| Literature DB >> 30070981 |
Eugene W Liu, Brian S Schwartz, Nicholas D Hysmith, John P DeVincenzo, Derek T Larson, Ryan C Maves, Debra L Palazzi, Chelsea Meyer, Haidee T Custodio, Mariejane M Braza, Roukaya Al Hammoud, Suchitra Rao, Yvonne Qvarnstrom, Michael J Yabsley, Richard S Bradbury, Susan P Montgomery.
Abstract
Angiostrongyliasis is caused by infection and migration to the brain of larvae of the parasitic nematode Angiostrongylus cantonensis, or rat lungworm. Adult A. cantonensis reside in the lungs of the definitive wild rodent host, where they produce larvae passed in feces, which are then ingested by snails and slugs (gastropods). Human infection typically occurs when gastropods containing mature larvae are inadvertently ingested by humans. Although human infection often is asymptomatic or involves transient mild symptoms, larval migration to the brain can lead to eosinophilic meningitis, focal neurologic deficits, coma, and death. The majority of cases of human angiostrongyliasis occur in Asia and the Pacific Islands, including Hawaii, but autochthonous and imported cases have been reported in the continental United States (1,2), underscoring the importance of provider recognition to ensure prompt identification and treatment. The epidemiologic and clinical features of 12 angiostrongyliasis cases in the continental United States were analyzed. These cases were identified through A. cantonensis polymerase chain reaction (PCR) testing (3) of cerebrospinal fluid (CSF) submitted to CDC from within the continental United States. Six cases were likely a result of autochthonous transmission in the southern United States. All 12 patients had CSF pleocytosis and eosinophilia, consistent with eosinophilic meningitis. Health care providers need to be aware of the possibility of angiostrongyliasis in patients with eosinophilic meningitis, especially in residents in the southern United States or persons who have traveled outside the continental United States and have a history of ingestion of gastropods or contaminated raw vegetables.Entities:
Mesh:
Year: 2018 PMID: 30070981 PMCID: PMC6072054 DOI: 10.15585/mmwr.mm6730a4
Source DB: PubMed Journal: MMWR Morb Mortal Wkly Rep ISSN: 0149-2195 Impact factor: 17.586
Exposures reported in 16 patients with presumed angiostrongyliasis with detectable Angiostrongylus cantonensis DNA on polymerase chain reaction testing at CDC — continental United States, January 2011–January 2017
| Exposure | No. of exposures | ||
|---|---|---|---|
| Yes (%)* | Possible | No | |
| Raw vegetables† | 6/11 (55) | 0 | 5 |
| Prawns | 2/9 (22) | 0 | 7 |
| Snails | 2/12 (17) | 2 | 8 |
| Crabs | 1/9 (11) | 0 | 8 |
| Slugs | 1/11 (9) | 1§ | 9 |
| Frogs | 0/8 (0) | 0 | 8 |
* Percentages were calculated using denominators based on availability of complete exposure data.
Three patients were known to have consumed vegetables from a local garden.
§ This patient was a toddler who was often permitted to crawl in a yard known to contain slugs.
Symptoms, physical exam findings, and laboratory results for 12 patients with angiostrongyliasis with detectable Angiostrongylus cantonensis DNA on polymerase chain reaction testing at CDC — continental United States, January 2011–January 2017
| Observation/Finding* | Present, No. | Absent, No. | Proportion with symptom/sign present (%)† |
|---|---|---|---|
|
| |||
| Subjective fever | 8 | 2 | 8/10 (80) |
| Generalized weakness | 7 | 2 | 7/9 (78) |
| Headache | 6 | 2 | 6/8 (75) |
| Numbness/Tingling | 3 | 3 | 3/6 (50) |
| Photophobia | 4 | 5 | 4/9 (44) |
| Visual changes | 3 | 4 | 3/7 (43) |
| Vomiting | 3 | 6 | 3/9 (33) |
| Stiff neck | 2 | 7 | 2/9 (22) |
| Rash | 2 | 7 | 2/9 (22) |
| Nausea | 1 | 5 | 1/6 (17) |
| Phonophobia | 1 | 6 | 1/7 (14) |
| Abdominal pain | 1 | 7 | 1/8 (13) |
| Itching | 1 | 8 | 1/9 (11) |
| Diarrhea | 3 | NA | NA |
| Hyperesthesias/diffuse allodynia | 2 | NA | NA |
|
| |||
|
| |||
| Fever (temperature ≥100.4°F [≥38.0°C]) | 3 | 8 | 3/11 (27) |
| Tachycardia (>100 bpm in adults aged ≥16 yrs, age-dependent in persons aged <16 yrs) | 1 | 10 | 1/11 (9) |
| Hypoxia (O2 saturation <90%) | 0 | 10 | 0/10 (0) |
|
| |||
| Cranial nerve deficits | 5 | 6 | 5/11 (45) |
| Nuchal rigidity | 4 | 8 | 4/12 (33) |
| Focal weakness | 3 | 7 | 3/10 (30) |
| Paresthesias | 1 | 7 | 1/8 (12) |
| Loss of consciousness | 0 | 10 | 0/10 (0) |
| Irritability | 3 | NA | NA |
| Ataxia | 2 | 1§ | NA |
|
| |||
|
| |||
| Pleocytosis of CSF (≥6 WBC/mm3) | 12 | 0 | 12/12 (100) |
| CSF eosinophilia (eosinophils ≥10% of all leukocytes in CSF or ≥10 eosinophils/mm3) | 10 | 2¶ | 10/12 (83) |
| Hypoglycorrhachia (CSF glucose <40 mg/dL) | 6 | 5 | 6/11 (54) |
|
| |||
| Peripheral eosinophilia (>600 eosinophils/mm3) | 8 | 2 | 8/10 (80) |
| Leukocytosis (>11x103 WBC/mm3 in persons aged >21 yrs, age-dependent in persons aged ≤21 yrs) | 3 | 9 | 3/12 (25) |
Abbreviations: bpm = beats per minute; CSF = cerebrospinal fluid; NA = not available; O2 = oxygen; WBC = white blood cells.
*Confirmed by the patient’s health care provider
† Percentages were calculated with different denominators based on availability of complete clinical data.
§ This patient developed ataxia 20 days after initial evaluation.
¶ These two patients were found to have CSF eosinophilia on repeat lumbar puncture.