Orbital Aspergillosis

From EyeWiki
Revision as of 11:08, July 1, 2019 by Rayna.Ungersma.AAO (talk | contribs) (Rayna.Ungersma.AAO moved page Orbital Apergillosis to Orbital Aspergillosis)

This page was enrolled in the Residents and Fellows contest.

Assigned editor:
Assigned status Update Pending
 by Jacquelyn Laplant, MD on June 30, 2019.

Article summary goes here.

Disease Entity


Orbital aspergillosis

  • ICD-10-CM B44.9 Aspergillosis, unspecified


Aspergillosis and mucormycosis are the most common orbital fungal infections while aspergillosis is the most common cause of paranasal mycoses. [1] Orbital mycoses most commonly occurs via extension from the paranasal sinuses; however, organisms can also gain access to the orbit from direct trauma or hematogenous spread from distant sites.[2]

Risk Factors

Orbital aspergillosis occurs primarily in immunocompromised hosts; however, infections in immunocompetent patients is well-documented.[3][4] Paranasal mycoses is an obvious risk factor for orbital involvement, and others include diabetic ketoacidosis, neutropenia, neutrophil dysfunction, prosthetic devices, trauma, severe burns, alcoholism, intravenous drug use, HIV infection, hematologic malignancy, bone marrow transplantation, liver cirrhosis, corticosteroid use, antibiotics, and chemotherapy. Smoking contaminated marijuana has also been reported to increase the risk for development of sino-orbital aspergillosis in immunocompromised patients.[5]

Environmental exposures such as hospital construction, demolition sites, or compost, and exposure in endemic areas such as Sudan and Saudi Arabia are also important to consider.6 For example, aspergilloma or “fungus ball” is the leading cause of secondary proptosis in Sudan.[6][7]

General Pathology

Aspergillosis is caused by the genus Aspergillus which are spore-forming, septate filamentous molds. The two species Aspergillus flavus and Aspergillus fumigatus most commonly affect the orbit. Aspergillus grows well in warm, moist environments, and it often colonizes the respiratory tract without causing disease in immunocompetent individuals.

Orbital aspergillosis is divided into noninvasive and invasive forms with the latter more common in immunocompromised patients, and several clinical entities have been further described based on the patterns of tissue involvement.6 Invasive aspergillosis is characterized by fungal tissue or bone invasion behaving similar to an inflammatory or malignant process.[8] This can present in a variety of ways: as a localized process, it can invade nearby structures and/or blood vessels causing thrombosis and tissue necrosis, or it can be fulminant with embolization and multiorgan involvement and possible death.[4]

In contrast, fungal infiltration of tissue is not characteristic of noninvasive aspergillosis, but it can still cause tissue destruction secondary to a chronic inflammatory reaction. For example, allergic aspergillus sinusitis occurs in young, atopic individuals who often have a history of recurrent sinusitis, nasal congestion, or allergic rhinitis. It is a chronic sinus disease that often leads to accumulation of a thick material known as allergic mucin consisting of degenerated eosinophils, cellular debris, and Charcot-leyden crystals which can necessitate debridement.[7][9]

Another example would be sinonasal aspergilloma, also known as “fungus ball” seen primarily in immunocompetent patients in a noninvasive form although it can become invasive in immunocompromised patients.[6][9] Sinonasal fungus balls are noninvasive extramucosal mycotic proliferations that fill at least one paranasal sinus, typically the sphenoid or ethmoid. Patients typically present with nasal symptoms such as rhinorrhea or obstruction and retro or peri-orbital headaches. Occasionally vision loss is reported if the fungus ball is compressing the optic nerve.[10] If the fungus ball is located in the posterior sphenoid or ethmoid sinus a rare neuro-ophthalmic emergency called orbital apex syndrome (OAS) may present. Orbital apex syndrome presents with visual loss, ophthalmoplegia and ptosis. Early recognition and management with antifungals and/or sinus surgery are imperative to prevent permanent vision loss.[11]


Primary orbital aspergillosis is a rare entity, but it has been reported in the literature.[3] Orbital aspergillosis most commonly occurs as a result of contiguous spread from the paranasal sinuses with sinus disease being present in the majority of those affected.[3] Inhalation of fungal spores in the nasopharynx and paranasal sinuses in an immunocompromised host can then initiate a granulomatous reaction that can extend to the orbit.[12] Secondary involvement can also result from trauma or hematogenous spread.

