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Literature DB >> 24236688

Syndrome-associated soft tissue tumours.

Cheryl M Coffin¹, Jessica L Davis, Scott C Borinstein.

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.

Entities: Disease Species

Keywords: Gardner fibroma; Li-Fraumeni syndrome; desmoid-type fibromatosis; malignant peripheral nerve sheath tumour; malignant rhabdoid tumour; neurofibroma; neurofibromatosis type I; rhabdomyosarcoma; schwannoma

Mesh：

Year: 2013 PMID： 24236688 DOI： 10.1111/his.12280

Source DB: PubMed Journal: Histopathology ISSN： 0309-0167 Impact factor: 5.087

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Cited

6 in total

6. Clinical characteristics and outcomes of infants compared with children diagnosed with rhabdomyosarcoma: Analysis of surveillance, epidemiology and end results data from 2000 to 2016.

Authors: Hannah D Rees; Nancy K Hills; Amit J Sabnis; Asmin B Tulpule; Tom K Shimotake; Robert E Goldsby
Journal: Cancer Rep (Hoboken) Date: 2021-07-13

6 in total

Syndrome-associated soft tissue tumours.

Review 1. Sarcomas Associated With Genetic Cancer Predisposition Syndromes: A Review.

Review 2. Probing for a deeper understanding of rhabdomyosarcoma: insights from complementary model systems.

3. Common lesions in a rare entity - Gardner's syndrome.

4. Alveolar Rhabdomyosarcoma in a 69-Year-Old Woman Receiving Glucagon-Like Peptide-2 Therapy.

5. From Gardner fibroma diagnosis to constitutional APC mutation detection: a one-way street.

6. Clinical characteristics and outcomes of infants compared with children diagnosed with rhabdomyosarcoma: Analysis of surveillance, epidemiology and end results data from 2000 to 2016.