Necrolytic migratory erythema
(Redirected from Glucagonoma syndrome)
Necrolytic Migratory Erythema
Necrolytic migratory erythema (NME) is a rare skin condition often associated with Glucagonoma, a type of neuroendocrine tumor. It is characterized by the cyclic appearance of red, blistering and peeling skin lesions that migrate across the body.
Symptoms[edit | edit source]
The primary symptom of NME is the presence of skin lesions that appear, heal, and then reappear in new locations. These lesions are typically red, blistering, and peeling, and can cause significant discomfort. Other symptoms may include weight loss, diarrhea, and anemia.
Causes[edit | edit source]
NME is most commonly associated with glucagonoma, a rare type of pancreatic tumor that produces excessive amounts of the hormone glucagon. However, it can also occur in individuals with other types of tumors or liver disease.
Diagnosis[edit | edit source]
Diagnosis of NME is typically based on the characteristic appearance of the skin lesions and confirmed by a skin biopsy. Blood tests may also be performed to check for elevated levels of glucagon and other abnormalities.
Treatment[edit | edit source]
Treatment for NME primarily involves addressing the underlying cause, such as removing or treating the tumor causing the excess glucagon production. Topical creams and ointments may also be used to help manage the skin symptoms.
Prognosis[edit | edit source]
The prognosis for individuals with NME depends largely on the underlying cause. If the cause is a glucagonoma, prognosis can be significantly improved with early detection and treatment of the tumor.
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