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原发性免疫缺陷病中的恶性肿瘤和淋巴组织增生;难以明确,难以治疗。

Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat.

机构信息

Department of Pediatrics, Division of Pediatric Allergy and Immunology, School of Medical, Marmara University, Istanbul, Turkey.

Istanbul Jeffrey Modell Diagnostic and Research Center for Primary Immunodeficiencies, Istanbul, Turkey.

出版信息

Pediatr Blood Cancer. 2020 Feb;67(2):e28091. doi: 10.1002/pbc.28091. Epub 2019 Nov 17.

Abstract

BACKGROUND

Regarding the difficulties in recognition and management of the malignancies in primary immune deficiencies (PIDs), we aimed to present the types, risk factors, treatment options, and prognosis of the cancers in this specific group.

METHODS

Seventeen patients with PID who developed malignancies or malignant-like diseases were evaluated for demographics, clinical features, treatment, toxicity, and prognosis.

RESULTS

The median age of malignancy was 12.2 years (range, 2.2-26). Lymphoma was the most frequent malignancy (n = 7), followed by adenocarcinoma (n = 3), squamous cell carcinoma (n = 2), cholangiocarcinoma (n = 1), Wilms tumor (n = 1), and acute myeloid leukemia (n = 1). Nonneoplastic lymphoproliferation mimicking lymphoma was observed in five patients. The total overall survival (OS) was 62.5% ± 12.1%. The OS for lymphoma was 62.2% ± 17.1% and found to be inferior to non-PID patients with lymphoma (P = 0.001).

CONCLUSION

In patients with PIDs, malignancy may occur and negatively affect the OS. The diagnosis can be challenging in the presence of nonneoplastic lymphoproliferative disease or bone marrow abnormalities. Awareness of susceptibility to malignant transformation and early diagnosis with multidisciplinary approach can save the patients' lives.

摘要

背景

原发性免疫缺陷(PID)患者的恶性肿瘤识别和管理存在困难,因此我们旨在介绍此类患者恶性肿瘤的类型、风险因素、治疗选择和预后。

方法

对 17 名患有恶性肿瘤或恶性样疾病的 PID 患者进行评估,评估内容包括人口统计学、临床特征、治疗、毒性和预后。

结果

恶性肿瘤的中位年龄为 12.2 岁(范围,2.2-26 岁)。淋巴瘤是最常见的恶性肿瘤(n=7),其次是腺癌(n=3)、鳞状细胞癌(n=2)、胆管癌(n=1)、Wilms 瘤(n=1)和急性髓系白血病(n=1)。5 例患者存在非肿瘤性淋巴增生样淋巴瘤。总总体生存率(OS)为 62.5%±12.1%。淋巴瘤的 OS 为 62.2%±17.1%,明显低于非 PID 淋巴瘤患者(P=0.001)。

结论

PID 患者可能会发生恶性肿瘤,并对 OS 产生负面影响。在存在非肿瘤性淋巴增生性疾病或骨髓异常的情况下,诊断可能具有挑战性。了解恶性转化的易感性并通过多学科方法进行早期诊断可以挽救患者的生命。

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