FAMILIAL HYPERPARATHYROIDISM ASSOCIATED WITH JAW FIBROMA - CASE-REPORT AND LITERATURE-REVIEW

被引：16

作者：

INOUE, H

MIKI, H

OSHIMO, K

TANAKA, K

MONDEN, Y

KAGAWA, S

SANO, N

HAYASHI, E

NAGAYAMA, M

HAYASHI, Y

机构：

[1] UNIV TOKUSHIMA,SCH MED,DEPT UROL,TOKUSHIMA 770,JAPAN

[2] UNIV TOKUSHIMA,SCH MED,DEPT PATHOL 2,TOKUSHIMA 770,JAPAN

[3] UNIV TOKUSHIMA,SCH DENT,DEPT ORAL & MAXILLOFACIAL SURG 1,TOKUSHIMA 770,JAPAN

[4] UNIV TOKUSHIMA,SCH DENT,DEPT ORAL PATHOL,TOKUSHIMA 770,JAPAN

来源：

CLINICAL ENDOCRINOLOGY | 1995年 / 43卷 / 02期

关键词：

D O I：

10.1111/j.1365-2265.1995.tb01919.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

A 53-year-old female suffering from renal stones and hypercalcaemia was diagnosed as having primary hyperparathyroidism caused by hyperplasia of the parathyroid glands. She underwent total parathyroidectomy and implantation of parathyroid tissue, After one year, she underwent surgery for a jaw tumour. The pathological findings indicated it to be a cementifying fibroma, Jackson et al. (1990) reported the familial association of hyperparathyroidism with jaw tumours, and they suggested that this condition represents a new clinical syndrome. We believe that our case belongs to this syndrome.

引用

页码：225 / 229

页数：5

共 10 条

[1] PARATHYROID CARCINOMA IN FAMILIAL HYPERPARATHYROIDISM [J].