Total: 5 |
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PMID (PMCID) | ||
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23890147 |
FEMALE | Middle Aged |
Necrolytic migratory erythema and glucagonoma rising from pancreatic head. | ||
Tseng HC, Liu CT, Ho JC, Lin SH. Pancreatology. 2013;13(4):455-7. |
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Glucagonoma syndrome encompasses necrolytic migratory erythema (NME), hyperglucagonemia, diabetes mellitus, anemia, weight loss, glossitis, angular cheilitis, steatorrhea, diarrhea, venous thrombosis, and neuropsychiatric disturbance. | ||
15313692 |
MALE | Middle Aged |
Clinical experience in diagnosis and treatment of glucagonoma syndrome. | ||
Zhang M, Xu X, Shen Y, Hu ZH, Wu LM, Zheng SS. Hepatobiliary Pancreat Dis Int. 2004;3(3):473-5. |
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The clinical data of a case of pancreatic head tumor with typical glucagonoma syndrome of necrolytic migratory erythema (NME), diabetes mellitus (DM), anemia, and glossitis were retrospectively analyzed. | ||
10502856 |
MALE | Middle Aged |
Glucagonoma syndrome: a case report. | ||
Shyr YM, Su CH, Lee CH, Wu CW, Lui WY. Zhonghua Yi Xue Za Zhi (Taipei). 1999;62(9):639-43. |
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We present a case of pancreatic tail tumor with the typical glucagonoma syndrome of necrolytic migratory erythema (NME), diabetes mellitus (DM), anemia, weight loss and glossitis. | ||
7648942 |
MALE | Middle Aged |
[Report of a case of glucagonoma misdiagnosed as "eczema" and "hepatic angioma" for three years and review of literature]. | ||
Dai W, Shi Y, Cai L. Zhonghua Nei Ke Za Zhi. 1995;34(3):190-2. |
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Glucagonoma is a rare pancreatic tumor, necrolytic migratory erythema is its distinctive feature and it is often associated with diabetes mellitus, weight loss, anemia, hypoaminoacidemia, glossitis and stomatitis. | ||
218426 |
MALE | |
Metabolic studies and glucagon gel filtration pattern before and after surgery in a case of glucagonoma syndrome. | ||
von Schenck H, Thorell JI, Berg J, Bojs G, Dymling JF, Hallengren B, Ljungberg O, Tibblin S. Acta Med Scand. 1979;205(3):155-62. |
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A case of glucagonoma syndrome with necrolytic migratory erythema, glossitis, anemia, hyperglucagonemia and a malignant, pancreatic A-cell tumour in a 68-year-old male is described. |