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...
Published in: | Malaysian Journal of Medicine and Health Sciences |
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Universiti Putra Malaysia Press
2024
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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 |
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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 |
format |
Article |
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record_format |
scopus |
collection |
Scopus |
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1823296153606684672 |