Familial occurrence of a type 2 segmental manifestation of cutaneous leiomyomatosis;Familiäres auftreten einer segmentalen typ-2-manifestation der kutanen leiomyomatose

JDDG - Journal of the German Society of Dermatology

Volumn 3, Issue 9, 2005, Pages 695-699

  Renner, Regina ^a   Sticherling, Michael ^a  

^a UNIVERSITY HOSPITAL LEIPZIG   (Germany)

Author keywords

Familial occurrence; Multiple cutaneous leiomyomas; Segmental type 2 manifestation; Theory of dichotomy

Indexed keywords

AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC DISORDER; GENODERMATOSIS; GERIATRIC PATIENT; HUMAN; HYSTERECTOMY; LEIOMYOMA; LEIOMYOMATOSIS; MOTHER; PEDIGREE ANALYSIS; PROGENY; SKIN DISEASE; SKIN MANIFESTATION; SKIN TUMOR; UTERUS MYOMA; CHROMOSOME ABERRATION; CHROMOSOME MAP; DOMINANT GENE; GENETICS; GESTATIONAL AGE; HETEROZYGOSITY LOSS; MALE; MIDDLE AGED; MULTIPLE CANCER; PEDIGREE; PRENATAL DEVELOPMENT; UTERUS CANCER;

AGED; CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; FEMALE; GENES, DOMINANT; GESTATIONAL AGE; HUMANS; LEIOMYOMATOSIS; LOSS OF HETEROZYGOSITY; MALE; MIDDLE AGED; NEOPLASMS, MULTIPLE PRIMARY; PEDIGREE; SKIN NEOPLASMS; UTERINE NEOPLASMS;

EID: 33644788717     PISSN: 16100379     EISSN: 16100387     Source Type: Journal    
DOI: 10.1111/j.1610-0387.2005.05742.x     Document Type: Article

References (12)

1. Happle R. Segmentale Typ-2-Manifestation autosomal-dominater Hauterkrankungen. Hautarzt 2001; 52: 283-287.
2. Happle R. Loss of heterozygosity in human skin. J Am Acad Dermatol 1999; 41: 143-161.
3. Fearfield LA, Smith JR, Bunker CB, Staughton RCD. Association of multiple familial curaneous leiomyoma with a uterine symplastic leiomyoma. Clin Exp Dermatol 2000; 25: 44-47.
4. Tso G, Haralambis C, Ascvest C. Leiomyomatose cutanée hemicorporelle droite (1 cas). Ann Dermatol Venereol 1998; 125 (Supp 3): 175.
5. König A, Happle R. Two cases of type 2 segmental manifestation in a familiy with cutaneous leiomyomatosis. Eur J Dermatol 2000; 10: 590-592.
6. Fernández-Pugnaire MA, Delgado-Florencio V. Familial multiple cutaneous Leiomyomas. Dermatology 1995; 191: 295-298.
7. Rikihisa W, Kiryu H, Furue M. Multiple piloleiomyomas associated with solitary angioleiomyoma. Eur J Dermatol 1999; 9: 309-310.
8. García Muret MP, Pujol RM, Alomar A, Calaf J, de Moragas JM. Familial leiomyomatosis cutis et uteri (Reed's syndrome). Arch Dermatol Res 1988; 280 (Suppl): 29-32.
9. Straka BF, Wilson BB. Multiple Papules on the Leg. Multiple Piloleiomyomas. Arch Dermatol 1991; 127: 1717-1720.
10. Chuang GS, Martinez-Mir A, Geyer A, Engler DE, Glaser B, Cserhalmi-Friedman PB, Gordon D, Horev L, Lukash B, Herman E, Prieto Cid M, Brenner S, Landau M, Sprecher E, Muret MPG, Christiano AM, Zlotogorski A. Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata. J Am Acad Dermatol 2005; 52: 410-416.
11. Happle R. Muster auf der Haut. Hautarzt 2004; 55: 960-968.
12. Alam NA, Barclay E, Rowan AJ, Tyrer JP, Colonje E, Manek S, Kelsell D, Leigh I, Olpin S, Tomlinson IP. Clinical features of multiple cutaneous and uterine leiomyomatosis: an underdiagnosed tumor syndrome. Arch Dermatol 2005; 141: 199-206.