Nonsyndromic segmental multiple infundibulocystic basal cell carcinomas in an adolescent female

Dermatologic Surgery

Volumn 32, Issue 9, 2006, Pages 1202-1208

  Kelly, Susan C ^a   Ermolovich, Tanya ^b   Purcell, Stephen M ^b  

^a DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

^b LEHIGH VALLEY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IMIQUIMOD; TAZAROTENE;

ADOLESCENT; ANAMNESIS; ARTICLE; BASAL CELL CARCINOMA; CANCER CHEMOTHERAPY; CANCER DIAGNOSIS; CANCER SURGERY; CASE REPORT; CHEMOSURGERY; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DRUG FORMULATION; FEMALE; HUMAN; INFUNDIBULOCYSTIC BASAL CELL CARCINOMA; PHYSICAL EXAMINATION; PRIORITY JOURNAL; PUNCH BIOPSY; SKIN BIOPSY;

ADOLESCENT; BIOPSY; CARCINOMA, BASAL CELL; DIAGNOSIS, DIFFERENTIAL; FEMALE; FOLLOW-UP STUDIES; HUMANS; SKIN NEOPLASMS; SYNDROME; THORAX;

EID: 33748533152     PISSN: 10760512     EISSN: 15244725     Source Type: Journal    
DOI: 10.1111/j.1524-4725.2006.32267.x     Document Type: Article

References (34)

1. Tozawa T, Ackerman AB. Basal cell carcinoma with follicular differentiation. Am J Dermatopathol 1987;9:474-82.
2. Gorlin RJ, Goltz RW. Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib: a syndrome. N Engl J Med 1960;262:908-12.
3. Gorlin RJ. Nevoid basal-cell carcinoma syndrome. Medicine 1987;66:98-113.
4. Gorlin RJ. Nevoid basal cell carcinoma syndrome. Dermatol Clin 1995;13:113-25.
5. Kimonis VE, Goldstein AM, Pastakia B, et al. Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. Am J Med Genet 1997;69:299-308.
6. Michaëlsson G, Olsson E, Westermark P. The Rombo syndrome: a familial disorder with vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis. Acta Derm Venerol 1981;61:497-503.
7. Bazex A, Dupré A, Christol B. Atrophodermie folliculaire, proliférations baso-cellulaires et hypotrichose. Ann Derm Syph 1966;93:241-54.
8. Bazex A, Dupré A, Christol B. Génodermatose complexe detype indéterminé associant une hypotrichose, un état atrophodermique généralisé et des dégé́ nérescences cutanées multiples (épithéliomas- basocellulaires). Bull Soc Franc Derm Syph 1964;71:206.
9. Carney RG. Linear unilateral basal-cell nevus with comedones: report of a case. Arch Derm Syphil 1952;65:471-6.
10. Anderson TE, Best PV. Linear basal-cell naevus. Br J Derm 1962;74:20-3.
11. Moulin G, Guillard V, Ferrier E, Marcellin X. Épithé liomatose basocellulaire unis lateralis. Ann Dermatol Venerol 1988;115:1188-90.
12. Bouscarat F, Avril MF, Prade M, et al. Épithéliomatose baso-cellulaire unilatérale. Ann Dermatol Venerol 1990;117:864-6.
13. Guarneri B, Borgia F, Cannavò SP, et al. Multiple familial basal cell carcinomas including a case of segmental manifestion. Dermatology 2000;200:299-302.
14. Happle R. Nonsyndromic type of hereditary multiple basal cell carcinoma. Am J Med Genet 2000;95:161-3.
15. Yoshikawa Y, Takahata Y, Ichimiya M, et al. A case of multiple unilateral localized basal cell carcinomas. J Dermatol 2005;32:66-8.
16. Binkley GW, Johnson HH. Epithelioma adenoides cysticum: basal cell nevi, agenesis of the corpus callosum and dental cyst: a clinical and autopsy study. Arch Dermatol Syphilol 1951;63:73-84.
17. Jarish W. Zur Lehre von den Hautgeschwülsten. Arch Dermatol Syphilol 1894;28:162-222.
18. White JC. Multiple benign cystic epitheliomas. J Cutan Genitourin Dis 1894;12:477-84.
19. Johnson RL, Rothman AL, Xie J, et al. Human homolog of patched, a candidate gene for the basal cell nevus syndrome. Science 1996;272:1668-71.
20. Vabres P, Lacombe D, Rabinowitz LG, et al. The gene for Bazex-Dupré-Christol syndrome maps to chromosome Xq. J Invest Dermatol 1995;105:87-91.
21. Stieler W, Plewig G. Multiple basaliome bei myotonia atrophica Curschmann-Steinert. Hautarzt 1986;37:226-9.
22. Bañuls J, Botella R, Palau F, et al. Tissue and tumor mosaicism of the myotonin protein kinase gene trinucleotide repeat in a patient with multiple basal cell carcinomas associated with myotonic dystrophy. J Am Acad Dermatol 2004;50:S1-3.
23. Requena L, Fariña M, Robledo M, et al. Multiple hereditary infundibulocystic basal cell carcinomas: a genodermatosis different from nevoid basal cell carcinoma syndrome. Arch Dermatol 1999;135:1227-35.
24. Herman AR, Klaus JB, Greenberg RA, Nehal KS. Multiple infundibulocystic basal cell carcinomas: Case report of unique unilateral presentation. Dermatol Surg 2003;29:436-9.
25. Ackerman A, Kerl H, Sanchez J, et al. A clinical atlas of 101 common skin diseases. New York: Ardor Scribendi, 2000. p. 10.
26. Walsh N, Ackerman AB. Infundibulocystic basal cell carcinoma: a newly described variant. Mod Pathol 1990;3:599-608.
27. Kato N, Ueno H. Infundibulocystic basal cell carcinoma. Am J Dermatopathol 1993;15:265-7.
28. de Eusebio E, Sánchez Yus E, López Bran E, et al. Infundibulocystic basaloid neoplasm. J Cutan Pathol 1996;23:147-50.
29. Brown AC, Crounse RG, Winkelman RK. Generalized hair-follicle hamartoma: associated with alopecia, aminoaciduria, and myasthenia gravis. Arch Dermatol 1969;99:478-93.
30. Ridley CM, Smith N. Generalized hair follicle hamartoma associated with alopecia and myasthenia gravis: report of a second case. Clin Exp Dermatol 1981;6:283-9.
31. Weltfriend S, David M, Ginzburg A, Sandbank M. Generalized hair follicle hamartoma: the third case report in association with myasthenia gravis. Am J Dermatopathol 1987;9:428-32.
32. Brownstein MH. Basaloid follicular hamartoma: solitary and multiple types. J Am Acad Dermatol 1992;27:237-40.
33. Wheeler CE, Carroll MA, Groben PA, et al. Autosomal dominantly inherited generalized basaloid follicular hamartoma syndrome: report of a new disease in a North Carolina family. J Am Acad Dermatol 2000;43:189-206.
34. Jih DM, Shapiro M, James W, et al. Familial basaloid follicular hamartoma: lesional characterization and review of the literature. Am J Dermatopathol 2003;25:130-7.