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Facial Balamuthia mandrillaris infection with neurological involvement in an immunocompetent child
Zhen Zhang1, Jianying Liang1, Ruoqu Wei1
1Department of Dermatology, Xinhua Hospital, and Institute of Dermatology, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Abstract:
Cutaneous infection by Balamuthia mandrillaris is a rare condition that is sometimes complicated by life-threatening CNS involvement. It often evades timely diagnosis due to its rarity and non-specific clinical manifestations. Patients can be either immunocompetent or immunocompromised. It is probably transmitted via inhalation or inoculation through broken skin, and then spreads to the brain and other organs through haematogenous spread. It is important for clinicians to be aware of this disease because rapid diagnosis and subsequent therapy has, in some cases, been associated with survival. In this Grand Round, we report the case of a 7-year-old boy who presented with large, chronic plaques on his face. Several biopsies showed non-specific granulomatous inflammation. The patient deteriorated rapidly and died within 1 month of displaying abnormal symptoms in the CNS. Immunohistochemical staining of skin tissue identified B mandrillaris as the infectious agent. The diagnosis was confirmed with PCR, which detected B mandrillaris DNA in formalin-fixed skin tissue sections. B mandrillaris infection should be considered in the differential diagnosis of patients with chronic granulomatous lesions. We also reviewed the epidemiology, B mandrillaris in nature and in the laboratory, clinical manifestations, histopathology, diagnosis, and treatment of infection.
Insights
Balamuthia mandrillaris causes rare skin infections that can spread to the brain. Early diagnosis of this granulomatous inflammation is crucial for potential survival.
Area of Science:
- Infectious Diseases
- Neurology
- Dermatology
Background:
- Balamuthia mandrillaris is a rare amoeba causing infections, often with severe central nervous system (CNS) involvement.
- Diagnosis is challenging due to non-specific symptoms and rarity, affecting both immunocompetent and immunocompromised individuals.
Observation:
- A case report details a 7-year-old boy with chronic facial plaques initially showing non-specific granulomatous inflammation.
- The patient experienced rapid neurological deterioration and death within a month of CNS symptom onset.
Findings:
- Immunohistochemistry and PCR confirmed Balamuthia mandrillaris DNA in skin biopsies.
- This highlights the pathogen's role in chronic granulomatous skin lesions with potential systemic spread.
Implications:
- Clinicians should consider Balamuthia mandrillaris in the differential diagnosis of unexplained granulomatous skin conditions.
- Awareness and rapid diagnosis are critical for improving patient outcomes in Balamuthia mandrillaris infections.
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