Dysplastic nevus syndrome

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Dysplastic nevus syndrome
Classification and external resources
ICD-10 D48.5 (ILDS D48.520)
OMIM 155600
DiseasesDB 31106
The back of somebody with FAMM.
Someone with FAMM.

Dysplastic nevus syndrome (also known as "Atypical Mole Syndrome (AMS)", "Familial atypical multiple mole–melanoma (FAMMM) syndrome", "familial melanoma syndrome,"[1] and "B-K mole syndrome") is a cutaneous condition described in certain families, and characterized by unusual nevi and multiple inherited melanomas.[2]:692[3]

Historical background[edit]

In 1820 Norris reported the first case of what is now recognized as FAMMM (12). He described a 59-year-old man with melanoma, a high total body mole count, and family history of the same.[4]

Definition[edit]

AMS has been described by multiple authors and institutions, and various definitions have been adopted.[5] According to Newton et al., a scoring system allotting one point per feature establishes AMS with scores greater than or equal to 3. The features include: 1) two or more clinically atypical nevi, 2) more than 100 nevi in patients between 20 and 50 years of age, 3) more than 50 nevi in patients under 20 years of age or more than 50 years of age, 4) more than one nevus in buttocks or instep, 5) nevi on the anterior scalp, 6) one or more pigmented lesions in the iris.

The Classical (1990) definition uses the following criteria: 1) 100 or more melanocytic nevi, 2) one or more melanocytic nevi greater than or equal to 8mm in its largest diameter, and 3) one or more clinically atypical melanocytic nevi.

The National Institutes of Health (NIH) Consensus 1992 definition, which is still controversial, requires a family history of melanoma, in addition to a large number of melanocytic nevi (often greater than 50) and melanocytic nevi that present certain histological features.

Pathology[edit]

The histopathologic characteristics of melanoma in FAMMM kindreds are not different from those seen in sporadic cases of melanoma and, thus, are not useful in diagnosing the syndrome. Superficial spreading melanoma (SSM) and nodular melanoma are the most frequently encountered histological melanoma subtypes in patients with CDKN2A mutations, which is consistent with the relative early age of onset.

CDKN2A[edit]

The CDKN2A gene is located on chromosome 9p21.3. Two main transcripts, isoforms ‘1’ and ‘4’, each contain three exons and span 7288 and 26740 bp, respectively. They encode proteins of 156 and 173 amino acids; isoform ‘1’ encodes p16(INK4a), while isoform ‘4’ encodes p14(ARF), a protein that is structurally unrelated to p16(INK4) but acts in cell cycle G1 control by stabilizing the tumor suppressor protein p53.[6]

The penetrance for melanoma in kindreds with CDKN2A mutations is estimated at 58% to 92% by 80 years of age and varies with geography. The penetrance in CDKN2A mutation carriers for pancreatic cancer has been estimated to be 17% by 75 years of age. As noted above, there is wide variation in published estimates of the penetrance of CDKN2A mutations.

Management[edit]

Screening for melanoma in FAMMM kindreds should begin at age 10 with a baseline total body skin examination including scalp, eyes, oral mucosa, genital area, and nail, as family members may develop melanoma in their early teens.

At Mayo Clinic, FAMMM patients with a confirmed mutation and family history of pancreatic cancer are offered screening with either high-resolution pancreatic protocol CT, MRI, or endoscopic ultrasound starting at age 50 or 10 years younger than the earliest family member with pancreas cancer. They are counseled on the lack of evidence-based data to support screening, and on the limitations of our current technology to detect a lesion at a stage amenable to therapy.[6]

See also[edit]

References[edit]

  1. ^ http://www.clevelandclinicmeded.com/medicalpubs/diseasemanagement/dermatology/cutaneous-malignant-melanoma/
  2. ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: Clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0. 
  3. ^ Czajkowski, R., FAMMM Syndrome: Pathogenesis and Management, Dermatologic Surgery, Vol. 30 Issue 2 p2, p291-296, 2004.
  4. ^ "FAMMM : In Familial Cancer Syndromes. DL Riegert-Johnson and others. NCBI 2009". Retrieved 2009-07-21. 
  5. ^ "Atypical mole syndrome and dysplastic nevi: identification of populations at risk for developing melanoma - review article. Julia Hypolito Silva et al. NCBI 2011". Retrieved 2015-05-19. 
  6. ^ a b "FAMMM : In Familial Cancer Syndromes. DL Riegert-Johnson and others. NCBI 2009". Retrieved 2009-07-21. 

External links[edit]