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Familial Parathyroid Tumors: Diagnosis and Management

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Abstract

Background

The management of hyperparathyroidism (HPT) in the familial setting is complex. Due to the rarity of familial HPT and its different presentation within and between the familial syndromes and individual kindreds, treatment recommendations based on high levels of evidence cannot be made. However, based on the molecular genetic studies and case series from institutions with significant experience, important management principles (grade C recommendations) have been developed.

Methods

We conducted a systematic review of the literature using evidence-based criteria.

Results

Issue 1: initial operation in multiple endocrine neoplasia type 1 (MEN1), a grade C recommendation can be made for subtotal parathyroidectomy. Issue 2: initial surgery in MEN 2A, a grade C recommendation can be made for excision of enlarged glands only. Issue 3: surgery in familial isolated HPT and HPT-jaw tumor (HPT-JT) syndrome may be treated with parathyroidectomy that is subtotal or less, although the risk of parathyroid cancer in HPT-JT requires attention (no grade of recommendation). Issue 4: parathyroid surgery in familial HPT syndromes in the setting of underlying mutations in the calcium receptor (CASR) gene involves subtotal parathyroidectomy (no grade of recommendation). Issue 5: the use of intraoperative PTH measurements in familial HPT may guide the extent of parathyroid resection (no grade of recommendation).

Conclusions

The goals of parathyroidectomy in familial HPT are to achieve and maintain normocalcemia for the longest time possible, avoid both iatrogenic hypocalcemia and operative complications, and facilitate future surgery for recurrent disease.

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References

  1. Carling T, Udelsman R (2003) Parathyroid tumors. Curr Treat Options Oncol 4(4):319–328

    Article  PubMed  Google Scholar 

  2. Marx SJ, Simonds WF, Agarwal SK et al (2002) Hyperparathyroidism in hereditary syndromes: special expressions and special managements. J Bone Miner Res 17(Suppl 2):N37–N43

    PubMed  CAS  Google Scholar 

  3. Heinrich S, Schafer M, Rousson V et al (2006) Evidence-based treatment of acute pancreatitis: a look at established paradigms. Ann Surg 243(2):154–168

    Article  PubMed  Google Scholar 

  4. Sackett DL (1989) Rules of evidence and clinical recommendations on the use of antithrombotic agents. Chest 95(2 Suppl):2S–4S

    Article  PubMed  CAS  Google Scholar 

  5. Carling T (2005) Multiple endocrine neoplasia syndrome: genetic basis for clinical management. Curr Opin Oncol 17(1):7–12

    Article  PubMed  Google Scholar 

  6. Brandi ML, Gagel RF, Angeli A et al (2001) Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab 86(12):5658–5671

    Article  PubMed  CAS  Google Scholar 

  7. Georgitsi M, Raitila A, Karhu A et al (2007) Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia. J Clin Endocrinol Metab 92(8):3321–3325

    Article  PubMed  CAS  Google Scholar 

  8. Pellegata NS, Quintanilla-Martinez L, Siggelkow H et al (2006) Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proc Natl Acad Sci USA 103(42):15558–15563

    Article  PubMed  CAS  Google Scholar 

  9. Skogseid B, Rastad J, Öberg K (1994) Multiple endocrine neoplasia type 1: clinical features and screening. Endocrinol Metab Clin North Am 23(1):1–18

    PubMed  CAS  Google Scholar 

  10. Carling T (2001) Molecular pathology of parathyroid tumors. Trends Endocrinol Metab 12:53–58

    Article  PubMed  CAS  Google Scholar 

  11. Hellman P, Skogseid B, Oberg K et al (1998) Primary and reoperative parathyroid operations in hyperparathyroidism of multiple endocrine neoplasia type 1. Surgery 124(6):993–999

    PubMed  CAS  Google Scholar 

  12. Burgess JR, David R, Greenaway TM et al (1999) Osteoporosis in multiple endocrine neoplasia type 1: severity, clinical significance, relationship to primary hyperparathyroidism, and response to parathyroidectomy. Arch Surg 134(10):1119–1123

    Article  PubMed  CAS  Google Scholar 

  13. Norton JA, Cornelius MJ, Doppman JL (1987) Effect of parathyroidectomy in patients with hyperparathyroidism, Zollinger-Ellison syndrome, and multiple endocrine neoplasia type I: a prospective study. Surgery 102(6):958–966

