Surgical options in treating patients with primary hyperparathyroidism
Article Category: Review
Published Online: Feb 29, 2020
Page range: 22 - 32
Received: Nov 05, 2019
Accepted: Nov 15, 2019
DOI: https://doi.org/10.2478/raon-2020-0010
© 2020 Masa Majcen, Marko Hocevar, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Primary hyperparathyroidism (PHPT) is a disease of parathyroid glands that results from their over-activity. The estimated incidence of PHPT is approximately two cases per 1,000 persons per year.1 About 80% of patients have no symptoms; the disease is generally detected during random laboratory blood test. In countries where biochemical test are not commonly used, classical symptoms and signs tend to predominate. Surgical resection is the only potentially curative treatment and remains the leading treatment option for PHPT. If the patient does not meet surgical criteria or refuses surgery, specific pharmacological therapy or close monitoring is recommended.1
Parathyroid glands were first discovered in Indian rhinoceros by English biologist Sir Richard Owen in 1850.2,3 Only 30 years later, Ivar Sandstörm from Sweden was the first person to describe the location and blood flow of glands in humans and coined the term
It has taken many years for scientists to understand the mechanism of action of parathyroid glands. With the rapid development of thyroid surgery (thyroidectomy) in the early 20th century, common occurrences of tetany were observed.2 The fact that hypocalcaemia after parathyroid surgery is the definitive cause of tetany was not wholly accepted for several decades.3 It was not until 1909 that the first evidence of the relationship between parathyroid glands and the metabolism of calcium was published by MacCallum and Voegtil.2, 3, 4
Parathyroid surgery as a possible treatment of parathyroid disease was first mentioned in 1915.5 Through the years, several scientists insisted on the connection between parathyroid disease and bone disease. Schlagenhaufer suggested the removal of a solitary tumour of the parathyroid gland in attempt to cure bone disease (described as
After the first successful parathyroidectomy, the surgery became the main treatment of parathyroid disease. Like in any other surgery, how-ever, there are potential risks and complications. In the early 1930s, many surgeons noted the occurrence of severe, life-threatening hypocalcaemia after surgery.5,6 They (often unsuccessfully) tried to treat hypocalcaemia with a high-calcium and low-phosphate diet or intravenous calcium administration.7 Churchill and Cope’s detailed description of parathyroid surgery facilitated the development of surgical treatment. They employed frozen sections and routinely performed biopsy from normal tissue to rule out hyperplasia.4 They also wrote recommendations for the course of surgery (based on their experience in 30 observed patients) according to the likelihood of parathyroid hyperplasia or multiple adenomas. With the development of histology and the understanding of function of parathyroid glands, their variations in the number and location, surgical success rate slowly became higher.7 Near the end of the 20th century; high-tech diagnostic imaging techniques became powerful medical tools that allowed surgeons to operate with minimal invasion to the patient. Since then, the use of minimally invasive surgery has expanded widely and has almost completely replaced the conventional surgical techniques.5,6
The anatomy of parathyroid glands is highly variable.7,8 A fundamental understanding of both surgical anatomy and embryology of parathyroid glands is key to successful parathyroid surgery. Nowadays, precise preoperative localization facilitates successful surgical therapy, but a good knowledge of anatomy remains irreplaceable.7
Parathyroid glands are yellowish brown endocrine glands, measuring about 6 × 4 × 2 mm and weighing on average 20 to 40 mg.8,9 The majority of glands are oval, bean shaped or spherical and usually lie on the posterior aspect of the thyroid lateral lobes.9 Each gland is separated from the thyroid gland by a thin connective tissue capsule. Most people (85%) have four parathyroid glands7, 8, 9, 10:
Two superior glands, each of which embryo-logically arises from the fourth pharyngeal pouch. They lie 1–2 cm above the intersection of the inferior thyroid artery and the recurrent laryngeal nerve at the level of the inferior margin of the cricoid cartilage.
