Syndrome-associated soft tissue tumours

Cheryl M. Coffin, Jessica Davis, Scott C. Borinstein

Research output: Contribution to journalReview article

12 Citations (Scopus)

Abstract

Soft tissue neoplasms may be associated with a variety of genetic disorders and malformation syndromes, especially when they arise in children, adolescents and early adulthood. This review summarizes the principal histopathological types of soft tissue tumours which occur in various syndromes, with an emphasis on pathological features, genetic aspects and considerations for the diagnostic pathologist.

Original languageEnglish (US)
Pages (from-to)68-87
Number of pages20
JournalHistopathology
Volume64
Issue number1
DOIs
StatePublished - Jan 1 2014
Externally publishedYes

Fingerprint

Soft Tissue Neoplasms
Inborn Genetic Diseases
Neoplasms
Pathologists

Keywords

  • Desmoid-type fibromatosis
  • Gardner fibroma
  • Li-Fraumeni syndrome
  • Malignant peripheral nerve sheath tumour
  • Malignant rhabdoid tumour
  • Neurofibroma
  • Neurofibromatosis type I
  • Rhabdomyosarcoma
  • Schwannoma

ASJC Scopus subject areas

  • Histology
  • Pathology and Forensic Medicine

Cite this

Syndrome-associated soft tissue tumours. / Coffin, Cheryl M.; Davis, Jessica; Borinstein, Scott C.

In: Histopathology, Vol. 64, No. 1, 01.01.2014, p. 68-87.

Research output: Contribution to journalReview article

Coffin, CM, Davis, J & Borinstein, SC 2014, 'Syndrome-associated soft tissue tumours', Histopathology, vol. 64, no. 1, pp. 68-87. https://doi.org/10.1111/his.12280
Coffin, Cheryl M. ; Davis, Jessica ; Borinstein, Scott C. / Syndrome-associated soft tissue tumours. In: Histopathology. 2014 ; Vol. 64, No. 1. pp. 68-87.
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