Two patients with hailey-hailey disease, multiple primary melanomas, and other cancers

Archives of Dermatology

Volumn 147, Issue 2, 2011, Pages 211-215

  Mohr, Melinda R ^a   Erdag, Gulsun ^b   Shada, Amber L ^b   Williams, Michael E ^b   Slingluff Jr , Craig L ^b   Patterson, James W ^b  

^a EASTERN VIRGINIA MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF VIRGINIA HEALTH SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSQUAMOUS CARCINOMA; ADULT; AGED; ARTICLE; CANCER RISK; CARCINOGENICITY; CASE REPORT; DISEASE ASSOCIATION; ENVIRONMENTAL FACTOR; HAILEY HAILEY DISEASE; HEREDITY; HUMAN; IATROGENIC DISEASE; MALE; MELANOMA; MONOCYTIC LEUKEMIA; NERVE SHEATH TUMOR; NEURILEMOMA; PAROTID GLAND CARCINOMA; PRIORITY JOURNAL;

ADULT; AGED; CARCINOMA, MUCOEPIDERMOID; HUMANS; LEUKEMIA, MONOCYTIC, ACUTE; MALE; MELANOMA; NEOPLASMS, MULTIPLE PRIMARY; NERVE SHEATH NEOPLASMS; NEUROMA, ACOUSTIC; PAROTID NEOPLASMS; PEMPHIGUS, BENIGN FAMILIAL; SKIN NEOPLASMS;

EID: 79951966697     PISSN: 0003987X     EISSN: 15383652     Source Type: Journal    
DOI: 10.1001/archdermatol.2010.445     Document Type: Article

References (29)

