The incidence of nephrolithiasis and osteoporosis in patients with asymptomatic hyperparathyroidism

Author(s):  
Antonis Polymeris ◽  
Nikolaos Kalogeris ◽  
Apostolos Lafkas ◽  
Nektaria Papanikola ◽  
Eleni Herolidi ◽  
...  
1984 ◽  
Vol 147 (4) ◽  
pp. 498-502 ◽  
Author(s):  
Randall D. Gaz ◽  
Chiu-an Wang

1981 ◽  
Vol 2 (9) ◽  
pp. 452-452
Author(s):  
P. J. Phillips ◽  
A. R. Robertson ◽  
A. G. Need ◽  
P. E. Harding

JAMA ◽  
1977 ◽  
Vol 237 (20) ◽  
pp. 2186
Author(s):  
Elliott M. Antman

2009 ◽  
Vol 160 (4) ◽  
pp. 689-694 ◽  
Author(s):  
C Christopoulos ◽  
V Balatsos ◽  
E Rotas ◽  
I Karoumpalis ◽  
D Papavasileiou ◽  
...  

ObjectiveTo present evidence supporting the hypothesis that the coexistence of gastric carcinoids (GCs) and hyperparathyroidism may represent a distinct clinical entity, not related to multiple endocrine neoplasia type 1 (MEN1).MethodsWe studied a cohort of five young siblings (age range 26–42 years), one of whom had been found to have GC and hyperparathyroidism. All siblings underwent serial gastroscopies for the assessment of gastric neuroendocrine cell proliferations over a mean follow-up period of 31.2 months. Imaging, biochemical and hormonal as well as molecular genetic investigations were performed in the direction of MEN1 syndrome. The literature was searched for cases with coexistence of GCs and hyperparathyroidism not associated with MEN1.ResultsFour of the siblings, all male, were found to have GCs in a background of Helicobacter pylori-associated chronic atrophic gastritis and pernicious anaemia, with no serological evidence of gastric autoimmunity. In two of them, asymptomatic hyperparathyroidism was also present. Screening for MEN1 gene mutations or large deletions was negative, and hormone and imaging investigations did not support a diagnosis of familial MEN1 syndrome. A literature search revealed sporadic reports of cases with GC and hyperparathyroidism not attributable to MEN1.ConclusionsThe association of GCs and hyperparathyroidism appears to constitute a distinct syndrome that can be encountered in genetically predisposed individuals, and should not be regarded as ‘atypical’ or ‘incomplete’ expression of MEN1. Its prevalence and aetiology should be the subject of future studies. Screening for hyperparathyroidism seems to be justified in patients with GC of any type.


2016 ◽  
Vol 5 (2) ◽  
pp. 104-106
Author(s):  
Md Raziur Rahman ◽  
Mohammad Abdul Hannan ◽  
Samira Rahat Afroze ◽  
Sultana Marufa Shefin ◽  
Muhammad Abdur Rahim ◽  
...  

Primary hyperparathyroidism is often asymptomatic, may be detected during routine investigations or may present with features of hypercalcaemia. Vitamin D deficiency causing secondary hyperparathyroidism presents with musculoskeletal symptoms. Studies have shown an association between primary hyperparathyroidism and vitamin D deficiency. It has also been observed that when co-exist, these two conditions contribute to each other’s disease presentation and severity. This case report depicts initial asymptomatic hyperparathyroidism developing symptoms due to co-existing parathyroid adenoma and vitamin D deficiency in a 26-year-old muslim Bangladeshi female who responded well to adequate pre, per and post parathyroidectomy medical managementBirdem Med J 2015; 5(2): 104-106


2015 ◽  
Vol 173 (3) ◽  
pp. D13-D20 ◽  
Author(s):  
Bruno Niederle ◽  
Jean-Louis Wémeau

A large majority of the currently diagnosed patients with hyperparathyroidism (PHPT) are mild or asymptomatic, mainly women after menopause. Following the debate held at the 16th European Congress of Endocrinology in Wroclaw (Poland) from May 3–7, 2014, arguments are here presented by a surgeon and a medical practitioner considering these situations rather have to profit from surgery, or simply from survey. For the trained endocrine surgeon, it is evident that parathyroidectomy confirms the diagnosis and undoubtedly reduces the discomfort felt by certain patients, prevents all risks of complications, removes patients and medical teams from the monitoring and represents a real individual financial benefit. On the other hand, the medical practitioner considers that mild or asymptomatic PHPT is commonly stable, and very rare are the subjects at risk of complications, particularly of fractures; prevention of vascular and metabolic disorders, nephrolithiasis and bone rarefaction justify regular physical exercise, a safe alimentation, a sufficient calcium and high water intake, the correction of the frequent deficit in vitamin D; finally has also to be considered the impossibility to refer to specialized (endocrine) surgeons, the enormous cohort of subjects more than 50 years with ‘mild’ or ‘asymptomatic’ PHPT. The surgeon and the medical practitioner agree to consider that in patients with ‘mild’ or ‘asymptomatic’ disease, there is no place for medical treatments, in particular calcimimetics and bisphophonates. Both agree that further studies are needed to clarify the long-term prognosis of operated and non-operated PHPT in term of fractures, cardiovascular risk and mortality. Individual and collective cost/benefit ratios of surgery or survey are also still imperfectly evaluated.


Sign in / Sign up

Export Citation Format

Share Document