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免疫功能正常男性的单侧眼球突出作为系统性霍奇金淋巴瘤的初始临床表现。

Unilateral proptosis in an immunocompetent man as the initial clinical manifestation of systemic Hodgkin disease.

作者信息

Klapper S R, Jordan D R, McLeish W, Pelletier C

机构信息

University of Ottawa Eye Institute, Ontario, Canada.

出版信息

Ophthalmology. 1999 Feb;106(2):338-41. doi: 10.1016/S0161-6420(99)90073-8.

Abstract

OBJECTIVE

Orbital involvement in Hodgkin disease (HD) is rare. Previously reported cases of HD in patients without the acquired immunodeficiency syndrome have been diagnosed late in the course of established systemic disease. The authors describe an immunocompetent man with orbital infiltration as the initial manifestation of systemic HD.

DESIGN

Case report.

PARTICIPANTS

A 47-year-old man with acute progressive, painless proptosis of the left eye is described.

INTERVENTION

A well-defined, homogeneous soft tissue mass of the superior left orbit was evident on computed tomography, and an incisional biopsy of the nontender mass was performed.

RESULTS

The histopathologic findings were characteristic of HD. Systemic investigations showed clinical stage 3A HD. Ten months after completion of hybrid chemotherapy, the patient remained in complete remission from his HD.

CONCLUSION

Hodgkin disease presenting initially in the orbit of a patient with the acquired immunodeficiency syndrome has been described previously. The patient presented in this report is the first case of HD in the recent English literature with the initial manifestation in the orbit of an otherwise immunocompetent patient.

摘要

目的

霍奇金淋巴瘤(HD)累及眼眶罕见。既往报道的无获得性免疫缺陷综合征患者的HD病例,均在全身性疾病确诊后期才得以诊断。作者描述了1例有免疫功能的男性,其眼眶浸润为全身性HD的初始表现。

设计

病例报告。

研究对象

描述了1例47岁男性,其左眼急性进行性无痛性眼球突出。

干预措施

计算机断层扫描显示左眼眶上部有一个边界清晰、均匀的软组织肿块,对该无痛肿块进行了切开活检。

结果

组织病理学检查结果符合HD特征。全身检查显示为临床3A期HD。混合化疗完成10个月后,患者的HD仍处于完全缓解状态。

结论

既往曾描述过获得性免疫缺陷综合征患者眼眶最初出现HD的情况。本报告中的患者是近期英文文献中首例初始表现为眼眶受累的免疫功能正常患者的HD病例。

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