Literature DB >> 28930003

Angiostrongylus cantonensis Eosinophilic Meningitis in an Infant, Tennessee, USA.

Tim Flerlage, Yvonne Qvarnstrom, John Noh, John P Devincenzo, Arshia Madni, Bindiya Bagga, Nicholas D Hysmith.   

Abstract

Angiostrongylus cantonensis, the rat lungworm, is the most common infectious cause of eosinophilic meningoencephalitis worldwide. This parasite is endemic to Southeast Asia and the Pacific Islands, and its global distribution is increasing. We report A. cantonensis meningoencephalitis in a 12-month-old boy in Tennessee, USA, who had not traveled outside of southwestern Tennessee or northwestern Mississippi.

Entities:  

Keywords:  Angiostrongylus cantonensis; Tennessee; United States; eosinophil-predominant pleocytosis; meningitis/encephalitis; mild hypoglycorrhacia; parasites; rat lungworm

Mesh:

Substances:

Year:  2017        PMID: 28930003      PMCID: PMC5621543          DOI: 10.3201/eid2310.170978

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


In 2016, a 12-month-old, fully vaccinated boy was admitted to a hospital in Memphis, Tennessee, USA, for evaluation of 18 days of daily fever, irritability, decreased oral intake, and emesis. His medical history was unremarkable, and he had no known contact with sick persons. He had not traveled outside the area comprising southwestern Tennessee and northwestern Mississippi. He lived in a nonagricultural rural area and was exposed to a vaccinated family dog. Wild rats had been observed in and around the home, and rat droppings had been found in the child’s bed. Raccoons were seen on the property; however, contact, either direct or through fomites such as latrines, was not reported. During a 17-day period, 2 evaluations by his primary care physician and 4 emergency department visits resulted in the diagnosis of fever of unknown origin and inpatient admission. A cerebrospinal fluid (CSF) sample taken by lumbar puncture on day 20 of illness showed eosinophil-predominant pleocytosis, mild hypoglycorrhacia, and a mildly elevated protein level (Table). Magnetic resonance imaging of the brain and spine showed scattered areas of restricted diffusion throughout the brain parenchyma, leptomeningeal enhancement, and multifocal nodular enhancement along the ventral portion of multiple spinal levels. Serologic testing was negative for Toxocara canis/cati, Strongyloides stercoralis, Ehrlichia chaffeenis, Rickettsia rickettsiae, Epstein-Barr virus, HIV, and Toxoplasma gondii; a rapid plasma reagin was also negative. Tuberculin skin testing was negative. Results of CSF PCR for Streptococcus pneumoniae, herpes simplex virus, and enteroviruses were negative; CSF cryptococcal antigen testing was also negative. Due to concern for infection with Baylisascaris procyonis, the raccoon roundworm, physicians prescribed albendazole and dexamethasone. The patient’s temperature returned to normal, and his symptoms resolved. Upon discharge, he was to complete 3 weeks of albendazole and tapering doses of corticosteroids. Attending physicians repeated lumbar punctures on days 28, 41, and 56 (Table).
Table

Results of cerebrospinal fluid testing for 12-month-old boy with meningoencephalitis, Memphis, Tennessee, USA, 2016*

TestReference rangeDay of illness
20284156
Leukocytes, cells/mm30–8547552,979115
Polymorphonuclear cells, %0–104204
Lymphocytes, %0–544806564
Monocytes, %0–52061021
Eosinophils, %
NA
36
10
5
11
Erythrocytes<0014045
Glucose, mg/dL40–7037252227
Protein, mg/dL
15–45
67
74
164
104
Gram stain
NA
Few leukocytes; 0 organisms
Rare leukocytes; rare erythrocytes; 0 organisms
Moderate leukocytes; rare erythrocytes; 0 organisms
Rare leukocytes; 0 organisms
Bacterial cultureNASterileSterileSterileSterile

*NA, not applicable.

