Thursday, 30 April 2015

Fungal infection in lungs COPD ( Candida)

Fungal infection in lungs (Candida)

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I was diagnosed with COPD (asthma/emphasema) several years ago. Also have had to endure two very painful surgeries on this stubborn Hiatal Hernia that returns defiantly. My stomach surgeon used pig skin to patch my diaphram to ensure that the Hernia woguld not return. Well, here I am 1 1/2 years later with the Hernia returned. I have been taken to the ER three times in the last three months with an unbearable pain in my left back flank and difficulty breathing. I was diagnosed first two times with pneumonia caused by the hernia. This last time in July the ER doc said either Cancer or Pneumonia. After going to my Lung doc he wanted to do a lung cleanse and biopsy to make sure it was not cancer.
The biopsy came back as Candida (yeast infection) in my lungs. After having so many bouts of my Air way being completely cut off and many bouts of pneumonia being blamed on this very painful and hard to deal with Hernia for so many years, I am confused. What have I really had going on in my lungs all these years? Did the pig skin cause the yeast infection? I feel very ill all the time. The hernia does cause very painful Acid Reflux and very difficult attempts to eat, hard to swallow and loss of appitite. What doctor do I go to? I am so tired of being sick. My stomach surgeon said it is way too dangerous to go back in for Hernia repair. I would have to go to Southwestern Medical School for any studies or surgeries. Is this hernia going to be the death of me or has it all along been out of control fungus in my digestive track causing so much misery? I am very tired and deppressed. My brother just passed away with Lung Cancer last year. That also has me concerned. Why can I not get any relief? I do pray to God to PLEASE just take me home often. That is how deppressing my situation has become. I have also been diagnosed with Fibromyalgia, Osteopenia, Rhumatoid Arthitis, anemia, High blood pressure, High cholesterol, and very low Vitamin D. I am on 13 different scripts. I am sure I am missing something. Any advise would be appreciated. I have been placed in a behavioral hospital for an attempt to end my life by taking a massive amount of Soma. I want a reason to live. That should be my boys and my lovely grandchildren. But I am literally so exhausted from so much pain and discomfort from whatever is really wrong with me. [b:c67369f5c3]Please Help!!! And Please forgive me for being soo dramatic.[/b:c67369f5c3] It's so hard to enjoy life.
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  • taracap1979 ★1
    taracap1979 lorrie4dad •
    Hi, I hope this email finds you in. Better state than you were when you wrote it.  I am so sorry to hear all you have gone through and the pain you have endured.  I was diagnosed with multiple sclerosis 8 years ago.  The symptoms that I have been linking to my M.S, seem to actually be from a candida overgrowth in my body!  The tiredness, lack of energy p, depression, brain fog...  Either way it's a long story but I just wanted to tell you that you would look into a holistic approach.  There is something called coiling that a woman here in the NY is doing for me.  I have only done two treatments but I will tell you that I literally have candida being expelled from my body!!!  They say when there is a bad overgrowth it will take over your whole system!  Also and this is very important, you must stop feeding the fungi in your body!  I am on a NO sugar, NO simple carbs, NO dairy diet.  It's hard but I feel SOOOOOO much better.  I am obviously not a doctor but this is helping me a lot and maybe you should look into it as an option.  Good luck with everything!
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  • alva0000 ★1
    alva0000 lorrie4dad •
    Hello, sorry I came across this letter so late..maybe this info can help you..your main objective should be to remove yeast from your entire body...stop eating sugar, flours, alcohol immdiately...take large amounts of probiotics, and yogurt with the live cultures in it . Eat plenty of fish, but no red meat...this should help significantly..if you take anti biotics that makes your yeast count higher...blessings to you, and so sorry you have gone through this...also, yeast causes fibromyalga also..
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Candida and lung cancer

