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Clinical Case Report
34 (
5
); 279-280
doi:
10.25259/NMJI_251_20

An unusual presentation of conjunctival aspergillosis as a polyp in an immunocompetent child

Dr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110029, India

Correspondence to Neiwete Lomi; neiwete@gmail.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

To cite: Yadav S, Lomi N, Mukhija R, Kashyap S, Tandon R. An unusual presentation of conjunctival aspergillosis as a polyp in an immuno-competent child. Natl Med J India 2021;34:279–80.

Abstract

Fungi are a part of normal ocular flora and usually do not cause clinical infection in the absence of predisposing factors. We report a 7-year-old healthy boy from a rural area of India, who presented with a gradually increasing mass in the left eye. Excisional biopsy of the mass was performed, and pathological examination revealed multiseptate hyphae with acute-angle branching consistent with aspergillosis.

INTRODUCTION

Fungal infections of the conjunctiva are much less common compared to bacterial and are rarely reported in the literature. Although normal conjunctival flora includes fungi, they are rarely implicated in ocular adnexal infections in the absence of any predisposing factors, i.e. pre-existing ocular disease, trauma with organic matter, immunocompromised state. We report conjunctival aspergillosis in a young immunocompetent child without an antecedent trauma.

THE CASE

A healthy 7-year-old boy presented to our centre with a history of a reddish mass in the nasal part of his left eye for 20 days. He belonged to a rural, middle socioeconomic background and was accompanied by his father who was a farmer by occupation. The lesion began as a small lump on the conjunctiva, initially the size of a pin-head and gradually increased in size. There was no associated pain or discharge from the affected eye, and the patient did not have a history of even a minor preceding trauma, any surgery or use of any topical medication.

The unaided visual acuity in both eyes was 20/20. Ocular examination showed a 2 mm×2.5 mm pedunculated lesion in the inferonasal part of the left bulbar conjunctiva, just lateral to the caruncle with mild adjacent hyperaemia. Rest of the ocular and general physical examination did not reveal any abnormality. A provisional diagnosis of a papilloma was made, and the patient was planned for an excision biopsy after 2 weeks. Few days before the planned surgery, the patient reported again with a history of spontaneous bleeding from the lesion. An increase in size of the mass was noted along with the presence of black necrotic slough on it (Fig. 1a).

(a) Clinical photograph shows a fungating mass in the inferonasal part of the left eye. Clotted blood with necrotic tissue can be seen on its surface; (b) only minimal congestion is present at 1-week follow-up, and no residual lesion is detected
FIG 1.
(a) Clinical photograph shows a fungating mass in the inferonasal part of the left eye. Clotted blood with necrotic tissue can be seen on its surface; (b) only minimal congestion is present at 1-week follow-up, and no residual lesion is detected

An excisional biopsy of the lesion was done under general anaesthesia with cauterization of its base and primary closure of the conjunctiva using 8-0 vicryl suture (Fig. 1b). Postoperatively, the patient was started on topical antibiotic-lubricant regimen which was continued for 1 month. Histopathological examination of the mass revealed multiple, unstained fungal hyphae on the surface of the excised mass on haematoxylin and eosin stain (Fig. 2a). Silver methenamine stain showed numerous septate fungal hyphae with acute angle branching consistent with aspergillosis (Fig. 2b). Topical antifungal drugs were not started as there was no clinical evidence of any infection or residual lesion following excision.

(a) Light microscopic image of the excised lesion on haematoxylin and eosin stain (×200), reveals septate fungal hyphae; (b) numerous septate fungal hyphae with acute angle branching on silver methenamine stain (×400) provide a definitive diagnosis of aspergillosis
FIG 2.
(a) Light microscopic image of the excised lesion on haematoxylin and eosin stain (×200), reveals septate fungal hyphae; (b) numerous septate fungal hyphae with acute angle branching on silver methenamine stain (×400) provide a definitive diagnosis of aspergillosis

Surgical excision led to complete resolution without any topical antifungal therapy and no recurrence was noted till 1 year of follow-up.

DISCUSSION

Ocular mycoses in children are commonly seen in the form of fungal keratitis or keratoconjunctivitis, and most can be attributed to an exogenous source with an antecedent history of trauma, surgery or use of topical steroids.1,2 Even though fungi have been isolated from healthy conjunctival sacs, with a reported incidence of 2.9%–27.4% across various age groups, their frequency is found to be much lower (0.8%–2%) between 0 and 9 years of age.35 Mycotic flora of healthy ocular surface is mainly considered as transient aerial contaminants that can act as potential pathogens in the presence of altered tissue resistance. Aspergillus is a common mould present in the environment and has been reported to be the most commonly isolated fungus from eyes with no pre-existing diseases.5 In the presence of predisposing factors such as trauma and immunosuppressed states, Aspergillus species can cause a wide array of sight-threatening ocular infections (e.g. keratitis, endophthalmitis, scleritis and orbital cellulitis). Chen et al. reported a case of conjunctival aspergilloma presenting as chronic refractory conjunctivitis in an immunocompetent woman and proposed opportunistic subconjunctival seeding of the fungus as the factor responsible.6 We suspect a similar causal factor in our case. Tropical/subtropical countries with higher temperature and humidity have increased rates of fungal isolation, and contamination of external eye can occur more frequently during summer and harvesting season when more fungal spores are present in the environment. Arora and Tyagi reported that in India, a majority of the fungal infections were in agricultural workers.5

In our patient, the exact inciting cause for the fungal conjunctivitis could not be determined, but he was at an increased risk of developing the infection secondary to environmental factors. Coming from a rural area of a tropical country and agricultural background, the chance of exposure to fungal contaminants was high and even accidental rubbing of the eye could have been responsible for subconjunctival seeding and eventual development of aspergillosis. The presence of multiseptate filamentous hyphae on silver methenamine stain helped in providing a definitive diagnosis. Hence, we believe that this report will increase awareness for general practitioners to keep in mind the rare but possible differential diagnosis of conjunctival aspergillosis besides other more common causes of a conjunctival mass in a child.

To the best of our knowledge, this is the first report in a child of conjunctival aspergillosis presenting as a pedunculated polyp which was adequately managed by surgical excision without the need for antifungal therapy.

Conflicts of interest

None declared

References

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