Chen H, 1935. A new pulmonary nematode of rats, Pulmonema cantonensis ng.nsp from Canton. Ann Parasitol 13: 312–317.
Wang QP, Lai DH, Zhu XQ, Chen XG, Lun ZR, 2008. Human angiostrongyliasis. Lancet Infect Dis 8: 621–630.
Cowie RH, 2013. Pathways for transmission of angiostrongyliasis and the risk of disease associated with them. Hawaii J Med Public Health 72: 70–74.
Sawanyawisuth K, Chindaprasirt J, Senthong V, Limpawattana P, Auvichayapat N, Tassniyom S, Chotmongkol V, Maleewong V, Intapan PM, 2013. Clinical manifestations of eosinophilic meningitis due to infection with Angiostrongylus cantonensis in children. Korean J Parasitol 51: 735–738.
York EM, Butler CJ, Lord WD, 2014. Global decline in suitable habitat for Angiostrongylus (= Parastrongylus) cantonensis: the role of climate change. PLoS One 9: e103831.
Wang QP, Wu ZD, Wei J, Owen RL, Lun ZR, 2012. Human Angiostrongylus cantonensis: an update. Eur J Clin Microbiol Infect Dis 31: 389–395.
Punyagupta S, Juttijudata P, Bunnag T, 1975. Eosinophilic meningitis in Thailand. Clinical studies of 484 typical cases probably caused by Angiostrongylus cantonensis. Am J Trop Med Hyg 24: 921–931.
Morton NJ, Britton P, Palasanthiran P, Bye A, Sugo E, Kesson A, Ardern-Holmes S, Snelling TL, 2013. Severe hemorrhagic meningoencephalitis due to Angiostrongylus cantonensis among young children in Sydney, Australia. Clin Infect Dis 57: 1158–1161.
Hochberg NS, Park SY, Blackburn BG, Sejvar JJ, Gaynor K, Chung H, Leniek K, Herwaldt BL, Effler PV, 2007. Distribution of eosinophilic meningitis cases attributable to Angiostrongylus cantonensis, Hawaii. Emerg Infect Dis 13: 1675–1680.
Graber D, Jaffar-Bandjee MC, Attali T, Poisson J, Renouil M, Alessandri JL, Combes JC, 1997. Angiostrongylus in the infant at Reunion and Mayotte. Apropos of 3 cases of eosinophilic meningitis including 1 fatal radiculomyeloencephalitis with hydrocephalus. Bull Soc Pathol Exot 90: 331–332.
Teem JL, Qvarnstrom Y, Bishop HS, da Silva AJ, Carter J, White-McLean J, 2013. The occurrence of the rat lungworm, Angiostrongylus cantonensis, in non indigenous snails in the Gulf of Mexico region of the United States. Hawaii J Med Public Health 72: 11–14.
Kim DY, Stewart TB, Bauer RW, Mitchell M, 2002. Parastrongylus (= Angiostrongylus) cantonensis now endemic in Louisiana wildlife. J Parasitol 88: 1024–1026.
Iwanowicz DD, Sanders LR, Schill WB, Xayavong MV, da Silva AJ, Qvarnstrom Y, Smith T, 2015. Spread of the Rat Lungworm (Angiostrongylus cantonensis) in Giant African Land Snails (Lissachatina fulica) in Florida, USA. J Wildl Dis 51: 749–753.
Morassutti AL, Thiengo SC, Fernandez M, Sawanyawisuth K, Graeff-Teixeira C, 2014. Eosinophilic meningitis caused by Angiostrongylus cantonensis: an emergent disease in Brazil. Mem Inst Oswaldo Cruz 109: 399–407.
Padilla-Docal B, Dorta-Contreras AJ, Moreira JM, Martini-Robles L, Muzzio-Aroca J, Alarcoìn F, Magraner-Tarrau ME, Bu-Coifiu-Fanego R, 2011. Comparison of major immunoglobulins intrathecal synthesis patterns in Ecuadorian and Cuban patients with angiostrongyliasis. Am J Trop Med Hyg 84: 406–410.
Aguiar PH, Morera P, Pascual J, 1981. First record of Angiostrongylus cantonensis in Cuba. Am J Trop Med Hyg 30: 963–965.
