Case Reports in Endocrinology
Volume 2015 (2015), Article ID 757951, 8 pages
http://dx.doi.org/10.1155/2015/757951

Case Report

Atypical Parathyroid Adenoma Complicated with Protracted Hungry Bone Syndrome after Surgery: A Case Report and Literature Review

Óscar Alfredo Juárez-León,¹ Miguel Ángel Gómez-Sámano,¹ Daniel Cuevas-Ramos,¹ Paloma Almeda-Valdés,¹ Manuel Alejandro López-Flores A La Torre,² Alfredo Adolfo Reza-Albarrán,¹ and Francisco Javier Gómez-Pérez¹

¹Endocrinology and Metabolism Department, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, 14080 Mexico City, Mexico
²School of Medicine, Universidad Panamericana, 03920 Mexico City, Mexico

Received 10 August 2015; Accepted 26 October 2015

Academic Editor: Hidetoshi Ikeda

Copyright © 2015 Óscar Alfredo Juárez-León et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Hungry Bone Syndrome refers to the severe and prolonged hypocalcemia and hypophosphatemia, following parathyroidectomy in patients with hyperparathyroidism. We present the case of an eighteen-year-old woman with a four-year history of hyporexia, polydipsia, weight loss, growth retardation, and poor academic performance. The diagnostic work-up demonstrated primary hyperparathyroidism with hypercalcemia of 13.36 mg/dL, a PTH level of 2551 pg/mL, bone brown tumors, and microcalcifications within pancreas and kidneys. Neck ultrasonography revealed a parathyroid adenoma of 33 × 14 × 14 mm, also identified on ⁹⁹Tc-sestamibi scan. Bone densitometry showed decreased -Score values (total lumbar -Score of −4.2). A right hemithyroidectomy and right lower parathyroidectomy were performed. Pathological examination showed an atypical parathyroid adenoma, of 3.8 g of weight and 2.8 cm in diameter. After surgery she developed hypocalcemia with tetany and QTc interval prolongation. The patient required 3 months of oral and intravenous calcium supplementation due to Hungry Bone Syndrome (HBS). After 42 months, she is still under oral calcium. Usually HBS lasts less than 12 months. Therefore we propose the term “Protracted HBS” in patients with particularly long recovery of 1 year. We present a literature review of the diagnosis, pathophysiology, and treatment of HBS.

1. Introduction

The Hungry Bone Syndrome (HBS) was first described by Albright and Reifenstein in 1950, in patients with hyperparathyroidism with a severe and prolonged hypocalcemia after parathyroidectomy [1].

Most HBS definitions consider clinical manifestations of hypocalcemia and biochemical variables including hyperparathyroidism requiring surgery, hypophosphatemia, and hypomagnesemia. Some authors denote HBS when patients develop postoperative hypocalcemia (<8.5 mg/dL), a simultaneous inorganic phosphate value of <3.0 mg/dL [2], and hypocalcemia longer than 4 days requiring calcium supplementation, despite optimization of supportive therapy with normal vitamin D levels [3, 4].

Parathyroid hormone (PTH) and calcitriol (1α,25[OH]₂D₃) regulate calcium and phosphate homeostasis. PTH is secreted in response to hypocalcemia after being sensed by the parathyroid calcium-sensing receptor (CaSR) [5]. PTH receptors are mainly present in kidney and bone tissue [6], and when activated, they increase bone calcium efflux and decrease renal excretion to maintain normal serum calcium concentrations. The HBS pathophysiology begins with elevated PTH production (primary, secondary, or tertiary hyperparathyroidism) which augments bone metabolism and calcium turnover, leading to increased serum calcium levels. Treatment of primary hyperparathyroidism often requires surgical resection of an adenoma, causing a sudden halt in bone turnover. Consequently, a marked depletion of serum circulating calcium, phosphate, and magnesium is seen due to bone remineralization [2].

The most common etiologies associated with HBS are secondary and primary hyperparathyroidism [3, 7, 8]. Other less frequent causes are parathyroid carcinoma, drugs, multiple endocrine neoplasia, and metastatic prostate cancer [9–14].

