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Multiple Cutaneous Granular Cell Tumors and Neurofibromatosis in ChildhoodA Case Report and Review of the Literature
Robert W. Martin III, MD;
Kenneth H. Neldner, MD;
Alan S. Boyd, MD;
Penelope W. Coates, PhD
Arch Dermatol. 1990;126(8):1051-1056.
Abstract
Multiple cutaneous granular cell tumors have been previously reported in only 26 children or adolescents. An association of these tumors with neurofibromatosis has never been reported previously. We describe a 12-year-old black girl with multiple cutaneous granular cell tumors and neurofibromatosis. Although the histogenesis of these tumors is not completely clear, the findings of ultrastructural and immunohistochemical evaluation of our patient's tumors and the associated neurofibromatosis support a neural crest origin for granular cell tumors.
(Arch Dermatol. 1990;126:1051-1056)
Author Affiliations
From the Departments of Dermatology (Drs Martin, Neldner, and Boyd) and Cell Biology and Anatomy (Dr Coates), School of Medicine, Texas Tech University Health Sciences Center, Lubbock.
Footnotes
Accepted for publication March 28, 1990.
Presented in part at the 41st annual meeting of the Pacific Dermatologic Association, Honolulu, Hawaii, October 27, 1989.
Reprint requests to Department of Dermatology, School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX 79430 (Dr Martin).
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