Parathyroid ultrasonography: the evolving role of the radiologist

Article information

Ultrasonography. 2015;34(4):268-274
Publication date (electronic) : 2015 April 6
doi : https://doi.org/10.14366/usg.14071
Department of Radiology, Thyroid Center, Daerim St. Mary’s Hospital, Seoul, Korea
Correspondence to: Jin Yong Sung, MD, Department of Radiology, Thyroid Center, Daerim St. Mary’s Hospital, 657 Siheung-daero, Youngdeungpo-gu, Seoul 150-822, Korea Tel. +82-2-829-9364 Fax. +82-2-829-9166 E-mail: jysrad68@empas.com
Received 2015 January 1; Revised 2015 April 6; Accepted 2015 April 6.

Abstract

Previously, radiologists played a limited role in the treatment of parathyroid disease, primary focusing on the preoperative localization of parathyroid lesions responsible for hyperparathyroidism. But, the widespread use of high-resolution ultrasound has lead to the increasing detection of parathyroid incidentalomas (PTIs). Consequently, radiologists may be required to differentiate PTIs from thyroid lesions, which is most reliably accomplished through the fine needle aspiration-parathyroid hormone analysis. Various nonsurgical treatment modalities for hyperfunctioning parathyroid lesions have been developed with some efficacy. Especially for symptomatic nonfunctioning parathyroid cysts, simple aspiration is a first-line procedure for diagnosis and treatment, while ethanol ablation is a subsequent treatment modality for recurrent cases.

Introduction

The role of radiologists in the treatment of parathyroid disease was previously limited to the preoperative localization of hyperfunctioning parathyroid lesions [1]. However, radiologists have been required to play a more active role, because it is increasingly necessary to distinguish parathyroid incidentalomas (PTIs) detected during thyroid ultrasonography (US), from thyroid lesions [2-5]. Moreover, some alternative nonsurgical treatments for parathyroid lesions have also emerged [6-14]. This article reviews evolving role of radiologists in the treatment of parathyroid disease.

Normal Anatomy and US Examination of Parathyroid Glands

Normal parathyroid glands are very small, measuring approximately 6 mm in the craniocaudal dimension and 3-4 mm in the transverse dimension, with shape like a flattened disk. Normal-sized parathyroid glands are not usually identified by most imaging modalities. Therefore, a parathyroid gland that is visible in US is very suspicious for the presence of a pathological entity [15]. The superior parathyroid glands are typically located on the posterior aspect of the upper thyroid lobes, with little anatomic variation in the population. The inferior parathyroid glands have a more variable location due to their embryologic relationship to the thymus. The inferior parathyroid glands are located along the lateral lower pole of the thyroid gland in 50% of the population, whereas they are located 1 cm below the lower thyroid lobe in 15% of the population [1], although they can be located anywhere between the angle of the mandible and the upper mediastinum. The incidence of intrathyroidal parathyroid tissue is approximately 2% [16]. Most people have four parathyroid glands, although supernumerary glands have been found in 13% of the population, most commonly in the thymus [1]. An examination for suspected parathyroid enlargement should include bilateral longitudinal and transverse images from the carotid arteries to the midline, with the carotid artery bifurcation as the superior border and the thoracic inlet as the inferior border [17,18].

