| Literature DB >> 22584722 |
Francesco Tonelli1, Francesco Giudici, Tiziana Cavalli, Maria Luisa Brandi.
Abstract
Usually, primary hyperparathyroidism is the first endocrinopathy to be diagnosed in patients with multiple endocrine neoplasia type 1, and is also the most common one. The timing of the surgery and strategy in multiple endocrine neoplasia type 1/hyperparathyroidism are still under debate. The aims of surgery are to: 1) correct hypercalcemia, thus preventing persistent or recurrent hyperparathyroidism; 2) avoid persistent hypoparathyroidism; and 3) facilitate the surgical treatment of possible recurrences. Currently, two types of surgical approach are indicated: 1) subtotal parathyroidectomy with removal of at least 3-3 K glands; and 2) total parathyroidectomy with grafting of autologous parathyroid tissue. Transcervical thymectomy must be performed with both of these procedures. Unsuccessful surgical treatment of hyperparathyroidism is more frequently observed in multiple endocrine neoplasia type 1 than in sporadic hyperparathyroidism. The recurrence rate is strongly influenced by: 1) the lack of a pre-operative multiple endocrine neoplasia type 1 diagnosis; 2) the surgeon's experience; 3) the timing of surgery; 4) the possibility of performing intra-operative confirmation (histologic examination, rapid parathyroid hormone assay) of the curative potential of the surgical procedure; and, 5) the surgical strategy. Persistent hyperparathyroidism seems to be more frequent after subtotal parathyroidectomy than after total parathyroidectomy with autologous graft of parathyroid tissue. Conversely, recurrent hyperparathyroidism has a similar frequency in the two surgical strategies. To plan further operations, it is very helpful to know all the available data about previous surgery and to undertake accurate identification of the site of recurrence.Entities:
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Year: 2012 PMID: 22584722 PMCID: PMC3328832 DOI: 10.6061/clinics/2012(sup01)26
Source DB: PubMed Journal: Clinics (Sao Paulo) ISSN: 1807-5932 Impact factor: 2.365
Results after subtotal parathyroidectomy (SPTX) in multiple endocrine neoplasia type 1 (MEN1)-hyperparathyroidism (HPT).
| Author | Year | Period | Pts | Mean follow-up (yrs) | Persistent HPT (%) | Recurrent HPT (%) | Hypoparathyroidism (%) |
| Edis et al. ( | 1979 | 1959–76 | 55 | 3.9 | 13 | 0 | 35 |
| Prinz et al. ( | 1981 | 1955–76 | 12 | 9.5 | 33 | 0 | 25 |
| Van Heerden et al. ( | 1983 | 1960–83 | 45 | N.A. | 6.6 | 6.6 | 13 |
| Goretzki et al. ( | 1991 | 1986–90 | 18 | N.A. | 11 | 0 | 0 |
| Hellman et al. ( | 1992 | 1982–91 | 11 | 11.9 | 0 | 27.3 | 27.3 |
| Kraimps et al. ( | 1992 | 1966–88 | 14 | 8 | 14 | 36 | 10 |
| O' Riordain et al. ( | 1993 | 1970–91 | 54 | 10 | 0 | 16.4 | 8 |
| Janson et al. ( | 1994 | 1971–92 | 4 | 9.9 | 0 | 25 | 0 |
| Thompson et al. ( | 1994 | 1972–92 | 14 | 20 | 7 | 7 | 0 |
| Grant at al. ( | 1994 | 1980–93 | 15 | 4.7 | 0 | 13.3 | 0 |
| Nilsson et al. ( | 1994 | 1971–92 | 2 | 9 | 0 | 0 | 0 |
| Hellman et al. ( | 1998 | 1969–96 | 9 | 7.3 | 22 | 44 | 0 |
| Goudet et al. ( | 2001 | 1986–97 | 73 | N.A. | 16.8 | N.A. | N.A. |
| Dotzenrath et al. ( | 2001 | 1986–98 | 25 | 10 | N.A. | 8 | 12 |
| Arnalsteen et al. ( | 2002 | 1992–01 | 66 | 10 | N.A. | 33 | 12.7 |
| Elaraj et al. ( | 2003 | 1960–02 | 63 | 10 | N.A. | 51 | 26 |
| Hubbard et al. ( | 2006 | 1974–02 | 21 | 5 | 0 | 5 | 10 |
| Norton et al. ( | 2008 | 1970–05 | 41 | 7.9 | 12 | 44 | 10 |
Actuarial estimation.
N.A. = not applicable.
Results after total parathyroidectomy (TPTX) in multiple endocrine neoplasia type 1 (MEN1)-hyperparathyroidism (HPT).
| Author | Year | Period | Pts | Meanfollow-up(yrs) | PersistentHPT(%) | RecurrentHPT(%) | Hypoparathyroidism(%) |
| Wells et al. ( | 1980 | 1973–80 | 36 | 7 | 3 | 30 | 5.6 |
| Malmaeus et al. ( | 1986 | 1961–85 | 18 | 6.5 | 0 | 0 | 26 |
| Hellman et al. ( | 1992 | 1982–91 | 23 | 6.1 | 0 | 22 | 30 |
| Janson et al. ( | 1994 | 1971–92 | 6 | 9.9 | 0 | 0 | 0 |
| Dralle et al. ( | 1994 | 1976–92 | 4 | 6.3 | 0 | 0 | 50 |
| Nilsson et al. ( | 1994 | 1971–92 | 6 | 9 | 0 | 0 | 0 |
| Hellmann et al. ( | 1998 | 1969–96 | 15 | 10.2 | 0 | 20 | 47 |
| Elaraj et al. ( | 2003 | 1960–02 | 16 | 10 | N.A. | 16 | 46 |
| Hubbard et al. ( | 2006 | 1974–02 | 4 | 14 | 0 | 50 | 25 |
| Norton et al. ( | 2008 | 1970–05 | 9 | 9.9 | 0 | 55 | 22 |
| Tonelli et al. ( | 2007 | 1990–06 | 45 | 6.5 | 0 | 11 | 22 |
Actuarial estimation.
N.A. = not applicable.
ntraoperative parathyroid hormone (PTH) monitoring for prediction of multi-glandular parathyroid disease after removal of the first pathological parathyroid gland.
| Author | Decrease of intra-operative PTH from baseline | False positivepercentage |
| Clerici et al. ( | >50% at 10′ | 75% |
| Jaskowiak et al. ( | >50% at 10′ | 50% |
| Kivlen et al. ( | >50% at 10′ | 14% |
| Arnalsteen et al. ( | >50% at 5′ | 5% |
| Thompson et al. ( | >70% at 20′ | 0% |
Decrease below the cut-off point in the presence of other enlarged gland/s.
Patients with MEN1 only.
Figure 1Blood sampling after the removal of each parathyroid gland until the parathyroid hormone (PTH) values are practically undetectable in patients with HPT/MEN1 (6).