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Atypical fibroxanthoma arising in a young patient with Li-Fraumeni syndrome

  • Published:2013-12-24 Issue:3 Volume:41 Page:303-307
  • ISSN:0303-6987
  • Container-title:Journal of Cutaneous Pathology
  • language:en
  • Short-container-title:J Cutan Pathol

Author:

Lee Sun Mi1,Zhang Wei1,Fernandez Martin P.23

Affiliation:

1. Department of Pathology; University of Texas Health Science Center; San Antonio TX USA

2. Department of Pathology; Scott and White Memorial Hospital and Texas A&M University Health Science Center; Temple TX USA

3. Department of Dermatology; Scott and White Memorial Hospital and Texas A&M University Health Science Center; Temple TX USA

Publisher

Wiley

Subject

Dermatology,Histology,Pathology and Forensic Medicine

Reference18 articles.

1. Germ-line p53 mutations predispose to a wide spectrum of early onset cancers;Nichols;Cancer Epidemiol Biomarkers Prev,2001

2. Li-Fraumeni syndrome;Malkin;Genes Cancer,2011

3. Sebaceous gland carcinoma of the eyelid masquerading as a cutaneous horn in Li Fraumeni syndrome;Baumuller;Br J Ophthalmol,2011

4. Infantile cutaneous rhabdomyosarcoma (Li-Fraumeni syndrome): cytological presentation of fine-needle aspirate biopsy, report of a case;Perez-Guillermo;Diagn Cytopathol,1992

5. Atypical fibrous histiocytoma of the skin: clinicopathologic analysis of 59 cases with evidence of infrequent metastasis;Kaddu;Am J Surg Pathol,2002

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