Primary prevention

Prevention is targeted to those who are at higher risk of infection, including patients with a history of HIV/AIDS, organ transplantation, chronic chemotherapy, or hematologic malignancies. Certain populations may benefit from prophylactic antifungal therapy although this is not standardized. Some suggest prevention in endemic areas or hospital construction zones by using masks and air supply treatment.[13] Increased awareness among healthcare providers is also integral in prevention and recognition.


The diagnosis of orbital aspergillosis is based on a combination of clinical presentation, imaging, and biopsy.


The clinical history of orbital aspergillosis is nonspecific and can closely resemble several orbital inflammatory and neoplastic conditions (see differential diagnosis).[3] Because it depends on the immune status of the patient and the form of aspergillosis, the presentation is typically chronic and indolent in immunocompetent patients and more acute and progressive in immunocompromised patients. The most common chief complaints at presentation are pain, headache, and/or proptosis.[4][14][15] The description of the pain is often vague, usually being and in the retrobulbar area. Pain usually precedes ophthalmic findings and can become progressively severe. Patients with allergic fungal sinusitis commonly have a history of allergic rhinitis, nasal congestion, nasal polyposis or recurrent sinusitis and may not initially present with orbital signs or symptoms.

Physical examination

A full orbital and ophthalmological examination should be performed which includes best-corrected visual acuity (BCVA), color vision and stereopsis, formal visual field evaluation, pupillary function, ocular motility/pain with motions, facial sensation, intraocular pressure, slit lamp biomicroscopy, dilated fundus exam, orbital auscultation, and exophthalmometry. This should be supplemented with nasal and sinus examination and may include otolaryngological consultation.[6]


Clinical signs of orbital aspergillosis are highly variable and dependent on the disease entity. Involvement of the orbit can be primarily orbital, sino-orbital, or with central nervous system involvement.[4]

Acute invasive sino-orbital aspergillosis may present with signs characteristic of a bacterial cellulitis with periorbital inflammation that progresses to an orbital apex syndrome, presenting with ptosis, proptosis, painful ophthalmoplegia, and an optic neuropathy characterized by loss of visual acuity and an afferent pupillary defect. Proptosis can also be seen in noninvasive aspergillosis secondary to expansion of the sinus cavities. Fulminant aspergillosis can resemble mucormycosis with invasion into the blood vessels with subsequent thrombosis and tissue necrosis with a black eschar in late stages. Alteration in mental status may suggest central nervous system invasion or represent diabetic ketoacidosis.[13]


The most common presenting symptom of orbital aspergillosis is orbital and facial pain. Concomitant sinus involvement with congestion, rhinorrhea, epistaxis, and epiphora is often but not always present and contributes to the diagnostic challenges of this disease. Allergic fungal sinusitis patients do not usually present with orbital symptoms, but rather with symptoms of allergic rhinitis, chronic sinusitis and nasal obstruction.8 Patients with aspergillomas may present with facial pain or symptoms secondary to chronic sinusitis. Invasive aspergillosis patients may present acutely or over a period of weeks to months and may report a wide range of symptoms including naso-orbital pain, headache, proptosis, epistaxis, and worsening vision.[7]

Diagnostic procedures

Computed tomography (CT) of the orbit is the initial imaging modality of choice for diagnosing and characterizing the extent of orbital aspergillosis as it is quick and effective. Aspergillus appears as isodense, heterogenous lesions affecting the paranasal sinuses with calcification and bony erosion. The sphenoid sinus is the most commonly affected paranasal sinus which is postulated to be related to its’ low oxygen content and acidic environment. The presence of patchy hyperattenuation is also considered an indirect indicator of fungal disease.[16] MRI reveals hypointense lesions on T1 and T2-weight images in contrast to neoplastic and bacterial lesions which are hypertense on T-2 weighted images.[8] MRI is generally preferred to CT in evaluating the orbital apex, cavernous sinus, and optic nerve changes.

Incisional biopsy of both the center and periphery of the lesion with histopathological and microbiological studies is considered the gold standard for diagnosis. Aspergillus has a characteristic microscopic appearance as thin 2-3 𝜇m, septate hyphae with 45 degree branching, best seen on Gomori Methanamine silver and periodic acid Schiff stains.[15] Part of the biopsy should be sent for culture. If initial biopsy does not yield a diagnosis and suspicion remains high then a second biopsy should be obtained, especially if considering corticosteroids. High rates of negative biopsies have been reported due to a tendency of the fungus to only appear in late-stage samples.[17]

Interest has been growing for non-invasive laboratory based tests for diagnosing aspergillosis. The use of serum assays for galactomannan, an Aspergillus antigen present during fungal growth, may become a useful, noninvasive option to aid in earlier diagnosis of invasive aspergillosis, and polymerase chain reaction (PCR) testing is a quick and reliable modality which may offer the most sensitive and specific method for identifying Aspergillus infection.[18][19]