Here we present a clinical case of an unusual long-lasting HBS developed in a female patient with primary hyperparathyroidism after surgical treatment of an atypical adenoma.

2. Case Presentation

An 18-year-old previously healthy woman presented at our institution after a four-year history of hyporexia, polydipsia, weight loss, growth retardation, and poor academic performance. One month prior to presentation, outpatient laboratory analysis revealed increased serum calcium and parathyroid hormone (PTH). She did not have any other significant personal or family history.

She was admitted to our hospital in February 2010. On physical examination her height was 1.40 m and weight was 30 kg. Her vital signs were within normal limits. She presented with a marked cervical kyphosis.

Relevant laboratory results showed hypercalcemia (13.36 mg/dL, normal 8.6–9.9 mg/dL), elevated PTH (2551 pg/mL, normal 12–88 pg/mL), elevated alkaline phosphatase level (4410 IU/L, normal 34–104 IU/L), hypercalciuria (urinary calcium of 213 mg/24 H, normal 100–250 mg/24 H), low creatinine clearance (25.84 mL/min/1.73 m², normal ≥90 mL/min/1.73 m²), and low 25[OH]D₃ circulating level (13 ng/mL, normal 30–100 ng/mL). The laboratory findings at hospital admission and last follow-up visit are summarized in Table 1. Biochemical approach was further completed with prolactin 12.6 ng/mL, FSH 4.4 mIU/mL, LH 17 mIU/mL, estradiol 36.13 pg/mL, T3 1.78 nmol/L, T4 69.33 nmol/L, TSH 1.85 μUI/mL, thyroglobulin 5.7 ng/mL, ACTH 19 pg/mL, and morning cortisol 15.76 μg/dL, all within normal limits.

Table 1: Laboratory findings at hospital admission and at last outpatient follow-up visit.

Hospitalization [February 2010]
Follow-up [November 2013]
Reference values

Serum calcium [mg/dL]
12.1
8.9
8.6–9.9

Corrected serum calcium [mg/dL]
12.6
7.9

Serum phosphate [mg/dL]
2.7
3
2.7–4.5

Serum magnesium [mg/dL]
1.3
2
1.9–2.7

Serum albumin [g/dL]
3.4
5.2
3.5–5.7

Serum creatinine [mg/dL]
4.83
1.05
0.42–1.09

Creatinine clearance [ml/min/1.73 m²]
12
76
≥90

PTH [pg/mL]
2551
91.7
12–88

25-OH vitamin D [ng/mL]
13
25.9
30–100

Alkaline phosphatase [IU/L]
4410
126
34–104

Urinary calcium [mg/day]
213
22
100–300

Urinary phosphorus [mg/day]
413
524
<1000

Prolactin [ng/mL]
12.6
—
2.64–13.13

FSH [mIU/mL]
4.4
—
3.85–8.78

LH [mIU/mL]
17
—
2.12–10.89

Estradiol [pg/mL]
36.13
—
12–40

T3 [nmol/L]
1.78
—
0.64–1.81

T4 [nmol/L]
69.33
—
66–181

TSH [UI/mL]
1.85
—
0.3–5

Thyroglobulin [ng/mL]
5.7
—
0–36.8

ACTH [pg/mL]
19
—
10–100

Morning cortisol [µg/dL]
15.76

6.7–22.6

PTH parathyroid hormone.

Corrected calcium with albumin using the following formula: = + 0.8 [4 − albuminmeasured].

Skeletal X-rays showed skull with “salt and pepper” lesions, vertebral compression fractures, brown tumors within the left humerus, and profuse calcifications within the pancreas and kidneys (Figure 1). The patient did not refer to abdominal pain, nor any symptomatology related to endocrine and exocrine pancreatic insufficiency. The electrocardiogram was unremarkable. Abdominal ultrasound revealed kidney stones causing bilateral dilation of the renal pelvis. Neck ultrasonography showed microcalcifications within a large echogenic mass, posterior to the right lobe of the thyroid gland of 33 × 14 × 14 mm, Figure 2. A 25 mCi ⁹⁹Tc-sestamibi scintigraphy reported persistence of the radionuclide material at 120 minutes in the right inferior parathyroid gland at the same location of the mass shown in the US, Figure 3. Bone densitometry showed decreased -Score values (total lumbar -Score of −4.2), Table 2. Primary hyperparathyroidism secondary to a large parathyroid tumor was diagnosed.

