Familial atypical multiple mole melanoma syndrome

Last revised by Daniel J Bell on 30 Jun 2019

Citation, DOI, disclosures and article data

Citation:

Weerakkody Y, Bell D, Familial atypical multiple mole melanoma syndrome. Reference article, Radiopaedia.org (Accessed on 18 Apr 2024) https://doi.org/10.53347/rID-69146

DOI:

https://doi.org/10.53347/rID-69146

Permalink:

https://radiopaedia.org/articles/69146

rID:

69146

Article created:

30 Jun 2019, Yuranga Weerakkody ◉

Disclosures:

At the time the article was created Yuranga Weerakkody had no recorded disclosures.

View Yuranga Weerakkody's current disclosures

Last revised:

30 Jun 2019, Daniel J Bell ◉

Disclosures:

At the time the article was last revised Daniel J Bell had no recorded disclosures.

View Daniel J Bell's current disclosures

Revisions:

2 times, by 2 contributors - see full revision history and disclosures

Systems:

Gastrointestinal, Hepatobiliary, Oncology

Sections:

Syndromes

Synonyms:

Familial atypical multiple mole melanoma (FAMMM)
Familial atypical multiple mole melanoma syndrome
Familial atypical multiple mole melanoma (FAMMM) syndrome
Hereditary dysplastic nevus syndrome
FAMMM syndrome

Familial atypical multiple mole melanoma (FAMMM) syndrome is an autosomal dominant genodermatosis characterized by multiple melanocytic nevi (often more than 50) and a family history of melanoma.