A Review on Angiosarcoma of the Breast: Case Studies

Palvi Sharma, Vikrant Dalwal, Sunaina Rana, Shilpa Thakur, Anu Sharma
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Abstract

An uncommon kind of cancer called angiosarcoma originates in the lining of lymph and blood arteries. The immune system includes the lymphatic vessels. The lymph vessels remove waste materials, viruses, and germs from the body. Any region of the body can develop cancer of this kind. Angiosarcoma is an aggressive tumour, It is a form of soft tissue sarcoma. The treatment of angiosarcoma is very difficult. Breast cancer arises in the breast's lymphatic or blood vessel networks eventually migrating to the breast and the skin of the arms. Most angiosarcomas have unknown origins. Researchers have found a number of variables that could raise the disease's risk. Angiosarcoma develops when the DNA of cells lining a blood artery or lymph channel changes. The instructions that inform a cell what to do are encoded in its DNA. The adjustment which scientists refer to as mutations, instruct the cells to divide quickly. When healthy cells would perish, the alterations prevent the cells from dying. As a result, cancer cells can accumulate and spread outside of the blood vessel or lymph channel. Cancerous cells are able to infiltrate and obliterate healthy body tissue. Cancer cells could eventually separate and travel to different parts of the body. Angiosarcomas have a rapid development rate and body-wide dissemination. Breast angiosarcomas come in two varieties, primary and secondary, and they are both treated surgically by removing the tumour. Angiosarcoma can be spread in other part of body from breast. Primary breast angiosarcoma is an uncommon kind of breast cancer that only affects women, typically developing in the third to fourth decade. For diagnosis, biopsy, mammogram, breast MRI, PET Scan, ultrasound were performed and for the treatment of breast cancer surgery, chemotherapy, radiotherapy were performed. Only 0.04% of malignant breast tumours are primary breast angiosarcomas, making it a rare form of breast cancer. Secondary malignant tumour growth is one of the dangers of therapeutic radiation. In this paper, various cases are reported of angiosarcoma of the breast.
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乳腺血管肉瘤病例研究综述
一种罕见的癌症称为血管肉瘤,起源于淋巴和血液动脉的内膜。免疫系统包括淋巴管。淋巴管清除体内的废物、病毒和细菌。身体的任何部位都可能发展成这种癌症。血管肉瘤是一种侵袭性肿瘤,是软组织肉瘤的一种。血管肉瘤的治疗非常困难。癌症发生在乳房的淋巴或血管网络中,最终转移到乳房和手臂的皮肤。大多数血管肉瘤起源不明。研究人员发现了许多可能增加疾病风险的变量。血管肉瘤是在血动脉或淋巴管内壁细胞的DNA发生变化时发展起来的。告知细胞该做什么的指令被编码在其DNA中。科学家们称之为突变的调整,指示细胞快速分裂。当健康细胞死亡时,这些变化会阻止细胞死亡。因此,癌症细胞可以积聚并扩散到血管或淋巴管外。癌细胞能够浸润和抹杀健康的身体组织。癌症细胞最终可能分离并传播到身体的不同部位。血管肉瘤的发展速度很快,并在全身范围内传播。乳腺血管肉瘤有两种,原发性和继发性,它们都是通过手术切除肿瘤来治疗的。血管肉瘤可以从乳房扩散到身体的其他部位。原发性乳腺血管肉瘤是一种罕见的癌症,只影响女性,通常在第三到第四个十年发展。进行诊断、活组织检查、乳房X光检查、乳腺MRI、PET扫描、超声检查,并进行癌症手术、化疗、放疗治疗。只有0.04%的恶性乳腺肿瘤是原发性乳腺血管肉瘤,这使其成为癌症的一种罕见形式。继发性恶性肿瘤生长是治疗性辐射的危险之一。本文报告了各种乳腺血管肉瘤的病例。
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