Table 2: Densitometry values on admission and at the last follow-up visit as an outpatient. The most affected segment is presented.

Hospitalization
Follow-up

[February 2010]
[November 2013]

Lumbar BMD
L1
Total
L1
Total

[g/cm²]
0.53
0.551
1.061
1.07

-Score
—

1.4
0.4

score

1.2
0.2

Hip BMD
Neck
Total
Neck
Total

[g/cm²]
0.41
0.481
0.939
0.998

-Score
—
—
0.6
0.4

score

0.5
0.3

Osteoporosis is diagnosed in young adults when both -score <−2.0 and fractures are present.

Due to the age of presentation, baseline -scores could not be obtained with the equipment used in our patient.

(a)

(b)

Figure 1: Abdominal computed tomography (CT) on admission. (a) Diffuse pancreatic calcifications; (b) bilateral kidney calcifications on axial computed tomography. Findings are marked with white arrow heads.

(a)

(b)

Figure 2: Neck ultrasonography on admission. (a) Large echogenic mass dorsal to the right lobe of the thyroid gland. (b) Doppler effect showing polar vessel finding, present in most adenomas. Findings are marked with white arrow heads.

(a)

(b)

Figure 3: Neck scintigraphies with 25 mCi of ⁹⁹Tc-sestamibi with 0′ and 120′ wash-out sequences. (a) 2010 Admission Scintigraphy. 120′ washout sequence shows residual capitation from right lower thyroid lobe suggesting a parathyroid adenoma. (b) 2013 postparathyroidectomy control scintigraphy. 120′ wash-out sequence shows no apparent residual captation. Findings are marked with white arrow heads.

For HBS prophylaxis, before surgery, she received a 400,000 IU of vitamin D2 (Drisdol) (ergocalciferol) and 1 mg of calcitriol. Right hemithyroidectomy with right lower parathyroidectomy was performed. A tumor of 2.8 cm with 3.8 g of weight was resected. Pathological revision reported a focal lesion containing parathyroid tissue; it infiltrated the nodule capsule, without trespassing it, and the diagnosis was consistent with an atypical parathyroid adenoma. Two lymph nodes demonstrated follicular hyperplasia. Despite the administration of vitamin D (50,000 per week) and calcitriol 0.75 mg per day after surgery, the 25-hydroxyvitamin D levels never reached a value above 30. 1,25-dihydroxy vitamin D was not measured.

Postsurgical laboratory analysis showed PTH values of 31.3 pg/mL, serum calcium of 8.5 mg/dL, phosphate of 1.9 mg/dL, and magnesium of 1.8 mg/dL; on physical examination she presented upper extremity distal contractures, oromandibular dystonia, Chvostek and Trousseau signs, and QTc interval prolongation. PTH levels reached up to 48.6 pg/mL after 1 month, coexisting with hypophosphatemia of 2.7 mg/dL. At last follow-up, PTH serum levels were between 80 and 90 pg/mL, Table 2. She developed a prolonged and severe HBS that required 3 months with oral and intravenous calcium supplementation. The calcium IV infusion was stopped three months later. High PTH levels with hypocalcemia but also hypophosphatemia ruled out hypoparathyroidism. “Protracted” HBS was therefore diagnosed. During her hospitalization she underwent two episodes of lithotripsy as treatment for the kidney stones. Serum calcium, phosphate, and magnesium levels during hospitalization and follow-up are shown in Figure 4.

(a)

(b)

(c)

Figure 4: (a) Corrected serum calcium during hospitalization and as outpatient. (b) Serum phosphate values during hospitalization and as outpatient. (c) Serum magnesium values during hospitalization and as outpatient. area represents reference values. dotted line represents treatment beginning, which continued beyond last medical assessment at our institution.

