# Novel diagnostic approaches and therapeutic management of mucormycosis: insights from a retrospective monocentric cohort study

**Authors:** Othman Lemhamdi, Evelyne Willems, Frédéric Baron, Bernard De Prijck, Jo Caers, Antoine Bouquegneau, Julien Guiot, François Cousin, Alexandre Jadoul, Florence Rogister, Frederic Frippiat, Marie-Pierre Hayette, Adrien De Voeght

PMC · DOI: 10.3389/fmed.2026.1715663 · Frontiers in Medicine · 2026-02-04

## TL;DR

This study examines the diagnosis and treatment of mucormycosis in immunocompromised patients, highlighting the high mortality rate and the need for early diagnosis and tailored therapies.

## Contribution

The study provides insights into risk factors, treatment approaches, and outcomes in mucormycosis patients based on a monocentric cohort.

## Key findings

- Hematological malignancies and immunosuppressive therapy were the most common risk factors for mucormycosis.
- Pulmonary involvement was observed in 94% of cases, and surgery improved outcomes in half of the patients.
- Despite treatment, the mortality rate on day 84 was 35%, emphasizing the need for better diagnostic and therapeutic strategies.

## Abstract

Mucormycosis is a rare, opportunistic fungal infection with high mortality rates, predominantly affecting immunocompromised patients. Its management is challenging due to diagnostic complexity and limited therapeutic options.

This retrospective cohort study analyzed 21 cases of mucormycosis diagnosed at the University Hospital of Liège between July 2018 and August 2023. Clinical, microbiological, and radiological data were evaluated to identify risk factors, treatment modalities, and outcomes.

Hematological malignancies (82%) and immunosuppressive therapy (53%) were the most common risk factors. Pulmonary involvement occurred in 94% of cases. Liposomal Amphotericin B was the most frequently used antifungal therapy, and surgery improved outcomes in 50% of cases when it was performed. Despite these measures, the mortality rate on day 84 remained significant at 35%.

This study underscores the challenges of managing mucormycosis in immunocompromised patients. The high mortality rate emphasizes the importance of early diagnosis, tailored antifungal therapy, and standardized treatment protocols to improve survival outcomes.

## Linked entities

- **Chemicals:** Liposomal Amphotericin B (PubChem CID 44405442)
- **Diseases:** mucormycosis (MONDO:0019136)

## Full-text entities

- **Genes:** IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CABIN1 (calcineurin binding protein 1) [NCBI Gene 23523] {aka CAIN, KB-318B8.7, PPP3IN}, GGTLC4P (gamma-glutamyltransferase light chain 4 pseudogene) [NCBI Gene 729838] {aka GGT}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}
- **Diseases:** Mycosis (MESH:D015821), PD (MESH:D018450), tracheal mass (MESH:D014133), DILI (MESH:D056486), candidiasis (MESH:D002177), invasive aspergillosis (MESH:D055744), Renal toxicity (MESH:D007674), CT (MESH:C000719218), invasive (MESH:D009361), infectious disease (MESH:D003141), necrotic (MESH:D009336), IFD (MESH:D000072742), immune dysregulation (OMIM:614878), Aspergillus infections (MESH:D001228), fungal (MESH:D009181), Graft (MESH:D055589), Neutropenia (MESH:D009503), death (MESH:D003643), Co (MESH:D060085), Mucorales (MESH:D009091), malignant hypercalcemia (MESH:D006934), toxicity (MESH:D064420), bacteremia (MESH:D016470), COVID-19 (MESH:D000086382), immune dysfunction (MESH:D007154), infected (MESH:D007239), bacterial pneumonia (MESH:D018410), function (MESH:D003291), pleural effusion (MESH:D010996), chronic granulomatous disease (MESH:D006105), osteolytic (MESH:D030981), CR (MESH:D001766), Hematological malignancies (MESH:D019337), critically ill (MESH:D016638), Disease (MESH:D004194), GVHD (MESH:D006086), zygomycosis (MESH:D020096), diabetes (MESH:D003920), Lymphopenia (MESH:D008231), Cancer (MESH:D009369), opportunistic (MESH:D009894), hyperferritinemia (MESH:D000085583), AD (MESH:D000544)
- **Chemicals:** gadolinium (MESH:D005682), creatinine (MESH:D003404), L-AmB (MESH:C068538), tacrolimus (MESH:D016559), Sabouraud agar medium (-), 18F-fluorodeoxyglucose (MESH:D019788), Amphotericin (MESH:D000666), Isavuconazole (MESH:C508735), posaconazole (MESH:C101425), L (MESH:D007930), voriconazole (MESH:D065819), MMF (MESH:D009173), Deferasirox (MESH:D000077588), azole (MESH:D001393), bilirubin (MESH:D001663)
- **Species:** Rhizopus microsporus (species) [taxon 58291], Enterococcus faecium (species) [taxon 1352], Homo sapiens (human, species) [taxon 9606], Mucorales (pin molds, order) [taxon 4827], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], A. flavus [taxon 315677], Rhizopus pusillus (species) [taxon 1357711], Aspergillus fumigatus (species) [taxon 746128], Mus musculus (house mouse, species) [taxon 10090], Nakaseomyces glabratus (species) [taxon 5478], Rhizopus arrhizus (species) [taxon 64495]

## Full text

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## Figures

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## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913173/full.md

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Source: https://tomesphere.com/paper/PMC12913173