|Year : 2019 | Volume
| Issue : 2 | Page : 93-97
The gift of honeymoon: An interesting case of furuncular myiasis caused by Dermatobia Hominis in Taiwan and review of the literature
Yung-Wei Chang1, Han-Chi Tseng2
1 Department of Dermatology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan
2 Department of Dermatology, Kaohsiung Chang Gung Memorial Hospital; Department of Cosmetic Applications and Management, Yuh Ying Junior College of Healthcare and Management, Kaohsiung, Taiwan
|Date of Submission||05-Sep-2018|
|Date of Acceptance||19-Nov-2018|
|Date of Web Publication||23-May-2019|
Dr. Han-Chi Tseng
Department of Dermatology, Chang Gung Memorial Hospital, No. 123, Ta-Pei Road, Niaosong District, 83301 Kaohsiung
Source of Support: None, Conflict of Interest: None
Travel-related cutaneous diseases are very common, and among them, myiasis ranks in the fourth place. Hereby, we present a case of a 28-year-old Taiwanese woman infested by Dermatobia hominis during honeymoon trip to Amazonas region and Peru. The diagnosis was confirmed by extracting the larva intraoperatively. The epidemiology, distinctive life cycle, clinical features, auxiliary diagnostic tools, therapeutic methods, and prophylactic measures of human botfly infestation will be discussed in the article. Owing to the progressive increment of international travels and ecological explorations, raising awareness of tropical diseases should be more emphasized.
Keywords: Dermatobia hominis, furuncular myiasis, human botfly, Taiwan
|How to cite this article:|
Chang YW, Tseng HC. The gift of honeymoon: An interesting case of furuncular myiasis caused by Dermatobia Hominis in Taiwan and review of the literature. Dermatol Sin 2019;37:93-7
|How to cite this URL:|
Chang YW, Tseng HC. The gift of honeymoon: An interesting case of furuncular myiasis caused by Dermatobia Hominis in Taiwan and review of the literature. Dermatol Sin [serial online] 2019 [cited 2022 Jun 30];37:93-7. Available from: https://www.dermsinica.org/text.asp?2019/37/2/93/258935
| Introduction|| |
Myiasis, by definition, is the infestation of live humans or other vertebrate hosts by the larvae of the order Diptera. Among the classifications, the most common clinical presentation is furuncular myiasis. Dermatobia hominis which is endemic in South and Central America is the most common species found in returning travelers. Herein, we report a young Taiwanese woman suffering from human botfly infestation owing to recent travel from the Amazonas region and Peru. This is the second report of human botfly infestation in a Taiwanese tourist to the best of our knowledge.
| Case Report|| |
A 28-year-old Taiwanese female who has no systemic disease visited our outpatient department for the painful swelling nodule on the scalp. She also complained accompanying intermittent throbbing pain over the scalp in the recent weeks. Physical examinations revealed one coin-sized swelling nodule with central pore and serous discharge on the vertex of her scalp [Figure 1]a. She denied fever episode recently. No enlarged lymph nodes were palpated. Initially, the clinical diagnosis was inflamed epidermal inclusion cyst. After 2 weeks of antibiotics, the nodule showed no obvious improvement. Surgical removal was performed after discussing with the patient. Much necrotic tissue was noted intraoperatively. After careful debridement, one larva was extruded. It was identified as the larva of the botfly, D. hominis, based on its morphological characteristics [Figure 1]e. The histopathology revealed dense granulomatous inflammation, consisting of mainly histiocytes, lymphocytes, and eosinophils in the dermis [Figure 1]b and [Figure 1]c and characteristic structures of the larva of human botfly [Figure 1]d. Afterward, the patient recalled that during her honeymoon trip to Amazonas region and Peru last month, she did not wear hat on the cruise over Amazon River. After the operation, we prescribed ivermectin 12 mg once and baktar (sulfamethoxazole 800 mg + trimethoprim 160 mg) twice a day for 1 week. The swelling and wound discharge subsided and healed gradually. No recurrence was observed after 1 year of follow-up.
|Figure 1:(a) One swelling erythematous nodule with central punctum (black arrow) and serous discharge was found over the vertex of scalp. (b) Histopathology showed dense granulomatous inflammation without caseous necrosis in the deep dermis to superficial subcutis (H and E; ×20). (c) Higher magnification image revealed mixed inflammatory infiltrates composed of histiocytes, lymphocytes, and many eosinophils (H and E, ×400). (d) The histological section revealed the botfly larva encased by a thick chitinous exoskeleton with blackish spines. Internal striated muscles were also identifiable (Hematoxylin and eosin stain; original magnification, ×20). (e) An object had circular blackish spine-like structures that encircle the anterior-middle segment with a narrowing tail-like figure located posteriorly, and it was identified as a second instar larva (L2) of Dermatobia hominis|
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| Discussion|| |
Myiasis is the infestation of humans and vertebrate animals by the larvae of the order Diptera (two-winged flies). The classification is based on different areas infested. Thus, it can be categorized into cutaneous, ocular, auricular, nasal, oral, urogenital, and enteric type. Among these classifications, the most common is the cutaneous type, which can be further divided into furuncular, migratory/creeping, wound, and cavitary myiasis.