After 42 months of treatment, bone densitometry scores improved within normal limits, Table 2. As an outpatient since 2010 she has been receiving an average of 1197 mg of oral elemental calcium, 1600 units of vitamin D, and 3 grams of magnesium sulfate per day. She was kept under close medical evaluation as an outpatient. Unfortunately in November 2013 the patient stopped coming to our institution with no clear reason, Table 1.

3. Discussion

We described a case of “Protracted” HBS in a female patient following parathyroidectomy for primary hyperparathyroidism caused by an atypical parathyroid adenoma. The primary hyperparathyroidism remained undiagnosed for at least 4 years and was complicated by the occurrence of brown tumors, severe osteoporosis, nephrocalcinosis, and short stature.

Postoperative hypocalcemia following parathyroidectomy could be associated with numerous causes. Some common causes are transient hypoparathyroidism due to extensive surgical removal of parathyroid glands, disruption of blood supply to remnant parathyroid glands, radical neck exploration, and major remineralization of bone such as in HBS [2, 7, 15]. The main features that favor the diagnosis of hypoparathyroidism versus HBS are the extent of surgery, bilateral neck exploration, or prior neck surgery. Also hypoparathyroidism usually presents with hypocalcemia and hyperphosphatemia [2, 16]. HBS is associated with high and long term requirements of calcium and vitamin D supplementation with normal or high PTH levels [2, 7].

The lack of consensus for the definition of HBS hinders the comparison of reported cases, validation of risk factors, determination of severity and prognosis predictors, proposal of prophylaxis regimens, and delineation of treatment goals, as well as resolution criteria [4, 7].

Clinical and laboratory risk factors for HBS are older age, weight and volume of resected parathyroid glands, elevated alkaline phosphatase, evidence of significant bone disease, and blood urea nitrogen [2, 7]. The length of hospitalization has been associated with severity of hypocalcemia [2].

In order to prevent HBS, some authors suggest treatment with bisphosphonates in primary [17] and secondary hyperparathyroidism [18]; however, this approach may delay bone remodeling [19].

The lesion resected from our patient was compatible with atypical adenoma, because it presented capsule invasion without trespassing its boundaries, the rest of the surgical piece was analyzed finding normal thyroid and lymph nodes without invasion. According to the World Health Organization criteria (WHO, 2004) [20] an atypical adenoma refers to large glands with either excess mitotic cells and tumor capsule invasion without exceeding its boundaries, or with marked fibrotic divisions pattern. It is associated with neither spontaneous tumor necrosis, nor vascular invasion to surrounding tissues [21, 22]. These pathology characteristics have been usually associated with a benign course in terms of survival. Parathyroid carcinoma specimens have been associated with the development of HBS [8, 10–12].

Due to the sporadic nature, severity of symptoms, and young age at presentation, genetic abnormalities could be suspected as the cause of this clinical presentation, such as gain of function of protooncogenes (e. gr. cyclinD1/PRAD1), or inactivation of tumor suppressor genes (e. gr. MEN1, multiple endocrine neoplasia 1).

Primary hyperparathyroidism (PHPT) is the most common feature of MEN1 and presents in approximately 90% of MEN1 patients [23, 24]. The PHPT main manifestations reported as part of MEN1 syndrome are earlier age at onset (20 to 25 yrs versus 55 yrs), demineralization, and/or recurrent kidney stones [24], findings consistent with the presentation of our patient. Normal laboratory analysis ruled out functional pituitary adenoma at this time; however, she will continue to be under close observation.

Since the patient did not refer to any symptomatology for the suspicion of a functional pancreatic/gastrointestinal (GI) adenoma, no additional biochemical analyses were carried out. No apparent pancreatic tumors were found on the abdominal CT.

Clinical manifestations of hypocalcemia in HBS range from relative benign symptoms such as weakness, headache, paresthesias, ileus, malabsorption, and muscle cramps to life threatening features such as arrhythmias, seizures, laryngeal stridor, tetany, and overt severe heart failure [4, 7, 25]. Our patient presented mainly musculoskeletal manifestations.

