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Doege‐Potter syndrome in a facial solitary fibrous tumor: Diagnose and clinical management discussion
Author(s) -
FortCulillas Roser,
Barahona San Millán Rebeca,
GarciaFructuoso Isabel,
Quera González Angels,
Grau Martín Armand,
Puigdemont Guinart Montserrat,
RubióCasadevall Jordi,
Recasens Sala Mònica,
Porta Balanyà Rut
Publication year - 2021
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.4291
Subject(s) - medicine , malignancy , differential diagnosis , solitary fibrous tumor , hypoglycemia , pathology , radiology , dermatology , stem cell , biology , cd34 , insulin , genetics
Doege‐Potter syndrome is a rare hypoglycemic paraneoplastic disorder. This case describes that severe and symptomatic hypoglycemia can occasionally be due to a rare malignant neoplasm, and the differential diagnosis of malignancy should not be overlooked in this setting.

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