Vargas M, Gomez Perez JD, Malek EA, 1992. First record of Angiostrongylus cantonensis (Chen, 1935) (Nematoda: Metastrongylidae) in the Dominican Republic. Trop Med Parasitol 43: 253–255.
Raccurt CP, Blaise J, Durette-Desset M-C, 2003. Presence of Angiostrongylus cantonensis in Haiti [in French]. Trop Med Int Health 8: 423–426.
Andersen E, Gubler DJ, Sorensen K, Beddard J, Ash LR, 1986. First report of Angiostrongylus cantonensis in Puerto Rico. Am J Trop Med Hyg 35: 319–322.
Lindo JF, Waugh C, Hall J, Cunningham-Myrie C, Ashley D, Eberhard ML, Sullivan J, Bishop H, Robinson D, Holtz T, Robinson R, 2002. Enzootic Angiostrongylus cantonensis in rats and snails after an outbreak of human eosinophilic meningitis, Jamaica. Emerg Infect Dis 8: 324–326.
Chikweto A, Bhaiyat MI, Macpherson CNL, Deallie C, Pinckney RD, Richards C, Sharma RN, 2009. Existence of Angiostrongylus cantonensis in rats (Rattus norvegicus) in Grenada, West Indies. Vet Parasitol 162: 160–162.
Martiìnez-Delgado JF, Gonzaìlez-CortinÞas M, Taìpanes-Cruz TR, Ruiz-Meìndez A, 2000. Eosinophilic meningoencephalitis in Villa Clara (Cuba). A study of 17 patients [in Spanish]. Rev Neurol 31: 417–421.
Leone S, De Marco M, Ghirga P, Nicastri E, Esposito M, Narciso P, 2007. Eosinophilic meningitis in a returned traveler from Santo Domingo: case report and review. J Travel Med 14: 407–410.
Slom TJ, Cortese MM, Gerber SI, Jones RC, Holtz TH, Lopez AS, Zambrano CH, Sufit RL, Sakolvaree Y, Chaicumpa W, Herwaldt BL, Johnson S, 2002. An outbreak of eosinophilic meningitis caused by Angiostrongylus cantonensis in travelers returning from the Caribbean. N Engl J Med 346: 668–675.
Qvarnstrom Y, Xayavong M, Aramburu da Silva AC, Park SY, Whelen AC, Calimlim PS, Sciulli RH, Honda SA, Higa K, Kitsutani P, Chea N, Heng S, Johnson S, Graeff-Teixeira C, Fox LM, da Silva AJ, 2016. Real-time polymerase chain reaction detection of Angiostrongylus cantonensis DNA in cerebrospinal fluid from patients with eosinophilic meningitis. Am J Trop Med Hyg 94: 176–181.
Qvarnstrom Y, da Silva ACA, Teem JL, Hollingsworth R, Bishop H, Graeff-Teixeira C, da Silva AJ, 2010. Improved molecular detection of Angiostrongylus cantonensis in mollusks and other environmental samples with a species-specific internal transcribed spacer 1-based TaqMan assay. Appl Environ Microbiol 76: 5287–5289.
Sawanyawisuth K, Takahashi K, Hoshuyama T, Sawanyawisuth K, Senthong V, Limpawattana P, Intapan PM, Wilson D, Tiamkao S, Jitpimolmard S, Chotmongkol V, 2009. Clinical factors predictive of encephalitis caused by Angiostrongylus cantonensis. Am J Trop Med Hyg 81: 698–701.
Kuberski T, Wallace GD, 1979. Clinical manifestations of eosinophilic meningitis due to Angiostrongylus cantonensis. Neurology 29: 1566–1570.
Nuamtanong S, 1996. The evaluation of the 29 and 31 kDa antigens in female Angiostrongylus cantonensis for serodiagnosis of human angiostrongyliasis. Southeast Asian J Trop Med Public Health 127: 291–296.
Thanaviratananich S, Thanaviratananich S, Ngamjarus C, 2015. Corticosteroids for parasitic eosinophilic meningitis. Cochrane Database Syst Rev 2: CD009088.
Chotmongkol V, Kittimongkolma S, Niwattayakul K, Intapan PM, Thavornpitak Y, 2009. Comparison of prednisolone plus albendazole with prednisolone alone for treatment of patients with eosinophilic meningitis. Am J Trop Med Hyg 81: 443–445.
