Rhino-orbito-cerebral mucormycosis complicated with an ophthalmic artery occlusion followed by subarachnoid hemorrhage

Abstract

A 70-year-old female with poorly controlled diabetes developed sudden visual loss, ptosis and complete ophthalmoplegia of the right eye. Funduscopic examination showed the pale retina and the cherry red spot in the right eye. Fluorescein angiography and indocyanine green angiography demonstrated the absence of retinal arterial filling and choroidal perfusion in the right eye even 20 minutes after injecting the dye. The patient was diagnosed with right ophthalmic artery occlusion. Computed tomography (CT) showed diffuse mucosal thickening in the right ethmoidal sinus. Based on the clinical findings and endoscopic biopsy result, mucormycosis was confirmed. Amphotericin B (40 mg/day) and ceftriaxone (2 g/day) were intravenously administered. Despite the improvement of the right ethmoidal sinusitis and the right proptosis, the patient deteriorated into a comatose state after 19 days of systemic amphotericin B therapy. Although the previous CT showed no cerebral aneurysm, a repeated CT showed newly developed posterior communicating artery aneurysm and the subarachnoid hemorrhage. Despite the amphotericin B treatment and the improvement of the sinusitis, mucormycosis could cause sudden cerebral aneurysm rupture and subarachnoid hemorrhage resulting in coma.

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Kang, K. , Kwon, Y. , Shin, J. , Kim, I. and Park, D. (2013) Rhino-orbito-cerebral mucormycosis complicated with an ophthalmic artery occlusion followed by subarachnoid hemorrhage. Case Reports in Clinical Medicine, 2, 345-347. doi: 10.4236/crcm.2013.26093.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] Koc, Z., Koc, F., Yerdelen, D. and Ozdogu, H. (2007) Rhino-orbital-cerebral mucormycosis with different cerebral involvements: Infarct, hemorrhage, and ophthalmoplegia. International Journal of Neuroscience, 117, 1677-1690. doi:10.1080/00207450601050238
[2] Haliloglu, N.U., Yesilirmak, Z., Erden, A. and Erden, I. (2008) Rhino-orbito-cerebral mucormycosis: Report of two cases and review of the literature. Dentomaxillofacial Radiology, 37, 161-166. doi:10.1259/dmfr/14698002
[3] Yang, S.W., Kim, S.Y., Chung, J. and Kim, K.B. (2000) Two cases of orbital infarction syndrome. Korean Journal of Ophthalmology, 14, 107-111.
[4] Hussain, S., Salahuddin, N., Ahmad, I., Salahuddin, I. and Jooma, R. (1995) Rhinocerebral invasive mycosis: Occurrence in immunocompetent individuals. European Journal of Radiology, 20, 151-155. doi:10.1016/0720-048X(95)00644-6
[5] Zimmerman, C.F., Van Patten, P.D., Golnik, K.C., Kopitnik Jr., T.A. and Anand, R. (1995) Orbital infarction syndrome after surgery for intracranial aneurysms. Ophthalmology, 102, 594-598.
[6] Chimelli, L. and Mahler-Araujo, M.B. (1997) Fungal infections. Brain Pathology, 7, 613-627. doi:10.1111/j.1750-3639.1997.tb01078.x
[7] Peterus, T., Teguh, T. and Daofu, D. (2004) Fatal strokes in patients with rhino-orbito-cerebral mucormycosis and associated vasculopathy. Scandinavian Journal of Infectious Diseases, 36, 643-648. doi:10.1080/00365540410020794
[8] Asari, S., Nishimoto, A. and Murakami, M. (1988) A rare case of cerebral aspergillus aneurysm at the site of temporary clip application. No Shinkei Geka, 16, 1079-1082.
[9] Harris, J.S. (1955) Mucormycosis; report of a case. Pediatrics, 16, 857-867.
[10] Shah, P.D., Peters, K.R. and Reuman, P.D. (1997) Recovery from rhinocerebral mucormycosis with carotid artery occlusion: A pediatric case and review of the literature Pediatric Infectious Disease Journal, 16, 68-71. doi:10.1097/00006454-199701000-00015
[11] Toumi, A., Larbi Ammari, F., Loussaief, C., Hadhri, R., Ben Brahim, H., Harrathi, K., Ben Romdhane, F., Koubaa, J. and Chakroun, M. (2012) Rhino-orbito-cerebral mucormycosis: Five cases. Médecine et Maladies Infectieuses, 42, 591-598. doi:10.1016/j.medmal.2012.10.001

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