失控的火车:泄漏的放射敏感SCID与皮肤病变和多发性淋巴瘤。

Pub Date : 2018-05-14 eCollection Date: 2018-01-01 DOI:10.1155/2018/2053716
Børre Fevang, Unn Merete Fagerli, Hanne Sorte, Harald Aarset, Håkon Hov, Marit Langmyr, Thomas Morten Keil, Ellen Bjørge, Pål Aukrust, Asbjørg Stray-Pedersen, Tobias Gedde-Dahl
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引用次数: 4

摘要

核酸酶Artemis对t细胞和b细胞受体的发育和DNA双链断裂的修复至关重要,表达或功能的丧失将导致无功能t细胞或b细胞的放射敏感性严重联合免疫缺陷(T-B-SCID)。Artemis基因的半胚性突变可导致t细胞和b细胞库功能减少,其临床过程更为缓慢,称为“漏性”SCID。在这里,我们报告了一个年轻人的病例,他从2岁开始患有越来越严重的淋巴增生性皮肤病变,并发展为多发性EBV+ b细胞淋巴瘤,在使用全外显子组测序的诊断竞赛中发现了Artemis基因的次形突变。患者在淋巴瘤缓解期接受了单倍干细胞移植,尽管最初的治疗是成功的,但移植后5个月,他死于严重的乙氏肺囊虫肺炎。该病例强调了下一代测序在诊断疑似严重免疫缺陷患者中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Runaway Train: A Leaky Radiosensitive SCID with Skin Lesions and Multiple Lymphomas.

The nuclease Artemis is essential for the development of T-cell and B-cell receptors and repair of DNA double-strand breaks, and a loss of expression or function will lead to a radiosensitive severe combined immunodeficiency with no functional T-cells or B-cells (T-B-SCID). Hypomorphic mutations in the Artemis gene can lead to a functional, but reduced, T-cell and B-cell repertoire with a more indolent clinical course called "leaky" SCID. Here, we present the case of a young man who had increasingly aggressive lymphoproliferative skin lesions from 2 years of age which developed into multiple EBV+ B-cell lymphomas, where a hypomorphic mutation in the Artemis gene was found in a diagnostic race against time using whole exome sequencing. The patient was given a haploidentical stem cell transplant while in remission for his lymphomas and although the initial course was successful, he succumbed to a serious Pneumocystis jirovecii pneumonia 5 months after the transplant. The case underscores the importance of next-generation sequencing in the diagnosis of patients with suspected severe immunodeficiency.

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