1. Systemic mycoses

2. General characters Fungi that cause systemic mycoses are:
Histoplasma capsulatum causing histoplasmosis.
Blastomyces dermatidis causing blastomycosis.
Paracoccidiodes brasiliensis causing paracoccidiodomycosis.
Coccidiodes immitis causing coccidiodomycosis.
All these fungi are DIMORPHIC:
In the soil or culture at 25 degree: hyphae with spores.
In the tissues or culture at 37 degree: yeast cells.

3. Infection by these fungi occurs as follows:
These fungi grow as hyphae in the soil.
They release spores into air.
These spores are inhaled by man.
Inside the human body: spores will grow as yeast cells.

4. Epidemiology
Infection by these fungi is restricted to certain areas in the world.
So, SYSTEMIC mycoses is called ENDEMIC mycoses.
Histoplasmosis and blastomycosis are endemic in vast areas that drain into Mississippi river.
Paracoccidiodes brasiliensis is endemic in South America especially Brazil.
Coccidiodes immitis is endemic in Southwestern USA (Arizona, New Mexico, South California) and North Mexico.

5. Pathogenesis
These fungi are acquired by inhalation of spores residing in the soil. (NO PERSON TO PERSON)
Once inhaled, spores will grow as yeast cells that infect the lungs.
Dissemination may occur.
Histoplasma capsulatum (non capsulated ) grows in areas contaminated with birds & bats excreta. So, outbreaks of histoplasmosis occur during clearing chicken coops or spelunking.
Blastomyces dermatidis is isolated from the soil and rotten wood.

6. Histoplasma lesions may heal with calcification of granuloma
Clinical picture
Asymptomatic: the majority of cases.
Pneumonia:
Mild pneumonia with fever & coughing.
A small percent will develop severe pneumonia.
A smaller percent will progress to chronic cavitary pneumonia.
Histoplasma lesions may heal with calcification of granuloma

7. Blastomycosis is the hardest to get & the hardest to have
Disseminated lesion: occurs in immunodeficient patients. Spread occurs to:
Lung.
CNS causing meningitis.
Bone causing lytic lesions.
Skin causing ulcers.
Other organs.
NOTE THAT
Blastomycosis is the hardest to get & the hardest to have
Blastomycosis is the rarest systemic infection. Mostly present as chronic disseminated disease.

8. Blastomycosis

9. Blastomycosis
Skin lesions resulting from the dissemination of the fungus from the lungs

10. Laboratory diagnosis Tissue is the issue
Specimen: BIOPSY from the affected tissue.
Direct microscopic examination of the tissue after staining with PAS (periodic Acid Schiff), silver to see the yeast phase.
Culture on SDA at:
At 25 degree: hyphae with characteristic spores.
It converts to yeast after incubation at 37 degree.

11. Serological diagnosis: detect the antibodies against fungi.
The tests used are:
Complement fixation test.
Immunodiffusion test.
Serological diagnosis of blastomycosis is not reliable because these antigens are:
Poorly defined.
Cross reactive with other fungi.

12. PAS stain showing Histoplasma capsulatum yeast cells in liver specimen

13. Macroconidia and microconidia
Histoplasma capsulatum
Macroconidia and microconidia
Rough-walled macroconidia

14. Blastomycosis
Tissue sections showing large, broad-base, unipolar budding yeast-like cells

15. Blastomyces dermatitidis
One-celled conidia formed on short conidiophores.
Broad based budding and thickened cell walls and globose shape are characteristic of the yeast form of Blastomyces dermatitidis
Differential interference contrast microscopy, potato glucose agar, 25° C
Differential interference contrast microscopy, 37° C

16. COCCIDIOIDOMYCOSIS Disease Properties
Coccidioides immitis causes coccidioidomycosis.
Properties
C. immitis is a dimorphic fungus that exists as a mold in soil and as a spherule in tissue

17. Coccidioides immitis showing typical single-celled, hyaline, rectangular to barrel-shaped, alternate arthroconidia

18. Transmission & Epidemiology Coccidioide
The fungus is endemic in arid regions of the southwestern United States and Latin America.
People who live in Central and Southern California, Arizona, New Mexico, Western Texas, and Northern Mexico.
In soil, it forms hyphae with alternating arthrospores
and empty cells.
Arthrospores are very light and are carried by the wind.
They can be inhaled and infect the lungs.

19. Pathogenesis of Coccidioide
In the lungs, arthrospores form spherules that are large, have a thick, doubly refractive wall, and are filled with endospores.
Upon rupture of the wall, endospores are released
and differentiate to form new spherules.
The organism can spread within a person by direct extension or via the bloodstream.
Granulomatous lesions can occur in virtually any organ but are found primarily in bones and the central nervous system (meningitis)
Dissemination from the lungs to other organs occurs in people who have a defect in cell-mediated immunity.