Two inferior glands, each of which embryo-logically arises from the third pharyngeal pouch. They are usually (in 70
A small number of patients have three or even more than four glands.8 Rarely, parathyroid glands will be located elsewhere in the neck or in the chest. They are so-called ectopic parathyroid glands.9 Ectopic superior parathyroid glands can be found para- or retropharyngeal, retrotracheal or in the upper mediastinum, rarely also within the thyroid capsule.7 The location of the lower parathyroid glands is more variable due to their longer embryologic migration pathway. They can be found anywhere along this embryologic tract: along the thyrothymic ligament, the carotid sheath, in the anterior mediastinum etc.7, 8, 9
The upper and lower parathyroid glands are supplied by branches of the inferior thyroid artery, which is the major blood supply for lower poles of thyroid.7,8 To preserve the vascular supply to the parathyroid glands, the ligation of branches of inferior thyroid artery in thyroidectomy should be done with caution as close as possible to the thyroid capsule. Venous drainage is carried out by the inferior, middle, and superior thyroid veins, which drain into the internal jugular vein.7,8
Hyperparathyroidism is a common endocrine dis-order in which one or more parathyroid glands become overactive.1 They produce and secrete parathyroid hormone (PTH). PTH affects several organ systems through multiple mechanisms. Its main role is regulation of calcium homeostasis but is important as well in vitamin D and phosphate regulation (see Table 1).1,8,11, 12, 13, 14 The most common cause of hyperparathyroidism is excessive and unregulated production of PTH by parathyroid glands, so-called PHPT. More than 80% of PHPT is caused by a single benign parathyroid neoplasm – adenoma.8 According to epidemiological research data, PHPT is the third most common endocrine disorder.11,12 It affects 2 in 1,000 people per year in western world and its incidence increases with age, with a peak incidence in the seventh decade of life. The risk of developing PHPT is 4-fold higher in women.1,8 On the other hand, secondary hyperparathyroidism refers to compensatory physiological response of parathyroid glands to chronic hypocalcaemic state due to other pathological processes (mostly kidney disease).1,8,12 Unlike PHPT, a disease outside of the parathyroids causes all of the parathyroid glands to become enlarged and hyperactive. Patients with long-standing secondary hyperparathyroidism may develop autonomous parathyroid function due to random mutation in one of the parathyroid glands called tertiary hyperparathyroidism.12 The clinical picture is usually similar and difficult to distinguish from PHPT. The following paper focuses on the diagnosis and treatment of PHPT.
Biological actions of parathyroid hormone (PTH) in the body. PTH increases the serum calcium concentration and lowers the serum phosphate concentration
| Organ system | Function of PTH |
|---|---|
| Kidneys (leading role) | It increases calcium and decreases phosphate reabsorption, stimulates calcitriol production by increasing the synthesis of the enzyme 1-α hydroxylase in proximal tubules. |
| Skeletal | It raises calcium levels in blood by increasing bone destruction (via osteoblast-mediated activation of osteoclasts) and decreasing the formation of new bone. |
| Gastrointestinal system | It increases calcium absorption by stimulating the production of 1,25-dihydroxycholecalciferol. |
| Other (minor role, experimental) | Metabolic effects (reduced glucose tolerance, changes in fat metabolism), effects on the liver, adipose tissue, cardiovascular system, neuromuscular function. |
Nowadays, hyperparathyroidism is usually found accidentally during routine biochemical blood tests.15 Patient history and clinical presentation are often not helpful.16 Hyperparathyroidism should be considered in asymptomatic patients with elevated serum calcium levels. An atypical form of PHPT with normocalcemia and elevated PTH levels is rare (some authors argue that an atypical PHPT is an early form of the PHPT).1,7,15 Other possible causes of hypercalcaemia should always be ruled out.15 Occasionally, non-specific symptoms are found in presumed asymptomatic patients with a more detailed questioning (for example fatigue, depression, neuromuscular symptoms). In the past, the disease was diagnosed in the more advanced phase or so-called classical form, which is less commonly seen today.16 The developed clinical picture is very diverse due to the broad action of PTH and different calcium concentrations (Table 2).1,12,14, 15, 16
Clinical presentation of developed primary hyperparathyroidism (PHPT). Symptoms and clinical signs are associated with an elevated serum calcium concentration and/or increased secretion of parathyroid hormone (PTH)
