Kerns Austin T, Brakel Kelsey A, Premanandan Christopher, Saffire Ashlie, Moore Sarah A
Department of Veterinary Clinical Sciences, The Ohio State University College of Veterinary Medicine, Columbus, OH, USA.
Department of Veterinary Biosciences, The Ohio State University College of Veterinary Medicine, Columbus, OH, USA.
JFMS Open Rep. 2018 Feb 19;4(1):2055116918756724. doi: 10.1177/2055116918756724. eCollection 2018 Jan-Jun.
A 9-year-old spayed female domestic shorthair cat with clinical signs suggestive of chronic recurrent otitis media and recent seizures was presented with multifocal nervous system disease, including bilateral central and/or peripheral vestibular, cerebellar and forebrain deficits. Prior to presentation, there was inadequate improvement after 6 weeks of treatment for bilateral middle ear effusion from which a highly susceptible species was cultured. This was followed by the development of seizures. Results of a complete blood count and serum chemistry were unremarkable, and a previous feline leukemia virus/feline immunodeficiency virus ELISA was negative. The cat was hospitalized overnight and had multiple seizures. The following morning the cat's mentation worsened, and the cat lost ventilatory drive after induction for anesthesia in preparation for MRI. A brain herniation event was suspected, and the cat was euthanized prior to further diagnostics. On post-mortem examination both tympanic bullae were filled with a soft, tan-colored material. Histologically, this material was composed of neoplastic lymphocytes. In addition, neoplastic lymphocytes were found in the leptomeninges, brain parenchyma, submandibular lymph nodes and pancreas. The neoplastic lymphocytes were negative for both B- and T-lymphocyte immunohistochemical markers and PCR for antigen receptor rearrangements failed to amplify target DNA, indicating non-B, non-T-cell lymphoma.
To our knowledge, this is the first report of lymphoma with confirmed bilateral tympanic bulla involvement in the human and veterinary literature. Neoplasia should be considered in cases of middle-ear effusion that do not improve adequately with appropriate antimicrobial therapy.
一只9岁已绝育的雌性家养短毛猫,有慢性复发性中耳炎的临床症状且近期出现癫痫发作,表现为多灶性神经系统疾病,包括双侧中枢性和/或外周性前庭、小脑和前脑功能缺陷。在就诊前,针对双侧中耳积液进行了6周的治疗,积液中培养出一种高度敏感的菌种,但病情改善不明显。随后出现了癫痫发作。全血细胞计数和血清生化检查结果无异常,之前的猫白血病病毒/猫免疫缺陷病毒酶联免疫吸附测定呈阴性。这只猫住院过夜并多次癫痫发作。第二天早上,猫的精神状态恶化,在为进行磁共振成像诱导麻醉后失去了呼吸驱动力。怀疑发生了脑疝,在进一步诊断之前对猫实施了安乐死。尸检时,两个鼓泡都充满了柔软的棕褐色物质。组织学检查显示,这种物质由肿瘤性淋巴细胞组成。此外,在软脑膜、脑实质、下颌下淋巴结和胰腺中也发现了肿瘤性淋巴细胞。肿瘤性淋巴细胞的B淋巴细胞和T淋巴细胞免疫组化标记均为阴性,抗原受体重排的聚合酶链反应未能扩增出目标DNA,表明为非B、非T细胞淋巴瘤。
据我们所知,这是人类和兽医文献中首例确诊双侧鼓泡受累的淋巴瘤报告。对于经适当抗菌治疗后中耳积液改善不充分的病例,应考虑肿瘤形成。