The Candida Expert

Candida and Cancer

11 13 12'
Written by Jeff McCombs
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Candida and Cancer have been associated through many studies and clinical observations throughout the years. Fungal candida has been identified as the leading cause of deaths due to sepsis in hospital settings, but can occur in anyone. Severe suppression of the immune system leads to an increased risk of death, while less severe cases can lead to diabetes, asthma, allergies, and over 100 symptoms and conditions. Candidemia, candida in the blood, remains a major cause of morbidity and mortality in the health care setting.
In the oral cavity, candidiasis is the most frequent opportunistic fungal infection and is associated with pre-cancer and cancers. For those people who do have cancer, radiation and chemotherapy are the two main options for treatment put forth by the medical field. Researchers at the Regional Cancer Institute “revealed the presence of C. albicans fungi as most significant oral cavity pathogens in radiotherapy and radio chemotherapy cases.” Here we see that candida can cause cancer and medical treatments for cancer can cause candida, seeming to create a vicious cycle.
One of the means by which candida promotes cancers is through inflammation. Inflammation is one of the common links to all cancers and candida has been shown to promote inflammation in the body, and inflammation further promotes candida. One of the pathways that has been recently discovered by cancer researchers is via the release of pro-inflammatory IL-15 in response to chronic infections such as candida.
Another pathway is through blood sugar imbalances. Candida can cause blood sugar imbalances and these imbalances, high and low, are associated with causing immune system suppression. Immune system suppression is a part of all cancers. The vast majority of IFIs (Invasive Fungal Infections) in the ICU are due to Candida spp. The incidence of invasive candidiasis (IC) has increased over recent decades, especially in the ICU. Surgeries can cause immunosuppression and are typically associated with a higher incidence of candida infections. Most cancer patients lack the appropriate immune responses and candida increases immune system dysfunction.
Candida has been shown to be involved in lung cancer, which is one of the most common cancers worldwide and a leading cause of death. Lung cancer is the most common cancer worldwide, with “1.35 million incident cases annually, and consists one of the leading causes of mortality worldwide.”
One medical doctor, Dr. Simoncini, believes that cancer is caused by the fungal form of candida. This of course leaves out many other possible known causes such as chemicals and heavy metals, but it does align itself to a growing body of research on candida and cancers.
It’s important to note that both antibiotics and candida are associated with causing cancers, and antibiotic use is the major cause of fungal candida. Given this link, it is likely that candida plays a causative and supportive role in creating cancers. The more antibiotic exposure one has, the greater the likelihood of contracting cancer.
Reversing the effects of antibiotics, boosting immune system responses, and restoring balance to the flora of the body should be a part of everyone’s approach to addressing imbalances that can lead to cancer.
Take back your health.   Live the life you create.   Dr. McCombs Candida Plan.
Dr. Jeffrey S. McCombs, DC, is founder of the McCombs Center for Health, the Candida Plan, the Candida Library, and author of Lifeforce and The Everything Candida Diet Book.
https://twitter.com/DrMcCombs
https://www.facebook.com/groups/candidaplan/
Candida and Cancer
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Jeff McCombs

Founder / CEO at McCombs Center For Health
Dr. Jeffrey S. McCombs, DC, is a third generation graduate of Palmer College of Chiropractic (1984). He is licensed in the states of California, Illinois, and Arizona. He is a member of the California and Illinois Chiropractic Associations, the International Association for Specialized Kinesiologists, and the American Holistic Health Association. Dr. McCombs developed his Candida Plan which is a detoxification and dietary plan that counters the detrimental effects of antibiotics and reestablishes the normal body flora, detoxification pathways, and regeneration cycles of a vital, youthful, and healthy body. Connect on GooCandida and lung cancer
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Blastomycosis

Blastomycosis (also known as "North American blastomycosis", "Blastomycetic dermatitis", and "Gilchrist's disease"[2]) is a fungal infection of humans and other animals, notably dogs and occasionally cats, caused by the organism Blastomyces dermatitidis. Endemic to portions of North America, blastomycosis causes clinical symptoms similar to histoplasmosis.[3] The disease occurs in several endemic areas the most important of which is in eastern North America, particularly in the western and northern periphery of the Great Lakes Basin, extending eastward along the south shore of the St. Lawrence River Valley and southward in the territory spanned by the central Appalachian Mountains in the east, to the Mississippi River Valley in the west. Sporadic cases have been reported in continental Africa,[4] the Arabian Peninsula and the Indian subcontinent.


