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罕见病例:IgG4相关性慢性炎症性疾病累及肾脏。

A rare case: IgG4-related chronic inflammatory disease with kidney involvement.

作者信息

Mete Fatos, Mengeneci Tuba, Albayrak Emre, Ayar Yavuz, Nalbant Melike, Ozudeniz Mutlucan Ilknur, Fusun Baba Zeliha

机构信息

Department of Internal Medicine Bursa City Hospital Bursa Turkey.

Division of Nephrology, Department of Internal Medicine Bursa City Hospital Bursa Turkey.

出版信息

Clin Case Rep. 2023 Dec 28;12(1):e8164. doi: 10.1002/ccr3.8164. eCollection 2024 Jan.

Abstract

IgG4-related disease is an inflammatory, multisystemic disease that affects the immune system. The disease progresses to fibrosis due to inflammation. Retroperitoneal fibrosis is a serious complication. Pancreas, biliary tract, glands, thyroid, lymph nodes, etc. may be involved. Prognosis is usually subacute, and seen in middle age and advanced men. It is characterized histopathologically by IgG4 positive plasma cells, lymphoplasmocytic cell infiltration, and storiform fibrosis. In our case, we evaluated a patient who referred to our clinic from an external center with the complaints of generalized pain, itching, tearing and redness in eyes, involvement of bilateral large joints, and impaired renal function. Diagnosis, treatment and management of the disease are important. Response to glucocorticoid therapy is good.

摘要

IgG4相关疾病是一种影响免疫系统的炎症性多系统疾病。由于炎症,该疾病会进展为纤维化。腹膜后纤维化是一种严重的并发症。胰腺、胆道、腺体、甲状腺、淋巴结等可能会受累。预后通常为亚急性,多见于中年及老年男性。其组织病理学特征为IgG4阳性浆细胞、淋巴细胞和浆细胞浸润以及席纹状纤维化。在我们的病例中,我们评估了一名从外部中心转诊至我们诊所的患者,该患者主诉全身疼痛、眼睛瘙痒、流泪和发红、双侧大关节受累以及肾功能受损。该疾病的诊断、治疗和管理很重要。对糖皮质激素治疗反应良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0721/10753643/51413dbee509/CCR3-12-e8164-g001.jpg

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