Literature DB >> 19926768

From the archives of the AFIP: musculoskeletal fibromatoses: radiologic-pathologic correlation.

Mark D Murphey1, Chad M Ruble, Sean M Tyszko, Andrew M Zbojniewicz, Benjamin K Potter, Markku Miettinen.   

Abstract

Musculoskeletal fibromatoses represent a wide spectrum of fibroblastic and myofibroblastic neoplasms with similar pathologic appearances and variable clinical behavior. These lesions can be categorized by location (superficial or deep) or by the age group predominantly affected. Superficial fibromatoses in adults (palmar and plantar) and children (calcifying aponeurotic fibroma, lipofibromatosis, and inclusion body fibromatosis) are often small slow-growing lesions; their diagnosis is suggested by location. Deep fibromatoses in adults (desmoid type and abdominal wall) and children (fibromatosis colli and myofibroma and myofibromatosis) are frequently large and more rapidly enlarging; location of these lesions may be nonspecific. Radiographic findings typically are nonspecific. Cross-sectional imaging (ultrasonography, computed tomography, or magnetic resonance [MR] imaging) reveals lesion location, extent, and involvement of adjacent structures for staging and evaluation of local recurrence. MR imaging findings of predominantly low to intermediate signal intensity, nonenhancing bands of low signal intensity on long repetition time MR images that represent collagenized regions, and extension along fascial planes ("fascial tail" sign) add specificity for diagnosis. Additional features that aid in diagnostic specificity include an abdominal wall location related to pregnancy (abdominal wall fibromatosis), a lower neck location in a young child (fibromatosis colli), an adipose component (lipofibromatosis), or multiple lesions in young children (myofibromatosis). Treatment may be conservative or surgical resection, depending on the specific diagnosis. Local recurrence is common after surgical resection owing to the infiltrative growth of these lesions. Recognition that the appearances of the various types of musculoskeletal fibromatoses reflect their pathologic characteristics improves radiologic assessment and helps optimize patient management.

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Mesh:

Year:  2009        PMID: 19926768     DOI: 10.1148/rg.297095138

Source DB:  PubMed          Journal:  Radiographics        ISSN: 0271-5333            Impact factor:   5.333


  47 in total

1.  T2 signal intensity as an imaging biomarker for patients with superficial Fibromatoses of the hands (Dupuytren's disease) and feet (Ledderhose disease) undergoing definitive electron beam irradiation.

Authors:  James S Banks; Aaron H Wolfson; Ty K Subhawong
Journal:  Skeletal Radiol       Date:  2017-10-30       Impact factor: 2.199

2.  Radiotherapy in desmoid tumors : Treatment response, local control, and analysis of local failures.

Authors:  Kirsi Santti; Annette Beule; Laura Tuomikoski; Mikko Rönty; Anna-Stina Jääskeläinen; Kauko Saarilahti; Hanna Ihalainen; Maija Tarkkanen; Carl Blomqvist
Journal:  Strahlenther Onkol       Date:  2017-01-02       Impact factor: 3.621

3.  Abdominal wall fibromatosis associated with previous laparoscopic hernia repair.

Authors:  S B F Brown; E MacDuff; P J O'Dwyer
Journal:  Hernia       Date:  2013-04-09       Impact factor: 4.739

4.  Soft tissue angiofibroma: a case report.

Authors:  Jonathan J Lee; Miriam A Bredella; Dempsey S Springfield; Gunnlauger P Nielsen
Journal:  Skeletal Radiol       Date:  2013-10-10       Impact factor: 2.199

5.  Lipofibromatosis: magnetic resonance imaging features and pathological correlation in three cases.

Authors:  Daniela Vogel; Alberto Righi; Jennifer Kreshak; Angelo Paolo Dei Tos; Biagio Merlino; Eugenio Brunocilla; Daniel Vanel
Journal:  Skeletal Radiol       Date:  2014-02-08       Impact factor: 2.199

6.  Clinics in diagnostic imaging (195). Plantar fibromatosis.

Authors:  Felicia Teo; Mohammad Taufik Bin Mohamed Shah; Bak Siew Steven Wong
Journal:  Singapore Med J       Date:  2019-05       Impact factor: 1.858

7.  Diagnostic imaging and CEUS findings in a rare case of Desmoid-type fibromatosis. A case report.

Authors:  Massimo Valentino; Mauro Liberatore; Fabrizio Maghella; Valeria De Soccio; Carlo De Felice; Daniela Messineo; Francesco Maria Drudi
Journal:  J Ultrasound       Date:  2018-03-21

Review 8.  Desmoid type fibromatosis in the facet joint of lumbar spine: case report and review of literature.

Authors:  So Jung Kim; Doo Hoe Ha; Sang Min Lee; Haeyoun Kang
Journal:  Korean J Radiol       Date:  2013-08-30       Impact factor: 3.500

9.  Imaging findings in seven cases of congenital infantile myofibromatosis with cerebral, spinal, or head and neck involvement.

Authors:  Laura Holzer-Fruehwald; Susan Blaser; Andrea Rossi; Julia Fruehwald-Pallamar; Majda M Thurnher
Journal:  Neuroradiology       Date:  2012-11-16       Impact factor: 2.804

10.  Desmoid-type fibromatosis in the head and neck: CT and MR imaging characteristics.

Authors:  Jung Hyo Rhim; Ji-Hoon Kim; Kyung Chul Moon; Sun-Won Park; Chul-Ho Sohn; Seung Hong Choi; Tae Jin Yun; Kee-Hyun Chang
Journal:  Neuroradiology       Date:  2013-01-22       Impact factor: 2.804

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