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霍奇金病的临床表现模式。对病因学和发病机制的启示。

Patterns of presentation of Hodgkin disease. Implications for etiology and pathogenesis.

作者信息

Mauch P M, Kalish L A, Kadin M, Coleman C N, Osteen R, Hellman S

机构信息

Joint Center for Radiation Therapy, Brigham and Women's Hospital, Boston, MA 02115.

出版信息

Cancer. 1993 Mar 15;71(6):2062-71. doi: 10.1002/1097-0142(19930315)71:6<2062::aid-cncr2820710622>3.0.co;2-0.

Abstract

BACKGROUND

The etiology of Hodgkin disease remains uncertain. Patterns of presentation of Hodgkin disease are analyzed by histologic subtype with implications for etiology and pathogenesis.

METHODS

The authors performed a detailed analysis of anatomic sites of involvement, histopathologic findings, and clinical features in 719 patients with Hodgkin disease who underwent staging laparotomy with splenectomy between April 1969 and December 1986. The presence of disease in each of 17 sites of potential nodal involvement was determined for each patient from a combination of clinical and surgical staging. Association among nodal sites was assessed in 2 x 2 tables by estimating the odds ratio and testing the significance with the chi-square test. A strict significance level (P = 0.01) was used. Log-linear models were used for assessing association in 2 x 2 tables while adjusting for other factors.

RESULTS

The mediastinum, left side of neck, and right side of neck were the most common sites involved for patients with nodular sclerosing (NS) or mixed cellularity (MC) histologic subtypes. Each of these sites was involved 60% of the time. These sites were four or more times as common as other nodal sites above or below the diaphragm. In contrast, the mediastinum was involved in only 8% of patients with lymphocyte predominance (LP) histologic subtype. Significant associations were found between mediastinal disease and low cervical/supraclavicular lymph node disease, mediastinal disease and NS histologic subtypes, peripheral nodal disease and LP histologic subtypes, and between splenic disease and mixed cellularity/lymphocyte depletion (MC/LD) Hodgkin disease. The age at onset and sex of patients with Hodgkin disease and the patterns of nodal distribution were somewhat different for NS and MC/LD histologic subtypes. Even greater differences were seen between LP and other histologic subtypes.

CONCLUSIONS

This study supports the conclusion that NS and MC Hodgkin disease spread by continguity, most often originating in the neck or mediastinum, and is consistent with evidence suggesting an infectious agent in the pathogenesis of these subtypes of Hodgkin disease. In contrast, LP Hodgkin disease is characterized by different sites of presentation and patterns of spread. This suggests that two or perhaps three clinicopathologic subtypes of Hodgkin disease exist. Implications for etiology and pathogenesis are discussed.

摘要

背景

霍奇金病的病因仍不确定。通过组织学亚型分析霍奇金病的表现模式,以探讨其病因及发病机制。

方法

作者对1969年4月至1986年12月期间接受分期剖腹术及脾切除术的719例霍奇金病患者的受累解剖部位、组织病理学发现及临床特征进行了详细分析。通过临床和手术分期相结合的方式,确定每位患者17个潜在淋巴结受累部位中每个部位是否存在病变。通过估计比值比并使用卡方检验来检验显著性,在2×2列联表中评估淋巴结部位之间的关联。采用严格的显著性水平(P = 0.01)。使用对数线性模型在调整其他因素的同时评估2×2列联表中的关联。

结果

对于结节硬化型(NS)或混合细胞型(MC)组织学亚型的患者,纵隔、左侧颈部和右侧颈部是最常受累的部位。这些部位每次受累的比例为60%。这些部位比横膈上下的其他淋巴结部位常见四倍或更多。相比之下,淋巴细胞为主型(LP)组织学亚型的患者中只有8%累及纵隔。发现纵隔病变与低位颈部/锁骨上淋巴结病变、纵隔病变与NS组织学亚型、外周淋巴结病变与LP组织学亚型以及脾病变与混合细胞型/淋巴细胞消减型(MC/LD)霍奇金病之间存在显著关联。NS和MC/LD组织学亚型的霍奇金病患者的发病年龄、性别及淋巴结分布模式略有不同。LP与其他组织学亚型之间的差异更为明显。

结论

本研究支持以下结论,即NS和MC霍奇金病通过连续性扩散,最常起源于颈部或纵隔,这与提示这些霍奇金病亚型发病机制中存在感染因子的证据一致。相比之下LP霍奇金病具有不同的表现部位和扩散模式。这表明霍奇金病存在两种或可能三种临床病理亚型。并讨论了其对病因及发病机制的意义。

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