| Organ system | Symptoms and clinical signs |
|---|---|
| General | anorexia, polyuria, polydipsia, weight gain, anaemia |
| Skeletal | |
| Kidney | kidney stones, renal parenchymal calcifications, nephrocalcinosis, chronic renal impairment |
| Neuromuscular | proximal muscle weakness, depression, decline in cognitive ability, psychosis |
| Cardiovascular | arterial hypertension, arrhythmias, left ventricular hypertrophy, vascular wall and myocardial calcification |
| Gastrointestinal | nausea, vomiting, constipation, ulcer disease, pancreatitis |
| Rheumatological | gout, pseudogout |
Laboratory measurement of serum calcium concentrations should be obtained on at least two separate occasions. Hypercalcemia with concomitant elevated PTH levels confirms the diagnosis of PHPT.1,15 Some patients have atypical form of hyperparathyroidism with elevated PHT levels in the absence of hypercalcemia.16 This phenotype of PHPT is called normocalcemia with abnormally high PTH. Different secondary causes need to be excluded before diagnosis of atypical PTH is made.15 At least the serum concentration of phosphate, chlorine, alkaline phosphatase, vitamin D and the patient’s acid-base balance must be checked, as well as basic examination of urine and urinary sediment.1,15,16
All patients with diagnosis of PHPT (including asymptomatic patients) should undergo a urinary tract ultrasound.15 Other diagnostic procedures (dual-energy x-ray absorptiometry, bone x-ray, bone biopsy) should be performed only if there is reasonable clinical suspicion.1,15
After the diagnosis of PHPT is established, localization studies need to be done to determine if minimally invasive surgical treatment can be performed.13 The localization studies should not be used to diagnose the disease. Parathyroid glands can be imaged with multiple modalities. The neck ultrasound, CT, scintigraphy or newer hybrid imaging PET/CT and SPECT/CT can be used.17, 18, 19, 2099mTc-sestamibi scan (complemented with neck ultrasound) is still the most commonly used method in many countries.18 Sestamibi is a small protein labelled with the radio-pharmaceutical technetium-99m. The scan is performed by injecting small amount of radioactive material, which is then absorbed by overactive parathyroid gland. The gamma camera detects radioactive material and shows position of parathyroid glands. Different studies reported the sensitivity of 99mTc-sestamibi between 77% and 89%, but up to one-third of patients with adenomas could be sestamibi negative.18
PET/CT is a newer and promising tool for localization of parathyroid adenomas. Different PET tracers can be used (18F-fluorodeoxyglucose, 18F-fluorocholine (FCH) etc.).19,21 Many studies are comparing FCH PET/CT with conventional imaging modalities. Behera and Damle reported the incremental role of PET/CT over sestamibi scan in 2016 because of better spacial resolution, possible detection of smaller adenomas and reduced scanning time.18,20 Retrospective study by Hočevar
The surgery is indicated in all patients with clinical symptoms of PHPT who agree to be treated with surgery.22 Successful surgical intervention can completely cure the disease.15 On the other hand, not all authors agree that surgery is beneficial for asymptomatic patients with PHPT. Differences in opinion arise mainly due to poor knowledge of the natural course of the disease, benefits of the surgical procedure and appropriate timing of surgery.1,16,22 The indications for surgery in asymptomatic patient with PHPT according to the Fourth International Guidelines for the Management of Asymptomatic PHPT are presented in Table 3.23
The 2014 Fourth International Guidelines for the Management of Asymptomatic PHPT. Patients need to meet at least one of the following criteria to be advised to have surgery
| Measurement | Criteria |
|---|---|
| Age of patient | < 50 years |
| Serum calcium concentration (above the upper reference value) | > 0.25 mmol/L (1.0 mg/dL) |
| Skeletal injury | bone mineral density (DXA): T-score < -2.5 SD* |
| spinal fracture (proven by XR, CT, MRI or VFA) | |
| Renal impairment | creatinine clearance < 60 mL/min |
| kidney stones or nephrocalcinosis (proven by XR, US or CT) | |
| 24-hour calcium in urine > 10 mmol/L (400 mg/day) or increased risk for kidney stones based on biochemical analysis |
* measured on the lumbar spine, hip, femoral neck or distal third of the radius
CT = computed tomography; DXA = dual-energy x-ray absorptiometry; MRI = magnetic resonance imaging; SD = standard deviation; US = ultrasound; VFA = vertebral fracture assessment; XR = x-ray imaging
