双侧肾b细胞淋巴瘤伴葡萄膜炎和继发性红细胞增多症的一例杰克罗素梗

Shu-Fang Yang, Heng-Leng Yang, Hui-Wen Chang, Yun-Han Hsieh, Peng-Chen Wang, Kwo-Chen Hu, Jian-Xi Yu, S. Liang
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引用次数: 0

摘要

患者为8岁男性,被阉割,杰克罗素梗犬,临床表现为右眼(右眼)葡萄膜炎和青光眼,持续2-3个月。眼科检查发现外膜充血,角膜血管化,水状耀斑,虹膜爆炸和视力下降。经药物治疗,外伤性青光眼、葡萄膜炎均得到控制。8个月后,狗出现了左眼急性葡萄膜炎(oculus sinister (OS))。一般体格检查、血液检查、x线摄影和尿液分析无显著差异。葡萄膜炎治疗1个月后未见好转,建议进行更多检查。腹部超声显示双肾有几个低回声肿块或囊肿。计算机断层扫描(CT)显示双肾弥漫性无强化低密度斑块。肾肿瘤高度怀疑,但业主拒绝活检。CT检查10天后,犬突然出现厌食、虚弱、尿毒症、高钾血症、红细胞增多症。由于临床状况恶化,预后不良和经济拮据,狗被安乐死,并对两个肾脏进行了组织病理学活检。免疫组化结果:肿瘤细胞b细胞标志物(CD20)阳性,t细胞标志物(CD3)阴性。双侧肾b细胞源性淋巴瘤通过组织学和免疫表型检查诊断。总之,除了双侧葡萄膜炎外,双侧肾淋巴瘤可诊断为无全身体征。肾脏功能损害是急性发展与严重的临床症状,在终末期的疾病。强烈建议尽早、积极、全面的检查和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A CASE OF BILATERAL RENAL B-CELL LYMPHOMA WITH UVEITIS AND SECONDARY POLYCYTHEMIA IN A JACK RUSSELL TERRIER
An 8-year-old, castrated male, Jack Russell Terrier was presented with clinical signs of uveitis and glaucoma in the right eye (oculus dexter (OD)) for 2–3 months. Ophthalmic examination revealed OD episcleral congestion, corneal vascularization, aqueous flare, iris bombe, and vision loss. OD glaucoma and uveitis were under control by medical treatment. After 8 months, the dog had acute uveitis in the left eye (oculus sinister (OS)). General physical examination, blood examinations, radiography, and urinalysis were unremarkable. No improvement was observed after for 1 month of uveitis treatment, and more examinations were strongly suggested. Abdominal ultrasonography revealed several hypoechoic masses or cysts on both kidneys. Computed tomography (CT) showed diffuse nonenhancing hypodense patches in both kidneys. Renal tumor was highly suspected, but biopsy was declined by the owner. Ten days after CT examination, the dog suddenly developed anorexia, weakness, uremia, hyperkalemia, and polycythemia. The dog was euthanatized because of the worsening clinical condition, poor prognosis, and financial constraints, and both kidneys were biopsied for histopathology. Immunohistochemically, the neoplastic cells were positive for B-cell marker (CD20) and negative for T-cell marker (CD3). Bilateral renal B-cell origin lymphoma was diagnosed by histologic and immunophenotyping examinations. In conclusion, bilateral renal lymphoma may be diagnosed with no systemic signs except bilateral uveitis. Renal function impairment was acutely developed with severe clinical signs at the end stage of the disease. Early, aggressive, complete examinations, and treatments are strongly recommended.
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