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新生儿患有严重原发性甲状旁腺功能亢进且其父母一方有高钙血症:通过甲状旁腺全切术及同期异位自体移植进行治疗。

Severe primary hyperparathyroidism in a neonate having a parent with hypercalcemia: treatment by total parathyroidectomy and simultaneous heterotopic autotransplantation.

作者信息

Fujimoto Y, Hazama H, Oku K

机构信息

Department of Endocrine Surgery, Tokyo Women's Medical College, Japan.

出版信息

Surgery. 1990 Nov;108(5):933-8.

PMID:2237775
Abstract

Neonatal primary hyperparathyroidism is a life-threatening disease because of marked hypercalcemia and severe respiratory distress caused by the hypoplastic thorax and occasional rib fractures. We report a 29-day-old girl treated by total parathyroidectomy and simultaneous autotransplantation of parathyroid tissue (one fifth of each of the two glands) in the femoral quadriceps muscle near the groin. At the time of operation, all four of the parathyroid glands were markedly enlarged, and their total weight was 900 mg. Part of the resected parathyroid tissue was cryopreserved for further autotransplantation should hypoparathyroidism develop. Two years six months after surgery, the infant was well and had normal levels of serum calcium and immunoreactive parathyroid hormone in the absence of any supplementary treatment. Asymptomatic hypercalcemia in the presence of abnormally low fractional excretion of calcium was found in the father. Based on our experience and review of the literature, we recommend total parathyroidectomy, autotransplantation, and cryopreservation for the neonate with primary hyperparathyroidism.

摘要

新生儿原发性甲状旁腺功能亢进是一种危及生命的疾病,因为会出现明显的高钙血症以及由胸廓发育不全和偶尔的肋骨骨折引起的严重呼吸窘迫。我们报告了一名29天大的女孩,她接受了甲状旁腺全切术,并同时将甲状旁腺组织(两个腺体各五分之一)自体移植到腹股沟附近的股四头肌中。手术时,所有四个甲状旁腺均明显肿大,总重量为900毫克。切除的部分甲状旁腺组织被冷冻保存,以备甲状旁腺功能减退发生时进一步自体移植。术后两年六个月,该婴儿情况良好,在未进行任何补充治疗的情况下血清钙和免疫反应性甲状旁腺激素水平正常。在父亲身上发现了存在异常低钙分数排泄的无症状高钙血症。基于我们的经验和文献回顾,我们建议对患有原发性甲状旁腺功能亢进的新生儿进行甲状旁腺全切术、自体移植和冷冻保存。

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