*NA, not applicable. Physicians sent samples (CSF and serum) taken on day 20 to the Centers for Disease Control and Prevention (Atlanta, GA, USA) to test for B. procyonis roundworms and samples taken on day 56 to test for Angiostrongylus cantonensis, the rat lungworm. Results were negative for B. procyonis but positive for A. cantonensis. In addition, serum samples obtained at the time of the initial lumbar puncture were positive for A. cantonensis antibodies by investigational whole-worm Western blot. The first documented human infection with A. cantonensis worms occurred in 1944 in Taiwan. Since then, >2,800 cases among humans have been reported; most have been in Southeast Asia and the Pacific islands (; Technical Appendix). In the late 1950s, the first report of human A. cantonensis infection in the United States occurred in Hawaii. A. cantonensis worms have since become endemic to wide-ranging tropical and subtropical locales in the Western Hemisphere, including the Hawaiian Islands (), the Caribbean Islands (), and South America (). The first report of the rat lungworm in the continental United States was in 1987, when Kim et al. found that 18% of rats sampled on necropsy in New Orleans, Louisiana, were infected with the nematode (). First-stage A. cantonensis larvae from these rats produced infections in native gastropods, providing the potential for these parasites to become endemic to the region. A report ≈15 years later documented infection in vertebrates not only in New Orleans but also in other areas of Louisiana and Mississippi. A. cantonensis worms are now considered to be endemic to Louisiana (). Infection has since been documented in rats (), gastropods (), and vertebrates () across a large area of the southern United States, from Oklahoma () to Florida (,). Soon after the initial recognition in local animal reservoirs, the first reported A. cantonensis infection in a human acquired in the continental United States occurred in an 11-year-old boy residing in New Orleans. Since then, 3 additional cases have been reported in an 11-month-old, a 12-month-old, and a 19-month-old, all of whom resided in Houston, Texas, and had not traveled (). A. cantonensis infection causes a self-limited illness in which headaches, nonfocal neurologic findings, and cranial nerve involvement are the most common signs and symptoms. Optimal therapy has not been clearly defined, and symptomatic management is an option for this self-limited illness. When therapy is prescribed, corticosteroids alone or in combination with antihelminth medications are most commonly used. In a prospective study that followed up on 3 previous studies, Chotmongkol et al. confirmed that a 2-week course of corticosteroids shortened the duration of headache and reduced the need for repeated lumbar puncture (). The study concluded that corticosteroids plus albendazole was no better than corticosteroids alone. International shipping and the ability of A. cantonensis worms to use diverse species of gastropods as intermediate hosts have all contributed to this parasite becoming a pathogen of increasing public health concern (). Angiostrongyliasis should be considered in the differential diagnosis of prolonged fever of unknown origin with compatible clinical and laboratory findings.

Technical Appendix

Additional reports of human infection with Angiostrongylus cantonensis, the rat lungworm.
  10 in total

1.  Eosinophilic meningoencephalitis caused by a metastrongylid lung-worm of rats.

Authors:  L ROSEN; R CHAPPELL; G L LAQUEUR; G D WALLACE; P P WEINSTEIN
Journal:  JAMA       Date:  1962-02-24       Impact factor: 56.272

2.  An epidemiological study of A. cantonensis in Jamaica subsequent to an outbreak of human cases of eosinophilic meningitis in 2000.

Authors:  C A Waugh; J F Lindo; J Lorenzo-Morales; R D Robinson
Journal:  Parasitology       Date:  2016-08       Impact factor: 3.234

3.  Angiostrongylus cantonensis in Introduced Gastropods in Southern Florida.

Authors:  Heather D Stockdale-Walden; John Slapcinsky; Yvonne Qvarnstrom; Antoinette McIntosh; Henry S Bishop; Brent Rosseland
Journal:  J Parasitol       Date:  2015-01-07       Impact factor: 1.276

Review 4.  Human Angiostrongylus cantonensis: an update.

Authors:  Q-P Wang; Z-D Wu; J Wei; R L Owen; Z-R Lun
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2011-07-05       Impact factor: 3.267

5.  Parastrongylus (=Angiostrongylus) cantonensis now endemic in Louisiana wildlife.

Authors:  D Y Kim; T B Stewart; R W Bauer; M Mitchell
Journal:  J Parasitol       Date:  2002-10       Impact factor: 1.276

6.  Comparison of prednisolone plus albendazole with prednisolone alone for treatment of patients with eosinophilic meningitis.