    PubMed  CAS  Google Scholar 

  14. Norton JA, Venzon DJ, Berna MJ et al (2008) Prospective study of surgery for primary hyperparathyroidism (HPT) in multiple endocrine neoplasia-type 1 and Zollinger-Ellison syndrome: long-term outcome of a more virulent form of HPT. Ann Surg 247(3):501–510

    Article  PubMed  Google Scholar 

  15. Carling T, Udelsman R (2003) Advancements in the surgical treatment of primary hyperparathyroidism. Probl Gen Surg 20(3):31–37

    Article  Google Scholar 

  16. Wells SA Jr, Ellis GJ, Gunnells JC et al (1976) Parathyroid autotransplantation in primary parathyroid hyperplasia. N Engl J Med 295(2):57–62

    Article  PubMed  Google Scholar 

  17. Åkerström G, Malmaeus J, Bergström R (1984) Surgical anatomy of human parathyroid glands. Surgery 95(1):14–21

    PubMed  Google Scholar 

  18. Burgess JR, David R, Parameswaran V et al (1998) The outcome of subtotal parathyroidectomy for the treatment of hyperparathyroidism in multiple endocrine neoplasia type 1. Arch Surg 133(2):126–129

    Article  PubMed  CAS  Google Scholar 

  19. Thompson NW (1995) The surgical management of hyperparathyroidism and endocrine disease of the pancreas in the multiple endocrine neoplasia type 1 patient. J Intern Med 238(3):269–280

    Article  PubMed  CAS  Google Scholar 

  20. Goudet P, Cougard P, Verges B et al (2001) Hyperparathyroidism in multiple endocrine neoplasia type I: surgical trends and results of a 256-patient series from Groupe D’etude des Neoplasies Endocriniennes Multiples Study Group. World J Surg 25(7):886–890

    Article  PubMed  CAS  Google Scholar 

  21. O’Riordain DS, O’Brien T, Grant CS et al. (1993) Surgical management of primary hyperparathyroidism in multiple endocrine neoplasia types 1 and 2. Surgery 114(6):1031–1037 discussion 1037–1039

    Google Scholar 

  22. Elaraj DM, Skarulis MC, Libutti SK et al (2003) Results of initial operation for hyperparathyroidism in patients with multiple endocrine neoplasia type 1. Surgery 134(6):858–864 discussion 864–855

    Google Scholar 

  23. Kraimps JL, Denizot A, Carnaille B et al (1996) Primary hyperparathyroidism in multiple endocrine neoplasia type IIa: retrospective French multicentric study. Groupe d’Etude des Tumeurs a Calcitonine (GETC, French Calcitonin Tumors Study Group), French Association of Endocrine Surgeons. World J Surg 20(7):808–812 discussion 812–803

    Google Scholar 

  24. Hubbard JG, Sebag F, Maweja S et al (2006) Subtotal parathyroidectomy as an adequate treatment for primary hyperparathyroidism in multiple endocrine neoplasia type 1. Arch Surg 141(3):235–239

    Article  PubMed  Google Scholar 

  25. Wells SA Jr, Debenedetti MK, Doherty GM (2002) Recurrent or persistent hyperparathyroidism. J Bone Miner Res 17(Suppl 2):N158–N162

    PubMed  Google Scholar 

  26. Alexander HJ, Chen C, Shawker T et al (2002) Role of preoperative localization and intraoperative localization maneuvers including intraoperative PTH assay determination for patients with persistent or recurrent hyperparathyroidism. J Bone Miner Res 17(Suppl 2):N133–N140

    PubMed  Google Scholar 

  27. Udelsman R, Aruny JE, Donovan PI et al (2003) Rapid parathyroid hormone analysis during venous localization. Ann Surg 237(5):714-719 discussion 719-721

    Google Scholar 

  28. Udelsman R (1996) Parathyroid imaging: the myths and the reality. Radiology 201:317–318

    PubMed  CAS  Google Scholar 

  29. Civelek AC, Ozalp E, Donovan P (2002) Prospective evaluation of delayed technetium-99 m sestamibi SPECT scintigraphy for preoperative localization of primary hyperparathyroidism. Surgery 131(2):149–157

    Article  PubMed  Google Scholar 

  30. Casanova D, Sarfati E, De Francisco A et al (1991) Secondary hyperparathyroidism: diagnosis of site of recurrence. World J Surg 15(4):546-549 discussion 549-550

