Idiopathic multifocal calcinosis cutis presenting in a cat with vestibular syndrome: clinical, radiographic and histopathological findings.

IF 0.7 Q3 VETERINARY SCIENCES
Journal of Feline Medicine and Surgery Open Reports Pub Date : 2026-01-03 eCollection Date: 2026-01-01 DOI:10.1177/20551169251415120
Samil Bugra Kose, Faruk Emre Turk, Nilufer Kuruca, Berfin Eftelya Guder, Halis Hosaf, Ahmet Ozak
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引用次数: 0

Abstract

Case summary: A 2-year-old spayed female British Shorthair cat was presented with an acute onset of right-sided head tilt, circling and horizontal nystagmus. Neurological examination, CT and video-otoscopic evaluation confirmed a right-sided peripheral vestibular syndrome secondary to otitis media. The cat received cefixime (10 mg/kg PO q24h) and methylprednisolone (1 mg/kg PO q24h) for 2 weeks, resulting in marked improvement of vestibular signs by day 4. During the physical examination, multiple firm, non-painful subcutaneous nodules of varying sizes were palpated in different body regions, unrelated to the primary neurological complaint. Laboratory analysis revealed serum calcium, ionised calcium and phosphorus concentrations within reference intervals, with a calcium-phosphorus product below the threshold for metastatic calcification. Ultrasonographic and hormonal assessments excluded metabolic, iatrogenic and dystrophic causes. Histopathological examination of an excisional biopsy from the largest lesion revealed dermal collagen fibril calcification surrounded by a hypocellular fibrous capsule and mild lymphohistiocytic inflammation, consistent with calcinosis cutis.

Relevance and novel information: The clinical, laboratory and histopathological findings supported a diagnosis of multifocal idiopathic calcinosis cutis. To the authors' knowledge, this is the first report from Türkiye describing multifocal subcutaneous idiopathic calcinosis cutis in a cat. This case emphasises the importance of thorough physical examinations to detect concurrent, clinically silent dermatological conditions during neurological evaluations.

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特发性多灶性皮肤钙质沉着症出现在猫与前庭综合征:临床,影像学和组织病理学的发现。
病例总结:一只2岁的雌性英国短毛猫出现急性右侧头部倾斜,旋转和水平眼球震颤。神经学检查,CT和视频耳镜评估证实继发于中耳炎的右侧周围前庭综合征。猫接受头孢克肟(10mg /kg PO q24h)和甲基强的松龙(1mg /kg PO q24h)治疗2周,第4天前庭体征明显改善。体格检查时,在身体不同部位可扪及多个大小不等的坚固无痛的皮下结节,与原发神经系统疾病无关。实验室分析显示血清钙、离子钙和磷浓度在参考区间内,钙磷产物低于转移性钙化的阈值。超声检查和激素评估排除了代谢、医源性和营养不良的原因。最大病变的组织病理学检查显示真皮胶原纤维钙化,周围有低细胞纤维囊和轻度淋巴组织细胞炎症,与皮肤钙化症一致。相关性和新信息:临床,实验室和组织病理学结果支持多灶特发性皮肤钙质沉着症的诊断。据作者所知,这是来自 rkiye杂志的第一篇关于猫多灶性皮下特发性皮肤钙质沉着症的报道。该病例强调了在神经学评估期间进行彻底的体格检查以发现并发的、临床无症状的皮肤病的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.30
自引率
14.30%
发文量
57
审稿时长
15 weeks
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