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2.
Emerg Infect Dis ; 30(4): 803-805, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38526236

ABSTRACT

Primary amebic meningoencephalitis caused by Naegleria fowleri is a rare but nearly always fatal parasitic infection of the brain. Globally, few survivors have been reported, and the disease has no specific treatment. We report a confirmed case in Pakistan in a 22-year-old man who survived after aggressive therapy.


Subject(s)
Central Nervous System Protozoal Infections , Naegleria fowleri , Male , Humans , Young Adult , Adult , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/drug therapy , Brain , Pakistan/epidemiology , Survivors
3.
Infect Genet Evol ; 119: 105570, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38382768

ABSTRACT

INTRODUCTION: Balamuthia amoebic encephalitis (BAE), caused by Balamuthia mandrillaris, is a rare and life-threatening infectious disease with no specific and effective treatments available. The diagnosis of BAE at an early stage is difficult because of the non-specific clinical manifestations and neuroimaging. CASE DESCRIPTION: A 52-year-old male patient, who had no previous history of skin lesions, presented to the emergency department with an acute headache, walking difficulties, and disturbance of consciousness. The patient underwent a series of examinations, including regular cerebrospinal fluid (CSF) studies and magnetic resonance imaging, and tuberculous meningoencephalitis was suspected. Despite being treated with anti-TB drugs, no clinical improvement was observed in the patient. Following corticosteroid therapy, the patient developed a rapid deterioration in consciousness with dilated pupils. Metagenomic next-generation sequencing (mNGS) revealed an unexpected central nervous system (CNS) amoebic infection, and the patient died soon after the confirmed diagnosis. CONCLUSION: This study highlights the application of mNGS for the diagnosis of patients with suspected encephalitis or meningitis, especially those caused by rare opportunistic infections.


Subject(s)
Amebiasis , Balamuthia mandrillaris , Central Nervous System Protozoal Infections , Encephalitis , Infectious Encephalitis , Male , Humans , Middle Aged , Infectious Encephalitis/diagnosis , Encephalitis/diagnosis , Encephalitis/pathology , Balamuthia mandrillaris/genetics , Central Nervous System Protozoal Infections/diagnosis , Amebiasis/diagnosis , High-Throughput Nucleotide Sequencing
4.
Am J Trop Med Hyg ; 110(2): 246-249, 2024 Feb 07.
Article in English | MEDLINE | ID: mdl-38190743

ABSTRACT

Acanthamoeba spp. are rare etiological agents of meningoencephalitis with high mortality. We present three cases of Acanthamoeba meningoencephalitis in immunocompetent individuals from Eastern India. The first patient presented with fever and headache; the second with headache, visual disturbance, and squint; and the third presented in a drowsy state. The cases presented on March 3, 18, and 21, 2023 respectively. The first two patients had concomitant tubercular meningitis for which they received antitubercular therapy and steroid. Their cerebrospinal fluid showed slight lymphocytic pleocytosis and increased protein. The diagnosis was done by microscopy, culture, and polymerase chain reaction. They received a combination therapy comprising rifampicin, fluconazole, and trimethoprim-sulfamethoxazole. The first patient additionally received miltefosine. She responded well to therapy and survived, but the other two patients died despite intensive care. Detection of three cases within a period of 1 month from Eastern India is unusual. It is imperative to sensitize healthcare providers about Acanthamoeba meningoencephalitis to facilitate timely diagnosis and treatment of the disease.


Subject(s)
Acanthamoeba , Amebiasis , Central Nervous System Protozoal Infections , Meningoencephalitis , Humans , Female , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/drug therapy , Amebiasis/diagnosis , Amebiasis/drug therapy , Meningoencephalitis/diagnosis , Meningoencephalitis/drug therapy , India , Headache
5.
Parasitol Res ; 123(1): 84, 2024 Jan 06.
Article in English | MEDLINE | ID: mdl-38182931

ABSTRACT

Primary amebic meningoencephalitis (PAM) is a necrotizing and hemorrhagic inflammation of the brain and meninges caused by Naegleria fowleri, a free-living thermophilic ameba of freshwater systems. PAM remains a neglected disease that disproportionately affects children in tropical and subtropical climates, with an estimated mortality rate of 95-98%. Due to anthropogenic climate change, the average temperature in the USA has increased by 0.72 to 1.06 °C in the last century, promoting the poleward spread of N. fowleri. PAM is often misdiagnosed as bacterial meningitis or viral encephalitis, which shortens the window for potentially life-saving treatment. Diagnosis relies on the patient's history of freshwater exposure and the physician's high index of suspicion, supported by cerebrospinal fluid studies. While no experimental trials have been conducted to assess the relative efficacy of treatment regimens, anti-amebic therapy with adjunctive neuroprotection is standard treatment in the USA. We performed a literature review and identified five patients from North America between 1962 and 2022 who survived PAM with various degrees of sequelae.


