Two cases of pilomatrixoma in Turner's syndrome

Dermatology

Volumn 199, Issue 4, 1999, Pages 338-340

  Noguchi, H ^a   Kayashima, K ^a   Nishiyama, S ^a   Ono, Tomomichi ^a  

^a KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

Calcifying epithelioma; Pilomatrixoma; Turner's syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; FEMALE; HUMAN; LEG; MYOTONIC DYSTROPHY; PILOMATRIXOMA; PRIORITY JOURNAL; THORAX; TURNER SYNDROME;

EID: 0033407384     PISSN: 10188665     EISSN: None     Source Type: Journal    
DOI: 10.1159/000018286     Document Type: Article

References (17)

1. Ullrich O: Über typische Kombinationsbilder multipler Abartungen. Z Kinderheilkd 1930; 49:271.
2. Turner HH: A syndrome of infantilism, congenital webbed neck, and cubitus valgus. Endocrinology 1938;23:566-574.
3. Ford CE: A sex-chromosome anomaly in a case of gonadal dysgenesis. Lancet. 1959;i: 711-713.
4. DiGeorge AM: Hypergonadotropic hypogonadism in the female; in Behrman RE, Kliegman RM, Arvin AM, Nelson WE (eds): Nelson Textbook of Pediatrics, ed 15. Philadelphia, Saunders, 1996, pp 1635-1637.
5. Harper J: Genetics and Genodermatoses: Turner's syndrome; in Champion RH, Bulton JL, Ebling FJG (eds): Textbook of Dermatology, ed 5. London, Blackwell Scientific, 1992, pp 319-320.
6. Cantwell AR Jr, Reed WB: Myotoniaatrophica and multiple calcifying epithelioma of Malherbe. Ada Derm Venereol 1965;45:387-390.
7. Harper PS: Calcifying epithelioma of Malherbe. Association with myotonic muscular dystrophy. Arch Dermatol 1972;106:41-44.
8. Pujol RM, Casanova JM, Egido R, Pujol J, de Moragas JM: Multiple familial pilomatricomas: Cutaneous marker for Gardner syndrome? Pediatr Dermatol 1995;12:331-335.
9. Cambiaghi S, Ermacora E, Brusasco A, Canzi L, Caputo R: Multiple pilomatricomas in Rubinstein-Taybi syndrome: A case report. Pediatr Dermatol 1994;11:21-25.
10. Miller RW, Rubinstein JH: Tumors in Rubinstein-Taybi syndrome. Am J Med Genet 1995; 56:112-115.
11. Masuno M: Pilomatrixomas in Rubinstein-Taybi syndrome (letter). Am J Med Genet 1998;77:81-82.
12. Narisawa Y, Kohda H; Cutaneous cysts of Gardner's syndrome are similar to follicular stem cells. J Cutan Pathol 1995;22:115-121.
13. Petriji F, Giles RH, Dauwerse HG, Saris JJ, Hennekam RCM, Masuno M, Tommerup N, van Ommen G-JB, Goodman RH, Peters DJM, Breuing MH: Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Nature 1995;376:348-351.
14. Borrow J, Stanton VP Jr, Anderson JM, Becher R, Behm FG, Chaganti RSK, Civin CI, Disteche C, Dube I, Frischauf AM, Horsman D, Mitelman F, Volinia S, Watmore AE, Housman DE: The translocation t(8;16)(p11:p13) of acute myeloid leukaemia fuses a putative acetyl-transferase to CREB-hinding protein. Nat Genet 1996;14:33-41.
15. Taki T, Sako M, Tsuchida M, Hayashi Y: The t(11;16)(q23;p13) translocation in myelodysplastic syndrome fuses the MLL gene to the CBP gene. Blood 1997;89:3945-3950.
16. Moehlenbeck FW: Pilomatrixoma (calcifying epithelioma). Arch Dermatol 1973;108:532-534.
17. Noguchi H, Hayashibara T, Ono T: A statistical study of calcifying epithelioma, focusing on the site of origin. J Dermatol 1995;22:24-27.