[Diffuse thickening of bronchial walls with multiple nodular mucosal protrusions].

W. Y. Zhu, Y. H. Li, T. Zhang, M. Peng, R. Feng, J. Shi
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Abstract

A 58-year-old woman presented with a six-month history of nasal congestion, sore throat and cough, and a five-month history of dyspnea. She had a history of xerostomia for one year. On examination, the bilateral submandibular gland and parotid glands were enlarged. Parotid and anterior cervical lymph nodes were palpable. There were rales in both lungs. The rest of the physical examination was unremarkable. Sialographic analysis showed normal caliber in the main duct, stenosis in secondary ducts, and dilation in the proximal ducts. Minor salivary gland biopsy demonstrated periductal lymphocytic infiltration. Chest computed tomography (CT) showed diffuse thickening of the tracheal and bilateral bronchial walls. Bronchoscopy revealed macroscopic multiple nodules mainly in the trachea and bilateral main bronchus. Endobronchial biopsy showed lymphocytic infiltration in the bronchial submucosa. She was diagnosed with Sjögren's syndrome and treated with glucocorticoids. The dose of prednisone was started at 30 mg/d and tapered gradually. Following treatment, the patient's clinical condition improved dramatically, with shrinkage of the enlarged lymph nodes, bilateral submandibular and parotid glands. A repeated chest CT scan revealed improvement of the tracheal and bilateral bronchial thickening. Multiple nodules in the airway regressed, as evidenced by repeated bronchoscopic examination. The final diagnosis was a large-airway disease associated with Sjögren's syndrome.Among airway diseases in Sjögren's syndrome, peripheral airway diseases including bronchiolitis and bronchiectasis are common; however, central airway lesions in Sjögren's syndrome, especially with macroscopic nodules, are rare. In this case, we demonstrated tracheal and endobronchial nodules in Sjögren's syndrome as determined by clinical features, CT scan, bronchoscopy, and response to therapy.
[支气管壁弥漫性增厚,多发结节状粘膜突起]。
一名 58 岁的女性患者有六个月的鼻塞、咽喉痛和咳嗽病史,还有五个月的呼吸困难病史。她有一年的口腔干燥症病史。经检查,双侧颌下腺和腮腺肿大。可触及腮腺和颈前淋巴结。双肺有啰音。其他体格检查无异常。涎腺造影分析表明,主导管口径正常,副导管狭窄,近端导管扩张。小唾液腺活检显示导管周围有淋巴细胞浸润。胸部计算机断层扫描(CT)显示气管和双侧支气管壁弥漫性增厚。支气管镜检查显示,主要在气管和双侧主支气管内有大面积多发性结节。支气管内活检显示支气管粘膜下有淋巴细胞浸润。她被诊断为斯约恩综合征,并接受了糖皮质激素治疗。泼尼松的剂量从 30 毫克/天开始,然后逐渐减少。治疗后,患者的临床症状明显改善,肿大的淋巴结、双侧颌下腺和腮腺缩小。重复胸部 CT 扫描显示,气管和双侧支气管增厚的情况有所改善。反复的支气管镜检查显示,气管内的多个结节已经消退。在斯约格伦综合征的气道疾病中,包括支气管炎和支气管扩张在内的外周气道疾病很常见;但斯约格伦综合征的中央气道病变,尤其是伴有大结节的中央气道病变却很少见。在本病例中,我们通过临床特征、CT 扫描、支气管镜检查和对治疗的反应确定了斯约格伦综合征的气管和支气管内结节。
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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