Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man

Conidiobolomycosis is a fungal infection caused by Conidiobolus spp. Common symptoms include epistaxis, nasal discharge, nasal obstruction, sinus tenderness, and persistent extensive facial swelling leading to facial mutilation. Our case describes an indolent presentation of conidiobolomycosis in an...

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Published in:Malaysian Journal of Medicine and Health Sciences
Main Author: Jamalut Y.; Mustakim S.; Zaini A.B.; Ting T.X.; Mohd-Hatta N.; Amin-Nordin S.; Masri S.N.
Format: Article
Language:English
Published: Universiti Putra Malaysia Press 2024
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85213889639&doi=10.47836%2fmjmhs.20.s11.23&partnerID=40&md5=2e9c250d03b4dd6e8cb0031f320e1279
id 2-s2.0-85213889639
spelling 2-s2.0-85213889639
Jamalut Y.; Mustakim S.; Zaini A.B.; Ting T.X.; Mohd-Hatta N.; Amin-Nordin S.; Masri S.N.
Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man
2024
Malaysian Journal of Medicine and Health Sciences
20

10.47836/mjmhs.20.s11.23
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85213889639&doi=10.47836%2fmjmhs.20.s11.23&partnerID=40&md5=2e9c250d03b4dd6e8cb0031f320e1279
Conidiobolomycosis is a fungal infection caused by Conidiobolus spp. Common symptoms include epistaxis, nasal discharge, nasal obstruction, sinus tenderness, and persistent extensive facial swelling leading to facial mutilation. Our case describes an indolent presentation of conidiobolomycosis in an immunocompromised young man, resulting in delayed diagnosis and treatment. A 29-year-old Malay gentleman, a chef, who was hearing disabled and on anti-tuberculosis treatment, presented with a five-month history of unwellness, poor oral intake, and painless left nasal cavity swelling. Despite classic symptoms of conidiobolomycosis being absent, biopsy and PCR confirmed Conidiobolus megalotocus. After antifungal treatment initiation, his condition significantly improved, with resolution of facial swelling, after two months. This case highlights the importance of considering conidiobolomycosis in immunocompromised patients even with atypical presentations. © 2024 Universiti Putra Malaysia Press. All rights reserved.
Universiti Putra Malaysia Press
16758544
English
Article

author Jamalut Y.; Mustakim S.; Zaini A.B.; Ting T.X.; Mohd-Hatta N.; Amin-Nordin S.; Masri S.N.
spellingShingle Jamalut Y.; Mustakim S.; Zaini A.B.; Ting T.X.; Mohd-Hatta N.; Amin-Nordin S.; Masri S.N.
Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man
author_facet Jamalut Y.; Mustakim S.; Zaini A.B.; Ting T.X.; Mohd-Hatta N.; Amin-Nordin S.; Masri S.N.
author_sort Jamalut Y.; Mustakim S.; Zaini A.B.; Ting T.X.; Mohd-Hatta N.; Amin-Nordin S.; Masri S.N.
title Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man
title_short Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man
title_full Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man
title_fullStr Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man
title_full_unstemmed Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man
title_sort Rhinofacial Conidiobolomycosis Mimicking Facial Cellulitis: A Diagnostic Challenge in an Immunocompromised Man
publishDate 2024
container_title Malaysian Journal of Medicine and Health Sciences
container_volume 20
container_issue
doi_str_mv 10.47836/mjmhs.20.s11.23
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85213889639&doi=10.47836%2fmjmhs.20.s11.23&partnerID=40&md5=2e9c250d03b4dd6e8cb0031f320e1279
description Conidiobolomycosis is a fungal infection caused by Conidiobolus spp. Common symptoms include epistaxis, nasal discharge, nasal obstruction, sinus tenderness, and persistent extensive facial swelling leading to facial mutilation. Our case describes an indolent presentation of conidiobolomycosis in an immunocompromised young man, resulting in delayed diagnosis and treatment. A 29-year-old Malay gentleman, a chef, who was hearing disabled and on anti-tuberculosis treatment, presented with a five-month history of unwellness, poor oral intake, and painless left nasal cavity swelling. Despite classic symptoms of conidiobolomycosis being absent, biopsy and PCR confirmed Conidiobolus megalotocus. After antifungal treatment initiation, his condition significantly improved, with resolution of facial swelling, after two months. This case highlights the importance of considering conidiobolomycosis in immunocompromised patients even with atypical presentations. © 2024 Universiti Putra Malaysia Press. All rights reserved.
publisher Universiti Putra Malaysia Press
issn 16758544
language English
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