    Google Scholar 

  31. Knudsen L, Brandi L, Daugaard H et al (1996) Five to 10 years follow-up after total parathyroidectomy and autotransplantation of parathyroid tissue: evaluation of parathyroid function by use of ischaemic blockade manoeuvre. Scand J Clin Lab Invest 56(1):47–51

    Article  PubMed  CAS  Google Scholar 

  32. Kivlen MH, Bartlett DL, Libutti SK et al (2001) Reoperation for hyperparathyroidism in multiple endocrine neoplasia type 1. Surgery 130(6):991–998

    Article  PubMed  CAS  Google Scholar 

  33. Mulligan L, Ponder B (1995) Genetic basis of endocrine disease: Multiple endocrine neoplasia type 2. J Clin Endocrinol Metab 80:1989–1995

    Article  PubMed  CAS  Google Scholar 

  34. Eng C (1999) RET proto-oncogene in the development of human cancer. J Clin Oncol 17(1):380–393

    PubMed  CAS  Google Scholar 

  35. Eng C, Clayton D, Schuffenecker I et al (1996) The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. JAMA 276(19):1575–1579

    Article  PubMed  CAS  Google Scholar 

  36. Milos IN, Frank-Raue K, Wohllk N (2008) Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation. Endocr Relat Cancer 15(4):1035–1041

    Article  PubMed  CAS  Google Scholar 

  37. Raue F, Kraimps JL, Dralle H et al (1995) Primary hyperparathyroidism in multiple endocrine neoplasia type 2A. J Intern Med 238(4):369–373

    Article  PubMed  CAS  Google Scholar 

  38. Herfarth KK, Bartsch D, Doherty GM et al (1996) Surgical management of hyperparathyroidism in patients with multiple endocrine neoplasia type 2A. Surgery 120(6):966–973 discussion 973–964

    Google Scholar 

  39. Skinner MA, Norton JA, Moley JF et al (1997) Heterotopic autotransplantation of parathyroid tissue in children undergoing total thyroidectomy. J Pediatr Surg 32(3):510–513

    Article  PubMed  CAS  Google Scholar 

  40. Carpten JD, Robbins CM, Villablanca A et al (2002) HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet 32:676–680

    Article  PubMed  CAS  Google Scholar 

  41. Wassif WS, Moniz CF, Friedman E et al (1993) Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer. J Clin Endocrinol Metab 77(6):1485–1489

    Article  PubMed  CAS  Google Scholar 

  42. Szabo J, Heath B, Hill VM et al (1995) Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21–q31. Am J Hum Genet 56(4):944–950

    PubMed  CAS  Google Scholar 

  43. Haven CJ, Wong FK, van Dam EW et al (2000) A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 85(4):1449–1454

    Article  PubMed  CAS  Google Scholar 

  44. Simonds WF, James-Newton LA, Agarwal SK et al (2002) Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds. Medicine (Baltimore) 81(1):1–26

    Article  Google Scholar 

  45. Winer KK, Ko CW, Reynolds JC et al (2003) Long-term treatment of hypoparathyroidism: a randomized controlled study comparing parathyroid hormone-(1–34) versus calcitriol and calcium. J Clin Endocrinol Metab 88(9):4214–4220

    Article  PubMed  CAS  Google Scholar 

  46. Iacobone M, Barzon L, Porzionato A et al (2007) Parafibromin expression, single-gland involvement, and limited parathyroidectomy in familial isolated hyperparathyroidism. Surgery 142(6):984-991 discussion 984-991

    Google Scholar 

  47. Scillatini A, Muscarella L, Guarnieri V et al (2004) Preclinical diagnosis of parathyroid carcinoma in a subject with a germline mutation of the parafibromin gene. J Intern Med 255:716

    Google Scholar 

  48. Gunn IR, Gaffney D (2004) Clinical and laboratory features of calcium-sensing receptor disorders: a systematic review. Ann Clin Biochem 41(Pt 6):441–458

    Article  PubMed  CAS  Google Scholar 

  49. Thorgeirsson U, Costa J, Marx SJ (1981) The parathyroid glands in familial hypocalciuric hypercalcemia. Hum Pathol 12(3):229–237

    Article  PubMed  CAS  Google Scholar 

  50. Marx SJ, Stock JL, Attie MF et al (1980) Familial hypocalciuric hypercalcemia: recognition among patients referred after unsuccessful parathyroid exploration. Ann Intern Med 92(3):351–356

