• Title/Summary/Keyword: Ectopic parathyroid gland

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A Case of Ectopic Parathyroid Gland in the Hypopharyngeal Wall (하인두벽에 발생한 이소성 부갑상선 1예)

  • Jung, Jae Yeup;Park, Kye Hoon;Jang, Si-Hyong;Ban, Myung Jin
    • Korean Journal of Head & Neck Oncology
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    • v.34 no.1
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    • pp.29-32
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    • 2018
  • The parathyroid glands are usually located in the posterolateral area of the thyroid gland. Due to their embryologic origin, they are sometimes found in an ectopic position from the angle of the jaw to the mediastinum. However, their incidental detection in the hypopharyngeal wall is rare. Herein, we report a case of an ectopic parathyroid gland found in the hypopharyngeal wall of a 39-year old woman with no known endocrine abnormality.

A Case of Pseudohypoparathyroidism in a Premature Infant (미숙아에서 발견된 가성부갑상선 기능저하증 1례)

  • Yang, Jong Il;Seo, Jang Won;Kim, Ji Young
    • Clinical and Experimental Pediatrics
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    • v.46 no.10
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    • pp.1032-1035
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    • 2003
  • In pseudohypoparathyroidism as reported by Albright in 1942, the parathyroid gland can normally synthesize and secrete parathyroid hormone(PTH). Pseudohypoparathyroidism has a similar biochemical finding with hypoparathyroidisms like hypocalcemia and hyperphosphatemia due to target tissue resistance to PTH. Administered PTH does not raise the serum levels of calcium and urinary phosphate. PTH activates G-protein in peripheral tissue and adenylate cyclase through a second messenger, cAMP. Pseudohypoparathyroidism produces hyperphosphatemia and hypocalcemia because of the resistance to PTH in peripheral tissue due to a defect of G-protein, although it releases PTH normally. According to the mechanism of resistance, pseudohypoparathyroidism is classified into types : Ia, Ib, Ic and psedopseudohypoparathyroism. Type Ia is accompanied by congenital growth retardation and abnormal bony development that shows mental retardation, obesity, low height, round face, short metacarpal bone and metatarsal bone, ectopic calcification, etc. We report a case of pseudohypoparathyroidism in a premature who shows hypocalcemia, hyperphosphatemia, elevation of serum PTH and 24 hr urinary basal c-AMP in biochemical tests without Albright's hereditary osteodystrophy at physical examination, accompanied by a spontaneous fracture in the femur.