Primary hyperparathyroidism and monoclonal gammopathy.

Henry Ford Hospital medical journal Pub Date : 1991-01-01
D S Rao, R Antonelli, K R Kane, J E Kuhn, C Hetnal
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Abstract

Coexistent primary hyperparathyroidism and monoclonal gammopathy, although rare, has been reported previously by a number of investigators. We report four patients with such an occurrence who were seen between 1976 and 1988. Another patient with primary hyperparathyroidism also had multiple myeloma and was in remission for 12 years. These patients represent approximately 1% of the 386 patients with primary hyperparathyroidism seen during the same 12-year period. Although several mechanisms have been proposed to explain this concurrence, we believe it is the result of a chance occurrence. A review of the literature, an estimate of the chance occurrence of coincidental monoclonal gammopathy, benign or malignant, in patients with primary hyperparathyroidism, and some practical implications of this interesting coexistence are presented.

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原发性甲状旁腺功能亢进和单克隆伽玛病。
原发性甲状旁腺功能亢进症和单克隆伽玛病共存,虽然罕见,但以前有许多研究者报道过。我们报告了1976年至1988年间发生的4例此类病例。另一名原发性甲状旁腺功能亢进症患者也患有多发性骨髓瘤,缓解期为12年。这些患者约占同一12年间386例原发性甲状旁腺功能亢进症患者的1%。虽然已经提出了几种机制来解释这种并发,但我们认为这是偶然发生的结果。本文回顾文献,估计原发性甲状旁腺功能亢进患者发生偶发性单克隆γ病(良性或恶性)的机会,并提出这种有趣共存的一些实际意义。
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Extracellular Ca2+ sensing in C-cells and parathyroid cells. Proceedings of the Urban Health Care Symposium II. June 2-4, 1991. Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2. Unusual features of multiple endocrine neoplasia. Long-term follow-up in four large MEN 2 families in The Netherlands.
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