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Volume 32, Number 7—July 2026

Synopsis

Neurosurgical Biopsy and Resection for Diagnosis and Treatment of Balamuthia mandrillaris Amebic Encephalitis, United States

Beenish Rubbab1, Ammar Adenwalla1, Natasha Spottiswoode, Julia C. Haston, Sarah Firmani, Sumit Singh, Veena Rajaram, Jay Ramos, Ibne Karim M. Ali, Brett Whittemore, and Natasha W. HannersComments to Author 
Author affiliation: University of Texas Southwestern Medical Center, Dallas, Texas, USA (B. Rubbab, A. Adenwalla, S. Singh, V. Rajaram, B. Whittemore, N.W. Hanners); University of California San Francisco, San Francisco, California, USA (N. Spottiswoode); Centers for Disease Control and Prevention, Atlanta, Georgia, USA (J.C. Haston, I.K.M. Ali); Children’s Health, Dallas (S. Firmani, J. Ramos)

Main Article

Figure 3

Timeline of events and medications for patient in study of neurosurgical biopsy and resection for diagnosis and treatment of Balamuthia mandrillaris amebic encephalitis, United States. Gray bar shows days since initial evaluation; red diamonds indicate magnetic resonance imaging (MRI) obtained before and after surgical dates; gray diamonds indicate interval MRI; blue diamonds indicate MRI before and after end date of nitroxoline. Nitroxoline dosing was titrated over 1 week to a total of 30 mg/kg/day 3 times/day; other medication dosing was pentamidine, 4 mg/kg (80 mg) every 24 hours; sulfadiazine, 50 mg/kg (1,000 mg) every 6 hours; azithromycin, 20 mg/kg (400 mg) every 24 hours; fluconazole, 12 mg/kg (240 mg) every 24 hours; flucytosine, 37.5 mg/kg (750 mg) every 6 hours; and miltefosine, 2.5 mg/kg (50 mg) every 24 hours. Pentamidine was discontinued after 8 weeks because of concern for renal toxicity. Sulfadiazine was briefly switched to trimethoprim/sulfamethoxazole because of manufacturer supply shortage and ultimately discontinued because of cost and administration concerns. Because of persistent nausea, vomiting, dysgeusia, and anorexia, flucytosine, fluconazole, azithromycin, and miltefosine were each discontinued, and the patient remained on nitroxoline for a total of 19 months. N/V, nausea and vomiting; TMP/SMX, trimethoprim/sulfamethoxazole; uPCR, universal broad-range PCR amplicon sequencing.

Figure 3. Timeline of events and medications for patient in study of neurosurgical biopsy and resection for diagnosis and treatment of Balamuthia mandrillaris amebic encephalitis, United States. Gray bar shows days since initial evaluation; red diamonds indicate magnetic resonance imaging (MRI) obtained before and after surgical dates; gray diamonds indicate interval MRI; blue diamonds indicate MRI before and after end date of nitroxoline. Nitroxoline dosing was titrated over 1 week to a total of 30 mg/kg/day 3 times/day; other medication dosing was pentamidine, 4 mg/kg (80 mg) every 24 hours; sulfadiazine, 50 mg/kg (1,000 mg) every 6 hours; azithromycin, 20 mg/kg (400 mg) every 24 hours; fluconazole, 12 mg/kg (240 mg) every 24 hours; flucytosine, 37.5 mg/kg (750 mg) every 6 hours; and miltefosine, 2.5 mg/kg (50 mg) every 24 hours. Pentamidine was discontinued after 8 weeks because of concern for renal toxicity. Sulfadiazine was briefly switched to trimethoprim/sulfamethoxazole because of manufacturer supply shortage and ultimately discontinued because of cost and administration concerns. Because of persistent nausea, vomiting, dysgeusia, and anorexia, flucytosine, fluconazole, azithromycin, and miltefosine were each discontinued, and the patient remained on nitroxoline for a total of 19 months. N/V, nausea and vomiting; TMP/SMX, trimethoprim/sulfamethoxazole; uPCR, universal broad-range PCR amplicon sequencing.

Main Article

1These authors contributed equally to this article.

Page created: June 10, 2026
Page updated: June 23, 2026
Page reviewed: June 23, 2026
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