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Vesicocutaneous fistula formation during treatment with sunitinib malate: Case report

BACKGROUND: The oral multi-kinase inhibitor sunitinib malate improves the survival of patients with gastrointestinal stromal tumors (GIST) after the disease progresses or intolerance to imatinib mesylate develops. Urinary fistulae arising during treatment with sunitinib for GIST have not been descri...

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Autores principales: Watanabe, Koichiro, Otsu, Satoshi, Morinaga, Ryotaro, Kawano, Sakura, Hirashima, Yoshinori, Sakashita, Hiroyuki, Shirao, Kuniaki
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988710/
https://www.ncbi.nlm.nih.gov/pubmed/21040530
http://dx.doi.org/10.1186/1471-230X-10-128
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author Watanabe, Koichiro
Otsu, Satoshi
Morinaga, Ryotaro
Kawano, Sakura
Hirashima, Yoshinori
Sakashita, Hiroyuki
Shirao, Kuniaki
author_facet Watanabe, Koichiro
Otsu, Satoshi
Morinaga, Ryotaro
Kawano, Sakura
Hirashima, Yoshinori
Sakashita, Hiroyuki
Shirao, Kuniaki
author_sort Watanabe, Koichiro
collection PubMed
description BACKGROUND: The oral multi-kinase inhibitor sunitinib malate improves the survival of patients with gastrointestinal stromal tumors (GIST) after the disease progresses or intolerance to imatinib mesylate develops. Urinary fistulae arising during treatment with sunitinib for GIST have not been described. CASE PRESENTATION: We describe a 62-year-old female patient diagnosed with unresectable GIST that involved the abdominal wall, urinary bladder wall, bowel, mesentery and peritoneum in the pelvic cavity. Intestinocutaneous fistulae developed on a surgical lesion after orally administered imatinib was supplemented by an arterial infusion of 5-flurouracil. Sunitinib was started after the patient developed resistance to imatinib. On day 4 of the fourth course of sunitinib, a widely dilated cutaneous fistula discharged large amounts of fluid accompanied by severe abdominal pain. Urinary communication was indicated based on the results of an intravenous injection of indigo carmine. Computed tomography findings suggested a small opening on the anterior urinary bladder wall and fistulous communication between the bladder and abdominal walls bridged by a subcutaneous cavity. The fistula closed and the amount of discharge decreased when sunitinib was discontinued. Therefore, sunitinib might have been associated with the development of the vesicocutaneous fistula in our patient. CONCLUSION: This is the first description of a vesicocutaneous fistula forming while under sunitinib treatment. Clinicians should be aware of the possible complication of vesicocutaneous fistula formation during treatment with molecular targeting agents in patients with extravesical invasion and peritoneal dissemination of GIST.
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spelling pubmed-29887102010-11-20 Vesicocutaneous fistula formation during treatment with sunitinib malate: Case report Watanabe, Koichiro Otsu, Satoshi Morinaga, Ryotaro Kawano, Sakura Hirashima, Yoshinori Sakashita, Hiroyuki Shirao, Kuniaki BMC Gastroenterol Case Report BACKGROUND: The oral multi-kinase inhibitor sunitinib malate improves the survival of patients with gastrointestinal stromal tumors (GIST) after the disease progresses or intolerance to imatinib mesylate develops. Urinary fistulae arising during treatment with sunitinib for GIST have not been described. CASE PRESENTATION: We describe a 62-year-old female patient diagnosed with unresectable GIST that involved the abdominal wall, urinary bladder wall, bowel, mesentery and peritoneum in the pelvic cavity. Intestinocutaneous fistulae developed on a surgical lesion after orally administered imatinib was supplemented by an arterial infusion of 5-flurouracil. Sunitinib was started after the patient developed resistance to imatinib. On day 4 of the fourth course of sunitinib, a widely dilated cutaneous fistula discharged large amounts of fluid accompanied by severe abdominal pain. Urinary communication was indicated based on the results of an intravenous injection of indigo carmine. Computed tomography findings suggested a small opening on the anterior urinary bladder wall and fistulous communication between the bladder and abdominal walls bridged by a subcutaneous cavity. The fistula closed and the amount of discharge decreased when sunitinib was discontinued. Therefore, sunitinib might have been associated with the development of the vesicocutaneous fistula in our patient. CONCLUSION: This is the first description of a vesicocutaneous fistula forming while under sunitinib treatment. Clinicians should be aware of the possible complication of vesicocutaneous fistula formation during treatment with molecular targeting agents in patients with extravesical invasion and peritoneal dissemination of GIST. BioMed Central 2010-11-01 /pmc/articles/PMC2988710/ /pubmed/21040530 http://dx.doi.org/10.1186/1471-230X-10-128 Text en Copyright ©2010 Watanabe et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Watanabe, Koichiro
Otsu, Satoshi
Morinaga, Ryotaro
Kawano, Sakura
Hirashima, Yoshinori
Sakashita, Hiroyuki
Shirao, Kuniaki
Vesicocutaneous fistula formation during treatment with sunitinib malate: Case report
title Vesicocutaneous fistula formation during treatment with sunitinib malate: Case report
title_full Vesicocutaneous fistula formation during treatment with sunitinib malate: Case report
title_fullStr Vesicocutaneous fistula formation during treatment with sunitinib malate: Case report
title_full_unstemmed Vesicocutaneous fistula formation during treatment with sunitinib malate: Case report
title_short Vesicocutaneous fistula formation during treatment with sunitinib malate: Case report
title_sort vesicocutaneous fistula formation during treatment with sunitinib malate: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988710/
https://www.ncbi.nlm.nih.gov/pubmed/21040530
http://dx.doi.org/10.1186/1471-230X-10-128
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