Differential diagnosis

The differential diagnosis can be broadly divided into orbital infectious, orbital neoplastic, and orbital non-infectious granulomatous processes.[6]

  • Orbital fungal infections: aspergillus, mucor, bipolaris, alternaria, curvularia, coccidioides, blastomyces, histoplasma
  • Orbital bacterial infections: cellulitis, subperiosteal abscess, syphilis, mycobacteria
  • Orbital inflammatory disorders: idiopathic orbital inflammatory disease, Graves’ ophthalmopathy, sarcoidosis, polyarteritis nodosa, granulomatosis with polyangiitis, collagen-vascular disorders
  • Neoplasia: metastasis, primary tumor, lacrimal gland tumor, lymphoma, leukemia
  • Vascular disease: carotid-cavernous fistula, cavernous sinus thrombosis, varix
  • Neuro-ophthalmic disorders: optic neuritis, optic neuropathy, cranial neuropathy


General treatment

Management of aspergillosis consists of reversal of any immunosuppression, aeration and drainage of the paranasal sinuses involved, and treatment with systemic antifungals. Surgical debridement of the orbit, sinuses and skull base with intravenous and local irrigation of antifungals may be necessary for widespread invasive disease.[20] Unfortunately, orbital exenteration is occasionally necessary at the time of orbital debridement if severe retrobulbar or apical involvement is encountered.

Treatment of allergic aspergillosis involves surgical debridement of the involved sinuses concurrent with administration of systemic and topical corticosteroids. Systemic antifungals are not indicated unless the patient is immunocompromised.[21] In addition, patients with allergic aspergillosis may have nasolacrimal duct obstruction requiring surgical intervention in the future.

Similarly, management of Aspergilloma involves surgical debridement and aeration of the sinus involved without the need for antifungal therapy.[22]

Medical therapy

Intravenous amphotericin B is considered the gold standard for medical treatment of sino-orbital aspergillosis. A lipid formulation of amphotericin B is available for patients with impaired renal function. Oral itraconazole is also commonly used as an alternative to or in combination with amphotericin B.[23] Oral voriconazole has also been shown to be equally effective as primary therapy with fewer side effects.[24] The maximum daily dosage of the chosen antifungal agent(s) is used until the disease is controlled which is then followed by maintenance therapy with oral itraconazole (stevens et al). Newer classes of antifungals such as lipid complex nystatin and echinocandins are starting to be used more widespread.

Medical follow up

A multi-disciplinary approach is often necessary under the care of oculoplastic surgery, otolaryngology, ophthalmology , infectious disease, and neurosurgery.


Complications include optic neuropathy, brain abscess, cavernous sinus thrombosis, mycotic aneurysms with subsequent subarachnoid hemorrhage, meningitis, and death.[25][26]


The prognosis of invasive aspergillosis is significantly worse than the prognosis of other forms of sinus aspergillosis and mortality rate remains high, especially in the setting of cerebral involvement. A recent study reported a mortality rate of 40% associated with invasive orbital aspergillosis and 50% with CNS involvement.[20] This is thought to be due to invasion of bone and blood vessel walls which make surgical access and drug penetration challenging. Delayed diagnosis, initial treatment with corticosteroids, fever, intracranial extension, and demonstration of hyphal invasion on histopathology have been associated with a poorer prognosis.[15][20] With advancements in medical management there has been an overall improvement in disease control and survival.

