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Middle Cerebral Artery Occlusion Allowing Reperfusion via Common Carotid Artery Repair in Mice
Published on: January 23, 2019
Carotid artery occlusion by rhinoorbitocerebral mucormycosis
Faisal Al-Otaibi1, Monirah Albloushi, Hindi Alhindi
1Division of Neurosurgery, Neurosciences Department, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
Abstract:
Mucormycosis is the third most common invasive fungal infection that particularly occurs in immunocompromised patients. Intracranial and extracranial arteriovenous vasculopathy is a complication that makes this disease more complex and difficult to treat. We describe a 23-year-old female, who presented to her local hospital with acute blindness and diabetic ketoacidosis-induced coma requiring intensive care treatment. She was found to have lesions in the nasal sinuses, orbit, and frontal base. The left carotid artery was occluded from its origin in the neck to the supraclinoid segment and left cavernous sinus involvement. No cerebral infarction was noted. Biopsies obtained by endonasal debridement confirmed mucormycosis. In addition to antimicrobial therapy, she underwent several multidisciplinary approaches to treat her disease. Multiple endonasal, and cranial procedures were done including bilateral orbital exenteration. After prolonged treatment on the intensive care unit she made a remarkable recovery to the point where she was communicating verbally and had normal limb movements and later discharged home. She remained alive and well for two months, but later succumbed to a recurrence of her disease. In conclusion, mucormycosis-induced vasculopathy is a complex problem, which merits aggressive treatment of this invasive disease. It is normally regarded as an indicator of grave prognosis.
Insights
Mucormycosis, a severe fungal infection, can cause dangerous vasculopathy, especially in immunocompromised individuals. Aggressive multidisciplinary treatment is crucial for managing this complex condition, despite its grave prognosis.
Area of Science:
- Mycology
- Infectious Diseases
- Vascular Medicine
Background:
- Mucormycosis is a serious invasive fungal infection, ranking as the third most common type, predominantly affecting immunocompromised patients.
- Intracranial and extracranial arteriovenous vasculopathy complicates mucormycosis, significantly increasing treatment difficulty and patient mortality.
- The case highlights the severe manifestations of mucormycosis, including acute blindness and coma due to diabetic ketoacidosis.
Purpose of the Study:
- To present a case of mucormycosis with extensive vasculopathy in a young immunocompromised patient.
- To illustrate the challenges and multidisciplinary treatment approaches for this complex condition.
- To emphasize the critical need for aggressive management of mucormycosis-induced vasculopathy.
Main Methods:
- A 23-year-old female patient with acute blindness and diabetic ketoacidosis-induced coma was diagnosed with mucormycosis.
- Diagnostic imaging revealed nasal sinus, orbital, and frontal base lesions, with left carotid artery occlusion and cavernous sinus involvement.
- Confirmation of mucormycosis was achieved through endonasal debridement biopsies.
Main Results:
- The patient underwent extensive multidisciplinary treatment, including antimicrobial therapy and multiple surgical procedures (bilateral orbital exenteration).
- Initial recovery was remarkable, with the patient regaining verbal communication and motor function.
- Despite initial improvement, the patient experienced a disease recurrence and ultimately succumbed two months post-discharge.
Conclusions:
- Mucormycosis-induced vasculopathy presents a complex clinical challenge requiring aggressive and comprehensive treatment strategies.
- Early diagnosis and prompt, multidisciplinary intervention are vital for managing invasive fungal infections with vascular complications.
- While aggressive treatment can lead to temporary recovery, the prognosis for mucormycosis with vasculopathy remains grave due to the high risk of recurrence.
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