Human cutaneous myiasis can be travel or nontravel related. Many species of Diptera are observed in the cases of myiasis, and they have unique geographic distributions and correlated clinical presentations. Furuncular myiasis is the most common presentation. Human botfly D. hominis in South and Central America and tumbu fly Cordylobia anthropophaga in tropical Africa are the leading two causative species. The human botfly in our case is the most common in returning travelers [Table 1]. Despite being named as human botfly, the main hosts of this ectoparasitic disease are in fact mammals such as cattle, sheep, horses, and pigs. In a case series conducted by Lachish et al. in 2015, 54% of the 72 cases traveled to Madidi National Park in the Amazonas Basin and Bolivia, followed by Peru and Brazil. The literature review from 1999 to 2015 which performed by Villalobos et al., the countries where most of the foreign travelers were infected are Brazil, Bolivia, Costa Rica, Peru, and Belize.
D. hominis is an obligatory parasite which requires hosts for completing its life cycle. It is endemic in the neotropics. The distribution range from southern Mexico to northern Argentina. This species is florid mainly in humid, rainy, and warm environments such as rainforests and lowland forests. The botfly has its unique and interesting life cycle; the female adult botfly uses blood-sucking insects (e.g., mosquitoes, flies, and ticks) as mechanical vectors to infest hosts. This distinctive process of transportation is called phoresis. It deposits about 10–50 eggs to the underside of the abdomen of arthropods rather than laying onto the host directly. On contact with the host, the warmth of body temperature stimulates the eggs to hatch. Immediately after the hatch, the first instar (L1) penetrates the host skin through insect bite site or hair follicle painlessly. After infestation, it will develop to the second instar (L2) and then to the third instar larva (L3) during 5–10 weeks. The third instar will leave the host skin, falls to the soil, and pupates thereafter. It takes another 1 month after the pupation to mature into an adult fly. However, the lifespan of an adult fly is only 9–12 days. Its sole goal is to mate and repeat the life cycle. Therefore, it seems harmless if the infested patients can tolerate the natural life cycle.
With regard to the distinctive features of different stages of botfly larva, the first instar (L1) is bulbous form, size around with 1–1.5 mm in length. The second instar (L2) is flask-shaped, whereas the third instar (L3) is about 23 mm in length and cylinder-shaped. At the anterior segments of larvae, there are two mouth hooks which enable them to drill and feed. Several circular rows and backward protruding blackish spines surround the thoracic segments. The caudal parts are spiracles that function as respiration.
In human hosts, it appears that there are no significant differences in terms of age, gender, or race. However, there is slight predominant in male travelers (58%) in a review performed from 1999 to 2015. Our review which includes several case series at different countries from 1995 to 2017 [Table 1] shows 99 males versus 71 females (the percentage of male patients is 58.24), this result is similar to the study of Villalobos et al. in 2016. Moreover, most of the travelers are young people in our review (the mean age is 30.64 years).
After infestation, a furuncle-like lesion will develop, especially the exposed areas of the human bodies such as scalp and extremities. Unusual sites such as back, buttock, eye, mouth, and genitalia have also been reported, though. In a study which enrolled 25 people in Mexico, 9 of 25 cases (36%) were infected over the scalp, followed by the trunk (28%) and four limbs. According to the largest study to date performed by Lachish et al. in 2015, single furuncular myiasis accounts for 33 in the total 39 (85%) of D. hominis myiasis.
During the larval stage, the typical symptoms and signs in most reported cases include serosanguinous discharge, sense of peculiar movement, pruritus, and lancinating pain (often but not always nocturnal).
The diagnosis is mainly based on the following two criteria: identification of the typical clinical appearance and relevant travel history. The procedure of skin biopsy is usually not necessary for diagnosis, but imaging equipment such as dermoscopy and Doppler ultrasonography are helpful tools for auxiliary diagnosis.
The differential diagnoses of furuncular myiasis include ruptured epidermoid cyst, abscess, furunculosis, cutaneous larvae migrans, foreign-body reaction, and insect prurigo, etc. On the whole, constitutional symptoms such as fever, malaise, and regional lymphadenopathy are rarely presented. The blood examinations are not diagnostic for furuncular myiasis, but leukocytosis and eosinophilia have been reported.
