Case Report: Abdominal Lymph Node Metastases of Parathyroid Carcinoma: Diagnostic Workup, Molecular Diagnosis, and Clinical Management.
Antibodies, Monoclonal, Humanized
/ pharmacology
Calcium
/ metabolism
Cinacalcet
/ pharmacology
Disease Progression
Female
Fluorodeoxyglucose F18
Humans
Immune System
Immunotherapy
Liver Neoplasms
/ secondary
Lymphatic Metastasis
Middle Aged
Molecular Biology
Neoplasm Metastasis
Neoplasm Recurrence, Local
/ pathology
Parathyroid Hormone
/ metabolism
Parathyroid Neoplasms
/ metabolism
Positron Emission Tomography Computed Tomography
Tomography, X-Ray Computed
Treatment Outcome
Ultrasonography
[18F]FDG-PET-CT
abdominal lymph node metastases
immune check inhibitor
molecular diagnostics
parathyroid carcinoma
pembrolizumab
repeated surgery
Journal
Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782
Informations de publication
Date de publication:
2021
2021
Historique:
received:
17
12
2020
accepted:
04
02
2021
entrez:
9
4
2021
pubmed:
10
4
2021
medline:
8
1
2022
Statut:
epublish
Résumé
Parathyroid carcinoma (PC) is an orphan malignancy accounting for only ~1% of all cases with primary hyperparathyroidism. The localization of recurrent PC is of critical importance and can be exceedingly difficult to diagnose and sometimes futile when common sites of recurrence in the neck and chest cannot be confirmed. Here, we present the diagnostic workup, molecular analysis and multimodal therapy of a 46-year old woman with the extraordinary manifestation of abdominal lymph node metastases 12 years after primary diagnosis of PC. The patient was referred to our endocrine tumor center in 2016 with the aim to localize the tumor causative of symptomatic biochemical recurrence. In view of the extensive previous workup we decided to perform [18F]FDG-PET-CT. A pathological lymph node in the liver hilus showed slightly increased FDG-uptake and hence was suspected as site of recurrence. Selective venous sampling confirmed increased parathyroid hormone concentration in liver veins. Abdominal lymph node metastasis was resected and histopathological examination confirmed PC. Within four months, the patient experienced biochemical recurrence and based on high tumor mutational burden detected in the surgical specimen by whole exome sequencing the patient received immunotherapy with pembrolizumab that led to a biochemical response. Subsequent to disease progression repeated abdominal lymph node resection was performed in 10/2018, 01/2019 and in 01/2020. Up to now (12/2020) the patient is biochemically free of disease. In conclusion, a multimodal diagnostic approach and therapy in an interdisciplinary setting is needed for patients with rare endocrine tumors. Molecular analyses may inform additional treatment options including checkpoint inhibitors such as pembrolizumab.
Identifiants
pubmed: 33833736
doi: 10.3389/fendo.2021.643328
pmc: PMC8021949
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Parathyroid Hormone
0
Fluorodeoxyglucose F18
0Z5B2CJX4D
pembrolizumab
DPT0O3T46P
Calcium
SY7Q814VUP
Cinacalcet
UAZ6V7728S
Types de publication
Case Reports
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
643328Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2021 Lenschow, Fuss, Kircher, Buck, Kickuth, Reibetanz, Wiegering, Stenzinger, Hübschmann, Germer, Fassnacht, Fröhling, Schlegel and Kroiss.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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