Granulomatous invasive fungal sinusitis, sometimes termed granulomatous invasive fungal sinusitis, is a form of invasive fungal sinusitis. Reports describing the imaging findings have been uncommon 1.
It is rare and been mainly reported in Sudan, India, Pakistan and sometimes in the United States 2.
Unlike other forms of invasive fungal sinusitis (which affect only immunocompromised patients) granulomatous invasive fungal rhinosinusitis typically affects immunocompetent patients.
This disease presents with a focal expanding granulomatous mass arising from the sinonasal region, locally aggressive, destroying adjacent structures.
Clinical presentation is mainly due to the mass effect, with possible nasal obstruction or proptosis. If there is intracranial invasion, it tends to have scarce symptoms due to the slow growth. The disease often presents late, at advanced stages, due to the initial paucity of symptoms.
Granulomatous invasive fungal rhinosinusitis is usually confirmed on the basis of clinical and histopathologic findings where there is non-caseating granuloma formation and fibrosis. It is usually caused by Aspergillus flavus.
Affected individuals are generally immunocompetent (unlike other forms of invasive sinusitis, which affect mainly immunocompromised individuals).
Imaging shows a large expansive mass with bone destruction and invasion of adjacent structures including orbits, nasal cavity and cranial base.
CT optimally demonstrates the degree of bone destruction. The mass is typically intrinsically hyperdense, with homogenous contrast enhancement.
MRI demonstrates the same intense pattern of intense, homogenous enhancement. The most salient MRI finding is a characteristic T2 hypointensity, along with peripheral foci of susceptibility, due to the deposition of paramagnetic elements. DWI may show a “T2-blackout” effect secondary to the marked T2 hypodensity, which may limit the value of diffusion sequences. Often described are foci of enhancing parenchyma representing cerebritis, in the region of the brain immediately adjacent to the solid lesion 3,4.
Treatment and prognosis
There is scarce evidence regarding optimal management and follow up in the literature. However, generally initial conservative surgical excision of the mass is generally indicated, followed by medical treatment with antifungal agents (itraconazole/voriconazole), which appear to decrease the degree of disease relapse.
Prognosis is generally good, especially if there is no intracranial invasion.
Post-surgical relapse is common, especially if antifungal therapy is not established 5.
- sinonasal squamous cell carcinoma (or sinonasal carcinoma): often similar in appearance should always be considered in sinonasal malignancy.
- sinonasal adenoid cystic carcinoma: mostly affects maxillary sinus and nasal cavity; very high propensity for perineural tumour spread.
- sinonasal adenocarcinoma: more aggressive, heterogeneous enhancement pattern. Classically described in wood-workers (intestinal subtype).
- sinonasal undifferentiated carcinoma (SNUC): mostly affects ethmoid and nasal cavity; early nodal metastases.
- sinonasal lymphoma: mainly affects paranasal sinuses and simulates benignity, with frequent bone remodelling more than destruction; homogeneous contrast-enhancement with homogeneous diffusion restriction, with scarce or no necrosis, are characteristic.
- sinonasal melanoma: mainly affects the inferior nasal fossa; lesions are characteristically hypervascular and haemorrhagic; can sometimes simulate benignancy, with frequent bone remodelling instead of destruction; if the tumour is the melanotic subtype, they can have a slight characteristic T1 hyperintensity.
- esthesioneuroblastoma: centered on the cribriform plate, with characteristic dumbbell shape affecting ethmoid sinuses inferiorly and invading anterior cranial fossa superiorly; often show adjacent bone hyperostosis, bone remodelling and nasal cavity expansion; intracranial tumour-margins often show characteristic peripheral T2-hyperintense cysts.
- 1. Aribandi M, McCoy VA, Bazan C. Imaging features of invasive and noninvasive fungal sinusitis: a review. Radiographics. 2007;27 (5): 1283-96. doi:10.1148/rg.275065189 - Pubmed citation
- 2. Kim TH, Jang HU, Jung YY et-al. Granulomatous invasive fungal rhinosinusitis extending into the pterygopalatine fossa and orbital floor: A case report. Med Mycol Case Rep. 2012;1 (1): 107-11. doi:10.1016/j.mmcr.2012.10.004 - Free text at pubmed - Pubmed citation
- 3. Siddiqui AA, Bashir SH, Ali Shah A, et al. Diagnostic MR imaging features of craniocerebral Aspergillosis of sino-nasal origin in immunocompetent patients. Acta Neurochir (Wien) 2006; 148: 155–66; discussion 166. doi:10.1007/s00701-005-0659-3 Pubmed citation
- 4. Reddy CEE, Gupta AK, Singh P, et al. Imaging of granulomatous and chronic invasive fungal sinusitis: comparison with allergic fungal sinusitis. Otolaryngol Head Neck Surg 2010; 143: 294–300. doi:10.1016/j.otohns.2010.02.027
- 5. Halderman A, Shrestha R, Sindwani R. Chronic granulomatous invasive fungal sinusitis: an evolving approach to management. Int Forum Allergy Rhinol 2014; 4: 280–3. doi:10.1002/alr.21299
- inflammatory and infective conditions
- granulomatosis with polyangiitis (Wegener granulomatosis)
- paranasal sinus mucocoele
- silent sinus syndrome
- masses and neoplasms
- fibrous-osseous lesions
- inflammatory and infective conditions