Chen X-G, Li H, Lun Z-R, 2005. Angiostrongyliasis, mainland China. Emerg Infect Dis 11: 1645–1647.
Evans-Gilbert T, Lindo JF, Henry S, Brown P, Christie CDC, 2014. Severe eosinophilic meningitis owing to Angiostrongylus cantonensis in young Jamaican children: case report and literature review. Paediatr Int Child Health 34: 148–152.
Malhotra S, Mehta DK, Arora R, Chauhan D, Ray S, Jain M, 2006. Ocular angiostrongyliasis in a child-first case report from India. J Trop Pediatr 52: 223–225.
Lindo JF, Escoffery CT, Reid B, Codrington G, Cunningham-Myrie C, Eberhard ML, 2004. Fatal autochthonous eosinophilic meningitis in a Jamaican child caused by Angiostrongylus cantonensis. Am J Trop Med Hyg 70: 425–428.
Hidelaratchi MDP, Riffsy MTM, Wijesekera JC, 2005. A case of eosinophilic meningitis following monitor lizard meat consumption, exacerbated by anthelminthics. Ceylon Med J 50: 84–86.
Juminer B, Roudier M, Raccurt CP, Pujol HP, Gerry F, Bonnet R, 1990. 1992. Presence of abdominal angiostrongylosis in Guadeloupe. Apropos of 2 recent cases [in French]. Bull Soc Pathol Exot 85: 39–43.
Eamsobhana P, 2013. Angiostrongyliasis in Thailand: epidemiology and laboratory investigations. Hawaii J Med Public Health 72: 28–32.
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Infection by the rat lungworm Angiostrongylus cantonensis represents the most common cause of infectious eosinophilic meningitis in humans, causing central nervous system (CNS) angiostrongyliasis. Most of CNS angiostrongyliasis cases were described in Asia, Pacific Basin, Australia, and some limited parts of Africa and America. CNS angiostrongyliasis has been reported in the Caribbean but never in the Lesser Antilles. The primary objectives of this study were to depict the first case of CNS angiostrongyliasis in the Lesser Antilles and investigate the environmental presence of A. cantonensis in Guadeloupe, Lesser Antilles. In December 2013, a suspected case of CNS angiostrongyliasis in an 8-month-old infant in Guadeloupe was investigated by real-time polymerase chain reaction (PCR) testing on cerebral spinal fluid (CSF). The environmental investigation was performed by collecting Achatina fulica molluscs from different parts of Guadeloupe and testing the occurrence of A. cantonensis by real-time PCR. CSF from the suspected case of angiostrongyliasis was positive for A. cantonensis by real-time PCR. Among 34 collected snails for environmental investigation, 32.4% were positive for A. cantonensis. In conclusion, we report the first laboratory-confirmed case of CNS-angiostrongyliasis in the Lesser Antilles. We identified the presence and high prevalence of A. cantonensis in A. fulica in Guadeloupe. These results highlight the need to increase awareness of this disease and implement public health programs in the region to prevent human cases of angiostrongyliasis and improve management of eosinophilic meningitis patients.
Authors' addresses: Céline Dard, Laboratoire de Biologie Médicale, Centre Hospitalier de Basse-Terre, Basse-Terre, Guadeloupe, France, and Laboratoire de Parasitologie-Mycologie, Centre Hospitalier Universitaire de Grenoble Alpes, Grenoble, France, E-mail: cdard@chu-grenoble.fr. Jean-Eudes Piloquet and Jean-Christophe Hebert, Département de Pédiatrie, Centre Hospitalier de Basse-Terre, Basse-Terre, Guadeloupe, France, E-mails: rubjep@hotmail.com and jc.hebert@ch-labasseterre.fr. Yvonne Qvarnstrom and LeAnne M. Fox, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, E-mails: bvp2@cdc.gov and llf4@cdc.gov. Helmi M'kada, Didier Mattera, and Dorothée Harrois, Laboratoire de Biologie Médicale, Centre Hospitalier de Basse-Terre, Basse-Terre, Guadeloupe, France, E-mails: helmi.mkada@ch-labasseterre.fr, didier.mattera@ch-labasseterre.fr, and dorothee.harrois@ch-labasseterre.fr.