If the patient is a suitable candidate for surgery according to the guidelines, possible contraindications for surgery must be considered.23,24 Surgery is absolutely contraindicated in patients with familial hypocalciuric hypercalcemia (FHH), because it does not result in cure.25 FHH is an autosomal dominant disorder that is often confused with PHPT due to similar laboratory findings (normoor hypercalcemia with elevated PTH). The major feature that distinguishes FHH from PHPT is 24-hour urinary calcium excretion. Urinary calcium concentration below 100 mg in 24-hour urine is diagnostic for FHH.12,24.25 The relative contraindications are prior vocal cord injury, contralateral laryngeal nerve injury and symptomatic cervical disc herniation (parathyroid surgery is performed in neck hyperextension, which may worsen the condition).25 The contraindications listed above are common and apply to all types of surgical procedures on the parathyroid glands. Each surgical approach also has specific contraindications, which are mentioned in the descriptions of individual approaches.
Once the diagnosis of PHPT has been confirmed, determining the best approach for surgery depends on several factors. Before making any decision, the surgeon checks and evaluates the patient’s medical history, family medical history, patient’s regular treatment, the most recent laboratory results, etc.24,25 Specific tests (if not already performed) based on clinical symptoms may need to be done to check for the involvement of individual organs (kidney, bone, etc.). The preoperative examination should include at least the following1,24,25:
serum calcium levels and intact parathyroid hormone (iPTH);
serum value of 25-hydroxy vitamin D;
serum creatinine concentration;
24-hour urinary calcium concentration and creatinine values and
serum thyroid-stimulating hormone (TSH) and thyroxine levels.
Accurate preoperative localization is crucial for successful surgical outcomes (particularly for minimally invasive parathyroidectomy). It helps to determine the location and number of hyper-functioning parathyroid glands and it is very important in the case of recurrent neck procedures.18 In some western Europe countries conventional imaging with 99mTc-sestamibi was successfully replaced by neck ultrasound and FCH PET-CT imaging (Figure 1).21 In some cases, additional imaging (e.g. CT, MRI) is required. Invasive procedures (selective venous sampling, selective arteriography) are reserved for patients who have had prior neck surgery and require reoperative surgery18,23 Due to the frequent concomitant thyroid and parathyroid disease, preventive preoperative analysis of the thyroid gland is performed to avoid increased complications from reoperations.26
Figure 1
18F-fluorocholine (FCH) PET-CT fusion images of patient with pathologic uptake in the right lower parathyroid gland (solitary adenoma).
The surgeon decides on the type of surgical procedure based on the patient’s anamnesis, clinical status and results of preoperative examinations.24 The patient should be informed of the procedure that is indicated, possible surgical complications and the overall course of treatment.25 Today, there are several different surgical approaches that are further described below. With the development of medicine, classical surgical procedures are increasingly being replaced by new approaches that seek to minimize interventions into the human body.7 There are many different tools/procedures available today to perform surgery as accurately as possible, reduce the number of surgical complications and surgery repetitions, e.g. intraoperative neuromonitoring for identification of the recurrent laryngeal nerve, intraoperative iPTH assay, intra-operative frozen section when malignant tissue is suspected etc.7,24,25,27
Bilateral neck exploration (also standard, open, conventional parathyroidectomy) is a traditional surgical approach for the treatment of PHPT. Due to the development of less invasive procedures, its application is decreasing.7 During the operation, the surgeon exposes all four parathyroid glands, therefore precise preoperative localization is not required (but it may be helpful). Parathyroid glands identification can be challenging even for a skilled surgeon due to their unpredictable location.22,25 According to literature data the success rate of surgery is 95% in experienced hands (the success of the procedure depends directly on the experience of the surgeon).8,25 In the past, a biopsy of all four parathyroid glands was used to histologically prove pathological parathyroid tissue.28 Due to the high risk of bleeding and postoperative hypoparathyroidism, it is no longer recommended.25,28
Current indications for bilateral parathyroidectomy include25,28, 29, 30:
unreliable or inaccessible preoperative imaging;
preoperative imaging is contraindicated (pregnancy etc.);
multiple parathyroid lesions;
ectopic parathyroid glands location (inaccessibility with minimally invasive intervention),
familial PHPT;
concurrent thyroid surgery and
other contraindications for minimally invasive intervention (measurement of iPTH is not available etc.).
