Case Report: Abdominal Lymph Node Metastases of Parathyroid Carcinoma: Diagnostic Workup, Molecular Diagnosis, and Clinical Management.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
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

643328

Commentaires 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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Auteurs

Christina Lenschow (C)

Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.

Carmina Teresa Fuss (CT)

Department of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.

Stefan Kircher (S)

Institute of Pathology, University of Würzburg, Würzburg, Germany.

Andreas Buck (A)

Department of Nuclear Medicine, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.

Ralph Kickuth (R)

Department of Diagnostic and Interventional Radiology, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.

Joachim Reibetanz (J)

Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.

Armin Wiegering (A)

Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.

Albrecht Stenzinger (A)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Germany and German Cancer Consortium (DKTK), Heidelberg Partner Site, Heidelberg, Germany.

Daniel Hübschmann (D)

Computational Oncology, Molecular Diagnostics Program, NCT Heidelberg and Heidelberg University Hospital, Heidelberg, Germany.

Christoph Thomas Germer (CT)

Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.

Martin Fassnacht (M)

Department of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.
Comprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany.

Stefan Fröhling (S)

National Center for Tumor Diseases (NCT Heidelberg), Division of Translational Medical Oncology German Cancer Research Center (DKFZ), University Hospital Heidelberg, Heidelberg, Germany.

Nicolas Schlegel (N)

Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.

Matthias Kroiss (M)

Department of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.
Comprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany.
Department of Medicine IV, University Hospital Munich, Ludwig-Maximilians-Universität München, Munich, Germany.

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