Abstract #504: A Case of Hungry-Bone Syndrome in an 18-Year-Old Female After Removal of a Single Adenoma for Severe Hyperparathyroidism

2017 ◽  
Vol 23 ◽  
pp. 101
Author(s):  
Ben Brannick ◽  
Andrew Olinger ◽  
Helmut Steinberg
2021 ◽  
Vol 17 (5) ◽  
pp. 396-397
Author(s):  
M. Hamdaoui ◽  
S. Mchiouer ◽  
I. Haouli ◽  
H. Oujidi ◽  
K. Frikel ◽  
...  

2015 ◽  
Vol 11 (04) ◽  
Author(s):  
Daniela Tatiana Sala ◽  
Ioan Tilea

2018 ◽  
Vol 11 (1) ◽  
pp. e226696 ◽  
Author(s):  
Mohamed Hassanein ◽  
Heather Laird-Fick ◽  
Richa Tikaria ◽  
Saleh Aldasouqi

Calcific uremic arteriolopathy (CUA), widely known as calciphylaxis, is a rare and lethal disease that usually affects patients with end-stage renal disease. It is characterised by widespread vascular calcification leading to tissue ischaemia and necrosis and formation of characteristic skin lesions with black eschar. Treatment options include sodium thiosulfate, cinacalcet, phosphate binders and in resistant cases, parathyroidectomy. We report a case of recurrent, treatment-resistant CUA successfully treated with parathyroidectomy. Her postoperative course was complicated by hungry bone syndrome and worsening of her wounds before they completely healed. We then discuss the morbidity of CUA, including the controversy around the use of parathyroidectomy and risk of aggressive management of hungry bone syndrome.


2008 ◽  
Vol 27 (1) ◽  
pp. 101-104 ◽  
Author(s):  
Ediz Yeşilkaya ◽  
Peyami Cinaz ◽  
Aysun Bideci ◽  
Orhun Çamurdan ◽  
Fatma Demirel ◽  
...  

2014 ◽  
Vol 75 (5-6) ◽  
pp. 352
Author(s):  
S. Leghlimi ◽  
K. Rifai ◽  
S. Ech-Cherif El Kettani ◽  
S. Elmoussaoui ◽  
G. Belmejdoub

2017 ◽  
Vol 58 (1) ◽  
pp. 50
Author(s):  
Mohammad Naghavi-Behzad ◽  
Hamid Tayyebi-Khosroshahi ◽  
Farahnoush Farnood ◽  
Maryam Ghorbanian ◽  
Farid Karkon-Shayan

2019 ◽  
Vol 5 (4) ◽  
pp. 140-144
Author(s):  
Corina Pop Radu ◽  
Valentin Daniealopol ◽  
Ario Santini ◽  
Ruxandra Darie ◽  
Daniela Tatiana Sala

Abstract Introduction Hungry bone syndrome (HBS) refers to the rapid, profound, and prolonged hypocalcaemia associated with hypophosphatemia and hypomagnesaemia, and is exacerbated by suppressed parathyroid hormone (PTH) levels, which follows parathyroidectomy in patients with severe primary hyperparathyroidism (PHPT) and preoperative high bone turnover. [1] Case report This report concerns a dialysed patient who underwent surgical treatment for secondary refractory hyperparathyroidism. Haemodialysis was carried out pre-operatively, and subsequently, a total parathyroidectomy with auto-transplantation of parathyroid tissue in the sternocleidomastoid muscle (SCM) was performed. Rapid and progressive hypocalcaemia symptoms developed during the second day postoperatively. Acute cardiac symptoms with tachyarrhythmia, haemodynamic instability and finally asystole occurred, which required cardiopulmonary resuscitation (CPR). The ionic calcium level was 2.2 mg/dL being consistent with a diagnosis of HBS. A second cardiac arrest unresponsive to CPR followed an initial period of normal sinus rhythm. Death ensued shortly after. Before death, the ionic calcium was 3.1 mg/dL. Conclusion HBS, after parathyroidectomy in patients with secondary hyperparathyroidism (SHPT), may be severe, prolonged and sometimes fatal. Generally, HBS symptomatology is that of a mild hypocalcaemia. It can, however, include heart rhythm disturbances with haemodynamic alterations requiring intensive care measurements and even cardiopulmonary resuscitation. A close clinical and laboratory post-parathyroidectomy monitoring of dialysed patients is of the utmost importance.


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