IgG4-associated hypophysitis coexisting with MALT lymphoma and gangliocytoma: first case report and literature review

被引：1

作者：

Zou, Dongbo ^{[1
]}

Jiang, Li ^{[2
]}

Yang, Tao ^{[1
]}

Cheng, Jingmin ^{[1
]}

Ma, Yuan ^{[1
]}

机构：

[1] Gen Hosp Western Theater Command, Dept Neurosurg, Chengdu, Peoples R China

[2] Second Peoples Hosp Chengdu, Dept Rheumatol & Immunol, Chengdu, Peoples R China

来源：

FRONTIERS IN NEUROLOGY | 2023年 / 14卷

关键词：

IgG4-related hypophysitis; MALT lymphoma; gangliocytomas; sellar region; headaches; vision loss; PITUITARY-ADENOMA; DISEASE; CELL;

D O I：

10.3389/fneur.2023.1253821

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

IgG4-related or IgG4-associated hypophysitis is a rare disease characterized by the infiltration of IgG4-positive plasma cells into pituitary gland tissue. Gangliocytomas in the sellar region are also extremely rare and are associated with pituitary adenomas in the majority of cases. Sellar mucosa-associated lymphoid tissue (MALT) lymphoma is an exceedingly rare condition. In this study, we present a case of IgG4-associated hypophysitis coexisting with MALT lymphoma and gangliocytoma. However, to elucidate the potential pathophysiological relationship, it is imperative to gather additional cases of IgG4-related hypophysitis accompanied by MALT lymphoma and gangliocytoma.

引用

页数：6

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