Subject(s)
Central Nervous System Protozoal Infections , Naegleria fowleri , Child , Humans , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/drug therapy , Brain , Climate Change , Disease Progression
6.
Neuropathology ; 44(1): 68-75, 2024 Feb.
Article in English | MEDLINE | ID: mdl-37381626

ABSTRACT

A 76-year-old female with no apparent immunosuppressive conditions and no history of exposure to freshwater and international travel presented with headache and nausea 3 weeks before the presentation. On admission, her consciousness was E4V4V6. Cerebrospinal fluid analysis showed pleocytosis with mononuclear cell predominance, elevated protein, and decreased glucose. Despite antibiotic and antiviral therapy, her consciousness and neck stiffness gradually worsened, right eye-movement restriction appeared, and the right direct light reflex became absent. Brain magnetic resonance imaging revealed hydrocephalus in the inferior horn of the left lateral ventricle and meningeal enhancement around the brainstem and cerebellum. Tuberculous meningitis was suspected, and pyrazinamide, ethambutol, rifampicin, isoniazid, and dexamethasone were started. In addition, endoscopic biopsy was performed from the white matter around the inferior horn of the left lateral ventricle to exclude brain tumor. A brain biopsy specimen revealed eosinophilic round cytoplasm with vacuoles around blood vessels, and we diagnosed with amoebic encephalitis. We started azithromycin, flucytosine, rifampicin, and fluconazole, but her symptoms did not improve. She died 42 days after admission. In autopsy, the brain had not retained its structure due to autolysis. Hematoxylin and eosin staining of her brain biopsy specimen showed numerous amoebic cysts in the perivascular brain tissue. Analysis of the 16S ribosomal RNA region of amoebas from brain biopsy and autopsy specimens revealed a sequence consistent with Balamuthia mandrillaris. Amoebic meningoencephalitis can present with features characteristic of tuberculous meningitis, such as cranial nerve palsies, hydrocephalus, and basal meningeal enhancement. Difficulties in diagnosing amoebic meningoencephalitis are attributed to the following factors: (1) excluding tuberculous meningitis by microbial testing is difficult, (2) amoebic meningoencephalitis has low incidence and can occur without obvious exposure history, (3) invasive brain biopsy is essential in diagnosing amoebic meningoencephalitis. We should recognize the possibility of amoebic meningoencephalitis when evidence of tuberculosis meningitis cannot be demonstrated.


Subject(s)
Amebiasis , Amoeba , Balamuthia mandrillaris , Central Nervous System Protozoal Infections , Hydrocephalus , Infectious Encephalitis , Tuberculosis, Meningeal , Humans , Female , Aged , Tuberculosis, Meningeal/diagnosis , Tuberculosis, Meningeal/pathology , Central Nervous System Protozoal Infections/diagnosis , Rifampin , Amebiasis/diagnosis , Amebiasis/pathology , Brain/diagnostic imaging , Brain/pathology , Infectious Encephalitis/diagnosis , Infectious Encephalitis/pathology , Hydrocephalus/pathology
7.
Trop Doct ; 54(2): 165-166, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38130144

ABSTRACT

Annual reported cases of Naegleria fowleri (NF), popularly known as brain eating amoeba, are becoming a huge challenge for Pakistani health authorities. Karachi has seen cases regularly up till the present but Lahore has not. The spread of this amoeba in non-chlorinated water is a major concern for the authorities. NF is an amoeba commonly found in warm freshwater environments such as lakes, hot springs and poorly chlorinated swimming pools. It poses a significant risk during hot weather when water-related recreational activities are popular. Where there is a non-chlorinated water supply, its spread is aggravated.


