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[气道鼻窦组织细胞增生伴巨大淋巴结病(罗萨伊-多夫曼病):一例报告并文献复习]

[Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) of the airway: a case report and review of the literature].

作者信息

Xie Bao-Song, Li Rui-Hui, Yue Wen-Xiang, Zheng Guan-Ying, Jin Long

机构信息

Department of Respiratory Medicine, Fujian Provincial Hospital, Fuzhou 350001, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2009 Sep;32(9):670-3.

Abstract

OBJECTIVE

To improve the awareness of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) involving the airways.

METHODS

The clinical presentations, endoscopic findings in the airways, pathological characteristics, and diagnosis and treatment of a case of Rosai-Dorfman disease was reported, and related literatures were reviewed.

RESULTS

A 60-year-old female patient was admitted to this hospital because of recurrent wheezing for 18 months and aggravated for 1 month on March 6, 2007. The diagnosis of "bronchial asthma" had been made and oral prednisolone and inhaled budesonide resulted in symptom improvement. One month ago, she had wheezing again with inspiratory dyspnea, which was more obvious at recumbent position.She had been found to have high blood pressure and left adrenal adenoma 23 years ago, and as the diagnosis of "primary aldosteronism" was made but underwent no surgery. Left parotid gland tumor and left submandibular lymph nodes had been found, and surgical resection implemented in 1999. Lacrimal gland tumor resection of her eyes had been performed in 2000. Multiple subcutaneous nodules, rising and disappearing spontaneously, had been demonstrated in 2001. After admission, physical examination revealed nodules of 3.0 cm x 2.0 cm in her left submandibular area, and soybean sized nodules at both arms, back, chest, abdomen, buttocks and thighs. Chest CT scan and tracheal reconstruction showed that there were multiple nodules in the tracheal wall with narrow lumen, with no obvious enlargement of mediastinal lymph nodes. Lymph node biopsy showed faintly stained areas and the formation of plasma cells and lymphocytes of the deeply stained area, presenting as a sinus-like structure, and plasma cells and lymphocytes were engulfed in the plasma of the histiocytes, consistent with the diagnosis of Rosai-Dorfman disease.

CONCLUSIONS

Rosai-Dorfman disease involving the airway was a rare disease often misdiagnosed. Bronchoscopy was very helpful for the diagnosis. Histiocytosis with phagocytosis of plasma cells and lymphocytes was the pathological feature, and immunohistochemical staining positive for S100 protein and CD(68) was suggestive of the diagnosis. Surgical resection combined with corticosteroids or radiotherapy was effective treatment of the airway diseases.

摘要

目的

提高对累及气道的窦性组织细胞增生伴巨大淋巴结病(罗萨伊 - 多夫曼病)的认识。

方法

报告1例罗萨伊 - 多夫曼病患者的临床表现、气道内镜检查结果、病理特征及诊断与治疗情况,并复习相关文献。

结果

一名60岁女性患者因反复喘息18个月,于2007年3月6日加重1个月入院。曾诊断为“支气管哮喘”,口服泼尼松龙及吸入布地奈德后症状改善。1个月前,再次出现喘息伴吸气性呼吸困难,卧位时更明显。23年前发现患有高血压及左肾上腺腺瘤,诊断为“原发性醛固酮增多症”但未手术。1999年发现左腮腺肿瘤及左下颌下淋巴结,并进行了手术切除。2000年对其眼部进行了泪腺肿瘤切除术。2001年出现多个皮下结节,可自行隆起及消失。入院后体格检查发现左下颌下区有3.0 cm×2.0 cm结节,双臂、背部、胸部、腹部、臀部及大腿有黄豆大小结节。胸部CT扫描及气管重建显示气管壁有多个结节,管腔狭窄,纵隔淋巴结无明显肿大。淋巴结活检显示淡染区及深染区浆细胞和淋巴细胞形成,呈窦样结构,组织细胞胞质内可见吞噬的浆细胞和淋巴细胞,符合罗萨伊 - 多夫曼病诊断。

结论

累及气道的罗萨伊 - 多夫曼病是一种罕见疾病,常被误诊。支气管镜检查对诊断非常有帮助。组织细胞吞噬浆细胞和淋巴细胞是其病理特征,S100蛋白及CD(68)免疫组化染色阳性提示诊断。手术切除联合皮质类固醇或放疗是治疗气道疾病的有效方法。

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