多发性内分泌肿瘤
门1
甲状旁腺功能亢进
医学
甲状旁腺切除术
原发性甲状旁腺功能亢进
甲状旁腺腺瘤
甲状旁腺肿瘤
腺瘤
多发性内分泌肿瘤2型
内科学
内分泌学
甲状旁腺激素
病理
内分泌系统
种系突变
突变
生物
遗传学
激素
基因
钙
作者
Stephen J. Marx,William F. Simonds,Sunita Agarwal,A. Lee Burns,Lee S. Weinstein,Craig Cochran,Monica C. Skarulis,Allen M. Spiegel,Steven K. Libutti,H. Richard Alexander,Clara C. Chen,Richard Chang,Settara C. Chandrasekharappa,Francis S. Collins
出处
期刊:PubMed
日期:2002-11-01
卷期号:17 Suppl 2: N37-43
被引量:161
摘要
Hyperparathyroidism (HPT) in its hereditary variants assumes special forms, has special associations, and requires special managements. Familial hypocalciuric hypercalcemia (FHH or FBHH) and neonatal severe primary hyperparathyroidism (NSHPT) reflect heterozygous or homozygous mutations, respectively, in the calcium-sensing receptor. FHH and NSHPT represent the mildest and severest variants of HPT. Both cause hypercalcemia from birth and atypical HPT that always and uniquely persists after subtotal parathyroidectomy. Their HPT is likely polyclonal and nonneoplastic. In contrast, mono- or oligo-clonal parathyroid neoplasia underlays most other HPT variants: multiple endocrine neoplasia type 1 (MEN1), multiple endocrine neoplasia type 2A (MEN2A), and hyperparathyroidism-jaw tumor syndrome (HPT-JT). Familial-isolated HPT combines several diagnoses, including occult forms of the above syndromes. Each neoplastic variant has tumors in multiple parathyroids and a delayed, but still early age of onset for HPT (average age, 25-35 years). Each justifies special and similar approaches to parathyroidectomy: typically, identification of four glands, subtotal parathyroidectomy, rapid intraoperative parathyroid hormone (PTH) assays, and parathyroid cryopreservation. Outcomes of parathyroidectomy remain suboptimal in each. Each syndrome of parathyroid neoplasia associates with characteristic cancer(s): enteropancreatic neuroendocrine or foregut carcinoid tissues (MEN1), thyroidal C cells (MEN2A), or parathyroid (HPT-JT). HPT has promoted gene discovery more through its rare hereditary variants than through common adenoma; the main genes causing four of six hereditary variants are known. The RET mutation test became essential in management of MEN2A. The MEN1 test is less urgent, because it rarely guides a major patient benefit. The CASR test, perhaps least urgent, has largely been unavailable. Further progress in molecular genetics will enhance understandings, diagnosis, and therapy of HPT.
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