Subject(s)
Amebiasis , Central Nervous System Protozoal Infections , Infectious Encephalitis , Naegleria fowleri , Humans , Pakistan/epidemiology , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/epidemiology , Amebiasis/diagnosis , Amebiasis/epidemiology , Water
8.
ACS Infect Dis ; 9(12): 2622-2631, 2023 Dec 08.
Article in English | MEDLINE | ID: mdl-37943251

ABSTRACT

Primary amebic meningoencephalitis (PAM), a brain infection caused by a free-living ameba Naegleria fowleri, leads to an extensive inflammation of the brain and death within 1-18 (median 5) days after symptoms begin. Although natural products have played a significant role in the development of drugs for over a century, research focusing on identifying new natural product-based anti-N. fowleri agents is limited. We undertook a large-scale ATP bioluminescence-based screen of about 10,000 unique marine microbial metabolite mixtures against the trophozoites of N. fowleri. Our screen identified about 100 test materials with >90% inhibition at 50 µg/mL and a dose-response study found 20 of these active test materials exhibiting an EC50 ranging from 0.2 to 2 µg/mL. Examination of four of these potent metabolite mixtures, derived from our actinomycete strains CNT671, CNT756, and CNH301, resulted in the isolation of a pure metabolite identified as oligomycin D. Oligomycin D exhibited nanomolar potency on multiple genotypes of N. fowleri, and it was five- or 850-times more potent than the recommended drugs amphotericin B or miltefosine. Oligomycin D is fast-acting and reached its EC50 in 10 h, and it was also able to inhibit the invasiveness of N. fowleri significantly when tested on a matrigel invasion assay. Since oligomycin is known to manifest inhibitory activity against F1FO ATP synthase, we tested different F1FO ATP synthase inhibitors and identified a natural peptide leucinostatin as a fast-acting amebicidal compound with nanomolar potency on multiple strains.


Subject(s)
Amebicides , Central Nervous System Protozoal Infections , Naegleria fowleri , Humans , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/drug therapy , Rutamycin , Amphotericin B/pharmacology
9.
PLoS One ; 18(11): e0290394, 2023.
Article in English | MEDLINE | ID: mdl-37939056

ABSTRACT

Primary amoebic meningoencephalitis (PAM) is a rapidly progressing central nervous system (CNS) infection caused by Naegleria fowleri, a free-living amoeba found in warm freshwater. The disease progression is very rapid, and the outcome is nearly always fatal. We aim to describe the disease course in patients admitted with PAM in a tertiary care center in Karachi, Pakistan between the periods of 2010 to 2021. A total of 39 patients were included in the study, 33 males (84.6%). The median age of the patients was 34 years. The most frequent presenting complaint was fever, which was found in 37 patients (94.9%) followed by headache in 28 patients (71.8%), nausea and vomiting in 27 patients (69.2%), and seizures in 10 patients (25.6%). Overall, 39 patients underwent lumbar puncture, 27 patients (69.2%) had a positive motile trophozoites on CSF wet preparation microscopy, 18 patients (46.2%) had a positive culture, and 10 patients had a positive PCR. CSF analysis resembled bacterial meningitis with elevated white blood cell counts with predominantly neutrophils (median, 3000 [range, 1350-7500] cells/µL), low glucose levels median, 14 [range, 1-92] mg/dL), and elevated protein levels (median, 344 [range, 289-405] mg/dL). Imaging results were abnormal in approximately three-fourths of the patients which included cerebral edema (66.7%), hydrocephalus (25.6%), and cerebral infarctions (12.8%). Only one patient survived. PAM is a fatal illness with limited treatment success. Early diagnosis and prompt initiation of treatment can improve the survival of the patients and reduce mortality.


Subject(s)
Amebiasis , Central Nervous System Protozoal Infections , Meningoencephalitis , Naegleria fowleri , Male , Humans , Adult , Pakistan/epidemiology , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/epidemiology , Central Nervous System Protozoal Infections/drug therapy , Spinal Puncture , Amebiasis/diagnosis , Amebiasis/epidemiology , Meningoencephalitis/diagnosis , Meningoencephalitis/epidemiology
10.
Front Public Health ; 11: 1266400, 2023.
Article in English | MEDLINE | ID: mdl-37927850

ABSTRACT

The outbreak of Naegleria fowleri in Pakistan presents a significant public health concern due to its high fatality rate and limited treatment options. This review explores the impact of the outbreak on communities and the challenges faced in combating the disease. It evaluates available treatment options and highlights the need for early diagnosis and intervention. The study proposes recommendations to improve public health preparedness, including public awareness campaigns, enhanced healthcare infrastructure, and robust water surveillance systems. Collaboration between research institutions and public health organizations is emphasized to develop effective outbreak response strategies.


