Chromomycosis

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Overview

Chromomycosis (also called chromoblastomycosis) is a long-lasting fungal infection that mainly affects the skin and the tissue just beneath it. It is caused by several types of dark-pigmented fungi found in soil, rotting wood, and plant material. The infection usually starts when fungal spores enter the body through a small cut, scrape, or puncture wound — most often on the feet, legs, or hands. Over months or years, the infection slowly spreads outward from the original wound site. The most noticeable signs are raised, warty, or cauliflower-like skin growths that can be itchy or painful. The affected skin may turn dark, crusty, or develop open sores. In some cases, the infection can spread through the lymph system to nearby areas of skin. Serious complications include secondary bacterial infections, lymphedema (swelling caused by blocked lymph vessels), and in rare cases, transformation into a type of skin cancer after many years. Treatment is challenging and often takes a long time — sometimes years. Antifungal medicines such as itraconazole and terbinafine are the main treatments. Doctors may also use physical methods like cryotherapy (freezing the lesions), laser therapy, or surgery to remove affected tissue. A complete cure is possible, especially when the infection is caught early, but advanced cases are much harder to treat. Early diagnosis and consistent treatment give the best outcomes.

Also known as:

Key symptoms:

Raised, warty or cauliflower-like growths on the skinItchy or painful skin lesionsDark, crusty, or scaly patches on the skinOpen sores or ulcers that do not healSwelling of the affected limbSkin that becomes thickened and hardened over timeSmall pink or red bumps that slowly grow largerBlack dots visible on the surface of skin lesionsSpreading of lesions along the limb over months or yearsSecondary skin infections causing redness, warmth, or pus

Clinical phenotype terms (33)— hover any for plain English
Predominantly lower limb lymphedemaHP:0003550Verrucous papuleHP:0012500Erythematous maculeHP:0025475Serpiginous cutaneous lesionHP:0025527Annular cutaneous lesionHP:0025528HyperparakeratosisHP:0040009Hyperkeratotic papuleHP:0045059Vascular skin abnormalityHP:0011276
Inheritance

Sporadic

Usually appears on its own, not inherited from a parent

Age of Onset

Adult

Begins in adulthood (age 18 or older)

Orphanet ↗NORD ↗

Treatments

1 available

M.V.I.-12

multi-vitamin infusion without vitamin K· Mayne Pharma (USA) Inc.

Prevention of thromboembolic complications in people receiving home parenteral nutrition who also receive warfarin-type anticoagulant therapy

No actively recruiting trials found for Chromomycosis at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Chromomycosis community →

Specialists

16 foundView all specialists →
YK
Yuko Kono
SAN DIEGO, CA
Specialist
1 Chromomycosis publication
CD
Caique Costa Dias
Specialist
1 Chromomycosis publication
WO
Walmar Roncalli Pereira de Oliveira
Specialist
1 Chromomycosis publication
SI
Saki Ito
Specialist
1 Chromomycosis publication
KT
Kiyonobu Takatsuki
Specialist
1 Chromomycosis publication
MK
Masahiro Katsurada
Specialist
1 Chromomycosis publication
NK
Naoyuki Kojima
Specialist
1 Chromomycosis publication
TH
Teruaki Hyakudo
Specialist
1 Chromomycosis publication
MM
Maho Morikawa
Specialist
1 Chromomycosis publication
SY
Shun Yamazaki
Specialist
1 Chromomycosis publication
YY
Yuki Yamamoto
Specialist
1 Chromomycosis publication
TN
Takuya Naito
Specialist
1 Chromomycosis publication
KK
Kazumi Kaneshiro
Specialist
1 Chromomycosis publication
MM
Masataka Matsumoto
Specialist
1 Chromomycosis publication
IM
Isadora Zago Miotto
Specialist
1 Chromomycosis publication
DM
Daniel E Barquero Orias, MD
Specialist
PI on 1 active trial

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Chromomycosis.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Chromomycosis

No recent news articles for Chromomycosis.

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Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Questions for your doctor

Bring these to your next appointment

  • Q1.Which type of fungus is causing my infection, and does it affect which treatment I should receive?,How long will I need to take antifungal medication, and what side effects should I watch for?,Should I also have a physical treatment like cryotherapy or surgery alongside my medication?,How will we know if the treatment is working, and what happens if it does not respond?,What are the chances of the infection coming back after treatment, and how can I reduce that risk?,Are there any activities or exposures I should avoid to prevent the infection from spreading or worsening?,Are there any newer or combination treatments I should consider if standard therapy does not work?

Common questions about Chromomycosis

What is Chromomycosis?

Chromomycosis (also called chromoblastomycosis) is a long-lasting fungal infection that mainly affects the skin and the tissue just beneath it. It is caused by several types of dark-pigmented fungi found in soil, rotting wood, and plant material. The infection usually starts when fungal spores enter the body through a small cut, scrape, or puncture wound — most often on the feet, legs, or hands. Over months or years, the infection slowly spreads outward from the original wound site. The most noticeable signs are raised, warty, or cauliflower-like skin growths that can be itchy or painful. The

How is Chromomycosis inherited?

Chromomycosis follows a sporadic inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does Chromomycosis typically begin?

Typical onset of Chromomycosis is adult. Age of onset can vary across affected individuals.

Which specialists treat Chromomycosis?

16 specialists and care centers treating Chromomycosis are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.

What treatment and support options exist for Chromomycosis?

1 patient support program are currently tracked on UniteRare for Chromomycosis. See the treatments and support programs sections for copay assistance, eligibility, and contact details.