Evidence map›Paper›PMID 42267261›Full record

ArticleCase reports in infectious diseases2026

Lumbar Spine Mucormycosis Mimicking Pott's Spine: A Case Report.

Kanav Gupta, Kashif Qureshi, Sonal Gupta, Rakesh Dua, Shivanya Singh, Shaurya Darbari, Bipin Chaurasia, Kivanc Yangi

Abstract read
In one paragraph

Article in Case reports in infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Lumbar Spine Mucormycosis Mimicking Pott's Spine: A Case Report.Case reports in infectious diseases · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Kanav GuptaDepartment of Neurosurgery, All India Institute of Medical Sciences (AIIMS), Jammu, India, aiims.edu.ORCID https://orcid.org/0000-0002-3272-536X
Kashif QureshiDepartment of Neurosurgery, Yale School of Medicine, New Haven, Connecticut, USA, yale.edu.ORCID https://orcid.org/0009-0002-7734-0567
Sonal GuptaDepartment of Neurosurgery, Fortis Hospital, Shalimar Bagh, New Delhi, India, fortishealthcare.com.ORCID https://orcid.org/0009-0002-6489-7251
Rakesh DuaDepartment of Neurosurgery, Fortis Hospital, Shalimar Bagh, New Delhi, India, fortishealthcare.com.ORCID https://orcid.org/0009-0003-7569-0579
Shivanya SinghDepartment of Oncoanesthesia and Palliative Care, All India Institute of Medical Sciences (AIIMS), Bhopal, India, aiims.edu.ORCID https://orcid.org/0000-0002-5207-0655
Shaurya DarbariDepartment of Neurosurgery, All India Institute of Medical Sciences (AIIMS), Jammu, India, aiims.edu.ORCID https://orcid.org/0000-0002-2177-3403
Bipin ChaurasiaDepartment of Neurosurgery, Neurosurgery Clinic, Birgunj, 44200, Nepal.ORCID https://orcid.org/0000-0002-8392-2072
Kivanc YangiDepartment of Neurosurgery, Barrow Neurological Institute, Phoenix, Arizona, USA, thebarrow.org.ORCID https://orcid.org/0000-0003-0500-218X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Spinal mucormycosis is an exceptionally rare form of invasive fungal infection, with fewer than 12 confirmed cases reported in the prior literature. Immunocompromised patients are disproportionately affected, and mortality exceeds 50% in this population. Chronic liver disease as a primary predisposing condition is underrepresented in the existing case series. Case Presentation: A 54-year-old male with Child-Pugh Grade C chronic liver cirrhosis, diabetes mellitus, and hypothyroidism presented with progressive low back pain and bilateral lower limb weakness of one week duration. Lumbar MRI demonstrated L2-L3 spondylodiscitis with epidural abscess formation, initially attributed to Pott's spine, and antitubercular therapy (ATT) was initiated empirically. Rapid neurological deterioration prompted surgical re-evaluation. The patient underwent an L3 laminectomy with drainage of an L3-L4 anterior epidural abscess. Intraoperative microscopy revealed aseptate ribbon-like hyphae consistent with Mucorales species. Liposomal Amphotericin B (5 mg/kg/day), intravenous micafungin, and oral posaconazole were commenced. Antifungal therapy was complicated by progressive nephrotoxicity and hepatic decompensation requiring repeated dose modifications. The patient developed hepatic encephalopathy with sepsis and died on Postoperative day (POD) 12 from multiorgan failure. Conclusion: This case represents the 12th documented instance of spinal mucormycosis and the first attributable to Child-Pugh Grade C liver disease. In tuberculosis-endemic settings, mucormycosis must be considered in the differential diagnosis of apparent Pott's spine in immunocompromised patients, particularly those with progressive neurological deterioration despite empirical ATT. Concurrent hepatic and renal impairment substantially constrains antifungal options and worsens prognosis. Multidisciplinary coordination and early tissue diagnosis are critical to the management of this rare, life-threatening condition.

Indexed as

antifungal therapycase reportimmunocompromised hostmucormycosisspinal infectionspondylodiscitis

Identifiers

PMID42267261
PMCPMC13244248

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