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Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation
Genital arteriovenous malformations are rare and present unique surgical challenges in preserving urogenital function, abdominal wall integrity, and lower limb perfusion. A 32-year-old man with a giant abdominoscrotal arteriovenous malformation presented with recurrent heavy bleeding. Due to the hig...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253270/ https://www.ncbi.nlm.nih.gov/pubmed/32537371 http://dx.doi.org/10.1097/GOX.0000000000002725 |
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author | Danno, Kanako Narushima, Mitsunaga Iida, Takuya Banda, Chihena Todokoro, Takeshi Tashiro, Kensuke Ishiura, Ryohei Mitsui, Kohei Tone, Shine Mori, Harushi |
author_facet | Danno, Kanako Narushima, Mitsunaga Iida, Takuya Banda, Chihena Todokoro, Takeshi Tashiro, Kensuke Ishiura, Ryohei Mitsui, Kohei Tone, Shine Mori, Harushi |
author_sort | Danno, Kanako |
collection | PubMed |
description | Genital arteriovenous malformations are rare and present unique surgical challenges in preserving urogenital function, abdominal wall integrity, and lower limb perfusion. A 32-year-old man with a giant abdominoscrotal arteriovenous malformation presented with recurrent heavy bleeding. Due to the high risk of rebleeding and fatal hemorrhage, surgery with curative intent was proposed and the patient was counseled on the risks of ischemia to the lower limb, testes, and penis. Preoperative embolization of the feeding vessels was performed. Three days later, surgical excision of the mass with the affected scrotum, left rectus muscle, sheath, and overlying abdominal skin followed. The testes were dissected from the malformation and preserved along with the right internal pudendal artery. The left thigh skin was advanced to the scrotal remnants and a neoscrotum created. The resulting large abdominal wall defect was reconstructed in layers with a pedicled anterolateral thigh flap, including innervated vastus lateralis muscle, to prevent herniation. Recovery was uneventful, and a 4-year follow-up revealed no significant clinical or radiological recurrence with recovery of flap sensation, retained erectile function, and no herniation. We report this case due to rarity of giant abdominoscrotal arteriovenous malformations and present preoperative embolization, surgical resection, and functional anterolateral thigh flap reconstruction as a valuable treatment option of this life-threatening illness. |
format | Online Article Text |
id | pubmed-7253270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-72532702020-06-11 Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation Danno, Kanako Narushima, Mitsunaga Iida, Takuya Banda, Chihena Todokoro, Takeshi Tashiro, Kensuke Ishiura, Ryohei Mitsui, Kohei Tone, Shine Mori, Harushi Plast Reconstr Surg Glob Open Case Report Genital arteriovenous malformations are rare and present unique surgical challenges in preserving urogenital function, abdominal wall integrity, and lower limb perfusion. A 32-year-old man with a giant abdominoscrotal arteriovenous malformation presented with recurrent heavy bleeding. Due to the high risk of rebleeding and fatal hemorrhage, surgery with curative intent was proposed and the patient was counseled on the risks of ischemia to the lower limb, testes, and penis. Preoperative embolization of the feeding vessels was performed. Three days later, surgical excision of the mass with the affected scrotum, left rectus muscle, sheath, and overlying abdominal skin followed. The testes were dissected from the malformation and preserved along with the right internal pudendal artery. The left thigh skin was advanced to the scrotal remnants and a neoscrotum created. The resulting large abdominal wall defect was reconstructed in layers with a pedicled anterolateral thigh flap, including innervated vastus lateralis muscle, to prevent herniation. Recovery was uneventful, and a 4-year follow-up revealed no significant clinical or radiological recurrence with recovery of flap sensation, retained erectile function, and no herniation. We report this case due to rarity of giant abdominoscrotal arteriovenous malformations and present preoperative embolization, surgical resection, and functional anterolateral thigh flap reconstruction as a valuable treatment option of this life-threatening illness. Wolters Kluwer Health 2020-03-27 /pmc/articles/PMC7253270/ /pubmed/32537371 http://dx.doi.org/10.1097/GOX.0000000000002725 Text en Copyright © 2020 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Case Report Danno, Kanako Narushima, Mitsunaga Iida, Takuya Banda, Chihena Todokoro, Takeshi Tashiro, Kensuke Ishiura, Ryohei Mitsui, Kohei Tone, Shine Mori, Harushi Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation |
title | Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation |
title_full | Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation |
title_fullStr | Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation |
title_full_unstemmed | Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation |
title_short | Resection and Reconstruction of Giant Abdominoscrotal Arteriovenous Malformation |
title_sort | resection and reconstruction of giant abdominoscrotal arteriovenous malformation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253270/ https://www.ncbi.nlm.nih.gov/pubmed/32537371 http://dx.doi.org/10.1097/GOX.0000000000002725 |
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