In patients with HBS, serum electrolytes, such as calcium, phosphate, and magnesium, should be cautiously monitored over the first postoperative hours and days, as severe electrolytes disturbances may develop [2, 3]. During hospitalization the patient required up to 1289 mg of elemental calcium IV per day or 42.9 mg/kg of elemental calcium IV. Treatment of hypocalcemia is based on oral and intravenous calcium replacement. Reported daily requirements of calcium in patients with severe hypocalcemia range from 6 to 16 g of elemental calcium per day [7, 10, 26–28].

The preferred calcium administration route depends on signs and symptoms severity, promptness of the onset of manifestations, and serum calcium levels [29, 30]. Oral calcium supplementation could be reasonably used in patients with mild symptoms and serum calcium concentrations greater than 7.5 mg/dL. Intravenous treatment is required for patients with calcium below this level or prolonged QTc interval on electrocardiogram and may be necessary for those cases who are currently unable to swallow or absorb oral calcium [30–32].

Intravenous calcium gluconate is preferred over calcium chloride due to its lower association with local irritation. For acute hypocalcemia management, one or two 10 mL ampoules of 10% calcium gluconate (10 mL of a 10% solution = 93 mg elemental Ca or 1 ampule) should be diluted in 50–100 mL of 5% dextrose or saline in order to infuse it over 10 minutes [10, 31, 33]. After the patient is stable, a calcium infusion is continued adding 10 ampoules of calcium gluconate (100 mL of 10% calcium gluconate) to 1000 mL normal saline or 5% dextrose making up a solution containing 1 mg/mL of elemental calcium [33]. Typical patient requirements are 0.5 to 1.5 mg/kg of elemental calcium per hour [30]. Throughout hospitalization the patient required up to 43,113.6 mg of elemental calcium orally per day (equivalent to 108 tablets of 1 g of calcium carbonate; each tablet contains approximately 400 mg of elemental calcium).

In HBS, once the hyperparathyroid state is resolved, it is important to assess serum magnesium and phosphate circulating concentrations. Significant hypomagnesaemia and hypophosphatemia may develop and perpetuate hypocalcemia [34, 35]. Even though mild hypomagnesaemia habitually is asymptomatic, chronic deficiency may be associated with diverse comorbid situations, such as arrhythmias, hypertension, and an increase in progression of kidney disease [34]. Magnesium levels after parathyroidectomy may decrease secondary to increased bone mineralization, causing a lower PTH secretion and a relative tissue specific resistance, increasing risk of severe hypocalcemia. Therefore, magnesium should be also supplemented [36].

Hypophosphatemia in HBS is probably due to an increase in bone uptake to facilitate matrix remineralization [6]. The administration of phosphate in patients with HBS is generally avoided because phosphate can precipitate with calcium, decreasing even further the circulating calcium concentration. Phosphate administration is reserved to those patients with less than 1.0 mg/dL and severe symptoms such as muscle weakness or heart failure [5]. Phosphate availability increases secondary to the intestinal action of vitamin D.

HBS duration has been defined as the time taken to remineralize the skeleton and/or cessation of additional calcium supplementation [7], evidenced by normalization of bone turnover markers, healing of radiological features of osteitis fibrosa cystica and brown tumours, and significant gain in bone mass. Due to the lack of consensus on definitions for HBS length, we take into account two of the most cited terms found in HBS related literature: bone mineral density (BMD) recovery and calcium supplementation length.

Considering HBS resolution with BMD normalization criteria, HBS lasted from 4.5 to 16 months with a median of 10 months [2, 13, 37–40] (Table 3). Calcium replenishment has been reported throughout 0.5 months to 12 months, with a median of 5.1 months. [3, 10, 13, 26, 41, 42]. Using this information, HBS lasts between 10 and 12 months. We therefore propose the term of “Protracted Hungry Bone Syndrome” to refer to those cases with a particularly long recovery taking more than one year.