There are three published literatures to depict the characteristics of botfly larvae in human bodies by using dermoscopy.,, The dermoscopic features are mainly the below findings: a central pore contains a creamy-white structure with black spines and is surrounded by dilated vessels. Another paper describes the breathing spiracles of the posterior segment as bird's feet-like structures, and blackish spines surrounding the larvae are named as thorn crown. However, all of the above discoveries are observed by using contact dermoscopy with fluid media. However, Silva de Lima and Rovere proposed another method that utilizing cross-polarized dermoscopy without contact to diagnose the furuncular myiasis and has the advantage of reducing cross infection.
In an observational study from Mexico, Quintanilla-Cedillo et al., 25 cases of furuncular myiasis were identified by using Doppler sonography for evaluation and proved its usefulness. With the help of echography (even if not equipped with color Doppler), we can make use of it to evaluate and localize the number of subcutaneous larvae inside the furunculoid lesions, thereby avoiding misdiagnosis and unnecessary treatments.
The treatment of botfly infestation is to extract the larvae. Multiple therapeutic modalities have been proposed, the most common method is to asphyxiate the larvae by occluding the central punctum with objects like adhesive tapes, coal tar, paraffin, petroleum, chewing gum, wax, and nail polish. After that procedure, the larvae would be forced to emerge out spontaneously because of suffocation; therefore, we can also make use of forceps or tweezers to pull the larvae out easier. This method is called mechanical removal and is cheap with nearly no scar developed, but there is a possibility of incomplete removal of the larvae.
Other procedures have also been reported, included injecting lidocaine to create pressure to extrude the larvae and using snake venom extractor to extract them. There are two previously published reports for using snake venom extractor, and both of them are the third instar (L3) being extracted. This interesting method is easy, rapid, relatively noninvasive, and harmless; however, more data and evidence are needed to evaluate the efficacy., All of the procedures that mentioned previously have the risk of imperfect extraction. To ensure removing the larvae completely, surgical removal remains the most effective, ultimate method. In our review, it reveals that there are more cases using mechanical removal than surgical intervention [Table 1].
Ivermectin is a new and preventive therapy which has shown its efficacy in cattle infested by D. hominis, but there are only few case reports discussing the use of ivermectin in human bodies. In 2006, TH Wakamatsu reported an 11-year-old boy of ophthalmomyiasis externa caused by human botfly, he was treated with a single dose of oral ivermectin (200 μg/kg) and that larva was extracted successfully and easily. In addition, topical application of 1% ivermectin solution four times per day killed the larva of botfly and assisted the removal satisfactorily in an HIV-infected patient. It seems that oral ivermectin often prescribed for more severe conditions such as involvement of oral or orbital cavities where surgery is difficultly feasible. In this article, we prescribed oral ivermectin (200 μg/kg) once for preventing other parasites other than human botfly. However, more studies and research are still needed to evaluate the efficacy and indications of oral ivermectin in humans.
To prevent the infestation of furuncular myiasis, the prophylactic measures depended on the different pathogens and associated unique life cycles. Therefore, we should avoid exposure to the outside environment in endemic areas. Insect repellents or mosquito nets are useful to avert blood-sucking insects bite.
Lethal complications are rarely reported. Our review found only a 5-month-old infant died from fatal cerebral myiasis owing to the penetration to the brain by botfly larvae. Other major complications are often not fatal, such as tetanus and bacterial superinfection. Interestingly, localized secondary bacterial infection over infested lesions is not so common because the larvae may produce some substances that exhibit bacteriostatic activity.
The first case report of furuncular myiasis caused by D. hominis in a Taiwanese man was similar to our case. Both of them were young people and traveled in the Amazonas region. The infested areas were the same, but different instars of larvae were extracted by using different methods [Table 2]. To the best of our knowledge, this is the second case of botfly infestation in a Taiwanese traveler and clinicians should pay more attention to patients who have furuncle-like lesions with a pivotal travel history from endemic countries because of the growing trend of international travels and outdoor tourism.
|Table 2: Comparisons between two Taiwanese returning travelers of botfly infestation|
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Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Francesconi F, Lupi O. Myiasis. Clin Microbiol Rev 2012;25:79-105.
McGraw TA, Turiansky GW. Cutaneous myiasis. J Am Acad Dermatol 2008;58:907-26.
Lachish T, Marhoom E, Mumcuoglu KY, Tandlich M, Schwartz E. Myiasis in travelers. J Travel Med 2015;22:232-6.
Haruki K, Hayashi T, Kobayashi M, Katagiri T, Sakurai Y, Kitajima T, et al.
