Literature DB >> 7665068

[Spontaneous malignant transformation of extra-abdominal fibromatosis to fibrosarcoma].

J Schwickerath1, H J Künzig.   

Abstract

The desmoid tumour with infiltrative and destructive growth tendencies, is a rare benign alteration of the connective tissue from musculo-aponeurotic structures and fascial sheaths. The exact pathogenesis is unknown, however trauma (surgery), genetic (Gardener's Syndrome) or hormonal factors (pregnancy) have been implicated. A spontaneous malignant transformation of a desmoid (extra-abdominal fibromatosis) to a fibrosarcoma is a rarity. Only one case is recorded in the literature. We report on the second case in international literature and describe the coherence to an endocrine factor (pregnancy), the high recurrence rate and the difficulty of therapy with regard to the risk of late malignant transformation.

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Year:  1995        PMID: 7665068     DOI: 10.1055/s-2007-1022800

Source DB:  PubMed          Journal:  Geburtshilfe Frauenheilkd        ISSN: 0016-5751            Impact factor:   2.915


  2 in total

1.  Intrathoracic Desmoid Tumor Presenting as Multiple Lung Nodules 13 Years after Previous Resection of Abdominal Wall Desmoid Tumor.

Authors:  Gun Woo Koo; Sung Jun Chung; Joo Hee Kwak; Chang Kyo Oh; Dong Won Park; Hyeon Jung Kwak; Ji-Yong Moon; Sang-Heon Kim; Jang Won Sohn; Ho Joo Yoon; Dong Ho Shin; Sung Soo Park; Young-Ha Oh; Ju Yeon Pyo; Tae-Hyung Kim
Journal:  Tuberc Respir Dis (Seoul)       Date:  2015-06-30

2.  Case report: Trapezius Fibromatosis in the Elderly - An Extremely Rare Tumor.

Authors:  Praveen Ravi; S Sundar Suriyakumar
Journal:  J Orthop Case Rep       Date:  2020
  2 in total

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