Teh A, Robertson J, Donahoe S L, Crighton T, Boyd S, Malik R
Sydney School of Veterinary Science, The University of Sydney, Sydney, Australia.
Clayfield Veterinary Clinic, Clayfield, Queensland, Australia.
Aust Vet J. 2025 Mar;103(3):121-126. doi: 10.1111/avj.13410. Epub 2024 Dec 22.
In cats, mycobacteriosis tends to present in a syndromic manner, with cases either being due to tuberculosis (TB) (in countries where TB is endemic), one of the "leprosy-like" diseases affecting the skin and subcutis, panniculitis caused by infection of subcutaneous tissues generally with rapidly growing Mycobacteria spp. or widely disseminated granulomatous disease, which is usually caused by members of the Mycobacterium avium-intracellulare complex (MAC). Disseminated MAC disease is rare, but when it occurs, usually develops in immunocompromised hosts with defective cell-mediated immunity. This report describes a case of widely disseminated mycobacteriosis in a 10-year-old American Shorthair cat with an atypical multi-organ distribution including rarely documented thyroid gland involvement. The cat presented for a chronic history of inappetence and weight loss. Abdominal ultrasonography revealed a large mass on the left kidney, and an aspirate (FNA) from this mass showed abundant negative-staining bacilli which were confirmed to be acid-fast with Ziehl-Neelsen (ZN) staining. This was consistent with a mycobacterial aetiology. Necropsy revealed mycobacterial granulomas and/or granulomatous inflammation in the kidneys, thyroid gland, liver, spleen, lungs and left mandibular lymph node, with abundant intralesional acid-fast bacilli in all these tissues. Polymerase chain reaction (PCR) and culture on samples of all affected tissues were positive for M. avium. Collectively, the findings are consistent with disseminated mycobacteriosis due to M. avium with atypical distribution of lesions. Very likely, the cat had underlying immunodeficiency of undetermined cause, exacerbated by the administration of depot corticosteroid.
在猫中,分枝杆菌病往往以综合征的形式出现,病例要么是由结核病(TB)引起(在结核病流行的国家),要么是由影响皮肤和皮下组织的“类麻风”疾病之一引起,通常由快速生长的分枝杆菌属感染皮下组织导致的脂膜炎,要么是广泛播散的肉芽肿性疾病,这通常由鸟分枝杆菌-胞内分枝杆菌复合体(MAC)的成员引起。播散性MAC病很罕见,但一旦发生,通常在细胞介导免疫缺陷的免疫功能低下宿主中发展。本报告描述了一例10岁美国短毛猫广泛播散性分枝杆菌病的病例,其具有非典型的多器官分布,包括罕见的甲状腺受累记录。这只猫因食欲不振和体重减轻的慢性病史前来就诊。腹部超声检查显示左肾有一个大肿块,从这个肿块中抽取的样本(细针穿刺抽吸活检,FNA)显示有大量不着色杆菌,经齐-尼(ZN)染色证实为抗酸杆菌。这与分枝杆菌病因一致。尸检显示肾脏、甲状腺、肝脏、脾脏、肺和左下颌淋巴结有分枝杆菌肉芽肿和/或肉芽肿性炎症,所有这些组织内都有大量病灶内抗酸杆菌。对所有受影响组织的样本进行聚合酶链反应(PCR)和培养,结果显示鸟分枝杆菌呈阳性。总的来说,这些发现与由鸟分枝杆菌引起的播散性分枝杆菌病一致,病变分布不典型。很可能这只猫存在病因不明的潜在免疫缺陷,长效皮质类固醇的使用使其病情加重。