Subject(s)
Central Nervous System Protozoal Infections , Naegleria fowleri , Humans , Pakistan/epidemiology , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/epidemiology , Water , Disease Outbreaks
11.
Yonsei Med J ; 64(10): 641-645, 2023 Oct.
Article in English | MEDLINE | ID: mdl-37727924

ABSTRACT

Primary amebic meningoencephalitis (PAM) is a rare, but almost always fatal, central nervous system infection caused by Naegleria fowleri, which are thermophilic free-living amoeba. Here, we report the first case of PAM detected in South Korea, probably imported from Thailand. Despite antimicrobial treatment for N. fowleri infection with a combination of intravenous liposomal amphotericin B, fluconazole, azithromycin, and oral rifampin, the patient died 13 days after the onset of symptoms. Clinicians in South Korea treating severe meningoencephalitis, especially in individuals returning from tropical areas, are encouraged to include PAM in the differential diagnoses, given the accelerated global warming and increased overseas trips.


Subject(s)
Central Nervous System Protozoal Infections , Naegleria fowleri , Humans , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/drug therapy , Republic of Korea , Administration, Intravenous , Azithromycin
12.
Parasitol Res ; 122(10): 2451-2452, 2023 Oct.
Article in English | MEDLINE | ID: mdl-37555856

ABSTRACT

This case report describes a 62-year-old male fisherman who presented with persistent vomiting, headache, and behavior changes. Despite initial antibiotic and corticosteroid treatment, his condition worsened, leading to coma and subsequent death. Macro-genome sequencing of cerebrospinal fluid (CSF) revealed the presence of Naegleria fowleri infection, which had been missed during initial laboratory tests. The patient's exposure history included sea-swimming near Zhoushan Island.


Subject(s)
Amebiasis , Central Nervous System Protozoal Infections , Meningoencephalitis , Naegleria fowleri , Male , Humans , Middle Aged , Central Nervous System Protozoal Infections/diagnosis , Amebiasis/diagnosis , Swimming , Naegleria fowleri/genetics , Fatal Outcome , Seawater , Meningoencephalitis/diagnosis
13.
Am J Trop Med Hyg ; 109(2): 322-326, 2023 08 02.
Article in English | MEDLINE | ID: mdl-37460088

ABSTRACT

Primary amebic meningoencephalitis (PAM) is a rare and lethal infection caused by Naegleria fowleri. We report an epidemiological and environmental investigation relating to a case of PAM in a previously healthy boy age 8 years. An interview of the patient's family was conducted to determine the likely exposure site and to assess risk factors. Data from the United States Geological Survey site at Waterloo, NE, on the Elkhorn River were used to estimate water temperature and streamflow at the time and site of exposure. Data from the National Weather Service were used to estimate precipitation and ambient air temperature at the time and site of exposure. Despite conventional treatment, the patient died 2 days after hospital admission. The patient participated in recreational water activities in the Elkhorn River in northeastern Nebraska 5 days before symptom onset. In the week before exposure, water and ambient air high temperatures reached annual highs, averaging 32.4°C and 35.8°C, respectively. The day before infection, 2.2 cm of precipitation was reported. Streamflow was low (407 ft3/s). Infections in several northern states, including Nebraska, suggest an expanding geographic range of N. fowleri transmission, which may lead to increased incidence of PAM in the United States. Similar environmental investigations at suspected exposure sites of future cases will allow data aggregation, enabling investigators to correlate environmental factors with infection risk accurately.


Subject(s)
Amebiasis , Central Nervous System Protozoal Infections , Meningoencephalitis , Naegleria fowleri , Male , Humans , United States/epidemiology , Child , Nebraska , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/epidemiology , Water , Rivers , Meningoencephalitis/epidemiology , Meningoencephalitis/diagnosis , Amebiasis/epidemiology , Amebiasis/diagnosis
15.
Neurology ; 101(8): e845-e851, 2023 08 22.
Article in English | MEDLINE | ID: mdl-37156616

ABSTRACT

A wide variety of diseases present with intracranial lesions. In this case report, a 67-year-old man initially presented to an outside hospital with nausea, headache, and ataxia and was found to have multiple intracranial lesions. Diagnostic workup was ultimately unrevealing, and his condition improved after a course of steroids and antibiotics. Unfortunately, symptoms returned 3 months later. MRI of the brain revealed progression of his intracranial lesions. This case highlights a diagnostic approach and general management strategy for patients presenting with undifferentiated intracranial pathology. A final diagnosis is ultimately reached and raises further discussion.


