Nevus of Ito

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ORPHA:263432D22.6
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What is Nevus of Ito?

Nevus of Ito, also known as nevus fuscoceruleus acromiodeltoideus, is a benign dermal melanocytic condition characterized by blue-gray or brown-gray hyperpigmentation affecting the shoulder, upper arm, and supraclavicular regions. It is closely related to Nevus of Ota, which affects the face and periorbital area; however, Nevus of Ito specifically involves the skin innervated by the posterior supraclavicular and lateral cutaneous brachial nerves. The condition results from the presence of ectopic melanocytes in the dermis, which produce the characteristic mottled or patchy pigmentation. Nevus of Ito is typically present at birth or appears during early childhood, though onset during puberty has also been reported. It is more commonly observed in individuals of Asian descent and in females. The condition is generally unilateral, though bilateral cases have been described. The pigmentation is usually stable but may darken or expand during puberty or pregnancy due to hormonal influences. While Nevus of Ito is a benign condition with no systemic involvement in most cases, rare associations with melanoma arising within the nevus have been reported, warranting periodic clinical monitoring. Treatment is primarily pursued for cosmetic reasons, as the condition does not typically cause medical complications. Laser therapy, particularly Q-switched lasers (such as Q-switched alexandrite, Q-switched Nd:YAG, and Q-switched ruby lasers), has been the most effective treatment modality for reducing or eliminating the pigmentation. Multiple treatment sessions are usually required. Camouflage cosmetics may also be used for patients who prefer non-invasive options. Dermatological follow-up is recommended to monitor for any changes in the pigmented area.

Also known as:

Clinical phenotype terms:

  • NevusHP:0003764
  • Cutaneous melanomaHP:0012056
  • Ocular melanocytosisHP:0025534
Inheritance
Sporadic
Usually appears on its own, not inherited from a parent
Age of Onset
Variable
Can begin at different ages, from infancy through adulthood
Orphanet ↗NORD ↗

Treatments

Source: openFDA + DailyMed · NDA / BLA labels with structured indications · refreshed weekly

No FDA-approved treatments are currently listed for Nevus of Ito.

View clinical trials →

Source: ClinicalTrials.gov · synced daily · phases, status, and PI names normalized at ingest

No actively recruiting trials found for Nevus of Ito at this time.

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

Search ClinicalTrials.gov ↗Join the Nevus of Ito community →

Source: NPI Registry + PubMed · trial PI roles cross-referenced with ClinicalTrials.gov · ranked by match score (publications + PI activity + community signal)

No specialists are currently listed for Nevus of Ito.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

Treatment Centers

8 centers

Source: NORD Rare Disease Centers + NIH Undiagnosed Diseases Network (UDN) · centers verified active within last 12 months

🏨 Children's

Children's Hospital Colorado Rare Disease Program

Children's Hospital Colorado

📍 Aurora, CO

👤 Boston Children's Hospital Rare Disease Program

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Boston Children's Hospital Rare Disease Program

Boston Children's Hospital

📍 Boston, MA

👤 Boston Children's Hospital Rare Disease Program

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

🏨 Children's

Ann & Robert H. Lurie Children's Hospital Genetics

Lurie Children's Hospital

📍 Chicago, IL

👤 Boston Children's Hospital Rare Disease Program

🏥 NORD

Cincinnati Children's Hospital Medical Center

Cincinnati Children's

📍 Cincinnati, OH

👤 Boston Children's Hospital Rare Disease Program

🏨 Children's

Nationwide Children's Hospital Rare Disease Center

Nationwide Children's Hospital

📍 Columbus, OH

👤 Boston Children's Hospital Rare Disease Program

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

Travel Grants

No travel grants are currently matched to Nevus of Ito.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Nevus of Ito

Source: PubMed + NIH RePORTER + openFDA + clinical-journal RSS · last 30 days · disease-tagged at ingest by AI extraction with human QC

No recent news articles for Nevus of Ito.

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

Common questions about Nevus of Ito

What is Nevus of Ito?

Nevus of Ito, also known as nevus fuscoceruleus acromiodeltoideus, is a benign dermal melanocytic condition characterized by blue-gray or brown-gray hyperpigmentation affecting the shoulder, upper arm, and supraclavicular regions. It is closely related to Nevus of Ota, which affects the face and periorbital area; however, Nevus of Ito specifically involves the skin innervated by the posterior supraclavicular and lateral cutaneous brachial nerves. The condition results from the presence of ectopic melanocytes in the dermis, which produce the characteristic mottled or patchy pigmentation. Nevus

How is Nevus of Ito inherited?

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

Frequently asked questions about Nevus of Ito

Auto-generated from canonical disease facts (Orphanet, OMIM, ClinicalTrials.gov, openFDA, NPPES). Not a substitute for clinical guidance.

  1. What is Nevus of Ito?

    Nevus of Ito is a rare disease catalogued in international rare-disease ontologies (Orphanet ORPHA:263432). It is typically inherited as sporadic. Age of onset is generally variable. For verified primary sources, see the UniteRare Nevus of Ito page.

  2. How is Nevus of Ito inherited?

    Nevus of Ito follows sporadic inheritance. Genetic counseling is recommended for affected families to understand recurrence risk in offspring and the likelihood of unaffected siblings being carriers. Variants in the underlying gene(s) may be identified via clinical genetic testing.

  3. Are there FDA-approved treatments for Nevus of Ito?

    Approved treatments for Nevus of Ito are tracked from openFDA and DailyMed primary sources. Many rare diseases have no specific FDA-approved therapy; for those, supportive care and management of complications form the basis of clinical care. Orphan-drug-designation status is noted where applicable.

  4. Are there clinical trials for Nevus of Ito?

    Active clinical trials for Nevus of Ito are tracked daily from ClinicalTrials.gov. Trial availability changes frequently; check the UniteRare trial listings for the current count and recruitment status. Sponsors of rare-disease research often welcome inquiries even when a trial is not actively recruiting at a given moment.

  5. How do I find a specialist for Nevus of Ito?

    Verified Nevus of Ito specialists are identified through ClinicalTrials.gov principal-investigator records, peer-reviewed publication authorship (via PubMed), and the NPPES NPI registry. NORD-designated Centers of Excellence and NIH-affiliated rare-disease clinics are also tracked. UniteRare's specialist directory is updated continuously as new evidence becomes available.

See full Nevus of Ito page for complete clinical details, sources, and verified-specialist listings.

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