犬巨大淋巴管肉瘤1例报告

Q4 Veterinary
M. Seo, Yeon-Woo Choi, D. Jung, Hee-Chun Lee, I. Hong
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引用次数: 0

摘要

这是一篇在知识共享署名非商业许可(http://creativecommons)条款下发布的开放获取文章。org/licenses/bync/4.0/),允许在任何媒介上不受限制地进行非商业使用、分发和复制,前提是正确引用原始作品。淋巴管肉瘤是一种罕见的肿瘤,起源于人类和动物的淋巴管内皮细胞。文献中患淋巴管肉瘤的狗从8周龄到13岁不等,大多数报道的病例发生在中型到大型犬种,没有性倾向[2-4]。狗的淋巴管肉瘤通常表现为界限不清的皮下肿块或局灶性肿胀伴水肿组织。病变通常起源于腹股沟和腋窝区域的皮下组织;胸腔;纵隔;四肢;颈腹和中线区域[2,3,5]。然而,关于淋巴管肉瘤的治疗信息有限,由于其侵袭性和浸润性的特点,在人类和动物中预后被认为很差。虽然在狗、猫和马中都有报道,但在兽医学中报道的淋巴管肉瘤病例数量有限[1,2,7,8]。本病例报告描述了犬下颌骨区域进行性和转移性淋巴管肉瘤的临床病史和组织病理学特征。一只12岁的绝育雄性金毛寻回犬被送到动物医院,其下颌下区域的肿块逐渐扩大,已经快速增长了大约1个月。全血细胞计数和血清生化分析在正常范围内,但显示贫血。x线摄影和计算机断层扫描(CT)分析检查其他器官和检测转移。对肿块进行活检以进行组织病理学诊断。活检组织固定在10%中性缓冲福尔马林中,常规处理,并包埋在石蜡中。12岁绝育雄性金毛寻回犬下颌骨区域肿块逐渐增大。组织病理诊断证实为淋巴管肉瘤,并转移至肝脏及脾脏。肿瘤的多形性肿瘤内皮细胞直接生长在真皮胶原束上,形成许多裂缝和相互连接的通道,缺乏明显的血液成分。由于淋巴管肉瘤是一种罕见的恶性肿瘤,以往报道的病例数量和有关肿瘤的信息有限。本报告描述的临床历史和组织病理学诊断进展性淋巴管肉瘤在下颌骨区域转移的狗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Massive lymphangiosarcoma in a dog: a case report
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial license (http://creativecommons. org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Lymphangiosarcoma is a rare tumor arising from lymphatic endothelial cells in both humans and animals [1]. Dogs in the literature with lymphangiosarcoma range from 8 weeks to 13 years of age, and most reported cases occurred in medium to large breeds with no sexual predisposition [2-4]. Lymphangiosarcoma in dogs typically presents as a poorly demarcated subcutaneous mass or focal swelling with edema tissues. Lesions have been commonly reported to originate in the subcutaneous tissue in the inguinal and axillary regions; thoracic cavity; mediastinum; limbs; ventral cervical and midline areas [2,3,5]. However, information regarding the treatment of lymphangiosarcoma is limited, and the prognosis is considered to be poor in both humans and animals because of its aggressive and infiltrative characteristics [6]. Although it has been described in dogs, cats, and horses, the number of reported cases of lymphangiosarcoma is limited in veterinary medicine [1,2,7,8]. This case report describes the clinical history and histopathological features of a progressive and metastatic lymphangiosarcoma in the submandibular region of a dog. A 12-year-old neutered male Golden Retriever was presented to the animal hospital with a history of a progressively enlarging mass in the submandibular region, which had rapidly grown for approximately 1 month. Complete blood count and serum biochemistry analyses were within the normal ranges for the species but revealed anemia. Radiographic and computed tomographic (CT) analyses were performed for the examination of other organs and detection of metastasis. The mass was biopsied for histopathological diagnosis. The biopsied tissue was fixed in 10% neutral buffered formalin, processed routinely, and embedded in paraffin wax. The samples were sectioned 4-μm thick, stained with hematoxylin and eosin A 12-year-old neutered male Golden Retriever presented with a progressively enlarging mass in the submandibular region. Histopathological diagnosis confirmed lymphangiosarcoma with metastasis to the liver and spleen. The pleomorphic neoplastic endothelial cells of the tumor grow directly on bundles of dermal collagen, forming numerous clefts and interconnecting channels that are devoid of conspicuous hematic elements. As lymphangiosarcoma is an uncommon malignant neoplasm, the number of previously reported cases and information of the tumor is limited. The present report describes the clinical history and histopathological diagnosis of a progressive lymphangiosarcoma in the submandibular region with metastases in a dog.
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Korean Journal of Veterinary Research
Korean Journal of Veterinary Research Veterinary-Veterinary (all)
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