一名慢性淋巴细胞白血病患者的眼眶里克氏病变及继发眼眶 MALT 型淋巴瘤

IF 1.2 4区 医学 Q3 OPHTHALMOLOGY
Patrick J Hunt, Jeel Mehta, Matthew R Ehrenburg, Daniela P Reyes-Capó, Chen Chen, Arthur Zieske, Yuli Zu, Patricia Chévez-Barrios, Michael T Yen, Stephen C Pflugfelder
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引用次数: 0

摘要

一名 74 岁的男性患者曾患慢性淋巴细胞白血病(CLL),其操作系统的下穹窿和颞上结膜出现大面积鲑鱼色斑片状病变。患者接受了病变切口活检,结果显示其为伴有大 B 细胞淋巴瘤区域的 CLL,符合里氏转化。在对这些病变进行药物和放射治疗后,患者于3个月后复发,对侧眼球内侧隐窝前肿胀,活检证实为复发/耐药的低级别CLL,并伴有治疗后的结节外边缘区B细胞淋巴瘤形态。本病例是一种罕见的里氏转化CLL表现,也是治疗后复发/耐药的眼眶CLL,具有边缘区B细胞淋巴瘤样形态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Orbital Richter Transformation With Subsequent Orbital MALT-type Lymphoma in a Patient With Chronic Lymphocytic Leukemia.

A 74-year-old man with a history of chronic lymphocytic leukemia (CLL) presented with large salmon-colored patch lesions along the inferior fornix and superotemporal conjunctiva of the OS. The patient underwent an incisional biopsy of the lesions, which showed a CLL with areas of large B-cell lymphoma, consistent with Richter transformation. Following medical and radiation-based therapy of these lesions, the patient returned 3 months later with inferomedial preseptal swelling in the contralateral eye, which biopsy proved to be recurrent/resistant low-grade CLL with a posttreatment extranodal marginal zone B-cell lymphoma pattern. This case exemplifies a rare presentation of CLL with Richter transformation and a recurrent/resistant posttreatment orbital CLL with a marginal zone B-cell lymphoma-like pattern.

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来源期刊
CiteScore
2.50
自引率
10.00%
发文量
322
审稿时长
3-8 weeks
期刊介绍: Ophthalmic Plastic and Reconstructive Surgery features original articles and reviews on topics such as ptosis, eyelid reconstruction, orbital diagnosis and surgery, lacrimal problems, and eyelid malposition. Update reports on diagnostic techniques, surgical equipment and instrumentation, and medical therapies are included, as well as detailed analyses of recent research findings and their clinical applications.
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