Zygomycosis

Summary about Disease


Zygomycosis is a rare but serious fungal infection caused by a group of molds called zygomycetes. These molds live in the environment, particularly in decaying organic matter like soil, leaves, and rotting food. Zygomycosis most commonly affects people with weakened immune systems, such as those with uncontrolled diabetes, cancer, organ transplants, or those taking immunosuppressant medications. The infection can affect various parts of the body, including the sinuses, lungs, skin, and brain. It is a life-threatening infection that requires prompt diagnosis and treatment.

Symptoms


Symptoms of zygomycosis vary depending on the location of the infection:

Rhino-orbital-cerebral (sinus and brain) zygomycosis: Facial swelling, headache, nasal congestion, sinus pain, fever, blurred vision, double vision, eye swelling, drooping eyelids, tissue death (black lesions) in the nasal area or palate.

Pulmonary (lung) zygomycosis: Fever, cough, chest pain, shortness of breath, coughing up blood.

Cutaneous (skin) zygomycosis: Painful, rapidly spreading skin ulcers or blisters that may turn black, swelling, warmth, redness around the affected area.

Gastrointestinal zygomycosis: Abdominal pain, vomiting, gastrointestinal bleeding.

Disseminated zygomycosis: Occurs when the infection spreads through the bloodstream to multiple organs. Symptoms vary widely depending on the organs involved.

Causes


Zygomycosis is caused by molds belonging to the class Zygomycetes. Common genera include Rhizopus, *Mucor*, *Lichtheimia* (formerly *Absidia*), *Cunninghamella*, and *Apophysomyces*. Infection occurs when the fungal spores are inhaled, ingested, or enter the body through a break in the skin. People with weakened immune systems are more susceptible to infection because their bodies are less able to fight off the fungus. Risk factors include:

Uncontrolled diabetes (especially diabetic ketoacidosis)

Cancer, especially blood cancers

Organ transplant

Stem cell transplant

Iron overload (hemochromatosis)

Neutropenia (low white blood cell count)

Use of corticosteroids or other immunosuppressant medications

Trauma, burns, or surgery

Medicine Used


4. Medicine used The primary medications used to treat zygomycosis are antifungal drugs, mainly from the polyene and azole classes:

Amphotericin B: This is often the first-line treatment, particularly liposomal amphotericin B, which is less toxic than the traditional formulation.

Isavuconazole: This azole antifungal is often used as a primary treatment option and has good tissue penetration.

Posaconazole: Another azole antifungal that can be used, especially in those who cannot tolerate amphotericin B or isavuconazole. In addition to antifungal medications, surgery is often necessary to remove infected tissue.

Is Communicable


Zygomycosis is not communicable. It is not spread from person to person or from animals to people. The infection occurs from direct contact with the fungal spores in the environment.

Precautions


For individuals at high risk (immunocompromised), the following precautions can help reduce the risk of zygomycosis:

Control underlying medical conditions: Manage diabetes effectively, address iron overload, and optimize immune function where possible.

Avoid construction sites and dusty environments: Zygomycetes are commonly found in soil and dust.

Good hygiene: Practice thorough handwashing, especially after exposure to soil or outdoor environments.

Protect skin wounds: Clean and cover any open wounds, burns, or surgical incisions.

Monitor for early signs of infection: Be vigilant for symptoms such as facial swelling, sinus pain, or skin lesions, and seek medical attention promptly.

Use air filtration: HEPA filters may reduce the number of fungal spores in the air, especially in high-risk environments like hospitals.

How long does an outbreak last?


There is no defined "outbreak" duration for zygomycosis in the traditional sense, as it is not contagious. The duration of the infection itself depends on the following:

Early diagnosis and treatment: Prompt treatment is crucial for better outcomes.

Severity of the infection: More extensive infections will take longer to resolve.

Underlying health status: Individuals with severely compromised immune systems may have a prolonged and challenging course.

Response to antifungal therapy: Some fungal strains may be more resistant to certain medications.

Surgical intervention: Successful surgical removal of infected tissue can shorten the course of the infection. Treatment may last for weeks or months, and some individuals may require long-term maintenance antifungal therapy to prevent recurrence.

How is it diagnosed?


Diagnosis of zygomycosis typically involves a combination of the following:

Clinical Evaluation: Assessing symptoms, risk factors, and medical history.

Imaging Studies: CT scans or MRI scans of the affected areas (sinuses, lungs, brain) to identify signs of infection.

Tissue Biopsy: A sample of infected tissue is taken for microscopic examination and culture to identify the specific fungus. This is the gold standard for diagnosis.

Fungal Culture: Growing the fungus from the tissue sample in a laboratory to confirm the diagnosis and identify the specific species.

Molecular Tests: PCR (polymerase chain reaction) tests can be used to detect fungal DNA in tissue samples.

Blood Tests: Blood tests may be done to assess overall health, immune function, and to rule out other possible infections. Beta-D-glucan assay can be used but is often not specific and is not usually helpful.

Timeline of Symptoms


The timeline of symptoms can vary widely depending on the location of the infection and the individual's immune status. However, zygomycosis is generally a rapidly progressing infection.

Initial Stage (Days to Weeks):

Symptoms may start subtly, such as mild sinus pain, nasal congestion, or a small skin lesion.

Fever may be present.

Progression (Days to Weeks):

Symptoms worsen rapidly.

Facial swelling, headache, blurred vision, or eye pain may develop in rhino-orbital-cerebral zygomycosis.

Cough, chest pain, and shortness of breath may occur in pulmonary zygomycosis.

Skin lesions may rapidly enlarge and become necrotic (blackened).

Advanced Stage (Days to Weeks):

Severe symptoms such as mental status changes, seizures, or coma may occur in cases of brain involvement.

Dissemination to other organs can lead to a variety of symptoms.

Without prompt treatment, the infection can be fatal.

Important Considerations


Early diagnosis is critical: Zygomycosis progresses rapidly, and early treatment significantly improves the chances of survival.

Aggressive treatment is necessary: Treatment usually involves a combination of antifungal medications and surgery.

Underlying conditions must be managed: Controlling diabetes, correcting iron overload, and optimizing immune function are essential components of treatment.

Multidisciplinary approach is often required: Management often involves infectious disease specialists, surgeons, hematologists/oncologists, and other specialists.

Prognosis is guarded: Even with treatment, the mortality rate for zygomycosis remains high, especially in individuals with severely compromised immune systems.

Consider drug toxicities: Amphotericin B and other antifungal medications can have significant side effects, requiring careful monitoring.

Long-term follow-up is needed: Recurrence of zygomycosis can occur, so long-term monitoring and potential maintenance antifungal therapy may be necessary.

Zygomycosis is a medical emergency: Any suspected case should be evaluated and treated urgently.