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Mucormycosis

 

Mucormycosis

Mucormycosis
Classification and external resources
10 9 DiseasesDB MedlinePlus MeSH D009091

Mucormycosis is any fungal infection caused by fungi in the order Mucorales.[1]:328 Generally, species in the Mucor, Rhizopus, Absidia, and Cunninghamella genera are most often implicated.[2][3] This disease is often characterized by hyphae growing in and around vessels.[4]

"Mucormycosis" and "zygomycosis" are sometimes used interchangeably.[5] However, zygomycota has been identified as polyphyletic, and is not included in modern fungal classification systems.

Also, while Zygomycosis includes Entomophthorales, mucormycosis excludes this group.

Signs and symptoms

Mucormycosis frequently involves the sinuses, brain, or lungs as the areas of infection. While oral or cerebral mucormycosis are the most common types of the disease, this infection can also manifest in the gastrointestinal tract, skin, and in other organ systems.[6] In rare cases, the maxilla may be affected by mucormycosis.[7] The rich vascularity of maxillofacial areas usually prevents fungal infections, although more virulent fungi, such as those responsible for mucormycosis, can often overcome this difficulty.[7]

There are several key signs which point towards mucormycosis. One such sign is fungal invasion into the vascular network which results in thrombosis and death of surrounding tissue by loss of blood supply.[8] If the disease involves the brain then symptoms may include a one-sided headache behind the eyes, facial pain, fevers, nasal stuffiness that progresses to black discharge, and acute sinusitis along with swelling of the eye.[9] Affected skin may appear relatively normal during the earliest stages of infection. This skin quickly progresses to an erythemic (reddening, occasionally with edema) stage, before eventually turning black due to necrosis.[8] In other forms of mucormycosis, such as pulmonary, cutaneous, or disseminated mucormycosis, symptoms may also include dyspnea (difficulty breathing), and persistent cough; in cases of necrosis, symptoms include nausea and vomiting, coughing blood, and abdominal pain.[6][9]

Diagnosis

As swabs of tissue or discharge are generally unreliable, the diagnosis of Mucormycosis tends to be established by a biopsy specimen of the involved tissue.

Treatment

If mucormycosis is suspected, prompt amphotericin B therapy should be administered due to the rapid spread and mortality rate of the disease. Amphotericin B (which works by damaging the cell walls of the fungi) is usually administered for a further 4–6 weeks after initial therapy begins to ensure eradication of the infection. Posaconazole has been shown to be effective against mucormycosis, perhaps more so than amphotericin B, but has not yet replaced it as the standard of care.

Liposomal drug is also available in the market, but this drug is very expensive.

After administration of either amphotericin B or Posaconazole, surgical removal of the "fungus ball" is indicated. The disease must be monitored carefully for any signs of reemergence.[6][10]

Surgical therapy can be very drastic, and in some cases of Rhinocerebral disease removal of infected brain tissue may be required. In some cases surgery may be disfiguring because it may involve removal of the palate, nasal cavity, or eye structures.[9] Surgery may be extended to more than one operation.[6] It has been hypothesised that hyperbaric oxygen may be beneficial as an adjunctive therapy because higher oxygen pressure increases the ability of neutrophils to kill the organism.[8]

Prognosis

In most cases, the prognosis of mucormycosis is poor and has varied mortality rates depending on its form and severity. In the rhinocerebral form, the mortality rate is between 30% and 70%, whereas disseminated mucormycosis presents with the highest mortality rate in an otherwise healthy patient, with a mortality rate of up to 90%.[8] Patients with AIDS have a mortality rate of almost 100%.[10] Possible complications of mucormycosis include the partial loss of neurological function, blindness and clotting of brain or lung vessels.[9]

Epidemiology

Mucormycosis is a very rare infection, and as such it is hard to note histories of patients and incidence of the infection.[6] However, one American oncology center revealed that mucormycosis was found in 0.7% of autopsies and roughly 20 patients per every 100,000 admissions to that center.[10] In the United States, mucormycosis was most commonly found in rhinocerebral form, almost always with hyperglycemia and metabolic acidosis.[11] In most cases the patient is immunocompromised, although rare cases have occurred in which the subject was not; these are usually due to a traumatic inoculation of fungal spores. Internationally, mucormycosis was found in 1% of patients with acute leukemia in an Italian review.[6]

A cluster of infections occurred in the wake of the 2011 Joplin tornado. As of July 19, a total of 18 suspected cases of cutaneous mucormycosis had been identified, of which 13 were confirmed. A confirmed case was defined as 1) necrotizing soft-tissue infection requiring antifungal treatment or surgical debridement in a person injured in the tornado, 2) with illness onset on or after May 22, and 3) positive fungal culture or histopathology and genetic sequencing consistent with a Mucormycete. No additional cases have been reported since June 17. Ten patients required admission to an intensive-care unit, and five died.[12]

Cutaneous mucormycosis has been reported after previous natural disasters; however, this is the first known cluster occurring after a tornado. None of the infections were found in persons cleaning up debris; instead it is believed transmission occurred through penetrating injuries inflicted by contaminated objects (e.g. splinters from a woodpile). Health-care providers should consider environmental fungi as potential causes of necrotizing soft-tissue infections in patients injured during tornados and initiate early treatment for suspected infections.[13]

Predisposing factors for mucormycosis include AIDS, diabetes, malignancies such as lymphomas, renal failure, organ transplant, long term corticosteroid and immunosuppressive therapy, cirrhosis energy malnutrition,[6][7] and Deferoxamine therapy. Despite this, however, there have been cases of mucormycosis reported with no apparent predisposing factors present.[11]

Notable people affected

Joplin outbreak publication: NEJM 2012 Dec 6; 367:2214

References

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