Doege–Potter syndrome
Doege–Potter syndrome is a rare medical condition characterized by the presence of a non-islet cell tumor hypoglycemia (NICTH) due to a solitary fibrous tumor (SFT). The syndrome was first described by Karl Doege and Roy P. Potter in 1930.
Symptoms[edit | edit source]
The main symptom of Doege–Potter syndrome is hypoglycemia, or low blood sugar. This is caused by the production of insulin-like growth factor 2 (IGF-2) by the tumor. Other symptoms can include weight loss, weakness, and fatigue.
Diagnosis[edit | edit source]
Diagnosis of Doege–Potter syndrome can be challenging due to its rarity. It is typically diagnosed through a combination of clinical findings, laboratory tests, and imaging studies. The diagnosis is confirmed by the presence of a solitary fibrous tumor and hypoglycemia.
Treatment[edit | edit source]
Treatment for Doege–Potter syndrome typically involves surgical removal of the tumor. In some cases, medication may be used to manage symptoms of hypoglycemia.
Prognosis[edit | edit source]
The prognosis for Doege–Potter syndrome varies depending on the size and location of the tumor, as well as the patient's overall health. With treatment, some patients may experience a complete resolution of symptoms.
See also[edit | edit source]
References[edit | edit source]
External links[edit | edit source]
- Doege–Potter syndrome at WikiMD
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Contributors: Prab R. Tumpati, MD
