p>This case report highlights the critical link between chronic hyperprolactinemia, even when masked by the physiological state of puerperium, and severe, recurrent breast pathology. Hyperlactation and subsequent recurrent breast abscesses in the post-partum period represent an often-recognized presentation of an underlying endocrine disorder, such as prolactinoma. The primary clinical implication of this case is that recurrent or unusually severe mastitis/abscesses during lactation should not solely be managed as a routine infectious process. Clinicians, including obstetricians, pediatricians, and general practitioners, must maintain a high index of suspicion for systemic causes when standard treatments fail or symptoms are atypical. Measuring serum prolactin levels should be considered in the workup of patients with intractable hyperlactation or recurrent breast infections.</p>
  </sec><sec id="s5">
   <title>Informed Consent</title>
   <p>Informed consent was obtained from the patient for the publication of this case report and the associated images. However, she did not authorize the publication of images showing the breast abscesses. Anonymity was maintained in accordance with the ethical principles of the Declaration of Helsinki. No identifying information about the patient has been disclosed in this article.</p>
  </sec>
 </body><back>
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