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伴有异常蛋白血症的血管免疫母细胞性淋巴结病的血液学特征

Haematological features of angioimmunoblastic lymphadenopathy with dysproteinaemia.

作者信息

Brearley R L, Chapman J, Cullen M H, Horton M A, Stansfeld A G, Waters A H

出版信息

J Clin Pathol. 1979 Apr;32(4):356-60. doi: 10.1136/jcp.32.4.356.

Abstract

A study of seven patients with AILD has confirmed previously reported cytological and immunological changes in the peripheral blood. In themselves these changes should not be considered as specific. Histological examination of the bone marrow may show more characteristic lesions which involve haemopoietic, lymphoid, and stromal cells. Three patients had bone marrow features similar to myelofibrosis, which are considered to be diagnostic of AILD.

摘要

一项针对7例自身免疫性淋巴增殖性疾病(AILD)患者的研究证实了先前报道的外周血细胞学和免疫学变化。就其本身而言,这些变化不应被视为具有特异性。骨髓组织学检查可能显示出更具特征性的病变,累及造血细胞、淋巴细胞和基质细胞。3例患者的骨髓特征类似于骨髓纤维化,这被认为是AILD的诊断依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d11e/1145672/f69b5fb170fa/jclinpath00452-0046-a.jpg

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