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具有炎性假瘤样特征的免疫球蛋白G4相关性淋巴结病

Immunoglobulin G4-related lymphadenopathy with inflammatory pseudotumor-like features.

作者信息

Sato Yasuharu, Kojima Masaru, Takata Katsuyoshi, Huang Xingang, Hayashi Eiko, Manabe Akihiro, Miki Yukari, Yoshino Tadashi

机构信息

Department of Pathology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700-8558, Japan.

出版信息

Med Mol Morphol. 2011 Sep;44(3):179-82. doi: 10.1007/s00795-010-0525-0. Epub 2011 Sep 16.

Abstract

Immunoglobulin (Ig) G4-related disease has been recently described. This disease affects various organs, including lymph nodes. We describe the case of a 52-year-old Japanese man with IgG4-related lymphadenopathy with inflammatory pseudotumor (IPT)-like features. Five years ago, the patient noticed a painless mass in the mandible but did not consult a doctor. Recently, he noted that the mass had increased in size and consulted an oral surgeon in the hospital. Excisional biopsy was performed for diagnosis. Histopathological examination revealed that most of the enlarged lymph node was occupied by the hyalinized tissue. A few residual lymphoid follicles with hyperplastic germinal centers and infiltration of plasma cells and eosinophils were observed. Most of the plasma cells expressed IgG4, and the ratio of IgG4-positive cells to IgG-positive cells was 57.1%. These findings were consistent with IgG4-related lymphadenopathy. In conclusion, pathologists should consider IgG4-related lymphadenopathy when diagnosing a lesion with IPT-like features.

摘要

免疫球蛋白(Ig)G4相关疾病最近已被描述。这种疾病会影响包括淋巴结在内的各种器官。我们描述了一例52岁日本男性患有具有炎性假瘤(IPT)样特征的IgG4相关淋巴结病的病例。五年前,患者注意到下颌骨有一个无痛性肿块,但未就医。最近,他发现肿块增大,于是到医院咨询了口腔外科医生。为明确诊断进行了切除活检。组织病理学检查显示,大部分肿大的淋巴结被玻璃样变组织占据。观察到一些残留的具有生发中心增生的淋巴滤泡以及浆细胞和嗜酸性粒细胞浸润。大多数浆细胞表达IgG4,IgG4阳性细胞与IgG阳性细胞的比例为57.1%。这些发现符合IgG4相关淋巴结病。总之,病理学家在诊断具有IPT样特征的病变时应考虑IgG4相关淋巴结病。

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