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腺苷脱氨酶缺乏型重症联合免疫缺陷的病理发现。II. 胸腺、脾脏、淋巴结及胃肠道淋巴组织改变

Pathologic findings in adenosine deaminase deficient-severe combined immunodeficiency. II. Thymus, spleen, lymph node, and gastrointestinal tract lymphoid tissue alterations.

作者信息

Ratech H, Hirschhorn R, Greco M A

机构信息

Department of Pathology, New York University Medical Center, New York.

出版信息

Am J Pathol. 1989 Dec;135(6):1145-56.

Abstract

Eight autopsies of patients with adenosine deaminase deficient-severe combined immunodeficiency disease (ADA-SCID) were reviewed with special emphasis on the lymphoid tissues. The thymus histology in five cases was remarkably uniform, whether or not prior ADA enzyme replacement or immunologic reconstitution therapy had been administered. Lymph nodes and spleens in all cases examined showed a residual nonlymphoid architectural framework corresponding to usual T and B cell zones found in normals. The development of an extranodal, monoclonal IgA lambda B cell immunoblastic lymphoma as a terminal event in one patient after several years of successful ADA enzyme replacement therapy through multiple red blood cell transfusions is described. In another patient with long-term ADA enzyme replacement, a terminal autoimmune hemolytic anemia developed. Autopsy revealed severe deposits of iron in the B cell zones of the lymph nodes, which is an unusual location. In addition, iron deposits outlined the splenic trabeculae, as well as the ring fibers and bridging fibers of the splenic sinuses.

摘要

对8例腺苷脱氨酶缺乏型重症联合免疫缺陷病(ADA - SCID)患者的尸检进行了回顾,特别关注淋巴组织。5例患者的胸腺组织学表现非常一致,无论之前是否接受过ADA酶替代或免疫重建治疗。所有检查的病例中的淋巴结和脾脏均显示出与正常情况下发现的T和B细胞区域相对应的残余非淋巴结构框架。描述了1例患者在通过多次红细胞输血成功进行ADA酶替代治疗数年之后,发生结外单克隆IgA λ B细胞免疫母细胞淋巴瘤作为终末期事件。在另1例长期接受ADA酶替代治疗的患者中,发生了终末期自身免疫性溶血性贫血。尸检显示淋巴结B细胞区域有大量铁沉积,这是一个不寻常的部位。此外,铁沉积勾勒出脾小梁以及脾窦的环形纤维和桥接纤维。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a67/1880483/1b8a64912c3a/amjpathol00120-0185-a.jpg

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