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腮腺腺样囊性癌鞍内远处转移:病例报告

Intrasellar remote metastasis from adenoid cystic carcinoma of parotid gland: case report.

作者信息

Kawamata Takakazu, Harashima Shiho, Kubo Osami, Hori Tomokatsu

机构信息

Department of Neurosurgery, Neurological Institute, Tokyo Women's Medical University, Tokyo, Japan.

出版信息

Endocr J. 2006 Oct;53(5):659-63. doi: 10.1507/endocrj.k05-146. Epub 2006 Aug 11.

Abstract

Adenoid cystic carcinoma is a tumor of exocrine glands originating primarily from the minor and major salivary glands, lacrimal gland, bronchus, breast, and intestinal and genital tracts. Intracranial remote metastasis from adenoid cystic carcinoma in salivary gland is quite rare. The authors encountered a case of intrasellar remote metastasis from an adenoid cystic carcinoma of parotid gland origin, presenting with hyponatremia secondary to the syndrome of inappropriate secretion of antidiuretic hormone (SIADH). To our knowledge, this is the first reported case of metastasis from an adenoid cystic carcinoma to intrasellar area. A 78-year-old woman had an adenoid cystic carcinoma in the left parotid gland, which was resected surgically followed by local radiation therapy of 60 Gy. After 4 years, the patient presented with general malaise, followed by disturbed consciousness caused by hyponatremia. The clinical data showed severe hyponatremia induced by SIADH. An intrasellar heterogenous mass lesion compressing the optic chiasm was resected subtotally via an endonasal transsphenoidal approach. Histopathological examination of the tumor specimens revealed adenoid cystic carcinoma, which had identical histological findings as those of the painful superficial cervical lymph nodes resected in the same operation. Tumors such as the present case are easily confused with pituitary adenoma or craniopharyngioma. Although rare, metastasis from tumors including those of salivary gland origin should be considered in the differential diagnosis of unusual pituitary tumors.

摘要

腺样囊性癌是一种外分泌腺肿瘤,主要起源于小唾液腺和大唾液腺、泪腺、支气管、乳腺以及肠道和生殖道。涎腺腺样囊性癌发生颅内远处转移颇为罕见。作者遇到一例起源于腮腺的腺样囊性癌鞍内远处转移病例,表现为抗利尿激素分泌不当综合征(SIADH)继发的低钠血症。据我们所知,这是首例报道的腺样囊性癌转移至鞍内区域的病例。一名78岁女性左侧腮腺患有腺样囊性癌,接受了手术切除,随后进行了60 Gy的局部放射治疗。4年后,患者出现全身不适,随后因低钠血症导致意识障碍。临床资料显示SIADH诱发了严重低钠血症。通过鼻内镜经蝶窦入路部分切除了一个压迫视交叉的鞍内异质性肿块病变。肿瘤标本的组织病理学检查显示为腺样囊性癌,其组织学表现与同一次手术中切除的颈部浅表疼痛淋巴结的组织学表现相同。像本例这样的肿瘤很容易与垂体腺瘤或颅咽管瘤混淆。尽管罕见,但在不寻常垂体肿瘤的鉴别诊断中,应考虑包括涎腺起源肿瘤在内的肿瘤转移。

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