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伴有巨大淋巴结病的窦组织细胞增生症(罗萨伊-多夫曼病):一例独特病例报告

Sinus histiocytosis with massive lymphadenopathy Rosai-Dorfman disease: a unique case presentation.

作者信息

Kaltman Jordan M, Best Steven P, McClure Shawn A

机构信息

Department of Oral and Maxillofacial Surgery, Nova Southeastern University, College of Dental Medicine, Broward General Medical Center, Fort Lauderdale, FL 33314, USA.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011 Dec;112(6):e124-6. doi: 10.1016/j.tripleo.2011.06.018. Epub 2011 Sep 9.

Abstract

Rosai and Dorfman first described sinus histiocytosis with massive lymphadenopathy (SHML) in 1969 with an article detailing 4 cases in which they differentiated this disease entity from the grouping of diseases categorized as histiocytosis X, where it was previously classified. Also known as Rosai-Dorfman disease (RDD), it is clinically characterized as massive, painless, bilateral, symmetric cervical lymphadenopathy, with fever and leukocytosis. An 11-year-old African American boy was referred to our clinic for extraction of a severely decayed tooth #30 and evaluation of a large right-sided neck mass. Initially, the patient had been seen by his general dentist who had diagnosed the mass as an odontogenic abscess. After 2 courses of different antibiotics, no changes in the mass were noted. Subsequently, the patient was sent to the emergency department where CT revealed multiple right-sided neck masses with the largest measuring 4 × 2 cm. The patient underwent an incisional biopsy by otolaryngology and a diagnosis of necrotic lymph tissue was made. Upon our examination, the carious tooth #30 was felt to be an incidental finding and fine-needle aspiration cytology of the largest mass was performed in 2 places. This also provided a diagnosis of necrotic lymph tissue. In concert with the patient and his mother, the decision was made to excise the mass because of psychosocial concerns. A massive right-sided lymph node attached to the submandibular gland was found and excised without complication. Histologic examination with S-100 stain confirmed a diagnosis of RDD. The patient healed well following surgery and has experienced no further lymphadenopathy. This case presentation and review of the literature is unique, as the patient presented with unilateral cervical lymphadenopathy only. Open biopsy and 2 fine-needle aspirations all returned as necrotic lymph tissue. Obtaining the correct diagnosis was additionally hampered by coincidental dental pathology on the affected side and final diagnosis was made only by excisional biopsy, which is not necessarily indicated in cases of RDD.

摘要

罗萨伊和多尔夫曼于1969年首次描述了伴巨大淋巴结病的窦组织细胞增生症(SHML),他们在一篇文章中详细介绍了4例病例,将这种疾病实体与之前归类于组织细胞增生症X的一组疾病区分开来。它也被称为罗萨伊 - 多尔夫曼病(RDD),临床特征为巨大、无痛、双侧对称的颈部淋巴结病,伴有发热和白细胞增多。一名11岁的非裔美国男孩因拔除严重龋坏的30号牙并评估右侧颈部的一个大肿块而被转诊至我们的诊所。最初,患者的全科牙医诊断该肿块为牙源性脓肿。在使用了两个疗程的不同抗生素后,肿块未见变化。随后,患者被送往急诊科,CT显示右侧颈部有多个肿块,最大的直径为4×2厘米。患者接受了耳鼻喉科的切开活检,诊断为坏死性淋巴组织。在我们的检查中,发现龋坏的30号牙是一个偶然发现,并在最大肿块的两个部位进行了细针穿刺细胞学检查。这也诊断为坏死性淋巴组织。考虑到心理社会因素,与患者及其母亲协商后决定切除肿块。发现一个附着于下颌下腺的巨大右侧淋巴结并将其切除,未出现并发症。S - 100染色的组织学检查确诊为RDD。患者术后恢复良好,未再出现淋巴结病。该病例报告及文献复习具有独特性,因为患者仅表现为单侧颈部淋巴结病。开放活检和两次细针穿刺结果均为坏死性淋巴组织。患侧同时存在的牙科病理情况进一步阻碍了正确诊断的得出,最终仅通过切除活检才做出诊断,而在RDD病例中不一定需要进行切除活检。

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