Should postviral anosmia be further investigated? A. Obando, I. Alobid, F. Gastón, J. Berenguer, C. Marin, J. Mullol* Key words: hyposmia; meningioma; postviral anosmia; rhinitis. Distortions in olfactory function are common in the general population, hyposmia affect- ing 16–19% and anosmia 0.5– 2%. Three of the most common causes for the loss of smell are: chronic rhinosi- nusitis and nasal polyposis (1), head trauma and upper respira- tory tract infec- tion (URTI) (2). Some authors (3) have also re- ported higher odour thresholds in allergic rhinitis patients than in the control groups. Recently, Guilemany et al. (4) have demonstrated that persis- tent allergic rhinitis induces a moderate loss of the sense of smell mainly in the moderate-to-severe disease. Nevertheless, there are more than 200 conditions that have been associated with changes in olfaction, which explain that there could be more than one cause for the loss of smell in an individual patient. Allergolo- gists, otolaryngologists and general practitioners very often have to manage patients with smell impairment related or not to acute and chronic nose inflamma- tory diseases. We present the case of a 43-year-old woman who visited our Rhinology Unit & Smell Clinic complaining of persistent anosmia that suddenly appeared during the winter of 2005 after three episodes of viral URTI. Past medical history was positive for hypotyroidism, which was well controlled with oral medication, and gestational diabetes in 1996, which was well controlled after giving birth. There was a negative clinical history of sinonasal or neurological symptoms, previous head trauma or ear–nose–throat surgery. Physical examination was normal, except for lower right turbinate hyper- trophy diagnosed by nasal endoscopy. Due to a suspected diagnosis of postviral anosmia, a smell test using the Barcelona Smell Test 24 (5) and a paranasal sinus and brain CT scan were performed following the smell protocol used by our institution. Subjective olfactometry confirmed anosmia (0% in odour detection, memory and identifi- cation), with no taste problems. Skin Prick test was negative for the most common aeroallergens. The CT scan showed no pathology in the paranasal sinuses while some osteolitic changes were observed in the ethmoid bone. Further imaging investigation of these osteolitic changes with MRI demon- strated a giant olfactory grove meningi- oma (55 · 42 mm) (Fig. 1). Three weeks after the diagnosis, resection of the lesion was performed via a transfrontal approach. While waiting for the indi- cated surgery, the patient developed visual loss in her right eye that com- pletely recovered after surgery. After her last follow-up in September 2008, her only remaining complaint was persistant anosmia. There are several important issues, which can be learnt from this case report. Despite other aetiologies, three main causes should always be investigated: nasal inflammatory diseases (allergic rhi- nitis and chronic rhinosinusitis, with or without nasal polyps), postviral anosmia and head trauma. Detailed clinical his- tory, subjective olfactometry and imaging (e.g. CT scan or/and MRI) should always be performed in patients with anosmia to discriminate different potential life threatening causes such as intracranial tumours. In conclusion, because hypos- mia and anosmia are highly prevalent symptoms in the general population and there could be more than one cause for the loss of smell, this case study demon- strates that patients experiencing these symptoms require the physicianÕs special attention and further investigation must be performed. The loss of the sense of smell is a very prevalent symptom in the general population. Postviral anosmia is one of the three main causes. We report a case of an anosmic patient related with two different aetiolo- gies: postviral and an olfactory grove meningioma. A B Figure 1. (A) Coronal CT image shows the focal hyperostosis in both cribiform plates (white arrow). (B) Contrast enhanced T1-weighted image shows a giant olfactory grove meningioma (black arrow). No pathology in nasal and paranasal regions was observed. ALLERGY Net 1556 Ó 2009 John Wiley & Sons A/S Allergy 2009: 64: 1554–1561