Additional Resources


  1. Chakrabarti A, Sharma SC, Chander J. Epidemiology and pathogenesis of paranasal sinus mycoses. Otolaryngology–Head and Neck Surgery. 1992;107(6_part_1):745-750.
  2. Klotz SA, Penn CC, Negvesky GJ, Butrus SI. Fungal and Parasitic Infections of the Eye. Clinical Microbiology Reviews. 2000;13(4):662-685.
  3. 3.0 3.1 3.2 3.3 Aggarwal E, Mulay K, Menon V, Sundar G, Honavar SG, Sharma M. Isolated Orbital Aspergillosis in Immunocompetent Patients: A Multicenter Study. American Journal of Ophthalmology. 2016;165:125-132.
  4. 4.0 4.1 4.2 4.3 Mody KH, Ali MJ, Vemuganti GK, Nalamada S, Naik MN, Honavar SG. Orbital aspergillosis in immunocompetent patients. British Journal of Ophthalmology. 2014;98(10):1379-1384.
  5. Johnson TE. Sino-orbital Aspergillosis in Acquired Immunodeficiency Syndrome. Archives of Ophthalmology. 1999;117(1):57.
  6. 6.0 6.1 6.2 6.3 Levin LA, Avery R, Shore JW, Woog JJ, Baker AS. The spectrum of orbital aspergillosis: a clinicopathological review. Survey of Ophthalmology. 1996;41(2):142-154.
  7. 7.0 7.1 7.2 Kirszrot J, Rubin PAD. Invasive Fungal Infections of the Orbit. International Ophthalmology Clinics. 2007;47(2):117-132.
  8. 8.0 8.1 Mukherjee B, Raichura N, Alam M. Fungal infections of the orbit. Indian Journal of Ophthalmology. 2016;64(5):337.
  9. 9.0 9.1 Slavin ML. Primary Aspergillosis of the Orbital Apex. Archives of Ophthalmology. 1991;109(11):1502.
  10. Chen B-N, Chang K-M. Sphenoid sinus fungus ball presenting with bilateral visual disturbance. Int J Clin Exp Med. 2018;11(11):12763-12767.
  11. Cho SH, Jin BJ, Lee YS, Paik SS, Ko MK, Yi H-J. Orbital Apex Syndrome in a Patient with Sphenoid Fungal Balls. Clinical and Experimental Otorhinolaryngology. 2009;2(1):52.
  12. Stevens DA, Kan VL, Judson MA, et al. Practice Guidelines for Diseases Caused by Aspergillus. Clinical Infectious Diseases. 2000;30(4):696-709.
  13. 13.0 13.1 Ribes JA, Vanover-Sams CL, Baker DJ. Zygomycetes in Human Disease. Clinical Microbiology Reviews. 2000;13(2):236-301.
  14. Khan AR, Dutta U. Orbital Aspergillosis A Rare Case of Proptosis. Asian Pacific Journal of Health Sciences. 2018;5(4):39-42.
  15. 15.0 15.1 15.2 Sivak-Callcott JA. Localised invasive sino-orbital aspergillosis: characteristic features. British Journal of Ophthalmology. 2004;88(5):681-687.
  16. Zinreich SJ, Kennedy DW, Malat J, et al. Fungal sinusitis: diagnosis with CT and MR imaging. Radiology. 1988;169(2):439-444.
  17. Mauriello JA, Yepez N, Mostafavi R, et al. Invasive Rhinosino-orbital Aspergillosis with Precipitous Visual Loss. Ophthalmic Plastic & Reconstructive Surgery. 1997;13(4):293.
  18. Pinel C, Fricker-Hidalgo H, Lebeau B, et al. Detection of Circulating Aspergillus fumigatus Galactomannan: Value and Limits of the Platelia Test for Diagnosing Invasive Aspergillosis. Journal of Clinical Microbiology. 2003;41(5):2184-2186.
  19. Singh R, Singh G, Urhekar A. Detection of Aspergillus Species by Polymerase Chain Reaction. International Journal of Current Microbiology and Applied Sciences. 2016;5(10):254-260.
  20. 20.0 20.1 20.2 Choi HS, Choi JY, Yoon JS, Kim SJ, Lee SY. Clinical Characteristics and Prognosis of Orbital Invasive Aspergillosis. Ophthalmic Plastic & Reconstructive Surgery. 2008;24(6):454-459.
  21. Carter KD, Graham SM, Carpenter KM. Ophthalmic manifestations of allergic fungal sinusitis. Am J Ophthalmol. 1999;127:189–95.
  22. Klapper SR, Lee AG, Patrinely JR, Stewart M, Alford EL. Orbital involvement in allergic fungal sinusitis. Ophthalmology. 1997;104:2094–100.
  23. Massry GG, Hornblass A, Harrison W. Itraconazole in the Treatment of Orbital Aspergillosis. Ophthalmology. 1996;103(9):1467-1470.
  24. Herbrecht R, Denning DW, Patterson TF, Bennett JE, Greene RE, Oestmann JW, et al. Voriconazole versus amphotericin B for primary therapy of invasive aspergillosis. N Engl J Med. 2002;347:408–15
  25. Hedges TR, Leung L-SE. Parasellar and orbital apex syndrome caused by aspergillosis. Neurology. 1976;26(2):117-117.
  26. Baeesa SS, Bakhaidar M, Ahamed NA, Madani TA. Invasive Orbital Apex Aspergillosis with Mycotic Aneurysm Formation and Subarachnoid Hemorrhage in Immunocompetent Patients. World Neurosurgery. 2017;102:42-48.