医学
垂体腺瘤
头痛
神经外科
颅咽管瘤
垂体炎
病变
视交叉
囊肿
放射科
腺瘤
肢端肥大症
垂体瘤
垂体
病理
外科
视神经
解剖
内科学
激素
生长激素
作者
Miguel A. Del Toro-Colín,Martha Lilia Tena‐Suck,Alberto Santiago-Balmaseda,Citlaltépetl Salinas-Lara,Germán Velázquez-Garcia,Maria de Lourdes Aguilar-Gómez,Elsa Yazmín León-Marroquín,Carlos Sánchez-Garibay,Alma Ortíz-Plata,Roger Antonio Carrillo-Meza,Noemí Gelista-Herrera,Lesly Hernández-Roque,Luis O. Soto-Rojas
标识
DOI:10.1007/s10014-025-00504-4
摘要
Abstract The coexistence of three lesions in the sellar region is exceedingly rare. Only two cases with three histopathologically distinct lesions have been reported. However, here, we present a unique case of a 54-year-old female with pituitary adenoma (PA), xanthogranulomatous hypophysitis (XGH), and a Rathke cleft cyst (RCC). Clinically, the patient manifested symptoms of mass compression, such as moderate-intensity headaches and progressive visual acuity decrease. Relevant endocrinological evaluation revealed elevated free thyroxine levels without clinical manifestations. MRI revealed a suprasellar mass compatible with a macroadenoma. The patient underwent transsphenoidal endoscopic resection, resulting in a non-functional macroadenoma with associated XGH due to the rupture of RCC. Furthermore, in this article, we analyze the possible mechanisms involved in the pathogenesis of these lesions, emphasizing the type of spectrum to which they belong and the manifestations present.
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