scholarly journals Day-case minimally invasive excision of a giant mediastinal parathyroid adenoma

2014 ◽  
Vol 96 (5) ◽  
pp. e21-e23 ◽  
Author(s):  
A Haldar ◽  
A Thapar ◽  
S Khan ◽  
S Jenkins

Inferior parathyroid adenomas in the mediastinum can be a troublesome cause for hypercalcaemia, requiring a full collar incision or, occasionally, a sternotomy. We report a case of a giant parathyroid adenoma in a 61-year-old woman on warfarin, which we excised via a minimally invasive transcervical approach after radiological localisation. The procedure was performed as a day case and, at six weeks, the patient had recovered fully with biochemical resolution of hypercalcaemia. This case demonstrates that focused transcervical excision of giant parathyroid adenomas is a viable option and should be considered prior to neck exploration or sternotomy.

2021 ◽  
Author(s):  
Xue Liu ◽  
lin Hui Wang

Abstract Background Giant ectopic mediastinal parathyroid adenoma with cystic degeneration and intratumoral hemorrhage is extremely rare, with low morbidity and a high misdiagnosis rate, and requires precise positioning and surgical resection. Case presentation: A 41-year-old woman presented with a sore throat for 3 days and hoarse voice for 1 day. The following chest computed tomography (CT) showed a large fusiform high-density mass in the posterior tracheal space (maximum cross-section of 34 x 25 mm). ultrasonography of the neck showed a low-echo solid mass. This patient had undergone 2 puncture treatments and 1 surgical treatment from the discovery of the lesion to the diagnosis of the cause over the span of more than a month. Subsequently, the final pathology was definitely diagnosed as parathyroid adenoma with cystic lesions. Six months after the operation, the patient did not relapse. Conclusions This case reported a rare and huge ectopic mediastinal parathyroid adenoma that was misdiagnosed as mediastinal tumor hemorrhage at an early stage. For ectopic mediastinal parathyroid adenomas, surgery is the preferred treatment option. Warn us that we should expand the scope of disease thinking for mediastinal tumors.


2018 ◽  
Vol 2 ◽  
pp. 75-75
Author(s):  
Senne Van Donink ◽  
Patrick Lauwers ◽  
Paul Van Schil ◽  
Jeroen Hendriks ◽  
Suresh Krishan Yogeswaran

2020 ◽  
pp. 014556132094202
Author(s):  
Ryan David Akin ◽  
A. Daniel Pinheiro

Hypercalcemic crisis is a rare endocrine emergency that occurs in a small percentage of patients with primary hyperparathyroidism. Although modern diagnostic capabilities allow timely diagnosis and intervention, hypercalcemic crisis still has a high potential for morbidity and mortality. We report an adult patient with a history of kidney stones who presented with heart palpitations, shortness of breath, fatigue, nausea, and 20-pound weight loss over 2 months. Workup revealed hypercalcemia, elevated parathyroid hormone (PTH), and a mediastinal mass on computed tomography angiography. This patient’s hypercalcemic crisis was treated with intravenous hydration using normal saline, zoledronate, and furosemide. After medical optimization, the patient underwent definitive treatment with surgical parathyroidectomy via a transcervical approach. At operation, a large parathyroid adenoma was removed from a posterior–superior mediastinal location dorsal to the recurrent laryngeal nerve with subsequent normalization of calcium and PTH. We discuss the timing of parathyroidectomy in cases of hypercalcemic crisis and the surgical approach to ectopic parathyroid glands in the mediastinum.


2006 ◽  
Vol 116 (3) ◽  
pp. 482-487 ◽  
Author(s):  
Mithran S. Sukumar ◽  
Christopher B. Komanapalli ◽  
James I. Cohen

2009 ◽  
Vol 19 (1) ◽  
pp. 78-81 ◽  
Author(s):  
Yoshifumi Ikeda ◽  
Yuzo Sasaki ◽  
Rika Miyabe ◽  
Naomi Morita ◽  
Hiroshi Takami

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