History[edit]

Blastomycosis was first described by Thomas Casper Gilchrist[5] in 1894 and sometimes goes by the eponym Gilchrist's disease.[6] It is also sometimes referred to as Chicago Disease.

Causative agent[edit]

Blastomycosis is caused by the dimorphic microfungus Blastomyces dermatitidis, a member of the phylum Ascomycota in the family Ajellomycetaceae. It has been recognised as the asexual state of Ajellomyces dermatitidis. In endemic areas, the fungus lives in soil and rotten wood near lakes and rivers. Although it has never been directly observed growing in nature, it is thought to grow there as a cottony white mold, similar to the growth seen in artificial culture at 25 °C. The moist, acidic soil in the surrounding woodland harbors the fungus.

Spectrum of disease[edit]

Blastomycosis manifests as a primary lung infection in about 70% of cases.[7] The onset is relatively slow and symptoms are suggestive of pneumonia, often leading to initial treatment with antibacterials. Occasionally, if a lesion is seen on X-ray in a cigarette smoker, the disease may be misdiagnosed as carcinoma, leading to swift excision of the pulmonary lobe involved. Upper lung lobes are involved somewhat more frequently than lower lobes.[7] If untreated, many cases progress over a period of months to years to become disseminated blastomycosis. In these cases, the large Blastomyces yeast cells translocate from the lungs and are trapped in capillary beds elsewhere in the body, where they cause lesions. The skin is the most common organ affected, being the site of lesions in approximately 60% of cases.[7] The signature image of blastomycosis in textbooks is the indolent, verrucous or ulcerated dermal lesion seen in disseminated disease. Osteomyelitis is also common (12–60% of cases). Other recurring sites of dissemination are the genitourinary tract (kidney, prostate, epididymis; collectively ca. 25% of cases) and the brain (3–10% of cases).[7]
An uncommon but very dangerous type of primary blastomycosis manifests as acute respiratory distress syndrome (ARDS); for example, this was seen in 9 of 72 blastomycosis cases studied in northeast Tennessee.[8] Such cases may follow massive exposure, e.g., during brush clearing operations. The fatality rate in the ARDS cases in the Tennessee study was 89%, while in non-ARDS cases of pulmonary blastomycosis, the fatality rate was 10%.
Blastomycosis also affects an indefinitely broad range of mammalian hosts, and dogs in particular are a highly vulnerable sentinel species.[7] They generally suffer a disease that begins with acute respiratory symptoms and rapidly progresses to death. Cats are the animals next most frequently detected as infected.[9]

Pathogenesis[edit]

Large, broadly-based budding yeast cells characteristic of Blastomyces dermatitidis in a GMS-stained biopsy section from a human leg.
Inhaled conidia of B. dermatitidis are phagocytosed by neutrophils and macrophages in alveoli. Some of these escape phagocytosis and transform into yeast phase rapidly. Having thick walls, these are resistant to phagocytosis and express glycoprotein, BAD-1, which is a virulence factor as well as an epitope. In lung tissue, they multiply and may disseminate through blood and lymphatics to other organs, including the skin, bone, genitourinary tract, and brain. The incubation period is 30 to 100 days, although infection can be asymptomatic.

