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2.
Rev. méd. Chile ; 137(12): 1591-1596, dic. 2009. ilus, tab
Article in Spanish | LILACS | ID: lil-543136

ABSTRACT

Background: The aim of the surgical treatment of primary hyperparathyroidism (PHPT) is to achieve its complete cure, evidenced by normal serum calcium in the postoperative period. Measurement of intraoperative serum parathormone (PTH) can be useful to predict complete cure of the disease. Aim: To assess the usefulness of intraoperative PTH measurement to predict complete cure of PHPT Material and methods: Serum PTH was measured to all patients operated for PHPT between 2003 and 2008, before and five and ten minutes after the excision of the parathyroid gland causing the disease. The criteria for complete cure were normal serum calcium at 24 hours and 6 months after surgery and the pathological confirmation of parathyroid gland excision. Results: Eighty-eight operated patients, aged 58±15 years (72 females) were studied. Sixty four percent were asymptomatic and their preoperative serum calcium was 11.6± 1.2 mg/dl. A normal serum calcium was achieved in 86 patients (98 percent) at 24 hours and 50 of 52 patients followed for six months (96 percent). The pathological study disclosed an adenoma in 69 (78 percent), and multiglandular disease in 16 (18 percent), a parathyroid cancer in one and a normal gland in one patient. Intraoperative PTH predicted early and definitive cure in 97 percent and 100 percent of patients with a single adenoma, respectively. Among patients with multiglandular disease, the predictive figures were 94 percent and 100 percent, respectively. Conclusions: Intraoperative PTH measurement efficiently predicts early and definitive surgical cure of PHPT.


Subject(s)
Female , Humans , Male , Middle Aged , Adenoma/surgery , Calcium/blood , Hyperparathyroidism/surgery , Parathyroid Hormone/blood , Parathyroid Neoplasms/surgery , Adenoma/complications , Biomarkers/blood , Hyperparathyroidism/blood , Hyperparathyroidism/etiology , Intraoperative Care , Parathyroid Neoplasms/complications , Parathyroidectomy , Predictive Value of Tests , Treatment Outcome
3.
Rev. méd. Chile ; 135(6): 718-724, jun. 2007. tab
Article in Spanish | LILACS | ID: lil-459574

ABSTRACT

Background: Papillary thyroid carcinoma can have familial aggregation. Aim: To compare retrospectively familial non medullary thyroid carcinoma (FNMTC) with sporadic papillary thyroid carcinoma (PTC). Material and methods: Retrospective analysis of medical records of patients with thyroid carcinoma. An index case was defined as a subject with the diagnosis of differentiated thyroid carcinoma with one or more first degree relatives with the same type of cancer. Seventeen such patients were identified and were compared with 352 subjects with PTC. Results: The most common affected relatives were sisters. Patients with FNMTC were younger than those with PTC. No differences were observed in gender, single or multiple foci, thyroid capsule involvement, surgical border involvement, number of affected lymph nodes and coexistence of follicular hyperplasia. Patients with FNMTC had smaller tumors and had a nine times more common association with lymphocytic thyroiditis. Five patients with FNMTC had local recurrence during 4.8 years of follow up. Conclusions: Patients with FNMTC commonly have an associated chronic thyroiditis, are younger and have smaller tumors than patients with PTC.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Carcinoma, Medullary/genetics , Carcinoma, Papillary/genetics , Thyroid Neoplasms/genetics , Age Factors , Carcinoma, Medullary/pathology , Carcinoma, Medullary/surgery , Carcinoma, Papillary/pathology , Carcinoma, Papillary/surgery , Chile , Pedigree , Retrospective Studies , Thyroid Neoplasms/pathology , Thyroid Neoplasms/surgery
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