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Genodermatoses with Malignant Potential

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Dermato-Oncology Study Guide

Abstract

Genodermatoses with malignant potential often manifest cutaneous findings as the presenting feature (Table 1). In most cases, the diagnosis can be made by clinical criteria or genetic testing. Prompt diagnosis is critical to initiate appropriate screening for malignancy.

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Abbreviations

APC:

Adenomatous polyposis coli

BCC:

Basal cell carcinoma

BCCNS:

Basal cell carcinoma nevus syndrome

FAP:

Familial adenomatous polyposis

HLRCC:

Hereditary leiomyomatosis and renal cell cancer

MEN:

Multiple endocrine neoplasia

MPNST:

Malignant peripheral nerve sheath tumor

MTS:

Muir-Torre syndrome

NF:

Neurofibroma

TS:

Tuberous sclerosis

References

  1. Smith MJ, Beetz C, Williams SG, et al. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations. J Clin Oncol. 2014;32(36):4155–61. Epub 2014 Nov 17.

    Article  CAS  Google Scholar 

  2. Gupta N, Sunwoo BY, Kotloff RM. Birt-Hogg-Dube syndrome. Clin Chest Med. 2016;37(3):475–86.

    Article  Google Scholar 

  3. Holman JD, Dyer JA. Genodermatoses with malignant potential. Curr Opin Pediatr. 2007;19(4):446–54.

    Article  Google Scholar 

  4. Patel VM, Handler MZ, Schwartz RA, Lambert WC. Hereditary leiomyomatosis and renal cell cancer syndrome: an update and review. JAAD. 2017;77(1):149–58.

    Article  Google Scholar 

  5. Norton JA, Krampitz G, Jensen RT. Mulitple endrocrine neoplasia: genetics and clinical management. Surg Oncol Clin N Am. 2015;24(4):795–832.

    Article  Google Scholar 

  6. Thakker RV, Newey PJ, Walls GV, et al. Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1). J Clin Endocrinol Metab. 2012;97(9):2990–3011. https://doi.org/10.1210/jc.2012-1230. (Screening).

    Article  PubMed  CAS  Google Scholar 

  7. Mahdi J, Mester JL, Nizialek EA, et al. Germline PTEN, SDHB-D, and KLLN alterations in endometrial cancer patients Cowden and Cowden-like syndromes: an international, multicenter, prospective study. Cancer. 2015;121(5):688–96. https://doi.org/10.1002/cncr.29106. Epub 2014 Nov 5.

    Article  PubMed  CAS  Google Scholar 

  8. Soura E, Eliades PJ, Shannon K, et al. Hereditary melanoma: update on syndromes and management: genetics of familial atypical multiple mole melanoma syndrome. J Am Acad Dermatol. 2016;74(3):395–407.

    Article  Google Scholar 

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Hernandez Holt, M., Liu, V., Dyer, J. (2021). Genodermatoses with Malignant Potential. In: Liu, V. (eds) Dermato-Oncology Study Guide. Springer, Cham. https://doi.org/10.1007/978-3-030-53437-0_3

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  • DOI: https://doi.org/10.1007/978-3-030-53437-0_3

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-030-53436-3

  • Online ISBN: 978-3-030-53437-0

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