Subject(s)
Anti-Bacterial Agents , Brain , Central Nervous System Protozoal Infections , Hemianopsia , Humans , Male , Aged , Hemianopsia/etiology , Magnetic Resonance Imaging , Brain/diagnostic imaging , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/drug therapy , Naegleria fowleri , Anti-Bacterial Agents/therapeutic use , Treatment Outcome
16.
Parasites Hosts Dis ; 61(2): 183-193, 2023 May.
Article in English | MEDLINE | ID: mdl-37258265

ABSTRACT

Balamuthia mandrillaris amebic encephalitis (BAE) can cause a fatal condition if diagnosis is delayed or effective treatment is lacking. Patients with BAE have been previously reported in 12 provinces of China, with skin lesions being the primary symptom and encephalitis developing after several years. However, a significantly lower number of cases has been reported in Southwest China. Here we report an aggressive BAE case of a 64-year-old woman farmer with a history of skin lesions on her left hand. She was admitted to our hospital due to symptoms of dizziness, headache, cough, vomiting, and gait instability. She was initially diagnosed with syphilitic meningoencephalitis and received a variety of empirical treatment that failed to improve her symptoms. Finally, she was diagnosed with BAE combined with amebic pneumonia using next-generation sequencing (NGS), qRT-PCR, sequence analysis, and imaging studies. She died approximately 3 weeks after the onset. This case highlights that the rapid development of encephalitis can be a prominent clinical manifestation of Balamuthia mandrillaris infection.


Subject(s)
Amebiasis , Amoeba , Balamuthia mandrillaris , Central Nervous System Protozoal Infections , Encephalitis , Infectious Encephalitis , Humans , Female , Middle Aged , Central Nervous System Protozoal Infections/diagnosis , Encephalitis/diagnosis , Amebiasis/diagnosis , China
17.
Curr Opin Infect Dis ; 36(3): 186-191, 2023 06 01.
Article in English | MEDLINE | ID: mdl-37093056

ABSTRACT

PURPOSE OF REVIEW: Free-living amebae (FLA) including Naegleria fowleri , Balamuthia mandrillaris , and Acanthamoeba species can cause rare, yet severe infections that are nearly always fatal. This review describes recent developments in epidemiology, diagnosis, and treatment of amebic meningoencephalitis. RECENT FINDINGS: Despite similarities among the three pathogenic FLA, there are notable variations in disease presentations, routes of transmission, populations at risk, and outcomes for each. Recently, molecular diagnostic tools have been used to diagnose a greater number of FLA infections. Treatment regimens for FLA have historically relied on survivor reports; more data is needed about novel treatments, including nitroxoline. SUMMARY: Research to identify new drugs and guide treatment regimens for amebic meningoencephalitis is lacking. However, improved diagnostic capabilities may lead to earlier diagnoses, allowing earlier treatment initiation and improved outcomes. Public health practitioners should continue to prioritize increasing awareness and providing education to clinicians, laboratorians, and the public about amebic infections.


Subject(s)
Acanthamoeba , Amebiasis , Central Nervous System Protozoal Infections , Infectious Encephalitis , Meningoencephalitis , Humans , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/drug therapy , Central Nervous System Protozoal Infections/epidemiology , Amebiasis/diagnosis , Amebiasis/drug therapy , Amebiasis/epidemiology , Meningoencephalitis/diagnosis , Meningoencephalitis/drug therapy , Meningoencephalitis/epidemiology , Infectious Encephalitis/diagnosis , Infectious Encephalitis/drug therapy , Infectious Encephalitis/epidemiology
18.
BMC Infect Dis ; 23(1): 245, 2023 Apr 18.
Article in English | MEDLINE | ID: mdl-37072710

