{"title":"A case report of Saksenaea vasiformis mucormycosis infection of a lower segment caesarean section wound","authors":"Steven Nguyen , Hao Han Tan , Damian Fry","doi":"10.1016/j.ijscr.2025.111923","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Mucormycosis is a rare and difficult condition to diagnose, often requiring histological confirmation. Only two previous case reports of mucormycosis infections following caesarean section have been published to date.</div></div><div><h3>Case presentation</h3><div>A 24-year-old female from Australia presented with fevers, pain and discharge from her wound site seven days following a lower segment caesarean section. The patient failed to improve with broad-spectrum antibiotics and required radical surgical debridement. Tissue samples from the first debridement operation found necrotic fibroadipose tissue with fungal hyphae histologically. The hyphae were 90-degree branching with focal angioinvasion, a highly suggestive feature of mucormycosis, which eventually identified <em>Saksenaea vasiformis</em>.</div></div><div><h3>Discussion</h3><div>The mucormycosis infection was treated with amphotericin B and posaconazole as well as multiple surgical debridement operations. Following resolution of the infection, reconstruction was performed with Phasix™ mesh repair of the abdominal fascia, in addition to biodegradable temporizing matrix (BTM) and split-thickness skin grafting.</div></div><div><h3>Conclusion</h3><div>This case highlights the exceptionally rare diagnosis of mucormycosis in a caesarean section wound, especially in a developed country, and the complex multidisciplinary management required. Antifungal treatment and aggressive radical debridement were essential for treatment, as well as reconstruction in an infected setting.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"135 ","pages":"Article 111923"},"PeriodicalIF":0.7000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210261225011095","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"SURGERY","Score":null,"Total":0}
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Abstract
Introduction
Mucormycosis is a rare and difficult condition to diagnose, often requiring histological confirmation. Only two previous case reports of mucormycosis infections following caesarean section have been published to date.
Case presentation
A 24-year-old female from Australia presented with fevers, pain and discharge from her wound site seven days following a lower segment caesarean section. The patient failed to improve with broad-spectrum antibiotics and required radical surgical debridement. Tissue samples from the first debridement operation found necrotic fibroadipose tissue with fungal hyphae histologically. The hyphae were 90-degree branching with focal angioinvasion, a highly suggestive feature of mucormycosis, which eventually identified Saksenaea vasiformis.
Discussion
The mucormycosis infection was treated with amphotericin B and posaconazole as well as multiple surgical debridement operations. Following resolution of the infection, reconstruction was performed with Phasix™ mesh repair of the abdominal fascia, in addition to biodegradable temporizing matrix (BTM) and split-thickness skin grafting.
Conclusion
This case highlights the exceptionally rare diagnosis of mucormycosis in a caesarean section wound, especially in a developed country, and the complex multidisciplinary management required. Antifungal treatment and aggressive radical debridement were essential for treatment, as well as reconstruction in an infected setting.