Literature DB >> 7390807

[Familial malignant melanoma and atypical disseminated moles (BK-mole syndrome)].

M Hundeiker, R Ruppel, H Schmitt.   

Abstract

Report of a family with malignant melanomas and multiple atypical pigmented moles in three siblings. A 29 year old caucasian woman had a nodular melanoma. Twelve years ago, at the age of 23, her elder brother had been suffering from a melanoma with a solitary cerebral metastasis. Following radical surgical treatment, he has been well since that time. Their sister died with 21 years after inadequate treatment and generalisation of a melanoma in her temporal region. All patients had multiple atypical nevus cell nevus-like pigmented moles with irregular bizarre configuration, especially in the upper parts of the trunk. These findings correspond to the BK-mole syndrome. This heritable syndrome is not frequent, but important because of the necessity to keep all relatives of BK-mole patients under continuous dermatological control and to remove each suspicious lesion early enough.

Entities:  

Mesh:

Year:  1980        PMID: 7390807

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  2 in total

1.  Familial cutaneous malignant melanoma: autosomal dominant trait possibly linked to the Rh locus.

Authors:  M H Greene; L R Goldin; W H Clark; E Lovrien; K H Kraemer; M A Tucker; D E Elder; M C Fraser; S Rowe
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

2.  Cutaneous malignant melanoma and familial dysplastic nevi: evidence for autosomal dominance and pleiotropy.

Authors:  S J Bale; A Chakravarti; M H Greene
Journal:  Am J Hum Genet       Date:  1986-02       Impact factor: 11.025

  2 in total

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