Recurrence of atypical fibroxanthoma. Diagnosis and treatment

Introduction: The soft tissue sarcomas (SPM) accounts for only 1% of malignant tumors of the adult population. The SPM is the most frequent malignant fibrous histiocytoma (MFH) that exhibits behavior characterized by the tendency to invasion of adjacent tissue and metastatic spread early. One of its...

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Main Authors: Mattiola, Leandro Ricardo, Mattiola, Lyzandro, Mattiola, Giovani, Mattiola, Sandra Zucchi de Moraes, Moura, Carlos Eduardo, Kirschnick, Alexandre
Format: Article
Language:English
Published: Thieme Revinter Publicações Ltda. 2012-01-01
Series:International Archives of Otorhinolaryngology
Subjects:
Online Access:http://www.internationalarchivesent.org/additional/acervo_eng.asp?id=1322
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spelling doaj-78ebe50bec314080b3ad3fa556a39f322020-11-25T01:29:41ZengThieme Revinter Publicações Ltda.International Archives of Otorhinolaryngology1809-97771809-48642012-01-01164530532Recurrence of atypical fibroxanthoma. Diagnosis and treatmentMattiola, Leandro RicardoMattiola, LyzandroMattiola, GiovaniMattiola, Sandra Zucchi de MoraesMoura, Carlos EduardoKirschnick, AlexandreIntroduction: The soft tissue sarcomas (SPM) accounts for only 1% of malignant tumors of the adult population. The SPM is the most frequent malignant fibrous histiocytoma (MFH) that exhibits behavior characterized by the tendency to invasion of adjacent tissue and metastatic spread early. One of its variants is the atypical fibroxanthoma (FA). Objective: To describe a case of probable recurrence of AF underwent surgical treatment and presentation of a literature review. Case report: Patient female, 63 years, presenting with a mass in the face about four inches and a history of prior resection of the lesion in the same topography. The patient underwent surgical resection with a diagnosis of AF. Conclusion: The FA is a rare tumor histological diagnosis difficult. The correct histological diagnosis and patient follow-up are essential.http://www.internationalarchivesent.org/additional/acervo_eng.asp?id=1322sarcomamalignant fibrous histiocytomaneoplasms of soft tissue neoplasms ENT
collection DOAJ
language English
format Article
sources DOAJ
author Mattiola, Leandro Ricardo
Mattiola, Lyzandro
Mattiola, Giovani
Mattiola, Sandra Zucchi de Moraes
Moura, Carlos Eduardo
Kirschnick, Alexandre
spellingShingle Mattiola, Leandro Ricardo
Mattiola, Lyzandro
Mattiola, Giovani
Mattiola, Sandra Zucchi de Moraes
Moura, Carlos Eduardo
Kirschnick, Alexandre
Recurrence of atypical fibroxanthoma. Diagnosis and treatment
International Archives of Otorhinolaryngology
sarcoma
malignant fibrous histiocytoma
neoplasms of soft tissue neoplasms ENT
author_facet Mattiola, Leandro Ricardo
Mattiola, Lyzandro
Mattiola, Giovani
Mattiola, Sandra Zucchi de Moraes
Moura, Carlos Eduardo
Kirschnick, Alexandre
author_sort Mattiola, Leandro Ricardo
title Recurrence of atypical fibroxanthoma. Diagnosis and treatment
title_short Recurrence of atypical fibroxanthoma. Diagnosis and treatment
title_full Recurrence of atypical fibroxanthoma. Diagnosis and treatment
title_fullStr Recurrence of atypical fibroxanthoma. Diagnosis and treatment
title_full_unstemmed Recurrence of atypical fibroxanthoma. Diagnosis and treatment
title_sort recurrence of atypical fibroxanthoma. diagnosis and treatment
publisher Thieme Revinter Publicações Ltda.
series International Archives of Otorhinolaryngology
issn 1809-9777
1809-4864
publishDate 2012-01-01
description Introduction: The soft tissue sarcomas (SPM) accounts for only 1% of malignant tumors of the adult population. The SPM is the most frequent malignant fibrous histiocytoma (MFH) that exhibits behavior characterized by the tendency to invasion of adjacent tissue and metastatic spread early. One of its variants is the atypical fibroxanthoma (FA). Objective: To describe a case of probable recurrence of AF underwent surgical treatment and presentation of a literature review. Case report: Patient female, 63 years, presenting with a mass in the face about four inches and a history of prior resection of the lesion in the same topography. The patient underwent surgical resection with a diagnosis of AF. Conclusion: The FA is a rare tumor histological diagnosis difficult. The correct histological diagnosis and patient follow-up are essential.
topic sarcoma
malignant fibrous histiocytoma
neoplasms of soft tissue neoplasms ENT
url http://www.internationalarchivesent.org/additional/acervo_eng.asp?id=1322
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AT mattiolasandrazucchidemoraes recurrenceofatypicalfibroxanthomadiagnosisandtreatment
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