Literature DB >> 16917630

Aggressive intracranial fibromatosis: case report.

Oswaldo Inácio de Tella1, Luciano Ricardo França Silva, João Norberto Stavale, Marco Antonio Herculano, Manoel Antonio de Paiva Neto, Celso Agner.   

Abstract

UNLABELLED: Fibromatosis is a locally aggressive, proliferative fibroblastic lesion affecting musculoaponeurotic structures, most often in the limbs and trunk. Intracranial fibromatosis is extremely rare and requires aggressive treatment to prevent recurrence. CASE DESCRIPTION: We present the case of a 20 year old woman with aggressive skull base fibromatosis. The lesion extended through the sphenoid, ethmoid sinus and nasal cavity, destroying the right roof of the orbit and penetrating in anterior skull base. A combined anterior craniofacial approach was performed; complete resection with surgical margin was impossible due to the localization of the tumor and relation to important neurovascular structures. Complete resection with surgical margin is often impossible because of its widely infiltrative nature. Radiotherapy and chemotherapy are often required to improve local control of the lesion.

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Mesh:

Year:  2006        PMID: 16917630     DOI: 10.1590/s0004-282x2006000300031

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  3 in total

1.  Primary intracranial aggressive fibromatosis arising in sella turcica: illustrative case.

Authors:  Kenta Ujifuku; Eisakua Sadakata; Shiro Baba; Koichi Yoshida; Kensaku Kamada; Minoru Morikawa; Kuniko Abe; Kazuhiko Suyama; Yoichi Nakazato; Isao Shimokawa; Takayuki Matsuo
Journal:  J Neurosurg Case Lessons       Date:  2021-09-20

2.  A Rare Case of Aggressive Fibromatosis Infiltrating Dorsal Muscles in a 6-Year-Old Patient - CT, MRI and Elastography Evaluation.

Authors:  Aleksander Pawluś; Kinga Szymańska; Krzysztof Kaczorowski; Dąbrówka Sokołowska-Dąbek; Cyprian Olchowy; Bartosz D Markiewicz; Urszula Zaleska-Dorobisz
Journal:  Pol J Radiol       Date:  2015-03-28

3.  Gradually shrinking intra-abdominal desmoid tumor derived from the stomach in a young boy: a case report.

Authors:  Kazushi Miyata; Masahide Fukaya; Masato Nagino
Journal:  Surg Case Rep       Date:  2017-04-20
  3 in total

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