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        <datestamp>2026-09-27T18:09:50Z</datestamp>
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          <dc:title>Disseminated melioidosis presenting as pre-septal cellulitis and multifocal abscesses in an adolescent with type 1 diabetes mellitus: a case report</dc:title>
          <dc:creator>Nikhil John (25116322)</dc:creator>
          <dc:creator>Pediredla Karunakar (25116325)</dc:creator>
          <dc:creator>Rajashree Choudhury (25116328)</dc:creator>
          <dc:creator>Arun Babu T (25116331)</dc:creator>
          <dc:creator>Sumit Rai (15143805)</dc:creator>
          <dc:creator>Debabrata Dash (616301)</dc:creator>
          <dc:subject>Space Science</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>Melioidosis</dc:subject>
          <dc:subject>Burkholderia pseudomallei</dc:subject>
          <dc:subject>type 1 diabetes mellitus</dc:subject>
          <dc:subject>preseptal cellulitis</dc:subject>
          <dc:subject>splenic abscess</dc:subject>
          <dc:subject>MALDI-ToF</dc:subject>
          <dc:subject>multifocal abscess</dc:subject>
          <dc:subject>case report</dc:subject>
          <dc:description>&lt;p&gt;Melioidosis, caused by &lt;i&gt;Burkholderia pseudomallei&lt;/i&gt;, produces a wide range of clinical manifestations and may be difficult to diagnose in the pediatric population. We describe the case of a 12-year-old girl with poorly controlled type 1 diabetes mellitus that posed diagnostic challenges. Over 4 months, she experienced relapsing fever, multiple splenic abscesses with a ‘target sign’ on ultrasonography, right-sided preseptal cellulitis, and a left thigh ulcer. Repeated cultures of superficial swabs and blood yielded no growth of bacteria. Radiological mimicry and culture-negative results raised concerns regarding a fungal etiology, leading to empiric amphotericin B therapy. The definitive diagnosis was made after incision and drainage of a 4 × 6 cm&lt;sup&gt;2&lt;/sup&gt; frontal abscess. Pus culture isolated &lt;i&gt;Burkholderia pseudomallei&lt;/i&gt;, identified by matrix‑assisted laser desorption/ionization time‑of‑flight mass spectrometry (MALDI‑ToF MS). Patient was treated with intravenous meropenem for 4 weeks followed by oral cotrimoxazole for a planned 3‑month eradication course. The patient recovered with no relapse on follow‑up. This case highlights the need to consider melioidosis in diabetic patients presenting with recurrent, culture-negative abscesses that display a target sign in endemic regions. Deep tissue culture remains essential for diagnosis, as superficial swabs may be misleading. Source control, coupled with dual-phase antimicrobial therapy, remain the cornerstones of effective management&lt;/p&gt;</dc:description>
          <dc:date>2026-09-27T18:09:50Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.34005442.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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