ABSTRACT

BACKGROUND: Balamuthia granulomatous amoebic encephalitis (GAE) is a peculiar parasitic infectious disease of the central nervous system, about 39% of the infected Balamuthia GAE patients were found to be immunocompromised and is extremely rare clinically. The presence of trophozoites in diseased tissue is an important basis for pathological diagnosis of GAE. Balamuthia GAE is a rare and highly fatal infection for which there is no effective treatment plan in clinical practice. CASE PRESENTATION: This paper reports clinical data from a patient with Balamuthia GAE to improve physician understanding of the disease and diagnostic accuracy of imaging and reduce misdiagnosis. A 61-year-old male poultry farmer presented with moderate swelling pain in the right frontoparietal region without obvious inducement three weeks ago. Head computed tomography(CT) and magnetic resonance imaging(MRI) revealed a space-occupying lesion in the right frontal lobe. Intially clinical imaging diagnosed it as a high-grade astrocytoma. The pathological diagnosis of the lesion was inflammatory granulomatous lesions with extensive necrosis, suggesting amoeba infection. The pathogen detected by metagenomic next-generation sequencing (mNGS) is Balamuthia mandrillaris, the final pathological diagnosis was Balamuthia GAE. CONCLUSION: When a head MRI shows irregular or annular enhancement, clinicians should not blindly diagnose common diseases such as brain tumors. Although Balamuthia GAE accounts for only a small proportion of intracranial infections, it should be considered in the differential diagnosis.


Subject(s)
Amebiasis , Central Nervous System Parasitic Infections , Central Nervous System Protozoal Infections , Encephalitis , Infectious Encephalitis , Male , Humans , Middle Aged , Encephalitis/diagnosis , Central Nervous System Protozoal Infections/diagnosis , Central Nervous System Protozoal Infections/parasitology , Amebiasis/diagnosis , Amebiasis/parasitology , Amebiasis/pathology , Brain/pathology , Central Nervous System Parasitic Infections/pathology , Granuloma/pathology , Fatal Outcome
19.
Article in English | MEDLINE | ID: mdl-36833715

ABSTRACT

INTRODUCTION: Primary amoebic meningoencephalitis (PAM) is a rare but lethal infection of the brain caused by a eukaryote called Naegleria fowleri (N. fowleri). The aim of this review is to consolidate the recently published case reports of N. fowleri infection by describing its epidemiology and clinical features with the goal of ultimately disseminating this information to healthcare personnel. METHODS: A comprehensive literature search was carried out using PubMed, Web of Science, Scopus, and OVID databases until 31 December 2022 by two independent reviewers. All studies from the year 2013 were extracted, and quality assessments were carried out meticulously prior to their inclusion in the final analysis. RESULTS: A total of 21 studies were selected for qualitative analyses out of the 461 studies extracted. The cases were distributed globally, and 72.7% of the cases succumbed to mortality. The youngest case was an 11-day-old boy, while the eldest was a 75-year-old. Significant exposure to freshwater either from recreational activities or from a habit of irrigating the nostrils preceded onset. The symptoms at early presentation included fever, headache, and vomiting, while late sequalae showed neurological manifestation. An accurate diagnosis remains a challenge, as the symptoms mimic bacterial meningitis. Confirmatory tests include the direct visualisation of the amoeba or the use of the polymerase chain reaction method. CONCLUSIONS: N. fowleri infection is rare but leads to PAM. Its occurrence is worldwide with a significant risk of fatality. The suggested probable case definition based on the findings is the acute onset of fever, headache, and vomiting with meningeal symptoms following exposure to freshwater within the previous 14 days. Continuous health promotion and health education activities for the public can help to improve knowledge and awareness prior to engagement in freshwater activities.


Subject(s)
Amoeba , Central Nervous System Protozoal Infections , Naegleria fowleri , Aged , Humans , Male , Brain , Central Nervous System Protozoal Infections/diagnosis , Fever , Headache
20.
J Pak Med Assoc ; 73(2): 396-398, 2023 Feb.
Article in English | MEDLINE | ID: mdl-36800735

ABSTRACT

Naegleria fowleri causes acute fatal primary amoebic meningoencephalitis in adults and children with a history of exposure to aquatic activities. However, several cases of Primary Amoebic Meningoencephalitis (PAM) have been reported from Karachi with no history of aquatic recreational activities suggesting the presence of N. fowleri in domestic water. This study reports a case of co-infection of N. fowleri with Streptococcus pneumoniae in an elderly hypertensive male.


Subject(s)
Central Nervous System Protozoal Infections , Meningoencephalitis , Naegleria fowleri , Adult , Child , Aged , Humans , Male , Streptococcus pneumoniae , Pakistan , Central Nervous System Protozoal Infections/diagnosis , Meningoencephalitis/diagnosis
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