多激素性垂体腺瘤与肉芽肿性垂体炎的独特共存。

IF 0.8 4区 医学 Q4 PATHOLOGY Indian Journal of Pathology and Microbiology Pub Date : 2023-07-01 DOI:10.4103/ijpm.ijpm_439_21
Sanjiban Patra, Priti Trivedi
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引用次数: 0

摘要

垂体的双重病理是一种独特的现象。垂体腺瘤与原发性垂体炎并存的报道很少,文献中很少有病例。在原发性垂体炎中,原发性肉芽肿亚型被认为是特发性和自身免疫性的。多发性垂体腺瘤产生一种以上不同垂体细胞谱系的激素。单一激素含量的垂体腺瘤已被记录为并发原发性肉芽肿性垂体炎。本病例描述了一名36岁女性鞍区多激素腺瘤与原发性肉芽肿性炎症的独特共存,该腺瘤表现为生长激素、乳细胞和促皮质激素谱系。
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A unique coexistence of a plurihormonal pituitary adenoma with granulomatous hypophysitis.

Dual pathology in the pituitary gland is a unique phenomenon. Coexistence of a pituitary adenoma with primary hypophysitis has been reported rarely with very few cases in the literature. Among the primary hypophysitis, primary granulomatous subtype has been proposed to be idiopathic and autoimmune in nature. Plurihormonal pituitary adenomas produce hormones of more than one different pituitary cell lineage. Pituitary adenoma with a single hormonal content has been documented with concurrent primary granulomatous hypophysitis. The present case describes the unique coexistence of a plurihormonal adenoma showing somatotroph, lactotroph, and corticotroph lineage with primary granulomatous inflammation in the sellar region in a 36-year-old woman.

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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
422
审稿时长
1 months
期刊介绍: The journal will cover studies related to pathology including morbid anatomy, surgical pathology, clinical pathology, diagnostic cytopathology including gynecologic cytology and aspiration cytology, hematology including immuno-hematology and medical microbiology. The journal gives preference to clinically oriented studies over experimental and animal studies. The Journal would publish peer-reviewed original research papers, case reports, systematic reviews, meta-analysis, letters to the editor and brief communications. Review articles on current topics usually are invited by the editor.
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