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耳硬化症的放大镜下。

Otosclerosis under the magnifying glass.

机构信息

Department V - Hematology, Victor Babeş University of Medicine and Pharmacy, Timişoara, Romania;

出版信息

Rom J Morphol Embryol. 2023 Apr-Jun;64(2):189-197. doi: 10.47162/RJME.64.2.09.

Abstract

Otosclerosis is a bone condition affecting the stapes bone within the otic capsule, and its exact cause is still unknown. It is characterized by a lack of proper remodeling of newly formed vascular and woven bone, leading to the development of abnormal osteons and the formation of sclerotic bone. Bilateral otosclerosis is seen in 80% of patients and 60% of otosclerosis patients have a family history of the condition. The etiology of this disease is still unknown, there are lots of theories to explain it. The histopathological (HP) studies of otosclerosis showed that osteoblasts, osteoclasts, vascular proliferation, fibroblasts, and histiocytes were observed in the stapes footplate. The onset of the symptoms occurs by the early third decade of life, usually it doesn't start later. In otosclerosis, the energy exerted by sound at the level of the tympanic membrane is reduced in the inner ear due to the fixation and rigidity of the ossicular chain, leading to hearing loss, especially for low frequencies. The primary clinical symptom of otosclerosis is conductive hearing loss but it is important to note that sensorineural hearing loss and mixed hearing loss can also occur as secondary symptoms of the condition. Another symptom present in patients with otosclerosis is tinnitus. The paper carried out a retrospective study of 70 patients diagnosed with otosclerosis in the Department of Otorhinolaryngology of Emergency City Hospital, Timişoara, Romania, between January 2021 to December 2022. Tissue fragments were processed at Service of Pathology by standard Hematoxylin-Eosin staining. The HP diagnosis was completed using Masson's trichrome staining, Giemsa histochemical staining, and immunohistochemical (IHC) reactions with anti-cluster of differentiation (CD)20, anti-CD3, anti-CD4, anti-CD8, anti-CD34, and anti-CD31 antibodies. The microscopic examination showed a chronic diffuse inflammatory infiltrate that consisted predominantly of mature T-lymphocytes, immunohistochemically positive for CD3, CD4 and CD8. There were also present rare CD20-positive B-lymphocytes. Among the lymphocytes, relatively numerous mast cells were identified, highlighted histochemically by the Giemsa staining. They had numerous purple-violet intracytoplasmic granules. In the connective tissue support, a relatively rich vascular network was identified, consisting of hyperemic capillaries, highlighted immunohistochemically with anti-CD31 and anti-CD34 antibodies. Bone tissues trabeculae showed extensive areas of fibrosis. The collagen fibers were highlighted by Masson's trichrome staining, being stained in green, blue, or bluish green.

摘要

耳硬化症是一种影响耳囊镫骨的骨骼疾病,其确切病因仍不清楚。它的特征是新形成的血管和编织骨的重塑不当,导致异常骨小梁的形成和硬化骨的形成。80%的患者双侧患有耳硬化症,60%的耳硬化症患者有该病的家族史。该病的病因仍不清楚,有很多理论试图解释它。耳硬化症的组织病理学(HP)研究表明,镫骨足板中观察到成骨细胞、破骨细胞、血管增殖、成纤维细胞和组织细胞。症状的发作发生在生命的第三个十年早期,通常不会更晚开始。在耳硬化症中,由于听骨链的固定和僵硬,鼓膜水平传递的声音能量在内耳中减少,导致听力损失,特别是低频。耳硬化症的主要临床症状是传导性听力损失,但值得注意的是,感音神经性听力损失和混合性听力损失也可能作为该病的继发症状出现。耳硬化症患者的另一个症状是耳鸣。本文对罗马尼亚蒂米什瓦拉紧急城市医院耳鼻喉科 2021 年 1 月至 2022 年 12 月期间诊断为耳硬化症的 70 例患者进行了回顾性研究。组织碎片由病理学科通过标准的苏木精-伊红染色进行处理。使用 Masson 三色染色、吉姆萨组织化学染色以及用抗分化群(CD)20、抗 CD3、抗 CD4、抗 CD8、抗 CD34 和抗 CD31 抗体的免疫组织化学(IHC)反应完成 HP 诊断。显微镜检查显示慢性弥漫性炎症浸润,主要由成熟的 T 淋巴细胞组成,免疫组织化学染色为 CD3、CD4 和 CD8 阳性。也存在罕见的 CD20 阳性 B 淋巴细胞。在淋巴细胞中,鉴定出相对较多的肥大细胞,吉姆萨染色显示为紫色-紫色细胞内颗粒。在结缔组织支持中,鉴定出相对丰富的血管网络,由充血的毛细血管组成,用抗 CD31 和抗 CD34 抗体的免疫组织化学染色突出显示。骨组织小梁显示出广泛的纤维化区域。胶原纤维用 Masson 三色染色突出显示,呈绿色、蓝色或蓝绿色。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a960/10520382/764ba0b36db5/RJME-64-2-189-fig1.jpg

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