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.

Case Reports in Surgery
|December 1, 2012
PubMed

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.