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Touraine A (1941)
Une nouvelle neuro-ectodermosa congenitale la lentiginose centro-faciale et ses dysplasies associecsAnn Dermatol Syphiligr, 8
L. Lumpkin (1973)
Skin, Hereditary and Malignant NeoplasmsMilitary Medicine, 138
N. Perkinson (1957)
Melanoma arising in a café au lait spot of neurofibromatosis.American journal of surgery, 93 6
F. Crowe, W. Schull, J. Neel (1956)
A clinical, pathological, and genetic study of multiple neurofibromatosis
Kopf Aw, J. Yuppa (1968)
Becker's nevus.Archives of dermatology, 98 1
Moynahan EJ (1962)
Multiple symmetrical moles with psychic and somatic infantilism and genital hypoplasiaProc R Soc Med, 55
F. Crowe (1964)
AXILLARY FRECKLING AS A DIAGNOSTIC AID IN NEUROFIBROMATOSIS.Annals of internal medicine, 61
A. Capute, D. Rimoin, B. Konigsmark, N. Esterly, F. Richardson (1969)
Congenital deafness and multiple lentigines. A report of cases in a mother and daughter.Archives of dermatology, 100 2
R. Gorlin, Ray Anderson, M. Blaw (1969)
Multiple Lentigenes Syndrome: Complex Comprising Multiple Lentigenes, Electrocardiographic Conduction Abnormalities, Ocular Hypertelorism, Pulmonary Stenosis, Abnormalities of Genitalia, Retardation of Growth, Sensorineural Deafness, and Autosomal Dominant Hereditary PatternJAMA Pediatrics, 117
et al Reed WB (1965)
Giant pigmented nevi, melanoma and leptomeningeal melanocytosisArch Dermatol, 91
Rook A Frain-Bell W (1947)
Pigmented and hypertrichotic epidermal nevus transSt. John Hosp Derm Soc, 39
A. Zelickson (1967)
Ultrastructure of Normal and Abnormal Skin
J. Venable, R. Coggeshall (1965)
A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPYThe Journal of Cell Biology, 25
P. Polani, E. Moynahan (1972)
Progressive cardiomyopathic lentiginosis.The Quarterly journal of medicine, 41 162
J. Luft (1961)
IMPROVEMENTS IN EPOXY RESIN EMBEDDING METHODSThe Journal of Biophysical and Biochemical Cytology, 9
A. Allen (1954)
The skin : a clinicopathological treatise
A. Pipkin, S. Pipkin (1950)
A pedigree of generalized lentigo.The Journal of heredity, 41 3
B. Johnson, D. Charneco (1970)
Café au lait spot in neurofibromatosis and in normal individuals.Archives of dermatology, 102 4
P. Benedict, G. Szabó, T. Fitzpatrick, S. Sinesi (1968)
Melanotic macules in Albright's syndrome and in neurofibromatosis.JAMA, 205 9
Hamada Y Ito M (1952)
Nevus spilus en nappeTohoku J Exp Med, 55
W. Reed, S. Becker, S. Becker, W. Nickel (1965)
GIANT PIGMENTED NEVI, MELANOMA, AND LEPTOMENINGEAL MELANOCYTOSIS: A CLINICAL AND HISTOPATHOLOGICAL STUDY.Archives of dermatology, 91
Anderson RC Gorlin RJ (1969)
Multiple lentigenes syndromeAm J Dis Child, 117
Minkin W Cohen HJ (1970)
Nevus spilusArch Dermatol, 102
Abstract A new pigmentary disorder, which is characterized by the presence of a large, seemingly related band of hyperpigmentation together with multiple theques of type-B nevus (Mishima) cells, is described in a 16-year-old boy, a 13-year-old girl, and a 12-year-old girl. The lesion, which had not been present since infancy, must be considered a probably new, undescribed entity that has been noted but not reported at various dermatological meetings. It is distinct from the giant, hairy, pigmented nevus, nevus spilus, Becker nevus, and the more involved systemic disorders that are genetic. References 1. Benedict PH, et al: Melanotic macules in Albright's syndrome and in neurofibromatosis . JAMA 205:618-626,1968.Crossref 2. Cohen HJ, Minkin W, Frank SB: Nevus spilus , Arch Dermatol 102:433-437,1970.Crossref 3. Ito M, Hamada Y: Nevus spilus en nappe . Tohoku J Exp Med 55 ( (suppl 1) ): 44,1952.Crossref 4. Luft JH: Improvements in epoxy resin embedding methods . J Biophys Biochem Cytol 9: 409-414,1961.Crossref 5. Venable JH, Coggeshall R: A simplified lead citrate stain for use in electron microscopy . J Cell Biol 25 (pt (1) ):407-408,1965.Crossref 6. Zelickson AS: Ultrastructure of Normal and Abnormal Skin . Philadelphia, Lea & Febiger Publishers, 1967, p 395. 7. Moynahan EJ: Multiple symmetrical moles with psychic and somatic infantilism and genital hypoplasia . Proc R Soc Med 55:959-960,1962. 8. Polani PE, Moynahan EJ: Progressive car- diomyopathic lentiginosa . Q J Med 41:205-225, 1972. 9. Gorlin RJ, Anderson RC, Blaw M: Multiple lentigenes syndrome . Am J Dis Child 117:652-662,1969.Crossref 10. Crowe FW, Schull WJ, Neel JU: A Clinical, Pathological and Genetic Study of Multiple Neurofibromatosis , Springfield, IL, Charles C Thomas Publisher, 1956. 11. Crowe FW: Axillary freckling as a diagnostic aid in neurofibromatosis . Ann Intern Med 61:1142-1143, 1964.Crossref 12. Allen AC: The Skin, a Clinicopathological Treatise . St. Louis, CV Mosby Co, 1954, p 966. 13. Johnson BL, Charneco DR: Cafe-au-lait spot in neurofibromatosis and in normal individuals . Arch Dermatol 102:442-446,1970.Crossref 14. Capute AJ, et al: Congenital deafness and multiple lentigines: A report of cases in a mother and daughter . Arch Dermatol 100:207-213, 1969.Crossref 15. Reed WB, et al: Giant pigmented nevi, melanoma and leptomeningeal melanocytosis . Arch Dermatol 91:100-119,1965.Crossref 16. Kopf WF: Becker's nevus . Arch Dermatol 98:97-98, 1968.Crossref 17. Frain-Bell W, Rook A: Pigmented and hypertrichotic epidermal nevus trans . St. John Hosp Derm Soc 39:51,1947. 18. Pipkin AC, Pipkin SB: A pedigree of generalized lentigo . J Hered 41:79-82,1950. 19. Touraine A: Une nouvelle neuro-ectodermosa congenitale la lentiginose centro-faciale et ses dysplasies associecs . Ann Dermatol Syphiligr 8:453-473,1941. 20. Perkinson NG: Melanoma arising in a cafe-au-lait spot of neurofibromatosis . Am J Surg 93:1018-1020,1957.Crossref 21. Lynch HT: Skin, Hereditary and Malignant Neoplasms . Flushing, NY, Medical Examination Publishing Co Inc, 1972, p 69.
Archives of Dermatology – American Medical Association
Published: Jun 1, 1973
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