Apophysomyces

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Apophysomyces[edit | edit source]

Microscopic image of Apophysomyces

Apophysomyces is a genus of filamentous fungi belonging to the order Mucorales. It is commonly found in soil, decaying organic matter, and various environmental sources. This genus is known for causing severe infections in humans, particularly in immunocompromised individuals.

Taxonomy[edit | edit source]

Apophysomyces was first described by G.L. Hoffman in 1979. It belongs to the family Mucoraceae, which comprises several other genera of fungi. The genus name "Apophysomyces" is derived from the Greek words "apophysis" meaning "outgrowth" and "myces" meaning "fungus," referring to the characteristic outgrowths observed in the fungal colonies.

Morphology[edit | edit source]

Apophysomyces species are characterized by their filamentous hyphae, which are typically septate and branched. The hyphae can grow rapidly and invade various tissues, leading to invasive infections. The colonies of Apophysomyces are usually cottony or woolly in texture and can vary in color from white to gray or brown.

Pathogenicity[edit | edit source]

Apophysomyces species are opportunistic pathogens that can cause a range of infections in humans. The most common clinical manifestation is cutaneous or subcutaneous infection, often associated with trauma or surgical wounds. However, they can also cause invasive infections in the sinuses, lungs, brain, and other organs.

In immunocompromised individuals, such as those with poorly controlled diabetes, organ transplant recipients, or patients with hematological malignancies, Apophysomyces infections can be particularly severe and life-threatening. The fungus can invade blood vessels, leading to tissue necrosis and potential dissemination to other organs.

Clinical Presentation[edit | edit source]

Cutaneous or subcutaneous infections caused by Apophysomyces typically present as rapidly progressing, necrotic ulcers with surrounding erythema and edema. The affected area may be painful and exhibit black eschar formation. Invasive infections in other organs can manifest as sinusitis, pneumonia, or brain abscesses, depending on the site of infection.

Diagnosis[edit | edit source]

The diagnosis of Apophysomyces infections can be challenging, as it requires a combination of clinical, radiological, and laboratory findings. Microscopic examination of infected tissues or cultures can reveal the characteristic hyphae and sporangia of the fungus. Molecular techniques, such as polymerase chain reaction (PCR), can also be employed for accurate identification.

Treatment[edit | edit source]

The management of Apophysomyces infections involves a multidisciplinary approach, including surgical debridement of infected tissues and antifungal therapy. Surgical intervention is crucial to remove necrotic tissue and improve the penetration of antifungal agents. The choice of antifungal drugs depends on the susceptibility profile of the specific Apophysomyces isolate, but commonly used agents include amphotericin B and posaconazole.

Prevention[edit | edit source]

Preventing Apophysomyces infections primarily involves maintaining good hygiene practices and avoiding exposure to contaminated environments. Individuals with compromised immune systems should take extra precautions to minimize the risk of infection. Prompt and appropriate wound care is essential, especially in individuals with diabetes or other conditions that impair wound healing.

References[edit | edit source]


See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD