Isolated idiopathic hypoparathyroidism that developed in adulthood: a case report

Hypoparathyroidism is a rare endocrine disease. In most cases in adult patients, the cause of hypoparathyroidism is damage or removal of parathyroid glands during surgical interventions on the neck; other causes are rarely observed.Case report. A 52-year-old man with episodes of seizures, intense mu...

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Main Authors: G. E. Runova, A. V. Oderiy, I. V. Glinkina, Yu. P. Sych, S. E. Moshenina, V. V. Fadeev
Format: Article
Language:Russian
Published: Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University) 2021-12-01
Series:Сеченовский вестник
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Online Access:https://www.sechenovmedj.com/jour/article/view/369
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author G. E. Runova
A. V. Oderiy
I. V. Glinkina
Yu. P. Sych
S. E. Moshenina
V. V. Fadeev
author_facet G. E. Runova
A. V. Oderiy
I. V. Glinkina
Yu. P. Sych
S. E. Moshenina
V. V. Fadeev
author_sort G. E. Runova
collection DOAJ
description Hypoparathyroidism is a rare endocrine disease. In most cases in adult patients, the cause of hypoparathyroidism is damage or removal of parathyroid glands during surgical interventions on the neck; other causes are rarely observed.Case report. A 52-year-old man with episodes of seizures, intense muscle pain, progressing for 7 years and resistance to treatment with myorelaxant, anxiolytics and nonsteroidal anti-inflammatory drugs was examined and hypocalcemia associated with low parathyroid hormone and excessive urinary calcium excretion was found. Ultrasound examination didn't reveal any changes in parathyroid glands. The patient was diagnosed with idiopathic hypoparathyroidism. Treatment with calcium supplements and active metabolites of vitamin D led to an improvement in clinical symptoms and laboratory parameters.Discussion. Hypoparathyroidism as part of several genetic syndromes was excluded due to the late- onset of the disease and the absence of concomitant diseases. Ultrasound of the parathyroid glands made it possible to rule out metastasis and storage diseases. It is recommended to perform genetic testing of the chromosomes 22 and 10 to exclude rare variants of syndromic hypoparathyroidism with the late-onset in the form of isolated hypocalcemia.
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language Russian
publishDate 2021-12-01
publisher Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)
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spelling doaj-art-b6a002011eff4b8d94f8c5b3f08643ed2025-08-03T13:30:20ZrusFederal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)Сеченовский вестник2218-73322658-33482021-12-01123687510.47093/2218-7332.2021.187.05190Isolated idiopathic hypoparathyroidism that developed in adulthood: a case reportG. E. Runova0A. V. Oderiy1I. V. Glinkina2Yu. P. Sych3S. E. Moshenina4V. V. Fadeev5Sechenov First Moscow State Medical University (Sechenov University)Sechenov First Moscow State Medical University (Sechenov University)Sechenov First Moscow State Medical University (Sechenov University)Sechenov First Moscow State Medical University (Sechenov University)Sechenov First Moscow State Medical University (Sechenov University)Sechenov First Moscow State Medical University (Sechenov University)Hypoparathyroidism is a rare endocrine disease. In most cases in adult patients, the cause of hypoparathyroidism is damage or removal of parathyroid glands during surgical interventions on the neck; other causes are rarely observed.Case report. A 52-year-old man with episodes of seizures, intense muscle pain, progressing for 7 years and resistance to treatment with myorelaxant, anxiolytics and nonsteroidal anti-inflammatory drugs was examined and hypocalcemia associated with low parathyroid hormone and excessive urinary calcium excretion was found. Ultrasound examination didn't reveal any changes in parathyroid glands. The patient was diagnosed with idiopathic hypoparathyroidism. Treatment with calcium supplements and active metabolites of vitamin D led to an improvement in clinical symptoms and laboratory parameters.Discussion. Hypoparathyroidism as part of several genetic syndromes was excluded due to the late- onset of the disease and the absence of concomitant diseases. Ultrasound of the parathyroid glands made it possible to rule out metastasis and storage diseases. It is recommended to perform genetic testing of the chromosomes 22 and 10 to exclude rare variants of syndromic hypoparathyroidism with the late-onset in the form of isolated hypocalcemia.https://www.sechenovmedj.com/jour/article/view/369isolated hypoparathyroidismisolated hypocalcemialate-onset of hypoparathyroidismconvulsive syndromecalcification of the basal gangliafahr's syndromeseizures in an adult patient
spellingShingle G. E. Runova
A. V. Oderiy
I. V. Glinkina
Yu. P. Sych
S. E. Moshenina
V. V. Fadeev
Isolated idiopathic hypoparathyroidism that developed in adulthood: a case report
Сеченовский вестник
isolated hypoparathyroidism
isolated hypocalcemia
late-onset of hypoparathyroidism
convulsive syndrome
calcification of the basal ganglia
fahr's syndrome
seizures in an adult patient
title Isolated idiopathic hypoparathyroidism that developed in adulthood: a case report
title_full Isolated idiopathic hypoparathyroidism that developed in adulthood: a case report
title_fullStr Isolated idiopathic hypoparathyroidism that developed in adulthood: a case report
title_full_unstemmed Isolated idiopathic hypoparathyroidism that developed in adulthood: a case report
title_short Isolated idiopathic hypoparathyroidism that developed in adulthood: a case report
title_sort isolated idiopathic hypoparathyroidism that developed in adulthood a case report
topic isolated hypoparathyroidism
isolated hypocalcemia
late-onset of hypoparathyroidism
convulsive syndrome
calcification of the basal ganglia
fahr's syndrome
seizures in an adult patient
url https://www.sechenovmedj.com/jour/article/view/369
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AT ivglinkina isolatedidiopathichypoparathyroidismthatdevelopedinadulthoodacasereport
AT yupsych isolatedidiopathichypoparathyroidismthatdevelopedinadulthoodacasereport
AT semoshenina isolatedidiopathichypoparathyroidismthatdevelopedinadulthoodacasereport
AT vvfadeev isolatedidiopathichypoparathyroidismthatdevelopedinadulthoodacasereport