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一名性早熟女孩患分泌人绒毛膜促性腺激素的异位松果体瘤病例(作者译)

[A case of HCG-producing ectopic pinealoma in a girl with precocious puberty (author's transl)].

作者信息

Kubo O, Yamasaki N, Kamijo Y, Amano K, Kitamura K

出版信息

No Shinkei Geka. 1977 Apr;5(4):363-9.

PMID:558538
Abstract

HCG-producing ectopic pinealoma of two cell pattern type was demonstrated in a 5-year old girl who presented precocious puberty and bilateral choked discs. The tumor was localized at the anterior third ventricle and suprasellar region. Endocrinological findings are as following: Plasma basal LH was markedly elevated to 306 mIU/ml and HCG was elevated to 1,192 ng/ml. Provocative test of hypophyseal function revealed low response. Plasma estrogen was not detectable. HCG content of resected tumor tissue was elevated to 400 ng/mg. FSH, however, was not detectable. Histological findings of this tumor showed atypical teratoma, so-called two cell pattern pinealoma. Electron microscopic findings revealed two types of cells, dark and clear cells. Many secreting granules were found in the dark cells. In this case, HCG in plasma, CSF and tumor tissue was remarkably elevated. In addition, plasma FSH was also elevated to 8.9 mIU/ml. Precocious puberty associated with tumor in the pineal-suprasellar region has been seen only in boys. There has been no case report of precocious puberty in girls. This case is the first female case is which HCG-producing ectopic penealoma is caused in precocious puberty.

摘要

一名5岁女童被诊断为产生人绒毛膜促性腺激素(HCG)的两细胞型异位松果体瘤,该女童出现性早熟和双侧视乳头水肿。肿瘤位于第三脑室前部和鞍上区域。内分泌学检查结果如下:血浆基础促黄体生成素(LH)显著升高至306 mIU/ml,HCG升高至1192 ng/ml。垂体功能激发试验显示反应低下。血浆雌激素检测不到。切除的肿瘤组织中HCG含量升高至400 ng/mg。然而,促卵泡生成素(FSH)检测不到。该肿瘤的组织学检查结果显示为非典型畸胎瘤,即所谓的两细胞型松果体瘤。电子显微镜检查结果显示有两种细胞,即暗细胞和亮细胞。在暗细胞中发现了许多分泌颗粒。在该病例中,血浆、脑脊液和肿瘤组织中的HCG显著升高。此外,血浆FSH也升高至8.9 mIU/ml。松果体-鞍上区域肿瘤相关的性早熟仅在男孩中出现过。尚无女孩性早熟的病例报告。该病例是首例因产生HCG的异位松果体瘤导致性早熟的女性病例。

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