| Comunicación Nº: 097 | English version  |
| Comunicación Nº: 097 | English version |
Jose Luis Rodríguez Peralto, Santiago Madero*, Víctor M. Castellano, Ricardo Gil
[Título] [Introducción] [Material y Métodos] [Resultados] [Iconografía] [Discusión] [Comentarios]
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1.- Calonje E, Fletcher CDM. Cutaneous fibrohistiocytic tumors: An update. Advances in Anatomic Pathology 1994, 1: 2-15.
2.- Calonje E, Mentzel T, Fletcher CDM. Cellular benign fibrous histiocytoma: clinicopathologic analysis of 74 cases of a distinctive variant of cutaneous fibrous hiatiocytoma with frequent rtecurrence. Am J Surg Pathol 1994, 18:668-676.
3.- LeBoit PE, Barr RJ, Burrall S, Metcalf JS, Benedict Yen TS, and Wick MR. Primitive polypoid granular-cell tumor and other cutaneous granular-cell neoplasms of apparent nonneural origin. Am J Surg Pathol 1991, 15:48-58.
4.- Tsang WYW, and Chan JKC. KPI (CD 68) staining of granular cell neoplasms: is KPI a marker for lysosomes rather than the histiocytic lineage? Histopathology 1992, 21:84-86.
5.- Menzel T, Wadden C, and Fletcher CDM. Granular cell change in smooth muscle tumours of skin and soft tissue. Histopathology 1994; 24: 223-231.
6.- Rodríguez Peralto JL. Dermatofibroma con células granulares. / Curso de Patología San Sebastian 1995; pp188-192.
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