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菊池病:61例病例的回顾与分析

Kikuchi's disease: a review and analysis of 61 cases.

作者信息

Lin Hsin-Ching, Su Chih-Ying, Huang Chao-Cheng, Hwang Chung-Feng, Chien Chih-Yen

机构信息

Department of Otolaryngology, Kaohsiung Hsien, Taiwan Republic of China.

出版信息

Otolaryngol Head Neck Surg. 2003 May;128(5):650-3. doi: 10.1016/S0194-59980223291-X.

Abstract

OBJECTIVE

Kikuchi's disease (KD), or histiocytic necrotizing lymphadenitis, is a rare self-limiting disorder that typically affects the cervical lymph nodes. It has occasionally been misdiagnosed as malignant lymphoma or another serious diseases; hence, clinicians should be made more aware of this disease.

METHODS

From January 1986 to January 2001, a series of 61 patients who underwent a biopsy of a cervical lymph node and proved histologically to have KD were enrolled in this study. We retrospectively reviewed the clinical records and pathologic parameters of each patient. The patients were followed up from 6 months to 14.3 years (mean, 6.9 years).

RESULTS

There were 34 women and 27 men (1.26:1 ratio; age range, 6 to 46 years; mean age, 21 years). The affected cervical lymph nodes were commonly located in the posterior cervical triangle (54 of 61, or 88.5%). Unilateral and bilateral cervical lymph nodes were affected in 54 and 7 patients, respectively. The dimensions of affected lymph nodes were commonly in the range of 0.5 to 4 cm (57 of 61, or 93.4%). In 2 patients, the size of the enlarged lymph nodes was greater than 6 cm. Leukopenia was observed in 14 patients (23%); fever, in 18 patients (29.5%). Five patients had a past history of tuberculosis. Two patients developed systemic lupus erythematosus, 1 month and 5 years later, respectively. The cervical lymphadenopathy usually resolved without any medical treatment within 6 months after definite diagnosis was made. In 3 patients, the enlarged lymph nodes eventually disappeared after more than 1 year. No recurrence has since been noted.

CONCLUSION

The results of this study support the theory that KD is a self-limiting disorder that does not require any specific management. The female predominance was not as striking as in the studies performed in Western countries. We suggest that the patients with KD require a systemic survey and regular follow-up for several years; 2 of our patients developed systemic lupus erythematosus. An effective communication between the otolaryngologist and pathologist is needed because the clinical and pathologic characteristics of KD are essential in making an accurate diagnosis.

摘要

目的

菊池病(KD),即组织细胞坏死性淋巴结炎,是一种罕见的自限性疾病,通常累及颈部淋巴结。它偶尔会被误诊为恶性淋巴瘤或其他严重疾病;因此,临床医生应更加了解这种疾病。

方法

从1986年1月至2001年1月,本研究纳入了61例接受颈部淋巴结活检且组织学证实患有KD的患者。我们回顾性地查阅了每位患者的临床记录和病理参数。对患者进行了6个月至14.3年(平均6.9年)的随访。

结果

有34名女性和27名男性(比例为1.26:1;年龄范围为6至46岁;平均年龄21岁)。受累的颈部淋巴结通常位于颈后三角(61例中的54例,即88.5%)。单侧和双侧颈部淋巴结受累的患者分别为54例和7例。受累淋巴结的大小通常在0.5至4厘米范围内(61例中的57例,即93.4%)。2例患者肿大淋巴结的大小超过6厘米。14例患者(23%)出现白细胞减少;18例患者(29.5%)发热。5例患者有结核病史。2例患者分别在1个月和5年后出现系统性红斑狼疮。颈部淋巴结病通常在确诊后6个月内无需任何治疗即可消退。3例患者肿大的淋巴结在1年多后最终消失。此后未发现复发。

结论

本研究结果支持KD是一种无需任何特殊治疗的自限性疾病这一理论。女性优势不像西方国家的研究那样显著。我们建议KD患者需要进行全面检查并进行数年的定期随访;我们的2例患者出现了系统性红斑狼疮。耳鼻喉科医生和病理科医生之间需要进行有效的沟通,因为KD的临床和病理特征对于准确诊断至关重要。

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