由血片解释的ssamzary综合征-嗜酸性粒细胞增多症

IF 10.1 1区 医学 Q1 HEMATOLOGY
Merel T. A. Soeterik, Joris Janssen, Leo M. Budel, Anton W. Langerak, Yorick Sandberg, Barbara J. Bain
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引用次数: 0

摘要

一名无重要病史的 61 岁男子因乏力、瘙痒、盗汗和体重减轻前来就诊,病史长达六个月。体格检查显示他患有红斑和全身淋巴结病。实验室检查显示嗜酸性粒细胞增多(白细胞计数 10.6 × 109/L,嗜酸性粒细胞 2.9 × 109/L)。没有淋巴细胞增多(淋巴细胞计数 1.1 × 109/L)。乳酸脱氢酶(LDH)升高至 469 U/L。外周血涂片(左上和右上,May-Grünwald-Giemsa [MGG],×100 镜下)显示,嗜酸性粒细胞明显增多,同时伴有大量非典型淋巴细胞,细胞核呈卷曲和沟状。淋巴结活检证实有异常 T 细胞群浸润。骨髓检查显示非典型大 T 细胞占细胞总数的 14%,嗜酸性粒细胞占 25%(左下,MGG,×100)。皮肤打孔活检(右下,苏木精和伊红,×20)显示浅表血管周围淋巴细胞和嗜酸性粒细胞皮炎,无海绵状增生或表皮增生。免疫组化分析发现表达 CD4 的异常淋巴细胞,CD4:CD8 比值≥ 10,CD5 同时缺失,CD7 部分缺失。随后对外周血、骨髓和淋巴结进行免疫分型,证实存在相同的克隆 T 细胞群,同时还显示出 CD26 表达缺失。塞扎里综合征是一种侵袭性成熟 T 细胞白血病,以难治性症状和预后不良为特征。嗜酸性粒细胞增多经常发生[1],据信是由于肿瘤细胞分泌特定的 Th2 相关细胞因子所致[2]。嗜酸性粒细胞增多症的病因不胜枚举,塞扎里综合征就是其中之一,外周血检查可能会发现嗜酸性粒细胞增多症。即使淋巴细胞计数没有增加,也可能出现这种情况。此外,嗜酸性粒细胞计数可能对皮肤 T 细胞淋巴瘤的预后有重要意义[1]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sézary Syndrome—Eosinophilia Explained by a Blood Film
image

A 61-year-old man, with no significant medical history, presented with a six-month history of fatigue, pruritus, night sweats, and weight loss. Physical examination revealed erythroderma and generalized lymphadenopathy. Laboratory tests showed prominent eosinophilia (white blood cell count 10.6 × 109/L, eosinophils 2.9 × 109/L). There was no lymphocytosis (lymphocyte count 1.1 × 109/L). Lactate dehydrogenase (LDH) was elevated at 469 U/L. A peripheral blood smear (top left and top right, May–Grünwald–Giemsa [MGG], ×100 objective) highlighted marked eosinophilia alongside large, atypical lymphocytes with convoluted and grooved nuclei. Lymph node biopsy confirmed infiltration by an aberrant T-cell population. Bone marrow examination showed atypical large T cells accounting for 14% of the total cell population and an eosinophil fraction of 25% (bottom left, MGG, ×100). A skin punch biopsy (bottom right, hematoxylin and eosin, ×20) demonstrated superficial perivascular lymphocytic and eosinophilic dermatitis, with no spongiosis or epidermotropism. Immunohistochemical analysis identified abnormal lymphocytes expressing CD4 with a CD4:CD8 ratio ≥ 10 and concurrent loss of CD5 and partial loss of CD7. Subsequent immunophenotyping of peripheral blood, bone marrow, and lymph nodes confirmed the presence of an identical clonal T-cell population with loss of CD26 expression also being shown.

Based on these peripheral blood and histopathological findings in the context of erythroderma, the diagnosis of Sézary syndrome was established. Sézary syndrome is an aggressive form of mature T-cell leukemia, characterized by refractory symptoms and a poor prognosis. Eosinophilia occurs frequently [1] and is believed to result from the secretion of specific Th2-associated cytokines by neoplastic cells [2].

There are innumerable causes of eosinophilia. Sézary syndrome is one of a number of causes that may be revealed by peripheral blood examination. This may be so even when the lymphocyte count is not increased. In addition, the eosinophil count may be of prognostic significance in cutaneous T-cell lymphomas [1].

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来源期刊
CiteScore
15.70
自引率
3.90%
发文量
363
审稿时长
3-6 weeks
期刊介绍: The American Journal of Hematology offers extensive coverage of experimental and clinical aspects of blood diseases in humans and animal models. The journal publishes original contributions in both non-malignant and malignant hematological diseases, encompassing clinical and basic studies in areas such as hemostasis, thrombosis, immunology, blood banking, and stem cell biology. Clinical translational reports highlighting innovative therapeutic approaches for the diagnosis and treatment of hematological diseases are actively encouraged.The American Journal of Hematology features regular original laboratory and clinical research articles, brief research reports, critical reviews, images in hematology, as well as letters and correspondence.
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