# Case Report: Immune reconstitution–related neurological deterioration in advanced HIV infection with multiple opportunistic infections: a diagnostic challenge

**Authors:** Jesús Endara-Mina, Cristopher-Josué Escudero, Victor Samaniego, Karla Fuentes, William Tapia, Cesar Intriago

PMC · DOI: 10.3389/fmed.2026.1742917 · Frontiers in Medicine · 2026-02-23

## TL;DR

A 26-year-old man with advanced HIV developed severe neurological issues after starting treatment, highlighting the diagnostic challenges of immune reconstitution inflammatory syndrome.

## Contribution

This case report highlights the diagnostic complexity of IRIS in advanced HIV with multiple opportunistic infections.

## Key findings

- Neurological deterioration occurred shortly after ART initiation in a patient with advanced HIV.
- IRIS-related inflammation, possibly linked to CNS tuberculosis, was the most plausible diagnosis.
- The case illustrates the difficulty in distinguishing IRIS from other opportunistic infections like toxoplasmosis and syphilis.

## Abstract

Immune reconstitution inflammatory syndrome (IRIS) is a serious complication following antiretroviral therapy (ART) initiation in patients with advanced HIV infection, particularly when the central nervous system is involved and multiple opportunistic infections coexist. We report the case of a 26-year-old man with newly diagnosed advanced HIV infection who developed rapid neurological deterioration shortly after ART initiation during hospitalization. Neuroimaging revealed a necrotic central nervous system mass lesion with extensive edema and mass effect. Serological testing demonstrated prior exposure to Toxoplasma gondii and active Treponema pallidum infection. Despite broad antimicrobial therapy, corticosteroids, and supportive care, the patient experienced progressive clinical deterioration and died. Retrospective reassessment of the clinical course, imaging findings, epidemiological context, and treatment response suggested an IRIS-related inflammatory process, with central nervous system tuberculosis–associated IRIS representing the most plausible underlying mechanism, while toxoplasmosis and syphilis were considered potential concomitant or confounding conditions. This case underscores the diagnostic complexity of IRIS in advanced HIV infection and highlights the importance of a cautious, probabilistic, and evidence-based approach to avoid etiologic misclassification in severe neurological presentations.

## Linked entities

- **Diseases:** HIV infection (MONDO:0005109), tuberculosis (MONDO:0018076)
- **Species:** Toxoplasma gondii (taxon 5811), Treponema pallidum (taxon 160)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** toxoplasmosis (MESH:D014123), Neurological deterioration (MESH:D009422), Kaposi's sarcoma (MESH:D012514), Histoplasmosis (MESH:D006660), intracranial mass lesions (MESH:C536030), respiratory distress (MESH:D012128), fever (MESH:D005334), necrosis (MESH:D009336), TB (MESH:D014390), Cerebral toxoplasmosis (MESH:D016781), HIV (MESH:D015658), immune dysregulation (OMIM:614878), neurological deficits (MESH:D009461), CNS involvement (MESH:D002494), seizures (MESH:D012640), herniation (MESH:D004677), non-Hodgkin lymphoma (MESH:D008228), Tuberculosis (MESH:D014376), central nervous system tuberculosis (MESH:D020306), mediastinal lymphadenopathy (MESH:D008477), interstitial pneumonia (MESH:D017563), wheezing (MESH:D012135), nausea (MESH:D009325), autoimmune diseases (MESH:D001327), lymphadenopathy (MESH:D008206), cerebral edema (MESH:D001929), pleural effusion (MESH:D010996), AIDS (MESH:D000163), edema (MESH:D004487), hepatitis B and C (MESH:D006509), CNS mass lesions (MESH:D002493), cough (MESH:D003371), IRIS (MESH:D054019), toxicity (MESH:D064420), neurosyphilis (MESH:D009494), lymphopenia (MESH:D008231), opportunistic infection (MESH:D009894), Cancer (MESH:D009369), Central nervous system involvement (MESH:C538190), Treponema pallidum infection (MESH:D007239), viral infections (MESH:D014777), ventricular compression (MESH:D009408), central (MESH:D020210), photophobia (MESH:D020795), impairment of consciousness (MESH:D003244), brain lesions (MESH:D001927), death (MESH:D003643), diplopia (MESH:D004172), Syphilis (MESH:D013587), progressive multifocal leukoencephalopathy (MESH:D007968), inflammatory (MESH:D007249), headache (MESH:D006261)
- **Chemicals:** benzathine penicillin (MESH:D010401), trimethoprim-sulfamethoxazole (MESH:D015662), methylprednisolone (MESH:D008775), Lipoarabinomannan (MESH:C050016), dexamethasone (MESH:D003907), Antituberculous (-)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Toxoplasma gondii (species) [taxon 5811], Treponema pallidum (species) [taxon 160], Cryptococcus neoformans (Cryptococcus neoformans serotype A, species) [taxon 5207], Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773], Pseudomonas aeruginosa (species) [taxon 287]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12968018/full.md

## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968018/full.md

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Source: https://tomesphere.com/paper/PMC12968018