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Orbital lymphangioma: a surgical challenge

Bibliographic Details
Main Author: Ramalho, M
Publication Date: 2013
Other Authors: Santos, C, Pina, S, Coutinho, I, Vaz, F, Ferreira, M, Melo, A
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.10/1076
Summary: Lymphangioma is an uncommon venolymphatic lesion with dead-end lymphatic channels, also defined as vascular hamartoma of lymphatic origin. Orbital lymphangiomas present management challenges to the ophthalmologist due to the tendency to recur locally unless it is completely excised, this is often difficult, because lymphangiomas tend to be infiltrative. The recurrence of hemorrhage and expansion can lead to vision loss and disfigurement. Case report: A 22-year-old woman who had a right orbital lesion excised when she was 18 months, with the confirmation of the clinical suspicion of lymphangioma, had also undergone surgery for another 3 times with a different surgeon. The patient presented with conjunctival chemosis, proptosis, exotropia, and no vision in the right eye, this symptoms had been present for several years. On ophthalmic examination, visual acuity was light perception in the right eye and 10/10 in the left eye. The biomicroscopy of the right eye revealed a punctate keratitis and an exuberant chemosis. The patient had proptosis and a limitation on the adduction of the right eye. Extensive orbital excision of the lymphangioma was performed with symptomatic improvement. After 13 years of follow-up the symptoms recurred progressively associated with recurrent corneal ulcers and pain, an evisceration was performed. The patient presented with adherences and fibrosis in the anophtalmic socket with the need for 2 surgerys for the excision of adherences and 1 surgery for correction of ectropion. Functional as well as aesthetic outcome was obtained. Conclusion: Orbital lymphangiomas represent unique treatment challenges. These infiltrative lesions are prone to recurrence with bleeding, disfigurement, vision loss, and diplopia and can result in disfigurement. Complete surgical excision, as in this case, is typically unattainable without
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spelling Orbital lymphangioma: a surgical challengeOrbital neoplasmsNeoplasias da órbitaLymphangiomaLinfangiomaLymphangioma is an uncommon venolymphatic lesion with dead-end lymphatic channels, also defined as vascular hamartoma of lymphatic origin. Orbital lymphangiomas present management challenges to the ophthalmologist due to the tendency to recur locally unless it is completely excised, this is often difficult, because lymphangiomas tend to be infiltrative. The recurrence of hemorrhage and expansion can lead to vision loss and disfigurement. Case report: A 22-year-old woman who had a right orbital lesion excised when she was 18 months, with the confirmation of the clinical suspicion of lymphangioma, had also undergone surgery for another 3 times with a different surgeon. The patient presented with conjunctival chemosis, proptosis, exotropia, and no vision in the right eye, this symptoms had been present for several years. On ophthalmic examination, visual acuity was light perception in the right eye and 10/10 in the left eye. The biomicroscopy of the right eye revealed a punctate keratitis and an exuberant chemosis. The patient had proptosis and a limitation on the adduction of the right eye. Extensive orbital excision of the lymphangioma was performed with symptomatic improvement. After 13 years of follow-up the symptoms recurred progressively associated with recurrent corneal ulcers and pain, an evisceration was performed. The patient presented with adherences and fibrosis in the anophtalmic socket with the need for 2 surgerys for the excision of adherences and 1 surgery for correction of ectropion. Functional as well as aesthetic outcome was obtained. Conclusion: Orbital lymphangiomas represent unique treatment challenges. These infiltrative lesions are prone to recurrence with bleeding, disfigurement, vision loss, and diplopia and can result in disfigurement. Complete surgical excision, as in this case, is typically unattainable withoutEuropean Society of Ophthalmic Plastic and Reconstructive Surgery (ESOPRS)Unidade Local de Saúde Amadora / SintraRamalho, MSantos, CPina, SCoutinho, IVaz, FFerreira, MMelo, A2014-02-21T10:17:40Z20132013-01-01T00:00:00Zconference objectinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10400.10/1076enginfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-10T15:03:18Zoai:repositorio.hff.min-saude.pt:10400.10/1076Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T01:16:29.930490Repositórios 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 Orbital lymphangioma: a surgical challenge
title Orbital lymphangioma: a surgical challenge
spellingShingle Orbital lymphangioma: a surgical challenge
Ramalho, M
Orbital neoplasms
Neoplasias da órbita
Lymphangioma
Linfangioma
title_short Orbital lymphangioma: a surgical challenge
title_full Orbital lymphangioma: a surgical challenge
title_fullStr Orbital lymphangioma: a surgical challenge
title_full_unstemmed Orbital lymphangioma: a surgical challenge
title_sort Orbital lymphangioma: a surgical challenge
author Ramalho, M
author_facet Ramalho, M
Santos, C
Pina, S
Coutinho, I
Vaz, F
Ferreira, M
Melo, A
author_role author
author2 Santos, C
Pina, S
Coutinho, I
Vaz, F
Ferreira, M
Melo, A
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Unidade Local de Saúde Amadora / Sintra
dc.contributor.author.fl_str_mv Ramalho, M
Santos, C
Pina, S
Coutinho, I
Vaz, F
Ferreira, M
Melo, A
dc.subject.por.fl_str_mv Orbital neoplasms
Neoplasias da órbita
Lymphangioma
Linfangioma
topic Orbital neoplasms
Neoplasias da órbita
Lymphangioma
Linfangioma
description Lymphangioma is an uncommon venolymphatic lesion with dead-end lymphatic channels, also defined as vascular hamartoma of lymphatic origin. Orbital lymphangiomas present management challenges to the ophthalmologist due to the tendency to recur locally unless it is completely excised, this is often difficult, because lymphangiomas tend to be infiltrative. The recurrence of hemorrhage and expansion can lead to vision loss and disfigurement. Case report: A 22-year-old woman who had a right orbital lesion excised when she was 18 months, with the confirmation of the clinical suspicion of lymphangioma, had also undergone surgery for another 3 times with a different surgeon. The patient presented with conjunctival chemosis, proptosis, exotropia, and no vision in the right eye, this symptoms had been present for several years. On ophthalmic examination, visual acuity was light perception in the right eye and 10/10 in the left eye. The biomicroscopy of the right eye revealed a punctate keratitis and an exuberant chemosis. The patient had proptosis and a limitation on the adduction of the right eye. Extensive orbital excision of the lymphangioma was performed with symptomatic improvement. After 13 years of follow-up the symptoms recurred progressively associated with recurrent corneal ulcers and pain, an evisceration was performed. The patient presented with adherences and fibrosis in the anophtalmic socket with the need for 2 surgerys for the excision of adherences and 1 surgery for correction of ectropion. Functional as well as aesthetic outcome was obtained. Conclusion: Orbital lymphangiomas represent unique treatment challenges. These infiltrative lesions are prone to recurrence with bleeding, disfigurement, vision loss, and diplopia and can result in disfigurement. Complete surgical excision, as in this case, is typically unattainable without
publishDate 2013
dc.date.none.fl_str_mv 2013
2013-01-01T00:00:00Z
2014-02-21T10:17:40Z
dc.type.driver.fl_str_mv conference object
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dc.publisher.none.fl_str_mv European Society of Ophthalmic Plastic and Reconstructive Surgery (ESOPRS)
publisher.none.fl_str_mv European Society of Ophthalmic Plastic and Reconstructive Surgery (ESOPRS)
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