Signs and symptoms[edit]

Blastomycosis can present in one of the following ways:
  • a flu-like illness with fever, chills, arthralgia (joint pain), myalgia (muscle pain), headache, and a nonproductive cough which resolves within days.
  • an acute illness resembling bacterial pneumonia, with symptoms of high fever, chills, a productive cough, and pleuritic chest pain.
  • a chronic illness that mimics tuberculosis or lung cancer, with symptoms of low-grade fever, a productive cough, night sweats, and weight loss.
  • a fast, progressive, and severe disease that manifests as ARDS, with fever, shortness of breath, tachypnea, hypoxemia, and diffuse pulmonary infiltrates.
  • skin lesions, usually asymptomatic, can be verrucous (wart-like) or ulcerated with small pustules at the margins.
  • bone lytic lesions can cause bone or joint pain.
  • prostatitis may be asymptomatic or may cause pain on urinating.
  • laryngeal involvement causes hoarseness.
  • 40% immunocompromised individuals have CNS involvement and present as brain abscess, epidural abscess or meningitis.

Diagnosis[edit]

Once suspected, the diagnosis of blastomycosis can usually be confirmed by demonstration of the characteristic broad based budding organisms in sputum or tissues by KOH prep, cytology, or histology.[10] Tissue biopsy of skin or other organs may be required in order to diagnose extra-pulmonary disease. Blastomycosis is histologically associated with granulomatous nodules. Commercially available urine antigen testing appears to be quite sensitive in suggesting the diagnosis in cases where the organism is not readily detected. While culture of the organism remains the definitive diagnostic standard, its slow growing nature can lead to delays in treatment of up to several weeks. However, sometimes blood and sputum cultures may not detect blastomycosis.

Treatment[edit]

Itraconazole given orally is the treatment of choice for most forms of the disease. Ketoconazole may also be used. Cure rates are high, and the treatment over a period of months is usually well tolerated. Amphotericin B is considerably more toxic, and is usually reserved for immunocompromised patients who are critically ill and those with central nervous system disease. Patients who cannot tolerate deoxycholate formulation of Amphotericin B can be given lipid formulations. Fluconazole has excellent CNS penetration and is useful where there is CNS involvement after initial treatment with Amphotericin B.

Prognosis[edit]

Mortality rate in treated cases
  • 0-2% in treated cases among immunocompetent patients
  • 29% in immunocompromised patients
  • 40% in the subgroup of patients with AIDS
  • 68% in patients presenting as acute respiratory distress syndrome (ARDS)

Epidemiology[edit]

Distribution of blastomycosis in North America based on the map given by Kwon-Chung and Bennett,[7] with modifications made according to case reports from a series of additional sources.[11][12][13][14][15][16][17]
Incidences in most endemic areas are circa 0.5 per 100,000 population, with occasional local areas attaining as high as 12 per 100,000.[7][18][19][20] Most Canadian data fit this picture. In Ontario, Canada, considering both endemic and non-endemic areas, the overall incidence is around 0.3 cases per 100,000; northern Ontario, mostly endemic, has 2.44 per 100,000.[15] Manitoba is calculated at 0.62 cases per 100,000.[11] Remarkably higher incidences were shown for the Kenora, Ontario region: 117 per 100,000 overall, with aboriginal reserve communities experiencing 404.9 per 100,000.[12] In the United States, the incidence of blastomycosis is similarly high in hyperendemic areas. For example, the city of Eagle River, Vilas County, Wisconsin, which has an incidence rate of 101.3 per 100,000; the county as a whole has been shown in two successive studies to have an incidence of ca. 40 cases per 100,000.[21] An incidence of 277 per 100,000 was roughly calculated based on 9 cases seen in a Wisconsin aboriginal reservation during a time in which extensive excavation was done for new housing construction.[22] The new case rates are greater in northern states such as Wisconsin, where from 1986 to 1995 there were 1.4 cases per 100,000 people.[23]
The study of outbreaks as well as trends in individual cases of blastomycosis has clarified a number of important matters. Some of these relate to the ongoing effort to understand the source of infectious inoculum of this species, while others relate to which groups of people are especially likely to become infected. Human blastomycosis is primarily associated with forested areas and open watersheds;[7][24][25][26] It primarily affects otherwise healthy, vigorous people, mostly middle-aged,[27] who acquire the disease while working or undertaking recreational activities in sites conventionally considered clean, healthy and in many cases beautiful.[7][18] Repeatedly associated activities include hunting, especially raccoon hunting,[28] where accompanying dogs also tend to be affected, as well as working with wood or plant material in forested or riparian areas,[7][29] involvement in forestry in highly endemic areas,[30] excavation,[21] fishing[27][31] and possibly gardening and trapping.[12][21]

Urban infections[edit]

There is also a developing profile of urban and other domestic blastomycosis cases, beginning with an outbreak tentatively attributed to construction dust in Westmont, Illinois.[32] The city of Rockford, Illinois, was also documented as a hyperendemic area based on incidence rates as high as 6.67 per 100,000 population for some areas of the city. Though proximity to open watersheds was linked to incidence in some areas,[26] suggesting that outdoor activity within the city may be connected to many cases, there is also an increasing body of evidence that even the interiors of buildings may be risk areas. An early case concerned a prisoner who was confined to prison during the whole of his likely blastomycotic incubation period.[33] An epidemiological survey found that although many patients who contracted blastomycosis had engaged in fishing, hunting, gardening, outdoor work and excavation, the most strongly linked association in patients was living or visiting near waterways.[31] Based on a similar finding in a Louisiana study, it has been suggested that place of residence might be the most important single factor in blastomycosis epidemiology in north central Wisconsin.[34] Follow-up epidemiological and case studies indicated that clusters of cases were often associated with particular domiciles, often spread out over a period of years, and that there were uncommon but regularly occurring cases in which pets kept mostly or entirely indoors, in particular cats, contracted blastomycosis.[9][35] The occurrence of blastomycosis, then, is an issue strongly linked to housing and domestic circumstances.

Seasonal trends[edit]

Seasonality and weather also appear to be linked to contraction of blastomycosis. Many studies have suggested an association between blastomycosis contraction and cool to moderately warm, moist periods of the spring and autumn[7][12][36] or, in relatively warm winter areas.[37] However, the entire summer or a known summer exposure date is included in the association in some studies.[27][38] Occasional studies fail to detect a seasonal link.[39] In terms of weather, both unusually dry weather[40] and unusually moist weather[41] have been cited. The seemingly contradictory data can most likely be reconciled by proposing that B. dermatitidis prospers in its natural habitats in times of moisture and moderate warmth, but that inoculum formed during these periods remains alive for some time and can be released into the air by subsequent dust formation under dry conditions. Indeed, dust per se or construction potentially linked to dust has been associated with several outbreaks[8][32][42] The data, then, tend to link blastomycosis to all weather, climate and atmospheric conditions except freezing weather, periods of snow cover, and extended periods of hot, dry summer weather in which soil is not agitated.

Gender bias[edit]

Sex is another factor inconstantly linked to contraction of blastomycosis: though many studies show more men than women affected,[7][15] some show no sex-related bias.[12][31] As mentioned above, most cases are in middle aged adults, but all age groups are affected, and cases in children are not uncommon.[7][12][15]

Ethnic populations[edit]

Ethnic group or race is frequently investigated in epidemiological studies of blastomycosis, but is potentially profoundly conflicted by differences in residence and in quality and accessibility of medical care, factors that have not been stringently controlled for to date. In the USA, a disproportionately high incidence and/or mortality rate is occasionally shown for blacks;[19][20][43][44] whereas aboriginals in Canada are disproportionately linked to blastomycosis in some studies[12][45] but not others.[11] Incidence in aboriginal children may be unusually high.[12] The Canadian data in some areas may be confounded or explained by the tendency to establish aboriginal communities in wooded, riparian, northern areas corresponding to the core habitat of B. dermatitidis, often with known B. dermatitidis habitats such as woodpiles and beaver constructions in the near vicinity.