Localization of Hyperfunctioning Parathyroid Lesions

The pathologic lesions associated with primary hyperparathyroidism (HPT) include solitary adenoma (80%-85%), multiglandular disease (15%-20%), and carcinoma (<1%). Multiglandular diseases of the parathyroid are due to hyperplasia of all of the parathyroid glands or, occasionally, double adenomas [19]. Single adenomas can be cured by excision of the adenoma through unilateral neck exploration. However, patients with suspected multiglandular disease, as well as those with ambiguous localization of the lesion in preoperative imaging, may require bilateral neck exploration, because the sensitivity of imaging in the detection of multiglandular disease is lower [20]. Although exceptions exist to this generalization, parathyroid carcinomas tend to be larger than adenomas, with an average size of 3 cm. The only reliable imaging feature indicating malignancy is invasion of the surrounding structures [1,21]. The majority of primary HPT patients have single-gland disease, which has led to a shift from traditional, bilateral neck exploration involving the evaluation of all four glands to minimally invasive parathyroidectomy [22]. This change was driven by the potential of achieving decreased patient morbidity and lowering costs, with similar rates of surgical success [23,24]. Minimally invasive parathyroidectomy requires preoperative localization studies, in which US and technetium-99m sestamibi scintigraphy (SS) are traditionally employed [25,26]. SS and US are the major imaging techniques for the preoperative localization of hyperfunctioning parathyroid lesions. Using a dual-phase technique, SS represents hyperfunctioning parathyroid lesions as areas of sustained increased uptake on the delayed phase, in contrast the faster washout that is found in normal parathyroid and thyroid gland tissue (Fig. 1). US represents an abnormal parathyroid gland as an oval, bean-shaped, or infrequently, multilobulated hypoechoic mass with a well-defined margin, located posteriorly or inferiorly to the thyroid gland (Fig. 1) [27-29]. Parathyroid lesions are usually very vascular, typically showing a peripheral vascular arc and a prominent polar feeding vessel that arises from the branches of the inferior thyroidal artery (Fig. 2). The identification of a polar feeding artery can distinguish parathyroid glands from lymph nodes, which usually have a hilar blood supply. Other features include asymmetrically increased vascularity in the thyroid gland on the side of the lesion and in the hyperechoic capsule [30]. Numerous studies comparing SS and US suggest that they have similar sensitivities and specificities in the detection of solitary adenomas. The reported sensitivities of SS and US in the detection of single parathyroid adenomas are comparable, with a range of 68%-95% for SS and a range of 72%-89% for US. However these techniques have substantially lower sensitivities in the detection of multiglandular disease [1,24,27-29]. As expected, a preoperative approach that combines both SS and US is more accurate than either technique alone. De Feo et al. [31] reported a higher sensitivity of combined SS and US (96%) compared to the use of SS (71%) or US (67%) alone in the prospective subgroup of their study. SS and US can complement each other when both methods are applied [27,31-34]. While SS provides functional information about nodules and can visualize ectopic lesions, US can visualize the anatomic relationship of the enlarged parathyroid gland to surrounding structures in the neck.

Fig. 1.

A 55-year-old woman with parathyroid adenoma.

A, B. Coronal images from a technetium-99m sestamibi parathyroid scan (A, early phase; B, delayed phase) demonstrate a single area of increased uptake in the right lower neck. C, D. Gray-scale sonograms (C, axial scan; D, longitudinal scan) demonstrate a large well-defined hypoechoic solid mass posteroinferior to the right lobe of the thyroid gland.

Fig. 2.

A 73-year-old woman with parathyroid adenoma with characteristic feeding vessels.

A longitudinal sonogram shows a hypoechoic solid mass with multiple feeding vessels from the lower pole margin of the thyroid gland.

