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The CPT® Code 86732 refers to a laboratory test specifically designed to measure antibodies against mucormycosis, a serious fungal infection caused by mucoromycotina fungi. These fungi are commonly found in various environments, particularly in soil and decaying organic matter such as leaves, wood, fruit, and bread. Mucormycosis can lead to life-threatening infections, particularly in individuals with weakened immune systems or underlying health conditions. The infection can enter the body through inhalation or through breaks in the skin, leading to various clinical manifestations. These manifestations include pulmonary disease, which affects the lungs; rhinocerebral disease, which impacts the sinuses and brain; gastrointestinal disease; cutaneous disease, which involves the skin; and central nervous system disease. Symptoms associated with mucormycosis can vary but often include fever, headache, facial pain, periorbital cellulitis, and cough. In cases of cutaneous disease, patients may present with blisters, ulcers, redness, and swelling. Individuals with uncontrolled diabetes mellitus and those who are immunocompromised are particularly at high risk for developing this infection. The detection of antibodies to mucoromycotina can be accomplished through various laboratory techniques, including enzyme-linked immunosorbent assay (ELISA), immunoblot, and immunodiffusion, which are effective in identifying the immune response to the infection.
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The laboratory test associated with CPT® Code 86732 is indicated for the detection of antibodies to mucormycosis in patients who may be at risk for this serious fungal infection. The following conditions and symptoms warrant the performance of this test:
The procedure for testing antibodies to mucormycosis involves several key steps to ensure accurate results. The following outlines the procedural steps:
Post-procedure care for patients undergoing antibody testing for mucormycosis is generally minimal, as the procedure primarily involves blood collection. Patients may be advised to hydrate adequately and can typically resume normal activities immediately following the test. However, if the test results indicate the presence of antibodies, further clinical evaluation and management may be necessary, especially for those exhibiting symptoms or who are at high risk for mucormycosis. It is essential for healthcare providers to discuss the implications of the test results with the patient and determine any necessary follow-up actions or treatments based on the findings.
| Short Descr | MUCORMYCOSIS ANTIBODY | Medium Descr | ANTIBODY MUCORMYCOSIS | Long Descr | Antibody; mucormycosis | Status Code | Statutory Exclusion (from MPFS, may be paid under other methodologies) | Global Days | XXX - Global Concept Does Not Apply | PC/TC Indicator (26, TC) | 9 - Not Applicable | Multiple Procedures (51) | 9 - Concept does not apply. | Bilateral Surgery (50) | 9 - Concept does not apply. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 9 - Concept does not apply. | Co-Surgeons (62) | 9 - Concept does not apply. | Team Surgery (66) | 9 - Concept does not apply. | Diagnostic Imaging Family | 99 - Concept Does Not Apply | CLIA Waived (QW) | No | APC Status Indicator | Conditionally packaged laboratory tests | Type of Service (TOS) | 5 - Diagnostic Laboratory | Berenson-Eggers TOS (BETOS) | T1H - Lab tests - other (non-Medicare fee schedule) | MUE | 2 | CCS Clinical Classification | 235 - Other Laboratory |
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| 1993-01-01 | Added | First appearance in code book in 1993. |
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