Syndrome-associated soft tissue tumours

Cheryl M. Coffin; Jessica L. Davis; Scott C. Borinstein

doi:10.1111/his.12280

Syndrome-associated soft tissue tumours

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

Research output: Contribution to journal › Review article › peer-review

22 Scopus citations

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 language	English (US)
Pages (from-to)	68-87
Number of pages	20
Journal	Histopathology
Volume	64
Issue number	1
DOIs	https://doi.org/10.1111/his.12280
State	Published - Jan 2014
Externally published	Yes

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

Pathology and Forensic Medicine
Histology

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10.1111/his.12280

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title = "Syndrome-associated soft tissue tumours",

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.",

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

author = "Coffin, {Cheryl M.} and Davis, {Jessica L.} and Borinstein, {Scott C.}",

year = "2014",

month = jan,

doi = "10.1111/his.12280",

language = "English (US)",

volume = "64",

pages = "68--87",

journal = "Histopathology",

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T1 - Syndrome-associated soft tissue tumours

AU - Coffin, Cheryl M.

AU - Davis, Jessica L.

AU - Borinstein, Scott C.

PY - 2014/1

Y1 - 2014/1

N2 - 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.

AB - 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.

KW - Desmoid-type fibromatosis

KW - Gardner fibroma

KW - Li-Fraumeni syndrome

KW - Malignant peripheral nerve sheath tumour

KW - Malignant rhabdoid tumour

KW - Neurofibroma

KW - Neurofibromatosis type I

KW - Rhabdomyosarcoma

KW - Schwannoma

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DO - 10.1111/his.12280

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JO - Histopathology

JF - Histopathology

IS - 1

ER -

Syndrome-associated soft tissue tumours

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

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