The surgical approach has not changed significantly since the first bilateral parathyroidectomy in 1925.7 Surgery is usually performed under general anaesthesia, local anaesthesia is rarely used (depending on the experience of the surgical and anaesthesia team).30.31 The patient is lying on the operating room table in a supine position with his upper body at 30 degrees.25 The surgeon makes a 3 to 5 cm transverse incision (initially the incision was longer) about 2 cm above the collarbone. Subcutaneous fat and platysma are divided and the infrahyoid strap muscles are retracted for optimal exposure of thyroid. Using upward and medial digital retraction of the thyroid gland, the surgeon enters the “parathyroid” space.7,25 Once the important structures come into view (inferior thyroid artery and recurrent laryngeal nerve), the surgeon continues with the identification of the parathyroid glands.31 Caution should be used when removing the parathyroid tissue and during connective tissue manipulation, because the rupture of the parathyroid capsule can result in parathyromatosis.25 The surgeon must identify all four parathyroid glands but remove only the abnormal ones.31 When in any doubt, frozen section can be done to confirm that the tissue excised is parathyroid in origin. In the event of accidental removal of healthy parathyroid tissue, reimplantation of the tissue should be considered (usually into the brachioradial forearm muscle).7,25 After successful removal of pathological glands and proper haemostasis, the surgeon approximates the retracted infrahyoid strap muscles and closes the wound with a continuous intradermal suture.25,28, 29, 30, 31
The most common complication of bilateral neck exploration is recurrent or persistent hyperparathyroidism that results from missed adenoma or parathyromatosis. Rarely, the cause of recurrent hyperparathyroidism is new neoplasia (most commonly in previously unrecognized familial PHPT or multiglandular disease, for example multiple endocrine neoplasia [MEN syndrome]).25 As well as the success of the operation, the rate of complication depends directly on the experience of the surgeon (to be considered experienced, surgeon should perform at least 50 procedures per year).25 During the procedure, the superior or recurrent laryngeal nerves on either side can be damaged.8 Damage can cause long-term hoarseness or voice loss. According to the literature, permanent nerve injury occurs in less than 1% of patients.8,33 Transient nerve injuries (neuropraxia) are more common and have different recovery times, complete recovery generally occurs within the first six months. Postoperative hypocalcaemia is usually transient and occurs in 25% of patients.25,33 It is most often due to slow reactivation of healthy parathyroid glands, which have been suppressed by overactive pathological parathyroid glands. After removal of the adenoma, the remaining suppressed glands will eventually regain their functional capacity.8,25,32 Patients with low blood calcium levels complain of numbness and tingling in their fingertips and toes, very low concentrations can result in involuntary movements and severe muscle spasms.25,33 Postoperative bleeding is a rare but dangerous complication, which may lead to respiratory problems and wound infection.25,33
The term minimally invasive parathyroidectomy (also focal, selective parathyroidectomy) has been used since the 1990s to describe newer types of surgeries on parathyroid glands.34,35 There is no exact definition of the term, but some experts define it as a procedure with minimal dissection (excision of the adenoma without the removal of non-pathological parathyroid glands) and a wound smaller than 2.5 cm.7 Worldwide, the term currently includes the following procedures: directed parathyroidectomy, endoscopic parathyroidectomy (total endoscopic, video-assisted and robotic parathyroidectomy) and isotope-guided parathyroidectomy.34 In 2009, the European Society of Endocrine Surgeons (ESES) confirmed that in keeping with prescribed indications and contraindications, minimally invasive parathyroidectomy is a safe and reliable procedure.35
With the development and improvement of preoperative imaging diagnostics, parathyroid surgery is focused on minimally invasive surgery.5,6 Accurate preoperative localization (with neck ultrasound, sestamibi scan and/or FCH PET-CT) is critical to the success of this type of surgery.17, 18, 19, 20 Directed parathyroidectomy is a procedure recommended for patients with solitary adenoma.7 Worldwide, this type of surgery accounts for 70% of all minimally invasive procedures.34 The operation is usually performed under general anaesthesia but can be also performed under regional anaesthesia (usually deep cervical block). Regional anaesthesia prevents side effects of general anaesthesia and at the same time allows for intraoperative testing of superior and recurrent laryngeal nerve (by evaluating the patient’s speech).36 Depending on the location of the adenoma, a central or lateral 2 to 4 cm long incision is made at the neck (see Figure 2).7,13 The surgeon identifies and removes only the pathological parathyroid gland (or solitary adenoma).25 Other parathyroid glands are not exposed. Since preoperative imaging is not completely reliable, majority of surgeons use iPTH to determine the surgery’s success.13 iPTH levels are determined at anaesthesia induction (general or regional) and 5–10 min after adenoma removal. According to Miami criteria, successful parathyroidectomy was defined as a > 50% decrease of iPTH level compared to the level measured before removal. The half-life of iPTH in plasma is 3–5 min.37,38 Directed approach reduces the invasiveness of the surgery and shortens the surgery and hospitalization time.13,32,35 Published research also demonstrates a lower risk of operative complications (postoperative hypocalcaemia, recurrent laryngeal nerve damage) and death, compared to bilateral neck exploration.7,13,25 The patient recovers faster, with less pain and a better aesthetic result (smaller postoperative scar) (Figure 3).25,32 The procedure is not appropriate for patients with multiglandular disease, thyroid disease that also requires surgery or a family history of MEN syndrome.13,25,27,28
Figure 2
Directed parathyroidectomy. The image shows the incision site and the removed parathyroid tissue.
Figure 3
Appearance of the incision and surrounding skin 10 days after performing directed parathyroidectomy.
In the last five years, FCH PET-CT has proven to be the most sensitive and specific method in pre-operative localization of pathologically changed parathyroid glands.39 Its reliability to exclude multiglandular disease is so high that iPTH monitoring can be safely abandoned.40 This shortens the surgery time by 30 minutes, which is very significant given that the average duration of directed parathyroidectomy is less than 20 minutes.
According to a 2007 analysis by Westerdahl
Endoscopic parathyroidectomy is a surgical technique using an endoscope.7 It is divided into two types, depending on the course: total endoscopic and video-assisted parathyroidectomy, which is a combination of endoscopic intervention and open surgical approach.34 In addition to a directed approach, the endoscope also allows us to perform the entire procedure through small incision wound and with small tissue damage. PHPT is a disease that is otherwise an “ideal disease” for endoscopic surgery, since34,42, 43, 44:
in most cases, the cause is a benign tumour,
the tumour is mostly smaller than 3 cm and
there is no need for surgical reconstruction after removal of small amount of tissue.
Endoscopic surgery has similar advantages to bilateral parathyroidectomy as other minimally invasive procedures. Compared to directed parathyroidectomy, it is less invasive, it results in less postoperative pain and a better aesthetic result, but surgery is longer, technically more demanding, and requires more expensive surgical equipment.45 General anaesthesia is always required.34 Endoscopic intervention is indicated in patients with sporadic PHPT and solitary adenoma, which should be confirmed by preoperative imaging.43 The procedure is not appropriate in the case of intrathyroid parathyroid adenoma, multiple parathyroid involvement, previous neck surgery, suspected parathyroid cancer, familial PHPT, secondary and tertiary hyperparathyroidism, goitre and in the obese patients.25,34,43,45
Total endoscopic parathyroidectomy was first mentioned by Gagner
Figure 4
Total endoscopic parathyroidectomy.