Parathyroid Incidentalomas

The term ‘parathyroid incidentaloma’ was previously used to refer to unexpected parathyroid adenomas that are encountered during surgery, but with the advent of high-resolution US, the term has also been applied to images that are discovered incidentally during thyroid US and raise the suspicion of a pathological parathyroid [2-4]. The reported intraoperative incidence of PTIs is between 0.2% and 7.6% [3,4], while the US incidence is <1% [4,35]. In autopsy studies of patients without primary HPT or thyroid disease, the incidence of parathyroid adenoma or hyperplasia varied from 1.9% to 7.6% of cases [36,37]. PTIs are most often found in younger patients, do not weigh as much, and are biochemically and pathologically less hyperfunctioning than lesions involved in parathyroid disease, which suggests that PTIs may represent an early stage of parathyroid disease [4]. The possibility of an enlarged parathyroid gland should always be considered when a homogeneous hypoechoic, well-defined, oval nodule is seen along the thyroid capsule (Fig. 3) [4,36]. Fine needle aspiration (FNA) of suspected parathyroid lesions and parathyroid hormone (PTH) (FNA-PTH) estimation from saline washing of the needle play an important role in localizing primary HPT [5]. If US evidence suggests the presence of a PTI, serum calcium and PTH levels, as determined by FNA-PTH, are used to determine whether the suspected lesion in a PTI [2,4]. In previous studies, approximately 20% of sonographically suspected lesions were proven to be PTIs, based on FNA-PTH, and the frequency of hyperfunctioning PTIs was reported to be 12.5%-37.5%, as determined by serum calcium and PTH levels [4,36]. Multinodular goiter or perithyroidal lymph nodes, which are often present in chronic lymphocytic thyroiditis, may be factors leading to false positive diagnoses of PTI (Fig. 3) [35]. A positive correlation was found between the size of the PTI and serum PTH levels in the patients studied by Frasoldati et al. [36], who found that larger PTIs are more likely to result in parathyroid hyperfunction [2,38]. Most patients with hyperfunctioning PTIs do not show symptoms or signs specific to HPT, and therefore are classified as having asymptomatic primary HPT. Recent guidelines for the management of asymptomatic primary HPT suggest that the decision between performing surgery and monitoring without surgery should be made based on serum calcium levels, bone density, and the results of renal evaluation [39]. Nonfunctioning PTIs in patients with normal serum calcium and PTH levels are considered to be the early stage of the development of primary HPT. However, no prospective studies have assessed what percentage of nonfunctioning PTIs become hypersecreting over time [2].

Fig. 3.

A 63-year-old man (A) and a 34-year-old woman (B) with suspicious parathyroid incidentalomas (PTIs).

A. An axial sonogram depicts an oval, well-defined hypoechoic solid PTI (arrow). The lesion was proven to be a parathyroid lesion by a fine needle aspiration-parathyroid hormone (FNA-PTH) assay. B. An axial sonogram shows an enlarged thyroid gland with heterogeneous parenchymal echogenicity and a flat hypoechoic nodular lesion (arrow) located posterior to the gland. Many lymphocytes were found up on cytologic examination and an FNA-PTH assay found low level of parathyroid hormone. A flat nodular lesion, suspected to be a PTI, was proven to be an enlarged perithyroidal lymph node associated with chronic thyroiditis.

Nonsurgical Treatments of Parathyroid Lesions

Nonfunctioning Parathyroid Cyst: Simple Aspiration and Ethanol Ablation

Nonfunctioning parathyroid cysts (PCs) are divided into two categories: functioning and nonfunctioning cysts. Nonfunctioning PCs are true cysts and usually asymptomatic, whereas large cysts can cause symptoms such as neck bulging, dysphasia, pain, tracheal compression, and recurrent laryngeal nerve palsy [14,40-42]. US-guided simple aspiration is the preferred technique for diagnosing nonfunctioning PCs [14,43]. The fluid aspirated from these cysts is usually clear and colorless [14,41]. Elevated PTH levels in aspirated fluid is indicative of a PC [4,5]. Although simple aspiration has been used as an initial diagnosis and treatment for symptomatic nonfunctioning PCs, cases of recurrence after aspiration have been reported [14,43,44]. In patients with recurrent cysts, repeat aspiration, surgical excision, tetracycline treatment, and ethanol ablation (EA) have been performed [41,43,44]. About 33% of PCs have been reported to be successfully treated by simple aspiration alone, while recurring cases can be successfully treated by EA without major complications (Fig. 4) [14]. In order to minimize ethanol leakage during EA of PCs, transisthmic approach should be employed, in which the needle is inserted through a sufficient amount of normal thyroid parenchyma (Fig. 4) [14]. For symptomatic nonfunctioning PCs, simple aspiration is a first-line procedure for diagnosis and treatment, whereas EA is a subsequent treatment modality suitable for recurrent PCs.