Table 3

Time to reach normal bone density values
Time required of calcium replenishment
References

4.5 months
—
[2]

—
5 months
[41]

8 months
—
[37]

—
5.2 months
[26]

—
6 months
[10]

16 months
3 months
[13]

0.5 months
[3]

12 months
(i) 8 months
(ii) 12 months
(iii) 12 months

[7]
[38]
[39]
[40]

—
12 months
[42]

Median (months): 10
Median (months): 5.1
—

In a case series of patients with HBS, parathyroidectomy improved femoral neck bone mineral density (BMD) scores from 35 to 131% in 1 year after surgery, considering basal BMD values ranging from 0.234 to 0.564 g/cm², and 1 year follow-up values of 0.541–0.942 g/cm² [43]. The significant recovery from baseline pathologic findings to the value above normal found in our patient is consistent with previously reported BMD recovery (Table 3). Bone densitometries were only done at hospital admission and three years after surgery as outpatient (Table 2). The factors that contribute to this impressive BMD improvement in our case were the resolution of primary hyperparathyroidism and the high amounts of calcium and vitamin D administered for over 42 months to treat the HBS.

To the best of our knowledge, the case presented here is one of the longest HBS reported. In spite of the HBS criteria described that requires recovery of bone remineralization, we believe that our patient still has HBS, based on the fact that she continues with oral calcium and magnesium supplementation to maintain normal serum levels, normal circulating vitamin D, and normal high PTH levels.

4. Conclusion

HBS is a consequence of hyperparathyroidism following parathyroidectomy. It is an infrequent cause of hypocalcemia, hypophosphatemia, and hypomagnesemia that requires adequate therapy to avoid complications in the acute and chronic scenarios. We propose the term of “Protracted Hungry Bone Syndrome” to refer to those cases with a particularly prolonged course of recovery that takes more than one year.

Conflict of Interests

There was not any financial interest reported by the authors, nor any conflict of interests.

Authors’ Contribution

Óscar Alfredo Juárez-León and Miguel Ángel Gómez-Sámano contributed equally to this work.

Acknowledgments

Óscar Alfredo Juárez-León wants to acknowledge Gabriel Juarez and Guadalupe Leon for their support. Miguel Ángel Gómez-Sámano wants to acknowledge Luz del Carmen Abascal Olascoaga for her support.

References

“The parathyroid glands and metabolic bone disease,” Ulster Medical Journal, vol. 19, no. 1, pp. 130–131, 1950.

A. R. Brasier and S. R. Nussbaum, “Hungry bone syndrome: clinical and biochemical predictors of its occurrence after parathyroid surgery,” The American Journal of Medicine, vol. 84, no. 4, pp. 654–660, 1988.

J. Latus, M. Roesel, P. Fritz et al., “Incidence of and risk factors for hungry bone syndrome in 84 patients with secondary hyperparathyroidism,” International Journal of Nephrology and Renovascular Disease, vol. 6, pp. 131–137, 2013.

M. Goldfarb, S. S. Gondek, S. M. Lim, J. C. Farra, V. Nose, and J. I. Lew, “Postoperative hungry bone syndrome in patients with secondary hyperparathyroidism of renal origin,” World Journal of Surgery, vol. 36, no. 6, pp. 1314–1319, 2012.

M. Filopanti, S. Corbetta, A. M. Barbieri, and A. Spada, “Pharmacology of the calcium sensing receptor,” Clinical Cases in Mineral and Bone Metabolism, vol. 10, no. 3, pp. 162–165, 2013.

R. Dunlay and K. Hruska, “PTH receptor coupling to phospholipase C is an alternate pathway of signal transduction in bone and kidney,” The American Journal of Physiology—Renal Fluid and Electrolyte Physiology, vol. 258, no. 2, pp. F223–F231, 1990.

J. E. Witteveen, S. van Thiel, J. A. Romijn, and N. A. Hamdy, “Hungry bone syndrome: still a challenge in the post-operative management of primary hyperparathyroidism: a systematic review of the literature,” European Journal of Endocrinology/European Federation of Endocrine Societies, vol. 168, no. 3, pp. R45–R53, 2013.

R. Varma, Y. J. Kim, K. Garjian, and D. Barank, “Hyperparathy-roidism and hungry bone syndrome revisited,” Clinical Nuclear Medicine, vol. 39, no. 8, pp. 704–706, 2014.