According to the data, the conversion from endoscopic to traditional ‘open’ surgery is between 13.4% and 28%.46,47 The causes are different, most often due to difficult dissection, bleeding or persistence of elevated iPTH after removal of the suspected solitary adenoma.25,46,47 The success of the endoscopic approach is very favourable in the short term (with the exception of a large number of conversion to the open mode), but the results of long-term studies are not yet available (intermediate results are encouraging).46,47 Fouyuet
Video-assisted parathyroidectomy is a combination of endoscopic and open surgery. It was first described in 1999 by Miccoli
Video-assisted parathyroidectomy can be performed under local or general anaesthesia.49,50 The procedure is performed via a central incision located centrally above the collarbone. The endoscope of 5 mm in size is introduced (without a trocar) at an angle of 30 degrees via a lateral incision on the side of the pathological parathyroid gland.35
Gas insufflation is not used in comparison with total endoscopic surgery.50 The endoscope is more mobile, but it requires an additional assistant to manage it. The procedure is performed in the same way as directed parathyroidectomy.35,50 Some authors also use endoscopes for bilateral exploratory parathyroidectomy in patients with multiglandular disease.25,31,35
Radioguided parathyroidectomy is a type of minimally invasive surgery, during which the gamma probe is used to guide the surgeon towards the location of the pathological parathyroid gland.35 As with all minimally invasive procedures, good preoperative imaging plays an important role.17, 18, 19, 20 Good interaction between the entire surgical team and nuclear medicine experts is a prerequisite for this type of surgical intervention. The patient is given an intravenous dose of 99mTc-sestamibi approximately 2 to 4 hours before the surgery.35 The uptake of sestamibi into the parathyroid adenoma cells depends on their activity.20 Intraoperatively, a gamma probe is then used to trace the location with the highest radioactivity (which must be at least 20% higher than background neck activity). The surgeon thus determines the best incision site.35 However, the use of radioactivity to determine the location has its limitations. The thyroid pathology, which can have increased sestamibi uptake, may be mistaken for an abnormal parathyroid gland. When searching for radioactive ectopic parathyroids in the chest, high concentration of the isotope in the myocardium can be mistakenly detected. If the tissue resected is radioactive and the neck shows equal radioactivity after excision, the patient can be assumed cured.51 Nonetheless, iPTH assay is used to determine the complete excision of all hyperfunctioning tissue.21,51
The method described above is used only by few experienced surgeons.35 It is mostly used as an alternative method or just as an aid for the surgery. According to Burkey
Robotic-assisted parathyroidectomy is a modern technique and it represents the new generation in the evolution of minimally invasive parathyroidectomy techniques.52 The beginnings of telerobotic surgical technology go back to the early 21st century when a new established idea of robotic-assisted surgery offered solutions in overcoming the limitations associated with endoscopic techniques (two-dimensional view of the operative filed, limited manipulation with surgical instruments, need for carbon dioxide insufflation and assistants during surgery).52,53 In 2011, Tolley
As for every other minimal invasive surgical approach, preoperative imaging studies that assist in the localization of lesions have been key elements in patients’ selection for targeted robotic-assisted parathyroid surgeries.17, 18, 19, 20,54 Before robotic-assisted parathyroidectomy is preformed, parathyroid adenoma should be properly localized.54 Tolley
Parathyroid surgery is the only potentially curative treatment of PHPT. Over the last two decades, technological advances and better understanding of the disease have refined surgical techniques. Surgery represents the last step in the overall patient care. Disease recognition, a proper diagnostic process and preoperative preparation of the patient are crucial for choosing the best surgical procedure. The aim of this paper was to discuss newer surgical techniques and their advantages and limitations in comparison to classical methods.