FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS

Bibliographic Details
Main Author: Araújo, Catarina
Publication Date: 2015
Other Authors: Henriques, M. A., Vale, Esmeralda, Viana, Isabel
Format: Article
Language: por
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://doi.org/10.29021/spdv.73.1.346
Summary: Introduction: Fibrous histiocytoma represents a group of common benign lesions that occur mainly on the extremities. The location on the face is rare and here, more aggressive variants and higher local recurrence are described.Methods: We conducted a retrospective clinicopathological study of cases of fibrous histiocytoma arising on the face at the Dermatology Service of the Hospital Egas Moniz and the “Centro de Dermatologia Médico-Cirúrgica” in Lisbon, between January 2001 and December 2012.Results: In a total of 1307 fibrous histiocytoma (any location), 12 were located on the face. These lesions occurred in 8 females and 4 males (mean age 48.9 years). The preferred location was the nose (4 cases) followed by the chin (3 cases), interciliar (3 cases), infraorbital (1 case) and ear (1case). The most common clinical diagnosis was epidermoid cyst (5 cases). Histologically, the majority of tumors (10 cases) reached the deep dermis. Six cases showed common morphology. Three cases corresponded to the cellular variant of fibrous histiocytoma, two cases aneurysmal fibrous histiocytoma and one case hemosiderotic fibrous histiocytoma. In five cases mild pleomorphism and mitotic activity were evident. Necrosis, neural and / or vascular invasion were not identified. In seven lesions immunohistochemical studies for differential diagnosis were performed.Conclusion: In most cases correlation with the clinical diagnosis was not observed. Compared with common fibrous histiocytoma, involvement of deep structures, cell density and pleomorphism are more frequent, leading to a need of greater clinical vigilance and excision with wider safety margins.
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spelling FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSISHISTIOCITOFIBROMA NA FACE – UM DIAGNÓSTICO INESPERADOHistiocytomabenign fibrousFaceHistiocitoma fibroso benignoFaceIntroduction: Fibrous histiocytoma represents a group of common benign lesions that occur mainly on the extremities. The location on the face is rare and here, more aggressive variants and higher local recurrence are described.Methods: We conducted a retrospective clinicopathological study of cases of fibrous histiocytoma arising on the face at the Dermatology Service of the Hospital Egas Moniz and the “Centro de Dermatologia Médico-Cirúrgica” in Lisbon, between January 2001 and December 2012.Results: In a total of 1307 fibrous histiocytoma (any location), 12 were located on the face. These lesions occurred in 8 females and 4 males (mean age 48.9 years). The preferred location was the nose (4 cases) followed by the chin (3 cases), interciliar (3 cases), infraorbital (1 case) and ear (1case). The most common clinical diagnosis was epidermoid cyst (5 cases). Histologically, the majority of tumors (10 cases) reached the deep dermis. Six cases showed common morphology. Three cases corresponded to the cellular variant of fibrous histiocytoma, two cases aneurysmal fibrous histiocytoma and one case hemosiderotic fibrous histiocytoma. In five cases mild pleomorphism and mitotic activity were evident. Necrosis, neural and / or vascular invasion were not identified. In seven lesions immunohistochemical studies for differential diagnosis were performed.Conclusion: In most cases correlation with the clinical diagnosis was not observed. Compared with common fibrous histiocytoma, involvement of deep structures, cell density and pleomorphism are more frequent, leading to a need of greater clinical vigilance and excision with wider safety margins.Introdução: O histiocitofibroma é um dos tumores cutâneos benignos mais frequentes que ocorre sobretudo nas extremidades. A localização na face é rara onde estão descritas variantes mais agressivas e maior recorrência local.Métodos: Efetuou-se um estudo clínico-patológico retrospetivo, de histiocitofibromas da face diagnosticados nos laboratórios de Dermatopatologia do Serviço de Dermatologia do Hospital Egas Moniz e do Centro de Dermatologia Médico-Cirúrgica de Lisboa, entre Janeiro de 2001 e Dezembro de 2012.Resultados: Num total de 1307 histiocitofibromas (qualquer localização) detectaram-se 12 histiocitofibromas da face. As lesões ocorreram em 8 mulheres e 4 homens (idade média - 48.9 anos). A localização preferencial foi o nariz (4 casos) seguido da região mentoniana (3 casos), interciliar (3 casos), infraorbitária (1 caso) e pavilhão auricular (1 caso). O diagnóstico clínico mais frequente foi de quisto epidermóide (5 casos). Histologicamente a maioria (10 casos) atingia a derme profunda e 6 casos apresentavam padrão morfológico comum. Em três casos observou-se variante de histiocitofibroma celular, em dois casos variante aneurismática e num caso variante hemossiderótica. Em cinco casos foi observado pleomorfismo discreto e mitoses. Não foram identificados necrose e/ou invasão vascular ou nervosa. Em sete lesões realizou-se