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Erschienen in: Familial Cancer 2/2017

20.10.2016 | Original Article

Cystic parathyroid glands in MEN1: A rare entity?

verfasst von: Tiziana Cavalli, Francesco Giudici, Gabriella Nesi, Andrea Amorosi, Raffaella Santi, Maria Luisa Brandi, Francesco Tonelli

Erschienen in: Familial Cancer | Ausgabe 2/2017

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Abstract

Approximately 300 cases of sporadic parathyroid cyst (PCs) have been reported to date. Only two cases have been described in MEN1 so far. Detection by imaging could be challenging, especially in multiglandular primary hyperparathyroidism (HPT) and clinical outcome could be different. During the period 1990–2014, 71 MEN1 patients were operated for primary hyperparathyroidism in our centre. We report three cases of PCs in MEN1 patients affected by HPT, who underwent a total or subtotal parathyroidectomy with transcervical thymectomy. In our series, all three patients had an unsatisfactory postoperative course, at variance with the high percentage (over 90 %) of long-term success in MEN1 patients operated at our centre. One patient affected by cystic degeneration of all the four parathyroid glands reported persistent hypoparathyroidism, despite autografts of parathyroid tissue. For the other two cases, surgery failed to cure hyperparathyroidism, perhaps because of the presence of undetected ectopic parathyroid tissue. In the context of a multiglandular disease such as MEN1 syndrome, PCs seem rare but our experience shows about a 4 % incidence. Furthermore their presence, even in expert hands, could affect the preoperative identification of the parathyroid glands due to the difficult differential diagnosis between PC and other cystic lesions of the neck, and intraoperative detection of the glands as well as the postoperative outcome.
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Metadaten
Titel
Cystic parathyroid glands in MEN1: A rare entity?
verfasst von
Tiziana Cavalli
Francesco Giudici
Gabriella Nesi
Andrea Amorosi
Raffaella Santi
Maria Luisa Brandi
Francesco Tonelli
Publikationsdatum
20.10.2016
Verlag
Springer Netherlands
Erschienen in
Familial Cancer / Ausgabe 2/2017
Print ISSN: 1389-9600
Elektronische ISSN: 1573-7292
DOI
https://doi.org/10.1007/s10689-016-9936-y

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