Communicability[edit]

There are a very small number of cases of human-to-human transmission of B. dermatitidis related to dermal contact[46] or sexual transmission of disseminated blastomycosis of the genital tract among spouses.[7]

    Additional images[edit]

    • Budding yeasts in cytoplasm of giant cells at arrows. Broad-based budding and double countoured cell wall seen in the giant cell in the center is characteristic of Blastomyces dermatiditis.
    • Granuloma with early suppuration. Fungal organisms difficult to recognize at this low magnification.
    • Large yeast-like fungi seen within giant cells at arrows.
    • Nodular skin lesions of blastomycosis, one of which is a bullous lesion on top of a nodule.

    See also[edit]

    References[edit]

    1. ^ "South American Blastomycosis: Overview - eMedicine Dermatology". Retrieved 2009-03-08. 
    2. ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. p. 319. ISBN 0-7216-2921-0. 
    3. ^ Ryan KJ; Ray CG (editors) (2004). Sherris Medical Microbiology (4th ed.). McGraw Hill. pp. 676–8. ISBN 0-8385-8529-9. 
    4. ^ Alvarez G, Burns B, Desjardins M, Salahudeen S, AlRashidi F, Cameron D (2006). "Blastomycosis in a young African man presenting with a pleural effusion". Can Respir J 13 (8): 441–4. PMC 2683332. PMID 17149463. 
    5. ^ "Thomas Caspar Gilchrist (www.whonamedit.com)". Retrieved 2008-12-10. 
    6. ^ "Gilchrist's disease (www.whonamedit.com)". Retrieved 2008-12-10. 
    7. ^ a b c d e f g h i j k l m n Kwon-Chung, K.J., Bennett, J.E.; Bennett, John E. (1992). Medical mycology. Philadelphia: Lea & Febiger. ISBN 978-0812114638. 
    8. ^ a b Vasquez, JE; Mehta, JB; Agrawal, R; Sarubbi, FA (1998). "Blastomycosis in northeast Tennessee.". Chest 114 (2): 436–43. doi:10.1378/chest.114.2.436. PMID 9726727. 
    9. ^ a b Blondin, N; Baumgardner, DJ; Moore, GE; Glickman, LT (2007). "Blastomycosis in indoor cats: suburban Chicago, Illinois, USA.". Mycopathologia 163 (2): 59–66. doi:10.1007/s11046-006-0090-1. PMID 17262169. 
    10. ^ Veligandla SR, Hinrichs SH, Rupp ME, Lien EA, Neff JR, Iwen PC (October 2002). "Delayed diagnosis of osseous blastomycosis in two patients following environmental exposure in nonendemic areas". Am. J. Clin. Pathol. 118 (4): 536–41. doi:10.1309/JEJ0-3N98-C3G8-21DE. PMID 12375640. 
    11. ^ a b c Crampton, TL; Light, RB; Berg, GM; Meyers, MP; Schroeder, GC; Hershfield, ES; Embil, JM (2002). "Epidemiology and clinical spectrum of blastomycosis diagnosed at Manitoba hospitals.". Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 34 (10): 1310–6. doi:10.1086/340049. PMID 11981725. 
    12. ^ a b c d e f g h Dwight, P.J.; Naus, M; Sarsfield, P; Limerick, B (2000). "An outbreak of human blastomycosis: the epidemiology of blastomycosis in the Kenora catchment region of Ontario, Canada.". Canada communicable disease report = Releve des maladies transmissibles au Canada 26 (10): 82–91. PMID 10893821. 
    13. ^ Kane, J; Righter, J; Krajden, S; Lester, RS (1983). "Blastomycosis: a new endemic focus in Canada.". Canadian Medical Association journal 129 (7): 728–31. PMID 6616383. 