1. Hailey H, Hailey H. Report of 13 cases in 4 generations of a family and report of 9 additional cases in 4 generations of a family. Arch Derm Syphilol. 1939;39:679-685.
2. Burge SM. Hailey-Hailey disease: the clinical features, response to treatment and prognosis. Br J Dermatol. 1992;126(3):275-282.
3. Holst VA, Fair KP, Wilson BB, Patterson JW. Squamous cell carcinoma arising in Hailey-Hailey disease. J Am Acad Dermatol. 2000;43(2, pt 2):368-371. (Pubitemid 30636542)
4. Hu Z, Bonifas JM, Beech J, et al. Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease. Nat Genet. 2000;24(1):61-65. (Pubitemid 30041422)
5. Sudbrak R, Brown J, Dobson-Stone C, et al. Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump. Hum Mol Genet. 2000;9(7):1131-1140. (Pubitemid 30216019)
6. Szigeti R, Kellermayer R. Hailey-Hailey disease and calcium: lessons from yeast. J Invest Dermatol. 2004;123(6):1195-1196. (Pubitemid 39586846)
7. Slingluff CL Jr, Vollmer RT, Seigler HF. Multiple primary melanoma: incidence and risk factors in 283 patients. Surgery. 1993;113(3):330-339. (Pubitemid 23082254)
8. Chun SI, Whang KC, Su WP. Squamous cell carcinoma arising in Hailey-Hailey disease. J Cutan Pathol. 1988;15(4):234-237.
9. Cockayne SE, Rassl DM, Thomas SE. Squamous cell carcinoma arising in Hailey-Hailey disease of the vulva. Br J Dermatol. 2000;142(3):540-542. (Pubitemid 30159085)
10. Hirai A, Naka W, Kitamura K, et al. A case of squamous cell carcinoma developed in the lesion of Hailey-Hailey's disease [in Japanese]. Rinsyo Derma (Tokyo). 1983;25:205-210.
11. Inaba Y, Mihara I, Tanioka S. Squamous cell carcinoma and Bowen's carcinoma arising in the lesion of Hailey-Hailey disease [in Japanese]. Jpn J Clin Dermatol. 1991;45:557-560.
12. Bitar A, Giroux JM. Treatment of benign familial pemphigus (Hailey-Hailey) by skin grafting. Br J Dermatol. 1970;83(3):402-404.
13. Furue M, Seki Y, Oohara K, Ishibashi Y. Basal cell epithelioma arising in a patient with Hailey-Hailey's disease. Int J Dermatol. 1987;26(7):461-462. (Pubitemid 17126566)
14. Ochiai T, Honda A, Morishima T, Sata T, Sakamoto H, Satoh K. Human papillomavirus types 16 and 39 in a vulval carcinoma occurring in a woman with Hailey- Hailey disease. Br J Dermatol. 1999;140(3):509-513. (Pubitemid 29182887)
15. Okunade GW, Miller ML, Azhar M, et al. Loss of the Atp2c1 secretory pathway Ca(2+)-ATPase (SPCA1) in mice causes Golgi stress, apoptosis, and midgestational death in homozygous embryos and squamous cell tumors in adult heterozygotes. J Biol Chem. 2007;282(36):26517-26527. (Pubitemid 47443792)
16. Capiod T, Shuba Y, Skryma R, Prevarskaya N. Calcium signalling and cancer cell growth. Subcell Biochem. 2007;45:405-427.
17. Cialfi S, Oliviero C, Ceccarelli S, et al. Complex multipathways alterations and oxidative stress are associated with Hailey-Hailey disease. Br J Dermatol. 2010; 162(3):518-526.
18. Pinnix CC, Lee JT, Liu ZJ, et al. Active Notch1 confers a transformed phenotype to primary human melanocytes. Cancer Res. 2009;69(13):5312-5320.
19. Jazbec J, Todorovski L, Jereb B. Classification tree analysis of second neoplasms in survivors of childhood cancer. BMC Cancer. 2007;7:27.
20. Corpron C, Black C, Ross M, et al. Melanoma as a second malignant neoplasm after childhood cancer. Am J Surg. 1996;172(5):459-462. (Pubitemid 26415751)
21. Guérin S, Dupuy A, Anderson H, et al. Radiation dose as a risk factor for malignant melanoma following childhood cancer. Eur J Cancer. 2003;39(16):2379-2386. (Pubitemid 37214863)
22. Rao RD, Holtan SG, Ingle JN, et al. Combination of paclitaxel and carboplatin as second-line therapy for patients with metastatic melanoma. Cancer. 2006;106 (2):375-382. (Pubitemid 43100447)
23. Curtis RE, Rowlings PA, Deeg HJ, et al. Solid cancers after bone marrow transplantation. N Engl J Med. 1997;336(13):897-904. (Pubitemid 27137189)
24. Preston DL, Shimizu Y, Pierce DA, Suyama A, Mabuchi K. Studies of mortality of atomic bomb survivors: report 13: solid cancer and noncancer disease mortality: 1950-1997. Radiat Res. 2003;160(4):381-407.
25. Paulino AC, Fowler BZ. Secondary neoplasms after radiotherapy for a childhood solid tumor. Pediatr Hematol Oncol. 2005;22(2):89-101. (Pubitemid 40315508)
26. Pho L, Grossman D, Leachman SA. Melanoma genetics: a review of genetic factors and clinical phenotypes in familial melanoma. Curr Opin Oncol. 2006;18 (2):173-179. (Pubitemid 43740438)
27. Azizi E, Friedman J, Pavlotsky F, et al. Familial cutaneous malignant melanoma and tumors of the nervous system: a hereditary cancer syndrome. Cancer. 1995;76(9):1571-1578.
28. Randerson-Moor JA, Harland M, Williams S, et al. A germline deletion of p14 (ARF) but not CDKN2A in a melanoma-neural system tumour syndrome family. Hum Mol Genet. 2001;10(1):55-62. (Pubitemid 32051568)
29. Bahuau M, Vidaud D, Kujas M, et al. Familial aggregation of malignant melanoma/ dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness. Ann Genet. 1997;40(2):78-91. (Pubitemid 27334326)