Fig. 4.

A 51-year-old woman with very large nonfunctioning parathyroid cyst.

A. An axial sonogram shows the parathyroid cyst (PC) (6.2 cm, 58.1 mL) below the right lower pole of the thyroid gland. The PC recurred two 2 months after simple aspiration. B. An axial sonogram shows the transisthmic approach of an 18-gauge needle (arrow) into the PC. C. An axial sonogram shows the PC after it was filled with instilled ethanol via an 18-gauge needle (arrow) after the complete evacuation of the cystic fluid. D. An axial sonogram shows the PC with a much smaller size (2.5 cm, 3.3 mL) 1 month after ethanol ablation. T, trachea; C, common carotid artery.

EA, Laser Thermal Ablation, Radiofrequency Ablation, and High-Intensity Focused Ultrasound for the Treatment of Hyperfunctioning Parathyroid Lesions

The conventional treatment of patients with primary HPT is neck surgery. However, some patients with HPT cannot undergo surgery due to the presence of unacceptable risks associated with the surgical procedure and/or anesthesia, while others refuse surgical treatment. Several nonsurgical treatment modalities have been developed to treat such patients. For over 20 years, EA has been used by specialists to treat patients with primary HPT as well as patients with secondary or tertiary HPT due to renal disease. The success rate of EA is inversely correlated with the size of the parathyroid tumor and the duration of follow-up. However, side effects are common, including pain, vocal cord palsy, and extraparathyroid fibrosis, which would be likely to interfere with any possible subsequent surgery [6,13]. Since 2001, laser thermal ablation has been suggested as a possible therapy, and has shown some efficacy in controlling serum levels of calcium and PTH in HPT patients [7-9]. In a recent study assessing the long-term effectiveness of laser thermal ablation, the serum PTH levels of the six patients included the study were temporarily reduced, but were above the normal range in all patients at the last follow-up examination, which took place at a mean of 54±34 months after the procedure [7]. Very limited information is available about the experiences of HPT patients treated by radiofrequency ablation, because only three case reports have been documented. However, in all three reports, serum levels of PTH and calcium were reduced after ablation [10,11]. High-intensity focused ultrasound is a noninvasive ablative method based on the generation of extracorporeal ultrasound waves focused on target tissue [12,13]. Kovatcheva et al. [13] reported results of high-intensity focused ultrasound treatment in 13 patients with primary HPT. EA, laser thermal ablation, radiofrequency ablation, and high-intensity focused ultrasound have been reported to show some efficacy in controlling serum calcium and PTH levels and in reducing the volume of the parathyroid. However, these treatments either involve some side effects or do not show evidence of good long-term efficacy [6-13]. More studies are needed to verify the utility and general applicability of these techniques.

Conclusion

This article has described the role of radiologist in the diagnosis and the treatment of parathyroid lesions. US examination plays an important role in patients with primary HPT in the preoperative localization of hyperfunctioning parathyroid lesions. Careful US examination and the use of an FNA-PTH assay can distinguish incidental parathyroid lesions from thyroid lesions. Symptomatic nonfunctioning PCs can be nonsurgically cured by US-guided simple aspiration and EA. More studies are needed to verify the utility of the nonsurgical treatment modalities that have been developed to treat hyperfunctioning parathyroid lesions.

Notes

No potential conflict of interest relevant to this article was reported.