    14. ^ Lester, RS; DeKoven, JG; Kane, J; Simor, AE; Krajden, S; Summerbell, RC (2000). "Novel cases of blastomycosis acquired in Toronto, Ontario.". CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 163 (10): 1309–12. PMID 11107469. 
    15. ^ a b c d Morris, SK; Brophy, J; Richardson, SE; Summerbell, R; Parkin, PC; Jamieson, F; Limerick, B; Wiebe, L; Ford-Jones, EL (2006). "Blastomycosis in Ontario, 1994-2003.". Emerging Infectious Diseases 12 (2): 274–9. doi:10.3201/eid1202.050849. PMC 3373107. PMID 16494754. 
    16. ^ Sekhon, AS; Jackson, FL; Jacobs, HJ (1982). "Blastomycosis: report of the first case from Alberta Canada.". Mycopathologia 79 (2): 65–9. doi:10.1007/bf00468081. PMID 6813742. 
    17. ^ Vallabh, V; Martin, T; Conly, JM (1988). "Blastomycosis in Saskatchewan.". The Western journal of medicine 148 (4): 460–2. PMID 3388850. 
    18. ^ a b Rippon, John Willard (1988). Medical mycology : the pathogenic fungi and the pathogenic actinomycetes (3rd ed. ed.). Philadelphia: W.B. Saunders Co. ISBN 9780721624440. 
    19. ^ a b Manetti, AC (1991). "Hyperendemic urban blastomycosis.". American Journal of Public Health 81 (5): 633–6. doi:10.2105/ajph.81.5.633. PMID 2014867. 
    20. ^ a b Cano, MV; Ponce-de-Leon, GF; Tippen, S; Lindsley, MD; Warwick, M; Hajjeh, RA (2003). "Blastomycosis in Missouri: epidemiology and risk factors for endemic disease.". Epidemiology and infection 131 (2): 907–14. doi:10.1017/s0950268803008987. PMID 14596532. 
    21. ^ a b c Baumgardner, DJ; Brockman, K (1998). "Epidemiology of human blastomycosis in Vilas County, Wisconsin. II: 1991-1996.". WMJ : official publication of the State Medical Society of Wisconsin 97 (5): 44–7. PMID 9617309. 
    22. ^ Baumgardner, DJ; Egan, G; Giles, S; Laundre, B (2002). "An outbreak of blastomycosis on a United States Indian reservation.". Wilderness & environmental medicine 13 (4): 250–2. doi:10.1580/1080-6032(2002)013[0250:aooboa]2.0.co;2. PMID 12510781. 
    23. ^ Centers for Disease Control and Prevention (CDC) (1996). "Blastomycosis--Wisconsin, 1986-1995". MMWR Morb. Mortal. Wkly. Rep. 45 (28): 601–3. PMID 8676851. 
    24. ^ DiSalvo, A.F. (1992). Al-Doory, Y., DiSalvo, A.F., ed. Ecology of Blastomyces dermatitidis. Plenum. pp. 43–73. 
    25. ^ Baumgardner, DJ; Steber, D; Glazier, R; Paretsky, DP; Egan, G; Baumgardner, AM; Prigge, D (2005). "Geographic information system analysis of blastomycosis in northern Wisconsin, USA: waterways and soil.". Medical mycology : official publication of the International Society for Human and Animal Mycology 43 (2): 117–25. doi:10.1080/13693780410001731529. PMID 15832555. 
    26. ^ a b Baumgardner, DJ; Knavel, EM; Steber, D; Swain, GR (2006). "Geographic distribution of human blastomycosis cases in Milwaukee, Wisconsin, USA: association with urban watersheds.". Mycopathologia 161 (5): 275–82. doi:10.1007/s11046-006-0018-9. PMID 16649077. 
    27. ^ a b c Klein, Bruce S.; Vergeront, James M.; Weeks, Robert J.; Kumar, U. Nanda; Mathai, George; Varkey, Basil; Kaufman, Leo; Bradsher, Robert W.; Stoebig, James F.; Davis, Jeffrey P. (1986). "Isolation of Blastomyces dermatitidis in Soil Associated with a Large Outbreak of Blastomycosis in Wisconsin". New England Journal of Medicine 314 (9): 529–534. doi:10.1056/NEJM198602273140901. 