Myiasis with dermatobia hominis in a traveler returning from costa rica: Review of 33 cases imported from South America to Japan. J Travel Med 2005;12:285-8.
Quintanilla-Cedillo MR, León-Ureña H, Contreras-Ruiz J, Arenas R. The value of Doppler ultrasound in diagnosis in 25 cases of furunculoid myiasis. Int J Dermatol 2005;44:34-7.
Caumes E, Carrière J, Guermonprez G, Bricaire F, Danis M, Gentilini M, et al.
Dermatoses associated with travel to tropical countries: A prospective study of the diagnosis and management of 269 patients presenting to a tropical disease unit. Clin Infect Dis 1995;20:542-8.
McGarry JW, McCall PJ, Welby S. Arthropod dermatoses acquired in the UK and overseas. Lancet 2001;357:2105-6.
Zammarchi L, Viligiardi R, Strohmeyer M, Bartoloni A. Dermatobia hominis: Small migrants hidden in your skin. Ann Dermatol 2014;26:632-5.
Jelinek T, Nothdurft HD, Rieder N, Löscher T. Cutaneous myiasis: Review of 13 cases in travelers returning from tropical countries. Int J Dermatol 1995;34:624-6.
Schwartz E, Gur H. Dermatobia hominis myiasis: An emerging disease among travelers to the Amazon Basin of Bolivia. J Travel Med 2002;9:97-9.
Hu JM, Wang CC, Chao LL, Lee CS, Shih CM. First report of furuncular myiasis caused by the larva of botfly, dermatobia hominis, in a taiwanese traveler. Asian Pac J Trop Biomed 2013;3:229-31.
Villalobos G, Vega-Memije ME, Maravilla P, Martinez-Hernandez F. Myiasis caused by dermatobia hominis: Countries with increased risk for travelers going to neotropic areas. Int J Dermatol 2016;55:1060-8.
Jacobs B, Brown DL. Cutaneous furuncular myiasis: Human infestation by the botfly. Can J Plast Surg 2006;14:31-2.
Maier H, Hönigsmann H. Furuncular myiasis caused by dermatobia hominis, the human botfly. J Am Acad Dermatol 2004;50:S26-30.
Solomon M, Lachish T, Schwartz E. Cutaneous myiasis. Curr Infect Dis Rep 2016;18:28.
Bernardes Filho F, Martins G, Barbará EF, Paiva ML, Coelho Filho RL, Nery JA, et al.
Dermoscopy as an auxiliary tool for the diagnosis of furuncular myiasis. An Bras Dermatol 2014;89:663-5.
Bakos RM, Bakos L. Dermoscopic diagnosis of furuncular myiasis. Arch Dermatol 2007;143:123-4.
Abraham LS, Azulay-Abulafia L, Aguiar Dde P, Torres F, Argenziano G. Dermoscopy features for the diagnosis of furuncular myiasis. An Bras Dermatol 2011;86:160-2.
Silva de Lima A, Rovere RK. Furuncular myiasis: Dermoscopic features using a cross-polarized device without contact. J Am Acad Dermatol 2015;72:S6-7.
Richter J, Schmitt M, Müller-Stöver I, Göbels K, Häussinger D. Sonographic detection of subcutaneous fly larvae in human myiasis. J Clin Ultrasound 2008;36:169-73.
Kahn DG. Myiasis secondary to sermatobia hominis (human botfly) presenting as a long-standing breast mass. Arch Pathol Lab Med 1999;123:829-31.
West JK. Simple and effective field extraction of human botfly, dermatobia hominis, using a venom extractor. Wilderness Environ Med 2013;24:17-22.
Boggild AK, Keystone JS, Kain KC. Furuncular myiasis: A simple and rapid method for extraction of intact dermatobia hominis larvae. Clin Infect Dis 2002;35:336-8.
Garvin KW, Singh V. Case report: Cutaneous myiasis caused by dermatobia hominis, the human botfly. Travel Med Infect Dis 2007;5:199-201.
Wakamatsu TH, Pierre-Filho PT. Ophthalmomyiasis externa caused by dermatobia hominis: A successful treatment with oral ivermectin. Eye (Lond) 2006;20:1088-90.
Clyti E, Nacher M, Merrien L, El Guedj M, Roussel M, Sainte-Marie D, et al.
Myiasis owing to dermatobia hominis in a HIV-infected subject: Treatment by topical ivermectin. Int J Dermatol 2007;46:52-4.
Hohenstein EJ, Buechner SA. Cutaneous myiasis due to dermatobia hominis. Dermatology 2004;208:268-70.
Rossi MA, Zucoloto S. Fatal cerebral myiasis caused by the tropical warble fly, dermatobia hominis. Am J Trop Med Hyg 1973;22:267-9.
[Table 1], [Table 2]