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A case of mediastinal hyperparathyromatosis.
Spillane, Chloe; Calpin, Gavin; Singh, Sneha; O'Reilly, Kasie; Hehir, Cian; Hill, Arnold; Magee, Colm; Barrett, Helen.
Afiliação
  • Spillane C; Department of Surgery, Beaumont Hospital, Beaumont Road, Beaumont, Dublin 9, D09V2N0, Ireland.
  • Calpin G; Department of Surgery, Beaumont Hospital, Beaumont Road, Beaumont, Dublin 9, D09V2N0, Ireland.
  • Singh S; Department of Surgery, Beaumont Hospital, Beaumont Road, Beaumont, Dublin 9, D09V2N0, Ireland.
  • O'Reilly K; Department of Surgery, Beaumont Hospital, Beaumont Road, Beaumont, Dublin 9, D09V2N0, Ireland.
  • Hehir C; Department of Surgery, Beaumont Hospital, Beaumont Road, Beaumont, Dublin 9, D09V2N0, Ireland.
  • Hill A; Department of Surgery, Beaumont Hospital, Beaumont Road, Beaumont, Dublin 9, D09V2N0, Ireland.
  • Magee C; Department of Medicine, Beaumont Hospital, Beaumont Road, Beaumont, Dublin 9, D09V2N0, Ireland.
  • Barrett H; Department of Pathology, Beaumont Hospital, Beaumont Road, Beaumont, Dublin 9, D09V2N0, Ireland.
J Surg Case Rep ; 2024(1): rjad735, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38250132
ABSTRACT
Recurrent hyperparathyroidism (HPT) after initial parathyroid surgery occurs rarely in an ectopic location. The rare phenomenon of parathyromatosis may be the cause of this. We present the case of a 59-year-old woman with recurrent HPT, which presented as a new ectopic mediastinal parathyroid gland 13 years after initial 3.5 gland parathyroidectomy. A 1.5 × 1.3 cm lesion was discovered as an incidental finding in the pretracheal region, closely abutting the aortic arch. An aspirate revealed oncocytic cells, which were positive for parathyroid hormone, confirming a mediastinal parathyroid nodule. Sestamibi scan confirmed an avid nodule in the mediastinum. This patient had multiple co-morbidities but was asymptomatic of HPT. It was therefore decided at multi-disciplinary team discussion that she should undergo surveillance. To our knowledge, no such presentations have been reported in the literature. Thus, our case report is a unique addition of an atypical presentation of HPT.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Surg Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Irlanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Surg Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Irlanda
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