    28. ^ Armstrong, CW; Jenkins, SR; Kaufman, L; Kerkering, TM; Rouse, BS; Miller GB, Jr (1987). "Common-source outbreak of blastomycosis in hunters and their dogs.". The Journal of infectious diseases 155 (3): 568–70. doi:10.1093/infdis/155.3.568. PMID 3805778. 
    29. ^ Kesselman, EW; Moore, S; Embil, JM (2005). "Using local epidemiology to make a difficult diagnosis: a case of blastomycosis.". CJEM 7 (3): 171–3. PMID 17355674. 
    30. ^ Vaaler, AK; Bradsher, RW; Davies, SF (1990). "Evidence of subclinical blastomycosis in forestry workers in northern Minnesota and northern Wisconsin.". The American Journal of Medicine 89 (4): 470–6. doi:10.1016/0002-9343(90)90378-q. PMID 2220880. 
    31. ^ a b c Baumgardner, DJ; Buggy, BP; Mattson, BJ; Burdick, JS; Ludwig, D (1992). "Epidemiology of blastomycosis in a region of high endemicity in north central Wisconsin.". Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 15 (4): 629–35. doi:10.1093/clind/15.4.629. PMID 1420675. 
    32. ^ a b Kitchen, MS; Reiber, CD; Eastin, GB (1977). "An urban epidemic of North American blastomycosis.". The American Review of Respiratory Disease 115 (6): 1063–6. PMID 262101. 
    33. ^ Renston, JP; Morgan, J; DiMarco, AF (1992). "Disseminated miliary blastomycosis leading to acute respiratory failure in an urban setting.". Chest 101 (5): 1463–5. doi:10.1378/chest.101.5.1463. PMID 1582324. 
    34. ^ Lowry, PW; Kelso, KY; McFarland, LM (1989). "Blastomycosis in Washington Parish, Louisiana, 1976-1985.". American Journal of Epidemiology 130 (1): 151–9. PMID 2787106. 
    35. ^ Baumgardner, DJ; Paretsky, DP (2001). "Blastomycosis: more evidence for exposure near one's domicile.". WMJ : official publication of the State Medical Society of Wisconsin 100 (7): 43–5. PMID 11816782. 
    36. ^ Rudmann, DG; Coolman, BR; Perez, CM; Glickman, LT (1992). "Evaluation of risk factors for blastomycosis in dogs: 857 cases (1980-1990)". Journal of the American Veterinary Medical Association 201 (11): 1754–9. PMID 1293122. 
    37. ^ Arceneaux, KA; Taboada, J; Hosgood, G (1998). "Blastomycosis in dogs: 115 cases (1980-1995).". Journal of the American Veterinary Medical Association 213 (5): 658–64. PMID 9731260. 
    38. ^ Archer, JR; Trainer, DO; Schell, RF (1987). "Epidemiologic study of canine blastomycosis in Wisconsin.". Journal of the American Veterinary Medical Association 190 (10): 1292–5. PMID 3583882. 
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    External links[edit]

    Superficial and
    cutaneous
    (dermatomycosis):
    Tinea = skin;
    Piedra (exothrix/
    endothrix) = hair
    Ascomycota
    Dermatophyte
    (Dermatophytosis)
    By location
    By organism
    Other
    Basidiomycota
    Subcutaneous,
    systemic,
    and opportunistic
    Ascomycota
    Dimorphic
    (yeast+mold)
    Onygenales
    Other
    Yeast-like
    Mold-like
    Basidiomycota
    Zygomycota
    (Zygomycosis)
    Mucorales
    (Mucormycosis)
    Entomophthorales
    (Entomophthoramycosis)
    Microsporidia
    (Microsporidiosis)
    Mesomycetozoea
    Ungrouped
    Index of fungal disease
    Description
    Disease
    Treatment

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