Remission of Primary Hyperparathyroidism Due To Spontaneous Infarction of a Parathyroid Adenoma: Case Report and Review of the Literature
- 1 November 1998
- journal article
- case report
- Published by Wolters Kluwer Health in Medicine
- Vol. 77 (6) , 398-402
- https://doi.org/10.1097/00005792-199811000-00005
Abstract
Subclinical infarction of abnormal parathyroid tissue likely occurs relatively frequently, but remission of primary hyperparathyroidism due to spontaneous massive infarction of a parathyroid adenoma is a rare occurrence. We describe a patient who was unique in that spontaneous remission was accompanied by disappearance of the parathyroid adenoma on serial parathyroid scans. We identified 11 other patients in the literature with sufficient documentation of clinical remission of primary hyperparathyroidism due to spontaneous massive infarction of a parathyroid adenoma and review their clinical features as well. Manifestations varied according to the delay in diagnosis, alteration in serum calcium, location, and degree of associated hemorrhage. Ages ranged from 19 to 73 years, and both sexes were affected. Preceding symptoms suggestive of hypercalcemia and/or prior documentation of hypercalcemia were present in 10 cases. Neck pain was present at the time of infarction in 6/12 patients, and a neck mass in 7/12. Only 1 patient died. The initial calcium level done postinfarction was "normal" in 7/12 patients, low in 3/12, and high in 2/12. The parathyroid adenoma was 2 cm or larger in 8/12 patients. In all patients who had parathyroidectomy, histopathology confirmed extensive infarction (bland or hemorrhagic) of the adenoma. The clinical scenarios encountered were 3 hypocalcemic crises, 2 hypercalcemic crises ("acute parathyroid intoxication"), 1 respiratory arrest secondary to a mediastinal hematoma, 2 patients with neck pain as the major complaint, and 4 with no symptoms apart from the premorbid symptoms of hypercalcemia.Keywords
This publication has 24 references indexed in Scilit:
- Long-Term Treatment of Girls with Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1996
- Plasma glutamine concentration: A guide in the management of urea cycle disordersThe Journal of Pediatrics, 1992
- Prospective treatment of urea cycle disordersThe Journal of Pediatrics, 1991
- Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase LocusNew England Journal of Medicine, 1990
- False positive results from the alanine loading test for ornithine carbamoyltransferase deficiency heterozygosityThe Journal of Pediatrics, 1989
- Natural History of Symptomatic Partial Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1986
- Neurologic Outcome in Children with Inborn Errors of Urea SynthesisNew England Journal of Medicine, 1984
- Treatment of Inborn Errors of Urea SynthesisNew England Journal of Medicine, 1982
- Carrier detection in ornithine transcarbamylase deficiencyJournal of Inherited Metabolic Disease, 1980
- Carrier detection in ornithine transcarbamylase deficiencyThe Journal of Pediatrics, 1978