References

1. Lee JH, Anzai Y. Imaging of thyroid and parathyroid glands. Semin Roentgenol 2013;48:87–104.
2. Ghervan C, Silaghi A, Nemes C. Parathyroid incidentaloma detected during thyroid sonography: prevalence and significance beyond images. Med Ultrason 2012;14:187–191.
3. Shroff P, McGrath GA, Pezzi CM. Incidentalomas of the parathyroid gland: multiple presentations, variable function, and review of the literature. Endocr Pract 2005;11:363–369.
4. Kwak JY, Kim EK, Moon HJ, Kim MJ, Ahn SS, Son EJ, et al. Parathyroid incidentalomas detected on routine ultrasound-directed fine-needle aspiration biopsy in patients referred for thyroid nodules and the role of parathyroid hormone analysis in the samples. Thyroid 2009;19:743–748.
5. Owens CL, Rekhtman N, Sokoll L, Ali SZ. Parathyroid hormone assay in fine-needle aspirate is useful in differentiating inadvertently sampled parathyroid tissue from thyroid lesions. Diagn Cytopathol 2008;36:227–231.
6. Cappelli C, Pelizzari G, Pirola I, Gandossi E, De Martino E, Delbarba A, et al. Modified percutaneous ethanol injection of parathyroid adenoma in primary hyperparathyroidism. QJM 2008;101:657–662.
7. Andrioli M, Riganti F, Pacella CM, Valcavi R. Long-term effectiveness of ultrasound-guided laser ablation of hyperfunctioning parathyroid adenomas: present and future perspectives. AJR Am J Roentgenol 2012;199:1164–1168.
8. Adda G, Scillitani A, Epaminonda P, Di Lembo S, Motta F, Cecconi P, et al. Ultrasound-guided laser thermal ablation for parathyroid adenomas: analysis of three cases with a three-year follow-up. Horm Res 2006;65:231–234.
9. Bennedbaek FN, Karstrup S, Hegedus L. Ultrasound guided laser ablation of a parathyroid adenoma. Br J Radiol 2001;74:905–907.
10. Carrafiello G, Lagana D, Mangini M, Dionigi G, Rovera F, Carcano G, et al. Treatment of secondary hyperparathyroidism with ultrasonographically guided percutaneous radiofrequency thermoablation. Surg Laparosc Endosc Percutan Tech 2006;16:112–116.
11. Hansler J, Harsch IA, Strobel D, Hahn EG, Becker D. Treatment of a solitary adenoma of the parathyroid gland with ultrasound-guided percutaneous Radio-Frequency-Tissue-Ablation (RFTA). Ultraschall Med 2002;23:202–206.
12. Ambrosini CE, Cianferotti L, Picone A, Torregrossa L, Segnini G, Frustaci G, et al. High-intensity focused ultrasound as an alternative to the surgical approach in primary hyperparathyroidism: a preliminary experience. J Endocrinol Invest 2011;34:655–659.
13. Kovatcheva R, Vlahov J, Stoinov J, Lacoste F, Ortuno C, Zaletel K. US-guided high-intensity focused ultrasound as a promising noninvasive method for treatment of primary hyperparathyroidism. Eur Radiol 2014;24:2052–2058.
14. Sung JY, Baek JH, Kim KS, Lee D, Ha EJ, Lee JH. Symptomatic nonfunctioning parathyroid cysts: role of simple aspiration and ethanol ablation. Eur J Radiol 2013;82:316–320.
15. Policeni BA, Smoker WR, Reede DL. Anatomy and embryology of the thyroid and parathyroid glands. Semin Ultrasound CT MR 2012;33:104–114.
16. Feliciano DV. Parathyroid pathology in an intrathyroidal position. Am J Surg 1992;164:496–500.
17. American Institute of Ultrasound in Medicine; American College of Radiology, ; Society for Pediatric Radiology, ; Society of Radiologists in Ultrasound. AIUM practice guideline for the performance of a thyroid and parathyroid ultrasound examination. J Ultrasound Med 2013;32:1319–1329.
18. Phillips CD, Shatzkes DR. Imaging of the parathyroid glands. Semin Ultrasound CT MR 2012;33:123–129.
19. Haciyanli M, Lal G, Morita E, Duh QY, Kebebew E, Clark OH. Accuracy of preoperative localization studies and intraoperative parathyroid hormone assay in patients with primary hyperparathyroidism and double adenoma. J Am Coll Surg 2003;197:739–746.
20. Bartsch D, Nies C, Hasse C, Willuhn J, Rothmund M. Clinical and surgical aspects of double adenoma in patients with primary hyperparathyroidism. Br J Surg 1995;82:926–929.
21. Harari A, Waring A, Fernandez-Ranvier G, Hwang J, Suh I, Mitmaker E, et al. Parathyroid carcinoma: a 43-year outcome and survival analysis. J Clin Endocrinol Metab 2011;96:3679–3686.
22. Greene AB, Butler RS, McIntyre S, Barbosa GF, Mitchell J, Berber E, et al. National trends in parathyroid surgery from 1998 to 2008: a decade of change. J Am Coll Surg 2009;209:332–343.