20. Pathogenesis of Coccidioide
Most people who are infected by C. immitis develop a cell-mediated (delayed hypersensitivity) immune response that restricts the growth of the organism.
One way to determine whether a person has produced adequate cell-mediated immunity to the organism is to do a skin test (see below).
In general, a person who has a positive skin test reaction has developed sufficient immunity to prevent disseminated disease from occurring.
If, at a later time, a person's cellular immunity is suppressed by drugs or disease, disseminated disease can occur.

21. Clinical Findings of Coccidioide
Infection of the lungs is often asymptomatic and is evident only by a positive skin test and the presence of antibodies.
Some infected persons have an influenza like illness with fever and cough.
About. 50% have changes in the lungs (infiltrates, adenopathy, or effusions) as seen on chest x-ray.
10% develop erythema nodosum (see below) or arthralgias.
This syndrome is called "valley fever" or "desert rheumatism"; it tends to subside spontaneously.
Disseminated disease can occur in almost any organ; the meninges, bone, and skin are important sites.

22. Clinical Findings of Coccidioide
The overall incidence of dissemination in persons infected with C. imrnitis is 1%, although the incidence in Filipinos and African Americans is 10 times higher.
Women in the third trimester of pregnancy also have a markedly increased incidence of dissemination.
Erythema nodosum (EN) manifests as red, tender nodules ("desert bumps") on extensor surfaces such as the shins.
It is a delayed (cell-mediated) hypersensitivity response to fungal antigens and thus is an indicator of a good prognosis.

23. Clinical Findings of Coccidioide
There are no organisms in these lesions; they are not a sign of disseminated disease. EN is not specific for coccidioidomycosis; it occurs in other granulomatous diseases, eg, histoplasmosis, tuberculosis, and leprosy.
In infected persons, skin tests with fungal extracts cause at least a 5mm induration 48 hours after injection (delayed hypersensitivity reaction).
Skin tests become positive within 2-4 weeks of infection and remain so for years but are often negative in patients with disseminated disease.

24. Tissue section showing typical endosporulating spherules of C. immitis
Coccidioidomycosis
Tissue section showing typical endosporulating spherules of C. immitis

25. Chronic cutaneous granulomatous lesions of the face, neck and chin
Coccidioidomycosis
Extension of pulmonary coccidioidomycosis showing a large superficial ulcerated lesion
Chronic cutaneous granulomatous lesions of the face, neck and chin

26. Laboratory Diagnosis of Coccidioide
In tissue specimens, spherules are seen microscopically.
Cultures on Sabouraud's agar incubated at 25 °C show hyphae with arthrospores
(Caution: Cultures are highly infectious; precautions against inhaling arthrospores must be taken.)

27. Laboratory Diagnosis of Coccidioide
In serologic tests, [gM and IgG precipitins appear within 2-4 weeks of infection and then decline in subsequent months.
Complement-fixing antibodies occur at low titer initially, but the titer rises greatly if dissemination occurs

28. PARACOCCIDIOIDOMYCOSIS
Paracoccidioides brasiliensis causes paracoccidioidomycosis, also known as South American blastomycosis.

29. Properties of Paracoccidioides
P. brasiliensis is a dimorphic fungus that exists as a mold in soil and as a yeast in tissue.
The yeast is thick walled with multiple buds, in contrast to B. dermatidis, which has a single bud .

30. Transmission & Epidemiology of Paracoccidioides
The spores are inhaled, and early lesions occur in the lungs.
Asymptomatic infection is common.
Alternatively oral mucous membrane lesions, lymph node enlargement, and sometimes dissemination to many organs develop.

31. Paracoccidioidomycosis
Ulcerated lesion on the nasal mucosa
Extensive destruction of facial features
Ulcerated lesion on the pharyngeal mucosa

32. Laboratory Diagnosis of Paracoccidioides
In pus or tissues, yeast cells with multiple buds are seen microscopically.
A specimen cultured for 2-4 weeks may grow typical organisms.
Skin tests are rarely helpful.
Serologic testing shows that when significant antibody titers (by immunodiffusion or complement fixation) are found, active disease is present.

33. Paracoccidioidoes brasiliensis
Multiple, narrow base, budding yeast cells "steering wheels" of P. brasiliensis

34. Paracoccidioidoes brasiliensis
Multiple, narrow base, budding yeast cells "steering wheels" of P. brasiliensis

35. Summary Agent infection Dissemination Drug of choice
Blastomyces dermatitidis
Blastomycosis
Skin and bone
Later nervous system and visceral organs
Amphotericin B
itraconazole
Coccidioides immitis
Coccidioidomycosis
Skin, bones, joints, subcutaneous tissues, and visceral organs
Paracoccidioidoes brasiliensis
Paracoccidioidomycosis
Oro-nasal mucosa
latter spleen, liver, intestine and skin
Amphotericin B + sulfas or azoles
Histoplasma capsulatum
Histoplasmosis
Acute pneumonia (cave disease)
Chronic pneumonia (smoker)
Disseminated (immunocompromised)
Primary cutaneous
(lab accidents)

36. Systemic Mycoses
PARACOCCIDIOIDES
BLASTOMYCES
HISTOPLASMA
COCCIDIOIDE