Authors:  Verajit Chotmongkol; Suvicha Kittimongkolma; Kanigar Niwattayakul; Pewpan M Intapan; Yupa Thavornpitak
Journal:  Am J Trop Med Hyg       Date:  2009-09       Impact factor: 2.345

7.  Endemic angiostrongyliasis, Rio de Janeiro, Brazil.

Authors:  Raquel O Simoes; Fernando A Monteiro; Elizabeth Sanchez; Silvana C Thiengo; Juberlan S Garcia; Socrates F Costa-Neto; Jose L Luque; Arnaldo Maldonado
Journal:  Emerg Infect Dis       Date:  2011-07       Impact factor: 6.883

8.  Parastrongylus cantonensis in a nonhuman primate, Florida.

Authors:  Michael S Duffy; Christine L Miller; J Michael Kinsella; Alexander de Lahunta
Journal:  Emerg Infect Dis       Date:  2004-12       Impact factor: 6.883

9.  Geographic Range Expansion for Rat Lungworm in North America.

Authors:  Emily M York; James P Creecy; Wayne D Lord; William Caire
Journal:  Emerg Infect Dis       Date:  2015-07       Impact factor: 6.883

10.  Angiostrongylus cantonensis Meningitis and Myelitis, Texas, USA.

Authors:  Roukaya Al Hammoud; Stacy L Nayes; James R Murphy; Gloria P Heresi; Ian J Butler; Norma Pérez
Journal:  Emerg Infect Dis       Date:  2017-06       Impact factor: 6.883

  10 in total
  7 in total

1.  Metagenomic Next-Generation Sequencing in Central Nervous System Angiostrongyliasis.

Authors:  Qiong Liao; Yu Zhu; Yang Wen
Journal:  Indian Pediatr       Date:  2022-05-15       Impact factor: 3.839

2.  Angiostrongylus cantonensis Nematode Invasion Pathway, Mallorca, Spain.

Authors:  Sofia Delgado-Serra; Jessica Sola; Nieves Negre; Claudia Paredes-Esquivel
Journal:  Emerg Infect Dis       Date:  2022-06       Impact factor: 16.126

3.  TNF-α Triggers RIP1/FADD/Caspase-8-Mediated Apoptosis of Astrocytes and RIP3/MLKL-Mediated Necroptosis of Neurons Induced by Angiostrongylus cantonensis Infection.

Authors:  Hongli Zhou; Minyu Zhou; Yue Hu; Yanin Limpanon; Yubin Ma; Ping Huang; Paron Dekumyoy; Wanchai Maleewong; Zhiyue Lv
Journal:  Cell Mol Neurobiol       Date:  2021-03-08       Impact factor: 4.231

Review 4.  Clinical Efficacy and Safety of Albendazole and Other Benzimidazole Anthelmintics for Rat Lungworm Disease (Neuroangiostrongyliasis): A Systematic Analysis of Clinical Reports and Animal Studies.

Authors:  John Jacob; Argon Steel; Zhain Lin; Fiona Berger; Katrin Zöeller; Susan Jarvi
Journal:  Clin Infect Dis       Date:  2022-04-09       Impact factor: 9.079

5.  First cases of Angiostrongylus cantonensis infection reported in Martinique, 2002-2017.

Authors:  Céline Dard; Eve Tessier; Duc Nguyen; Loïc Epelboin; Dorothée Harrois; Christopher Swale; André Cabié; Katia de Meuron; Charline Miossec; Nicole Desbois-Nogard
Journal:  Parasite       Date:  2020-05-12       Impact factor: 3.000

6.  The genetic basis of adaptive evolution in parasitic environment from the Angiostrongylus cantonensis genome.

Authors:  Lian Xu; Meng Xu; Xi Sun; Junyang Xu; Xin Zeng; Dai Shan; Dongjuan Yuan; Ping He; Weiming He; Yulan Yang; Shiqi Luo; Jie Wei; Xiaoying Wu; Zhen Liu; Xiaomin Xu; Zhensheng Dong; Langui Song; Beibei Zhang; Zilong Yu; Lifu Wang; Chi Zhang; Xiaodong Fang; Qiang Gao; Zhiyue Lv; Zhongdao Wu
Journal:  PLoS Negl Trop Dis       Date:  2019-11-21

7.  Demographics of the semi-slug Parmarion martensi, an intermediate host for Angiostrongylus cantonensis in Hawai'i, during laboratory rearing.

Authors:  Lindsey J Hamilton; Yaeko Tagami; Lisa Kaluna; John Jacob; Susan I Jarvi; Peter Follett
Journal:  Parasitology       Date:  2020-08-03       Impact factor: 3.234

  7 in total

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