- Received September 25, 2022
- Accepted October 10, 2022
- Publication November 08, 2022
- Visibility 7 Views
- Downloads 0 Downloads
- DOI 10.18231/j.ijooo.2022.050
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CrossMark
- Citation
Living parasite in the eyelid
- Author Details:
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Syeed Mehbub Ul Kadir *
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Sharmin Ahmed
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Golam Haider
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Md. Ismail Hossain
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Tanjila Hossain
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Narayon Chandra Bhowmik
Introduction
Ocular parasitic infections are significant worldwide due to increased morbidity rate, if not treated on time, and it may lead to visual loss. An increasing number of sub conjunctival Loa loa cases are reported from non-endemic areas are due to increased travel and migration.[1] High index of clinical suspicion is required to establish the diagnosis of eyelid and adnexal parasitic infection. Occasionally the adult parasite is found in the eyelid subcutaneous tissue space and subconjunctival area of humans. Eyelid parasitic lesion often presented as like as presepteal cellulitis or diffuse or nodular swelling of the eyelid.[2] Subconjunctival parasite may be found in young adult with a history of swelling, redness and foreign body sensation in the conjunctiva, and mimic as subconjunctival granulomatous lesion. Often parasite is obviously seen on slit lamp examination.[3] The management depends on the causative parasite, mostly require surgical removal and antiparasitic medication may be needed in some cases.[1] Surgery is the treatment of choice for eyelid and subconjunctival parasitic lesion.[2], [3] The first line anti-parasitic medication like diethylcarbamazine (DEC) to kill both microfilaria and macrofilaria, [4], [5] and the second line treatment include albendazole or ivermectin, both have limited efficacy on adult worms.[6] Oral steroid may be used in combination with anti-parasitic drug to reduce inflammation and allergic reaction to parasite and adverse effects of anti-parasitic medication.[1], [3] Here, we attempt to report a rare case of atypical presentation of living parasite in the eyelid.
Materials and Methods
This case was treated at the Department of Oculoplastic service in National Institute of Ophthalmology and Hospital, Dhaka, Bangladesh from May 2018 to April 2019. We evaluated the patient thoroughly. Meticulous ophthalmic and systemic evaluation was performed after taken a clinical history of the patient. CT scan of the orbit was helped to take decision for exploring the eyelid surgically. Parasitological and histopathological analysis were helped to diagnose the case. Per operative video recording, preoperative and postoperative photograph was documented properly. We followed up the patient up to one year at 3 weekly for 3 months, then 3 monthly for 9 months.
Case Report
A 8-year-old-boy presented swelling of the right upper eyelid for the last one year. Parents of the boy also gave a history of occasional pain and redness of his right eyelid which was relieved by oral anti-inflammatory medications (NSAIDs) and oral antihistamine for 3-5 days. On examination, the skin overlying of the swelling area of the eyelid was intact and showed no blister or other skin lesions. We found a non tender lesion underneath right upper eyelid skin that was 1 cm x 1cm in diameter ([Figure 1]). Vision was 6/6 in both eyes. Anterior and posterior segment evaluation revealed normal study. CT Scan of the orbit revealed a heterogenous ill-defined lesion within a central hypodense lesion in the right upper eyelid ([Figure 2]a) which is suggestive of chronic inflammatory lesion with a cystic change. So, our radiological diagnosis was a cystic lesion with thicken hazy irregular outline. Our case, the unusual location, misleading history, and atypical appearance precluded us from considering cysticercosis. We advised for the exploration and excision biopsy of the lesion under general anaesthesia. After given an eyelid crease incision, a thick wall cystic lesion was identified under the orbicularis oculi muscle in the mid-preseptal area of the right upper eyelid, and the lesion was attached to the supra-orbital margin. An iatrogenic injury to the cystic wall was occurred. Then a live worm was coming out from the injured cystic cavity. One of the crucial steps of the surgery was to remove the whole parasite and cystic wall completely. The whole cyst was opened, and a live worm was revealed and extracted from the right upper eyelid per operatively ([Figure 2]b). The remaining cystic wall with the cystic mass was excised ([Figure 2]c) and sent for histopathological analysis. The operating area was cleaned with 5% povidone iodine followed by normal saline, then the wound was closed by interrupted 6-0 Vicryl suture in layers. The measured live worm was about 10 cm in length ([Figure 3]a). The live worm was kept in a normal saline filled container ([Figure 3]b) and sent for parasitological analysis. The parasitological analysis revealed the parasite infestation compatible with adult Loa worm, and the histopathological examination reported also for parasitic infestation ([Figure 3]c). Recurrence and any adverse effects were not reported in the one year follow up period.



Discussion
Loiasis is a filarial disease caused by the nematode Loa loa which is an undertreated infectious disease and restricted in Central and Western Africa.[3], [4], [5] It is transmitted to humans by the bites of mango flies or deerflies (Chrysops silica and Chrysops dimidiate), which introduce larvae into the subcutaneous tissues of human. Macrofilaria migrate in the subcutaneous and deep connective tissues, and the microfilariae are found in the blood. Development into adult worms within human subcutaneous tissues takes over six to twelve months, and they can survive up to seventeen years. The adult worm is about 30-70 millimeters in length and 0.3-0.5 mm in diameter.[4], [5], [7] The literature reported that adult worms may survive in human tissue for up to 21 years. [8], [9] The first clinical presentation may appear as soon as 5 months of post infection. [9] This case report notes a novel clinical presentation of Loa loa (Loiasis) of the eyelid in Bangladesh.
First published article on extracted Loa loa from a human eye was in 1770 (Grove 1990). In India, first published case report on periocular manifestation of Loa loa in 2011 according to PubMed search. [10] Literature reported two cases of Loa loa macrofilaria diagnosed in United states.[4] Total eight similar cases are reported in the literatures. [10], [11] This case represents the second case of periocular subcutaneous Loa loa macrofilaria of the eyelid in Bangladesh. Clinical diagnosis is important and diagnostic criteria would include exposure to an endemic area, Calabar swelling, and subconjunctival macrofilaria.
Adult Loa loa migrate actively throughout the subcutaneous tissue of the body. It is known as African eye worm because it may frequently occur in eyelid Calabar swelling and subconjunctiva and causes irritating when crossing the conjunctiva. Calabar swellings, is a nontender swelling can occur anywhere, but are more frequently found on the forearms. [12], [13]
The best diagnostic technique is PCR of the repeat-3 region of the gene encoding a 15-kDa protein for the detection of species-specific sequences. [7], [13] Loiasis can be effectively managed by complete surgical removal of the worms including the cystic wall. The standard dose (150 µg/kg) of Ivermectin can be used in the cases of microfilaria. [12] Our patient did not exhibit microfilaremia or other side effects on follow up times. Though rarely diagnosed in developed nations, practitioners in all medical specialties must be aware of the disease which may present in immigrants and travelers up to 21 years after their initial infection. Loa loa infection should be considered in the differential diagnosis of eyelid or conjunctival swelling for patients with eosinophilia and Calabar swelling especially those who travelling from Africa.
Conclusion
Ophthalmologists should be aware of atypical parasitic presentation of the eyelid and adnexa coupled with high index of clinical suspicion, may help in early management.
Conflict of Interest
The authors declare no Conflict interests regarding the publication of this article
Source of Funding
There was no financial support in terms of grants or funds for this study from any source.
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