R. K. Crowley, M. Kilbane, T. F. J. King, M. Morrin, M. O'Keane, and M. J. McKenna, “Hungry bone syndrome and normalisation of renal phosphorus threshold after total parathyroidectomy for tertiary hyperparathyroidism in X-linked hypophosphataemia: a case report,” Journal of Medical Case Reports, vol. 8, article 84, 2014.

M. S. Rathi, R. Ajjan, and S. M. Orme, “A case of parathyroid carcinoma with severe hungry bone syndrome and review of literature,” Experimental and Clinical Endocrinology & Diabetes, vol. 116, no. 8, pp. 487–490, 2008.

M. N. Ohe, R. O. Santos, F. Hojaij et al., “Parathyroid carcinoma and hungry bone syndrome,” Arquivos Brasileiros de Endocrinologia & Metabologia, vol. 57, no. 1, pp. 79–86, 2013.

K.-M. Kim, J.-B. Park, K.-S. Bae, and S.-J. Kang, “Hungry bone syndrome after parathyroidectomy of a minimally invasive parathyroid carcinoma,” Journal of the Korean Surgical Society, vol. 81, no. 5, pp. 344–349, 2011.

S. Tachibana, S. Sato, T. Yokoi et al., “Severe hypocalcemia complicated by postsurgical hypoparathyroidism and hungry bone syndrome in a patient with primary hyperparathyroidism, Graves' disease, and acromegaly,” Internal Medicine, vol. 51, no. 14, pp. 1869–1873, 2012.

S. A. Vogelgesang and J. M. McMillin, “Hypocalcemia associated with estrogen therapy for metastatic adenocarcinoma of the prostate,” The Journal of Urology, vol. 140, no. 5, pp. 1025–1027, 1988.

D. Shoback, “Hypoparathyroidism,” The New England Journal of Medicine, vol. 359, no. 4, pp. 391–403, 2008.

J. P. Bilezikian, A. Khan, J. T. Potts Jr. et al., “Hypoparathyroidism in the adult: epidemiology, diagnosis, pathophysiology, target-organ involvement, treatment, and challenges for future research,” Journal of Bone and Mineral Research, vol. 26, no. 10, pp. 2317–2337, 2011.

I.-T. Lee, W. H.-H. Sheu, S.-T. Tu, S.-W. Kuo, and D. Pei, “Bisphosphonate pretreatment attenuates hungry bone syndrome postoperatively in subjects with primary hyperparathyroidism,” Journal of Bone and Mineral Metabolism, vol. 24, no. 3, pp. 255–258, 2006.

A. Davenport and M. P. Stearns, “Administration of pamidronate helps prevent immediate postparathyroidectomy hungry bone syndrome,” Nephrology, vol. 12, no. 4, pp. 386–390, 2007.

M. Coco, D. Glicklich, M. C. Faugere et al., “Prevention of bone loss in renal transplant recipients: a prospective, randomized trial of intravenous pamidronate,” Journal of the American Society of Nephrology, vol. 14, no. 10, pp. 2669–2676, 2003.

R. A. DeLellis, Pathology and Genetics of Tumours of Endocrine Organs, IARC, Lyon, France, 2004.

Z. W. Baloch and V. A. LiVolsi, “Pathology of the parathyroid glands in hyperparathyroidism,” Seminars in Diagnostic Pathology, vol. 30, no. 3, pp. 165–177, 2013.

G. G. Fernandez-Ranvier, E. Khanafshar, K. Jensen et al., “Parathyroid carcinoma, atypical parathyroid adenoma, or parathyromatosis?” Cancer, vol. 110, no. 2, pp. 255–264, 2007.

R. V. Thakker, P. J. Newey, G. V. Walls et al., “Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1),” The Journal of Clinical Endocrinology and Metabolism, vol. 97, no. 9, pp. 2990–3011, 2012.

P. Grzegorz, C. Jerzy, and W. Andrzej, “Primary hyperparathyroidism in patients with multiple endocrine neoplasia type 1,” International Journal of Endocrinology, vol. 2010, Article ID 928383, 6 pages, 2010.