23. Beyer TD, Solorzano CC, Starr F, Nilubol N, Prinz RA. Parathyroidectomy outcomes according to operative approach. Am J Surg 2007;193:368–372.
24. Ruda JM, Hollenbeak CS, Stack BC Jr. A systematic review of the diagnosis and treatment of primary hyperparathyroidism from 1995 to 2003. Otolaryngol Head Neck Surg 2005;132:359–372.
25. Russell CF, Dolan SJ, Laird JD. Randomized clinical trial comparing scan-directed unilateral versus bilateral cervical exploration for primary hyperparathyroidism due to solitary adenoma. Br J Surg 2006;93:418–421.
26. Westerdahl J, Bergenfelz A. Unilateral versus bilateral neck exploration for primary hyperparathyroidism: five-year follow-up of a randomized controlled trial. Ann Surg 2007;246:976–980.
27. Johnson NA, Tublin ME, Ogilvie JB. Parathyroid imaging: technique and role in the preoperative evaluation of primary hyperparathyroidism. AJR Am J Roentgenol 2007;188:1706–1715.
28. Cheung K, Wang TS, Farrokhyar F, Roman SA, Sosa JA. A meta-analysis of preoperative localization techniques for patients with primary hyperparathyroidism. Ann Surg Oncol 2012;19:577–583.
29. Smith RB, Evasovich M, Girod DA, Jorgensen JB, Lydiatt WM, Pagedar NA, et al. Ultrasound for localization in primary hyperparathyroidism. Otolaryngol Head Neck Surg 2013;149:366–371.
30. Lane MJ, Desser TS, Weigel RJ, Jeffrey RB Jr. Use of color and power Doppler sonography to identify feeding arteries associated with parathyroid adenomas. AJR Am J Roentgenol 1998;171:819–823.
31. De Feo ML, Colagrande S, Biagini C, Tonarelli A, Bisi G, Vaggelli L, et al. Parathyroid glands: combination of (99m)Tc MIBI scintigraphy and US for demonstration of parathyroid glands and nodules. Radiology 2000;214:393–402.
32. Mazzeo S, Caramella D, Lencioni R, Molea N, De Liperi A, Marcocci C, et al. Comparison among sonography, double-tracer subtraction scintigraphy, and double-phase scintigraphy in the detection of parathyroid lesions. AJR Am J Roentgenol 1996;166:1465–1470.
33. Haber RS, Kim CK, Inabnet WB. Ultrasonography for preoperative localization of enlarged parathyroid glands in primary hyperparathyroidism: comparison with (99m)technetium sestamibi scintigraphy. Clin Endocrinol (Oxf) 2002;57:241–249.
34. Rodgers SE, Hunter GJ, Hamberg LM, Schellingerhout D, Doherty DB, Ayers GD, et al. Improved preoperative planning for directed parathyroidectomy with 4-dimensional computed tomography. Surgery 2006;140:932–940.
35. Ozdemir D, Arpaci D, Ucler R, Cuhaci N, Ersoy R, Cakir B. Suspected parathyroid lesions and incidentally detected parathyroid adenomas during thyroid ultrasonography. Endocr Abstr 2011;26:P506.
36. Frasoldati A, Pesenti M, Toschi E, Azzarito C, Zini M, Valcavi R. Detection and diagnosis of parathyroid incidentalomas during thyroid sonography. J Clin Ultrasound 1999;27:492–498.
37. Khanna S, Singh S, Khanna AK. Parathyroid incidentaloma. Indian J Surg Oncol 2012;3:26–29.
38. Locchi F, Tommasi M, Brandi ML, Tonelli F, Meldolesi U. A controversial problem: is there a relationship between parathyroid hormone level and parathyroid size in primary hyperparathyroidism? Int J Biol Markers 1997;12:106–111.
39. Bilezikian JP, Brandi ML, Eastell R, Silverberg SJ, Udelsman R, Marcocci C, et al. Guidelines for the management of asymptomatic primary hyperparathyroidism: summary statement from the Fourth International Workshop. J Clin Endocrinol Metab 2014;99:3561–3569.
40. Ippolito G, Palazzo FF, Sebag F, Sierra M, De Micco C, Henry JF. A single-institution 25-year review of true parathyroid cysts. Langenbecks Arch Surg 2006;391:13–18.
41. McCoy KL, Yim JH, Zuckerbraun BS, Ogilvie JB, Peel RL, Carty SE. Cystic parathyroid lesions: functional and nonfunctional parathyroid cysts. Arch Surg 2009;144:52–56.
42. Woo EK, Simo R, Conn B, Connor SE. Vocal cord paralysis secondary to a benign parathyroid cyst: a case report with clinical, imaging and pathological findings (2008:6b). Eur Radiol 2008;18:2015–2018.
43. Prinz RA, Peters JR, Kane JM, Wood J. Needle aspiration of nonfunctioning parathyroid cysts. Am Surg 1990;56:420–422.
44. Armstrong J, Leteurtre E, Proye C. Intraparathyroid cyst: a tumour of branchial origin and a possible pitfall for targeted parathyroid surgery. ANZ J Surg 2003;73:1048–1051.

