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伴有大量IgG4浆细胞的ALK-1阳性眼眶炎性肌纤维母细胞瘤(IMT)——病例报告

ALK-1 positive orbital inflammatory myofibroblastic tumour (IMT) associated with prominent numbers of IgG4 plasma cells - a case report.

作者信息

Mudhar Hardeep Singh, Nuruddin Murtuza

机构信息

National Specialist Ophthalmic Pathology Service, Department of Histopathology, Royal Hallamshire Hospital , Sheffield, England , United Kingdom and.

出版信息

Orbit. 2013 Oct;32(5):321-3. doi: 10.3109/01676830.2013.805789. Epub 2013 Aug 8.

Abstract

A 14-year-old boy presented with a 2-year history of a supraorbital mass, associated with loss of vision and phthisis. A lack of response to systemic steroids led to an incisional biopsy. This showed a spindle cell lesion with a prominent inflammatory component, with numerous plasma cells. The spindle cells were positive for anaplastic lymphoma kinase (ALK-1). Over 90% of the plasma cells were surprisingly positive for IgG4. The presence of ALK-1 positivity within the spindle cells, coupled with the prominent inflammation indicated a diagnosis of ALK-1 positive inflammatory myofibroblastic tumour (IMT-the neoplastic member of the so called inflammatory pseudotumours). However, the level of IgG4 positivity within the plasma cell population would have otherwise lead to a diagnosis of IgG4 related disease, if the ALK-1 positive spindle cells population was not represented. Recent literature from systemic IMT has alluded to the presence of IgG4 plasma cell positivity in IMT and argues that in the absence of other supporting histological features of IgG4 disease (phlebitis and lymphoid aggregates), as in this case, the presence of IgG4 plasma cells, even in high numbers should not lead to a kneejerk diagnosis of co-existing IgG4 disease. This case report is the first to make this association in the orbit and argues that in the presence of IMT, the IgG4 plasma cells are not necessarily pathogenic.

摘要

一名14岁男孩出现眶上肿块2年,伴有视力丧失和眼球痨。对全身用类固醇治疗无反应,遂进行切开活检。结果显示为梭形细胞病变,伴有明显的炎症成分,有大量浆细胞。梭形细胞间变性淋巴瘤激酶(ALK-1)呈阳性。令人惊讶的是,超过90%的浆细胞IgG4呈阳性。梭形细胞内ALK-1阳性,加上明显的炎症,提示诊断为ALK-1阳性炎性肌纤维母细胞瘤(IMT,即所谓炎性假瘤的肿瘤性成员)。然而,如果不存在ALK-1阳性梭形细胞群,浆细胞群中IgG4阳性水平本会导致IgG4相关疾病的诊断。系统性IMT的最新文献提到IMT中存在IgG4浆细胞阳性,并认为在不存在IgG4疾病的其他支持性组织学特征(静脉炎和淋巴样聚集)的情况下,如本病例,即使IgG4浆细胞数量很多,也不应贸然诊断为并存的IgG4疾病。本病例报告首次在眼眶中发现这种关联,并认为在存在IMT的情况下,IgG4浆细胞不一定具有致病性。

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