Cutaneous leishmaniasis
ICD-10 B55.1 · ICD-11 1F54.1

Treatment of American Mucosal Leishmaniasis with Laryngeal or Pharyngeal Disease and Risk of Respiratory Obstruction

Clinical Scenario

This protocol addresses clinically manifest American mucosal leishmaniasis in patients who have laryngeal or pharyngeal involvement and an increased risk for respiratory obstruction, as indicated by symptoms and otolaryngologic or radiologic examination findings.

Key concern: Initiation of antileishmanial therapy in this setting carries a risk of inflammatory reactions that can further compromise the airway. Inpatient monitoring is recommended for these patients.
Why This Situation Requires a Specific Approach

Laryngeal and pharyngeal mucosal disease creates potential for airway compromise that must be anticipated and managed proactively. Clinical assessment — including symptoms alongside otolaryngologic and radiologic findings — guides the determination of obstruction risk and shapes the treatment strategy accordingly.

Treatment Approach (Partial Overview)

Management involves prophylactic corticosteroid therapy administered before and during antileishmanial treatment, combined with systemic antileishmanial therapy. Several antileishmanial options exist — including parenteral agents and an oral alternative — but the choice, sequencing, and full regimen details go beyond what is summarised here.

Full regimen, agent selection, dosing, duration, and clinical decision points are in the structured protocol.

Treatment Goals

The primary goal is clinical cure of the mucosal disease — resolution of mucosal lesions assessed by clinical criteria. Follow-up over at least the first year is important, as the majority of relapses occur within that window.

Instant Access to Structured Evidence-Based Regimens

References

DOI: 10.1093/cid/ciw670

We recommend inpatient monitoring and prophylactic corticosteroid therapy for persons with laryngeal/pharyngeal disease and increased risk for respiratory obstruction, as indicated by symptoms and otolaryngologic/radiologic examinations, because of the potential for inflammatory reactions after initiation of antileishmanial therapy.

The traditional options for ML include treatment with a pentavalent antimonial (SbV) compound or with amphotericin B deoxycholate. More recently, the armamentarium has expanded to include lipid formulations of amphotericin B, as well as the oral agent miltefosine.

Response to antileishmanial treatment of ML typically is assessed by clinical criteria. The majority of relapses occur within the first year, but they may occur later.

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