    PubMed  CAS  Google Scholar 

  51. Cole D, Janicic N, Salisbury S et al (1997) Neonatal severe hyperparathyroidism, secondary hyperparathyroidism, and familial hypocalciuric hypercalcemia: multiple different phenotypes associated with an inactivating Alu insertion mutation of the calcium-sensing receptor gene. Am J Med Genet 71:202–210

    Article  PubMed  CAS  Google Scholar 

  52. Carling T, Szabo E, Bai M et al (2000) Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor. J Clin Endocrinol Metab 85(5):2042–2047

    Article  PubMed  CAS  Google Scholar 

  53. Szabo E, Hellman P, Lundgren E et al (2002) Parathyroidectomy in familial hypercalcemia with clinical characteristics of primary hyperparathyroidism and familial hypocalciuric hypercalcemia. Surgery 131(3):257–263

    Article  PubMed  Google Scholar 

  54. Szabo E, Carling T, Hessman O et al (2002) Loss of heterozygosity in parathyroid glands of familial hypercalcemia with hypercalciuria and point mutation in calcium receptor. J Clin Endocrinol Metab 87(8):3961–3965

    Article  PubMed  CAS  Google Scholar 

  55. Warner J, Epstein M, Sweet A et al (2004) Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications. J Med Genet 41(3):155–160

    Article  PubMed  CAS  Google Scholar 

  56. Carling T, Udelsman R (2008) Focused approach to parathyroidectomy. World J Surg 32(7):1512–1517

    Article  PubMed  Google Scholar 

  57. Carneiro DM, Solorzano CC, Nader MC et al (2003) Comparison of intraoperative iPTH assay (QPTH) criteria in guiding parathyroidectomy: which criterion is the most accurate? Surgery 134(6):973-979 discussion 979-981

    Google Scholar 

  58. Sokoll LJ, Drew H, Udelsman R (2000) Intraoperative parathyroid hormone analysis: a study of 200 consecutive cases. Clin Chem 46(10):1662–1668

    PubMed  CAS  Google Scholar 

  59. Di Stasio E, Carrozza C, Pio Lombardi C et al (2007) Parathyroidectomy monitored by intra-operative PTH: the relevance of the 20 min end-point. Clin Biochem 40(9–10):595–603

    PubMed  Google Scholar 

  60. Clerici T, Brandle M, Lange J et al (2004) Impact of intraoperative parathyroid hormone monitoring on the prediction of multiglandular parathyroid disease. World J Surg 28(2):187–192

    Article  PubMed  Google Scholar 

  61. Jaskowiak NT, Sugg SL, Helke J et al (2002) Pitfalls of intraoperative quick parathyroid hormone monitoring and gamma probe localization in surgery for primary hyperparathyroidism. Arch Surg 137(6):659-668 discussion 668-659

    Google Scholar 

  62. Tonelli F, Spini S, Tommasi M et al (2000) Intraoperative parathormone measurement in patients with multiple endocrine neoplasia type I syndrome and hyperparathyroidism. World J Surg 24(5):556-562; discussion 562-553

    Google Scholar 

  63. Weber CJ, Ritchie JC (1999) Retrospective analysis of sequential changes in serum intact parathyroid hormone levels during conventional parathyroid exploration. Surgery 126(6):1139–1143 discussion 1143-1134

    Google Scholar 

  64. Dackiw AP, Sussman JJ, Fritsche HA Jr et al (2000) Relative contributions of technetium 99 m sestamibi scintigraphy, intraoperative gamma probe detection, and the rapid parathyroid hormone assay to the surgical management of hyperparathyroidism. Arch Surg 135(5):550–555; discussion 555–557

    Google Scholar 

  65. Lal A, Bianco J, Chen H (2007) Radioguided parathyroidectomy in patients with familial hyperparathyroidism. Ann Surg Oncol 14(2):739–743

    Article  PubMed  Google Scholar 

  66. Dotzenrath C, Cupisti K, Goretzki PE et al (2001) Long-term biochemical results after operative treatment of primary hyperparathyroidism associated with multiple endocrine neoplasia types I and IIa: is a more or less extended operation essential? Eur J Surg 167(3):173–178

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Tobias Carling.

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Stålberg, P., Carling, T. Familial Parathyroid Tumors: Diagnosis and Management. World J Surg 33, 2234–2243 (2009). https://doi.org/10.1007/s00268-009-9924-6

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