Summary
Background
The association of a solitary tumor of the pleura with paraneoplastic refractory hypoglycemia is a very rare clinical condition.
Methods
An 86-year-old gentleman with an incidentally discovered large mass in the left chest and a long-standing history of refractory hypoglycemia was referred for surgical consultation. Computed tomography and PET (Positron Emission Tomography) scan confirmed the presence of a homogeneous mass leaning on the left hemidiaphragm with no tracer uptake.
Results
After tumor board discussion, the mass was radically excised through a left thoracotomy. Histopathology revealed a benign solitary fibrous tumor of the pleura. At 1‑year follow-up the patient was doing well and did not further complain of hypoglycemia-related symptoms.
Conclusion
Doege–Potter syndrome is a life-threatening condition associated with severely impaired quality of life. Prompt identification and surgical treatment are mandatory.
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C. A. Manzo, E. Asti, C. Froiio, B. Bruni, and L. Bonavina declare that they have no competing interests.
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All procedures performed in studies involving human participants or on human tissue were in accordance with the ethical standards of the institutional and/or national research committee and with the 1975 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from the patient included in the study. Internal review board approval HSD 2020-071.
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Manzo, C.A., Asti, E., Froiio, C. et al. Refractory hypoglycemia associated with giant solitary fibrous tumor of the pleura (Doege–Potter syndrome). Eur Surg 52, 296–299 (2020). https://doi.org/10.1007/s10353-020-00673-w
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DOI: https://doi.org/10.1007/s10353-020-00673-w