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Angiosarcoma of the breast with hypofibrinogenemia: A rare case report and review of the literature

BACKGROUND: Breast angiosarcoma is a rare malignant tumor, accounting for approximately 0.04% of all breast malignancies. Angiosarcoma of the breast with hypofibrinogenemia is even rarer and has not been described in man. Breast angiosarcoma is associated with high metastatic potential and poor prog...

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Autores principales: An, Ran, Ma, Jing-Yi, Ni, Xi-Hao, Wang, Chang-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698920/
https://www.ncbi.nlm.nih.gov/pubmed/36439505
http://dx.doi.org/10.3389/fonc.2022.1047935
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author An, Ran
Ma, Jing-Yi
Ni, Xi-Hao
Wang, Chang-Liang
author_facet An, Ran
Ma, Jing-Yi
Ni, Xi-Hao
Wang, Chang-Liang
author_sort An, Ran
collection PubMed
description BACKGROUND: Breast angiosarcoma is a rare malignant tumor, accounting for approximately 0.04% of all breast malignancies. Angiosarcoma of the breast with hypofibrinogenemia is even rarer and has not been described in man. Breast angiosarcoma is associated with high metastatic potential and poor prognosis, and there is no specific manifestation in imaging. At present, surgery is considered to be the only effective treatment. There is no unified standard for postoperative adjuvant radiotherapy and chemotherapy. CASE PRESENTATION: A 30-year-old female patient underwent left breast mass resection under local anesthesia on May 22, 2014. Postoperative pathology showed a vasogenic tumor. On November 10, 2017, she visited us again due to left breast swelling and pain during lactation, and underwent breast mass puncture. She was diagnosed with breast hematoma and fibrinogen reduction. On November 14, 2017, mastectomy was performed under tracheal intubation and general anesthesia, and the fibrinogen gradually returned to normal after surgery. Pathological examination showed a hemangiosarcoma with hematoma formation in the left breast. According to the pathological findings and after comprehensive evaluation, the patient underwent modified radical mastectomy for left breast cancer and right axillary sentinel lymph node biopsy on December 5, 2017. The patient died on January 28, 2018 due to rupture and hemorrhage of liver cancer and hemorrhagic shock. CONCLUSION: Breast angiosarcoma with hypofibrinogenemia is a rare and highly aggressive malignancy. Clinicians should be familiar with its clinicopathological features and diagnostic criteria. Multidisciplinary approach is recommended to benefit the patients.
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spelling pubmed-96989202022-11-26 Angiosarcoma of the breast with hypofibrinogenemia: A rare case report and review of the literature An, Ran Ma, Jing-Yi Ni, Xi-Hao Wang, Chang-Liang Front Oncol Oncology BACKGROUND: Breast angiosarcoma is a rare malignant tumor, accounting for approximately 0.04% of all breast malignancies. Angiosarcoma of the breast with hypofibrinogenemia is even rarer and has not been described in man. Breast angiosarcoma is associated with high metastatic potential and poor prognosis, and there is no specific manifestation in imaging. At present, surgery is considered to be the only effective treatment. There is no unified standard for postoperative adjuvant radiotherapy and chemotherapy. CASE PRESENTATION: A 30-year-old female patient underwent left breast mass resection under local anesthesia on May 22, 2014. Postoperative pathology showed a vasogenic tumor. On November 10, 2017, she visited us again due to left breast swelling and pain during lactation, and underwent breast mass puncture. She was diagnosed with breast hematoma and fibrinogen reduction. On November 14, 2017, mastectomy was performed under tracheal intubation and general anesthesia, and the fibrinogen gradually returned to normal after surgery. Pathological examination showed a hemangiosarcoma with hematoma formation in the left breast. According to the pathological findings and after comprehensive evaluation, the patient underwent modified radical mastectomy for left breast cancer and right axillary sentinel lymph node biopsy on December 5, 2017. The patient died on January 28, 2018 due to rupture and hemorrhage of liver cancer and hemorrhagic shock. CONCLUSION: Breast angiosarcoma with hypofibrinogenemia is a rare and highly aggressive malignancy. Clinicians should be familiar with its clinicopathological features and diagnostic criteria. Multidisciplinary approach is recommended to benefit the patients. Frontiers Media S.A. 2022-11-02 /pmc/articles/PMC9698920/ /pubmed/36439505 http://dx.doi.org/10.3389/fonc.2022.1047935 Text en Copyright © 2022 An, Ma, Ni and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
An, Ran
Ma, Jing-Yi
Ni, Xi-Hao
Wang, Chang-Liang
Angiosarcoma of the breast with hypofibrinogenemia: A rare case report and review of the literature
title Angiosarcoma of the breast with hypofibrinogenemia: A rare case report and review of the literature
title_full Angiosarcoma of the breast with hypofibrinogenemia: A rare case report and review of the literature
title_fullStr Angiosarcoma of the breast with hypofibrinogenemia: A rare case report and review of the literature
title_full_unstemmed Angiosarcoma of the breast with hypofibrinogenemia: A rare case report and review of the literature
title_short Angiosarcoma of the breast with hypofibrinogenemia: A rare case report and review of the literature
title_sort angiosarcoma of the breast with hypofibrinogenemia: a rare case report and review of the literature
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698920/
https://www.ncbi.nlm.nih.gov/pubmed/36439505
http://dx.doi.org/10.3389/fonc.2022.1047935
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