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一名库欣病患者合并分泌促卵泡生成素的大腺瘤。

FSH-producing macroadenoma associated in a patient with Cushing's disease.

作者信息

Oyama Ken-Ichi, Yamada Shozo, Hukuhara Noriaki, Hiramatsu Rikako, Taguchi Manabu, Yazawa Masako, Matsuda Akira, Ohmura Eiji, Imai Yasuo

机构信息

Department of Hypothalamic and Pituitary Surgery, Toranomon Hospital, Tokyo, and Division of Diabetes & Endocrinology, Saitama Medical Center, Saitama Medical University, Japan.

出版信息

Neuro Endocrinol Lett. 2006 Dec;27(6):733-6.

Abstract

OBJECTIVE AND IMPORTANCE

We encountered a Cushing's disease patient whose surgically removed pituitary macroadenoma was not an ACTH-producing, but rather a gonadotroph adenoma. Cure was obtained only after a tiny microadenoma, overlooked on preoperative studies, was removed by a 2nd operation from a compressed thin normal anterior pituitary gland.

CLINICAL PRESENTATION

This 45-year-old woman with Cushing syndrome presented with diabetes mellitus and steroid psychosis. Endocrinological examinations suggested Cushing's disease and MRI disclosed an invasive macroadenoma (22 mm in diameter) with suprasellar extension.

INTERVENTION

Despite total removal of the invasive macroadenoma by transsphenoidal surgery, her elevated serum cortisol- and ACTH levels failed to decrease. Histologic study of the surgical specimen disclosed that the tumor was a silent FSH-producing, rather than an ACTH-producing adenoma. Detailed re-evaluation of pre- and postoperative MRI suggested the presence of a 3-mm microadenoma on the left side of a thin compressed normal gland. Venous sampling of the cavernous sinus confirmed this suspicion. In a 2nd operation an ACTH-producing microadenoma was removed from inside the thin remaining compressed normal pituitary gland and endocrinological cure of Cushing's disease was achieved.

CONCLUSION

Although double adenomas, being a non-ACTH producing macroadenoma associated with an ACTH producing tiny microadenoma, are extremely rare in patients with Cushing's disease, detailed preoperative MRI evaluation is necessary to avoid missing tiny adenomas hidden in a compressed normal pituitary gland which is the cause of Cushing's disease, especially when a macroadenoma is found in patient with Cushing's disease.

摘要

目的与重要性

我们遇到一名库欣病患者,其经手术切除的垂体大腺瘤并非产生促肾上腺皮质激素(ACTH)的腺瘤,而是促性腺激素腺瘤。仅在第二次手术从受压变薄的正常垂体前叶中切除了术前检查遗漏的微小腺瘤后,病情才得以治愈。

临床表现

这位45岁患有库欣综合征的女性表现为糖尿病和类固醇精神病。内分泌检查提示库欣病,磁共振成像(MRI)显示有一个侵袭性大腺瘤(直径22毫米)并向鞍上扩展。

干预措施

尽管经蝶窦手术完全切除了侵袭性大腺瘤,但她升高的血清皮质醇和ACTH水平并未下降。手术标本的组织学研究表明,该肿瘤是一种不产生促卵泡生成素(FSH)的沉默腺瘤,而非产生ACTH的腺瘤。对术前和术后MRI进行详细重新评估提示,在变薄受压的正常腺体左侧存在一个3毫米的微腺瘤。海绵窦静脉采血证实了这一怀疑。在第二次手术中,从剩余变薄受压的正常垂体腺体内切除了产生ACTH的微腺瘤,库欣病的内分泌症状得以治愈。

结论

尽管双重腺瘤(即与产生ACTH的微小腺瘤相关的非产生ACTH的大腺瘤)在库欣病患者中极为罕见,但术前进行详细的MRI评估对于避免遗漏隐藏在受压正常垂体腺体内导致库欣病的微小腺瘤至关重要,尤其是在库欣病患者中发现大腺瘤时。

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