E. Mallet, “Hypocalcemia: clinical signs and mechanisms,” Archives de Pédiatrie, vol. 15, no. 5, pp. 642–644, 2008.

H. Demirci, E. Suyani, A. Karakoc et al., “A longstanding hungry bone syndrome,” The Endocrinologist, vol. 17, no. 1, pp. 10–12, 2007.

O. Laitinen, “Bone, calcium, and hydroxyproline metabolism in hyperparathyroidism and after removal of parathyroid adenoma,” Acta Medica Scandinavica, vol. 202, no. 1-2, pp. 39–42, 1977.

S. M. Corsello, R. M. Paragliola, P. Locantore et al., “Post-surgery severe hypocalcemia in primary hyperparathyroidism preoperatively treated with zoledronic acid,” Hormones, vol. 9, no. 4, pp. 338–342, 2010.

J. F. Tohme and J. P. Bilezikian, “Hypocalcemic emergencies,” Endocrinology and Metabolism Clinics of North America, vol. 22, no. 2, pp. 363–375, 1993.

J. Fong and A. Khan, “Hypocalcemia: updates in diagnosis and management for primary care,” Canadian Family Physician Médecin de Famille Canadien, vol. 58, no. 2, pp. 158–162, 2012.

M. S. Cooper and N. J. Gittoes, “Diagnosis and management of hypocalcaemia,” The British Medical Journal, vol. 336, no. 7656, pp. 1298–1302, 2008.

J.-J. Body and R. Bouillon, “Emergencies of calcium homeostasis,” Reviews in Endocrine & Metabolic Disorders, vol. 4, no. 2, pp. 167–175, 2003.

D. Shoback, “Hypocalcemia: definition, etiology, pathogenesis, diagnosis, and management,” in Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism, chapter 68, John Wiley & Sons, Hoboken, NJ, USA, 2009.

J. H. F. de Baaij, J. G. J. Hoenderop, and R. J. M. Bindels, “Magnesium in man: implications for health and disease,” Physiological Reviews, vol. 95, no. 1, pp. 1–46, 2015.

F. M. Hannan and R. V. Thakker, “Investigating hypocalcaemia,” British Medical Journal, vol. 346, no. 7911, Article ID f2213, 2013.

Z. S. Agus, “Hypomagnesemia,” Journal of the American Society of Nephrology, vol. 10, no. 7, pp. 1616–1622, 1999.

F. Ghanaat and J. A. Tayek, “Hungry bone syndrome: a case report and review of the literature,” Nutrition Research, vol. 24, no. 8, pp. 633–638, 2004.

K. Natsui, K. Tanaka, M. Suda et al., “Oxyphil parathyroid adenoma associated with primary hyperparathyroidism and marked post-operative hungry bone syndrome,” Internal Medicine, vol. 35, no. 7, pp. 545–549, 1996.

T. Y. Yong and J. Y. Z. Li, “Mediastinal parathyroid carcinoma presenting with severe skeletal manifestations,” Journal of Bone and Mineral Metabolism, vol. 28, no. 5, pp. 591–594, 2010.

T. França, L. Griz, J. Pinho et al., “Bisphosphonates can reduce bone hunger after parathyroidectomy in patients with primary hyperparathyroidism and osteitis fibrosa cystica,” Revista Brasileira de Reumatologia, vol. 51, no. 2, pp. 131–137, 2011.

C. Campusano and J. López, “Complete recovery of hungry bone syndrome using intravenous calcium infusion. Report of one case,” Revista Medica de Chile, vol. 131, no. 7, pp. 779–784, 2003.

G. Ghilardi and L. De Pasquale, “Hungry bone syndrome after parathyroidectomy for primary hyperthyroidism,” Surgery: Current Research, vol. 4, article 168, 2014.

T. C. P. T. de França, L. Griz, J. Pinho et al., “Bisphosphonates can reduce bone hunger after parathyroidectomy in patients with primary hyperparathyroidism and osteitis fibrosa cystica,” Revista Brasileira de Reumatologia, vol. 51, no. 2, pp. 131–137, 2011.