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Doege-Potter Syndrome In A Facial Solitary Fibrous Tumor: Diagnose And Clinical Management Discussion
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  • Roser Fort-Culillas,
  • Rebeca Barahona,
  • Isabel Garcia-Fructuoso,
  • Angels Quera,
  • Armand Grau,
  • Montserrat Puigdemont,
  • Jordi Rubió-Casadevall,
  • Monica Recasens,
  • Rut Porta
Roser Fort-Culillas
Institut Català d'Oncologia Girona
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Rebeca Barahona
Hospital Universitari de Girona Doctor Josep Trueta
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Isabel Garcia-Fructuoso
Institut Català d'Oncologia Girona
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Angels Quera
Hospital de Figueres
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Armand Grau
Hospital de Figueres
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Montserrat Puigdemont
Institut Català d'Oncologia Girona
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Jordi Rubió-Casadevall
Institut Català d'Oncologia Girona
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Monica Recasens
Hospital Universitari de Girona Doctor Josep Trueta
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Rut Porta
Institut Català d'Oncologia Girona
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Abstract

Doege Potter syndrome is a rare paraneoplastic clinical entity. A 31-year-old woman consulted with a right indurated malar mass and hypoglycemia. Blood test showed a non-insulin-mediated hypoglycemia. CT scan revealed a solid tumor from the right temporal region with liver metastasis. The histopathological diagnosis revealed a solitary fibrous tumor.

Peer review status:ACCEPTED

04 Dec 2020Submitted to Clinical Case Reports
18 Dec 2020Submission Checks Completed
18 Dec 2020Assigned to Editor
09 Jan 2021Reviewer(s) Assigned
15 Jan 2021Review(s) Completed, Editorial Evaluation Pending
19 Jan 2021Editorial Decision: Revise Minor
05 Feb 20211st Revision Received
06 Feb 2021Submission Checks Completed
06 Feb 2021Assigned to Editor
06 Feb 2021Review(s) Completed, Editorial Evaluation Pending
08 Feb 2021Reviewer(s) Assigned
18 Feb 2021Editorial Decision: Revise Minor
01 Apr 20212nd Revision Received
02 Apr 2021Assigned to Editor
02 Apr 2021Submission Checks Completed
02 Apr 2021Review(s) Completed, Editorial Evaluation Pending
03 Apr 2021Reviewer(s) Assigned
20 Apr 2021Editorial Decision: Accept