2004, Number 2
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Rev Cent Dermatol Pascua 2004; 13 (2)
Solitary neurofibroma. Two cases report
Venadero-Albarrán F, Rodríguez AM, Merelo V, Cervantes AAM, Ramos-Garibay A
Language: Spanish
References: 11
Page: 99-102
PDF size: 84.02 Kb.
ABSTRACT
Neurofibromas can be classified either as solitary or multiple. Solitary neurofibromas are incidental findings and usually are not associated with systemic manifestations. Multiple neurofibromas could be find in patients with neurofibromatosis or Von Recklinghausen´s disease. Clinical manifestation of solitary neurofibromas are most commonly observed in the second and third decade of life, they are soft, not associated to any other clinical symptomatology lesions. It exist a plenty of types of neurofibromas we review them in this article.
REFERENCES
Eniko K, Riccardi V. Las neurofibromatosis. In: Fitzpatrick TB, Risen A. Dermatology in General Medicine. 5a. ed. McGraw-Hill, New York EUA, 1999: 2281-2290.
Mosaad M. Histopathological variants of neurofibroma. Am J Dematopathol 1996; 16: 486-499.
Ahn, Sung K, Hyung J, Kim T et al. Intratumoral fat in neurofibroma. Am J Dermatopathol 2002; 24: 326-329.
Dangoise C, Andre J, Dobbeleer G. Solitary subungual neurofibroma. Ac Terap Dermatol 2003; 26: 116.
Richard J. Tumores de tejido neural. En: Lever Histopatología de la piel. 8ª ed. Intermédica Editorial. Buenos Aires Argentina, 1999: 843-856.
Inaba, Mayumi, Yamamoto, Tetsuji et al. Pigmented neurofibroma: Report of two cases and literature review. Path Internal 2001; 51: 565-569.
Bhushan M, Telfer NR. Subungal neurofibroma: an unusual cause of nail dystrophy. Br J Dermatol 1999; 140: 777-778.
Enzinger FM, Weiss S. Soft tissue tumors. St. Louis: Mosby, 1998.
Prichard R, Custer R. Pacinian neurofibroma. Cancer 1952; 5: 297-301.
Jaimes V. Tumores neurales cutáneos. Tesis de posgrado. Centro Dermatológico Pascua 2000: 6-38.
Linares S, Vega ME. Tumores de la vaina nerviosa periférica. Estudio de 62 casos. Dermatol Rev Mex 1998; 42: 52-7.