estudo imunohistoquímico para diagnóstico diferencial com outros tumores, nomeadamente dermatofibrossarcoma protuberans e leiomiossarcoma.Conclusão: Na maioria dos casos a concordância com o diagnóstico clínico não foi observada. Em comparação com a forma comum de histiocitofibroma há maior envolvimento de estruturas profundas, densidade celular e pleomorfismo pelo que é necessário maior vigilância clínica e excisão com maior margem de segurança.Sociedade Portuguesa de Dermatologia e Venereologia2015-06-06T00:00:00Zjournal articleinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://doi.org/10.29021/spdv.73.1.346oai:ojs.revista.spdv.com.pt:article/346Journal of the Portuguese Society of Dermatology and Venereology; Vol 73 No 1 (2015): Janeiro - Março; 79-88Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 73 n. 1 (2015): Janeiro - Março; 79-882182-24092182-2395reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPporhttps://revista.spdv.com.pt/index.php/spdv/article/view/346https://doi.org/10.29021/spdv.73.1.346https://revista.spdv.com.pt/index.php/spdv/article/view/346/315Araújo, CatarinaHenriques, M. A.Vale, EsmeraldaViana, Isabelinfo:eu-repo/semantics/openAccess2022-10-06T12:34:51Zoai:ojs.revista.spdv.com.pt:article/346Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T10:31:04.647776Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS
HISTIOCITOFIBROMA NA FACE – UM DIAGNÓSTICO INESPERADO
title FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS
spellingShingle FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS
Araújo, Catarina
Histiocytoma
benign fibrous
Face
Histiocitoma fibroso benigno
Face
title_short FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS
title_full FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS
title_fullStr FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS
title_full_unstemmed FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS
title_sort FIBROUS HISTIOCYTOMA ARISING ON THE FACE – AN UNEXPECTED DIAGNOSIS
author Araújo, Catarina
author_facet Araújo, Catarina
Henriques, M. A.
Vale, Esmeralda
Viana, Isabel
author_role author
author2 Henriques, M. A.
Vale, Esmeralda
Viana, Isabel
author2_role author
author
author
dc.contributor.author.fl_str_mv Araújo, Catarina
Henriques, M. A.
Vale, Esmeralda
Viana, Isabel
dc.subject.por.fl_str_mv Histiocytoma
benign fibrous
Face
Histiocitoma fibroso benigno
Face
topic Histiocytoma
benign fibrous
Face
Histiocitoma fibroso benigno
Face
description Introduction: Fibrous histiocytoma represents a group of common benign lesions that occur mainly on the extremities. The location on the face is rare and here, more aggressive variants and higher local recurrence are described.Methods: We conducted a retrospective clinicopathological study of cases of fibrous histiocytoma arising on the face at the Dermatology Service of the Hospital Egas Moniz and the “Centro de Dermatologia Médico-Cirúrgica” in Lisbon, between January 2001 and December 2012.Results: In a total of 1307 fibrous histiocytoma (any location), 12 were located on the face. These lesions occurred in 8 females and 4 males (mean age 48.9 years). The preferred location was the nose (4 cases) followed by the chin (3 cases), interciliar (3 cases), infraorbital (1 case) and ear (1case). The most common clinical diagnosis was epidermoid cyst (5 cases). Histologically, the majority of tumors (10 cases) reached the deep dermis. Six cases showed common morphology. Three cases corresponded to the cellular variant of fibrous histiocytoma, two cases aneurysmal fibrous histiocytoma and one case hemosiderotic fibrous histiocytoma. In five cases mild pleomorphism and mitotic activity were evident. Necrosis, neural and / or vascular invasion were not identified. In seven lesions immunohistochemical studies for differential diagnosis were performed.Conclusion: In most cases correlation with the clinical diagnosis was not observed. Compared with common fibrous histiocytoma, involvement of deep structures, cell density and pleomorphism are more frequent, leading to a need of greater clinical vigilance and excision with wider safety margins.
publishDate 2015
dc.date.none.fl_str_mv 2015-06-06T00:00:00Z
dc.type.driver.fl_str_mv journal article
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format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.29021/spdv.73.1.346
oai:ojs.revista.spdv.com.pt:article/346
url https://doi.org/10.29021/spdv.73.1.346
identifier_str_mv oai:ojs.revista.spdv.com.pt:article/346
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://revista.spdv.com.pt/index.php/spdv/article/view/346
https://doi.org/10.29021/spdv.73.1.346
https://revista.spdv.com.pt/index.php/spdv/article/view/346/315
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Sociedade Portuguesa de Dermatologia e Venereologia
publisher.none.fl_str_mv Sociedade Portuguesa de Dermatologia e Venereologia
dc.source.none.fl_str_mv Journal of the Portuguese Society of Dermatology and Venereology; Vol 73 No 1 (2015): Janeiro - Março; 79-88
Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 73 n. 1 (2015): Janeiro - Março; 79-88
2182-2409
2182-2395
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