Ma Shi-hong, Liu Qin-jiang, Wang Jun, Yang Rong
Department of Head Neck Surgery, Tumor Hospital of Gansu Province, Lanzhou 730050, China.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Mar;44(3):223-6.
To improve the diagnosis and management level of giant lymph node hyperplasia (Castleman's disease).
To retrospective analyze 10 misdiagnosed cases with Castleman's disease in order to give some suggestions for clinical diagnosis and differential diagnosis.
Ten patients with neck giant lymph node hyperplasia underwent surgical treatment after misdiagnosis. There were 8 localized Castleman's disease constituted of 6 cases with hyaline vascular type and 2 cases with mixture type and 2 multicentric Castleman's disease constituted of 1 cases with plasma cell type and 1 cases with mixture type were classified according to the criteria described by Frizzera. Ten cases were diagnosed by secondary operation after misdiagnosis and were clinically characterized by painless neck lymphadenectasis, 2 cases with multicentric Castleman's disease accompanied with aspecific systemic symptom and (or) multi-system damage. Ten cases survived for 4 - 17 years during follow-up periods in which 1 case with plasma cell type, multicentric Castleman's disease was recurrent 2 years later and underwent lymphadenectomy and chemotherapy and have no local recurrence so far.
Castleman's disease on neck is seldom seen and liable to misdiagnose. The diagnosis of Castleman's disease is based on its histopathological characteristics by lymph node resection biopsy. It should be considered in the differential diagnosis with lymph node tuberculosis, lymphadenitis, sarcoidosis and granuloma. Operation is the first choice for patient with localized type and multicentric type without serious involvement of multiple system functions.
提高巨大淋巴结增生症(Castleman病)的诊断与治疗水平。
回顾性分析10例Castleman病误诊病例,为临床诊断及鉴别诊断提供建议。
10例颈部巨大淋巴结增生症患者误诊后接受手术治疗。根据Frizzera描述的标准分类,其中8例为局限性Castleman病,包括6例透明血管型和2例混合型;2例为多中心性Castleman病,包括1例浆细胞型和1例混合型。10例均经误诊后二次手术确诊,临床表现为颈部无痛性淋巴结肿大,2例多中心性Castleman病伴有非特异性全身症状和(或)多系统损害。10例随访4~17年,其中1例浆细胞型多中心性Castleman病术后2年复发,再次行淋巴结切除及化疗,目前无局部复发。
颈部Castleman病少见,易误诊。其诊断依靠淋巴结切除活检的组织病理学特征,鉴别诊断时应考虑与淋巴结结核、淋巴结炎、结节病及肉芽肿等疾病相鉴别。对于局限性及多中心性且无严重多系统功能受累的患者,手术是首选治疗方法。