Article information Continued

Fig. 1.

A 55-year-old woman with parathyroid adenoma.

A, B. Coronal images from a technetium-99m sestamibi parathyroid scan (A, early phase; B, delayed phase) demonstrate a single area of increased uptake in the right lower neck. C, D. Gray-scale sonograms (C, axial scan; D, longitudinal scan) demonstrate a large well-defined hypoechoic solid mass posteroinferior to the right lobe of the thyroid gland.

Fig. 2.

A 73-year-old woman with parathyroid adenoma with characteristic feeding vessels.

A longitudinal sonogram shows a hypoechoic solid mass with multiple feeding vessels from the lower pole margin of the thyroid gland.

Fig. 3.

A 63-year-old man (A) and a 34-year-old woman (B) with suspicious parathyroid incidentalomas (PTIs).

A. An axial sonogram depicts an oval, well-defined hypoechoic solid PTI (arrow). The lesion was proven to be a parathyroid lesion by a fine needle aspiration-parathyroid hormone (FNA-PTH) assay. B. An axial sonogram shows an enlarged thyroid gland with heterogeneous parenchymal echogenicity and a flat hypoechoic nodular lesion (arrow) located posterior to the gland. Many lymphocytes were found up on cytologic examination and an FNA-PTH assay found low level of parathyroid hormone. A flat nodular lesion, suspected to be a PTI, was proven to be an enlarged perithyroidal lymph node associated with chronic thyroiditis.

Fig. 4.

A 51-year-old woman with very large nonfunctioning parathyroid cyst.

A. An axial sonogram shows the parathyroid cyst (PC) (6.2 cm, 58.1 mL) below the right lower pole of the thyroid gland. The PC recurred two 2 months after simple aspiration. B. An axial sonogram shows the transisthmic approach of an 18-gauge needle (arrow) into the PC. C. An axial sonogram shows the PC after it was filled with instilled ethanol via an 18-gauge needle (arrow) after the complete evacuation of the cystic fluid. D. An axial sonogram shows the PC with a much smaller size (2.5 cm, 3.3 mL) 1 month after ethanol ablation. T, trachea; C, common carotid artery.