英文摘要 |
Tumor-induced hypoglycemia (TIH) or non-islet cell tumor hypoglycemia (NICTH) is described as a tumor-induced hypoglycemia other than insulinoma which is also a manifestation of paraneoplastic syndrome. In most cases, NICTH occurs in subjects with a large solid tumor of mesenchymal or epithelial origins over 10 cm in diameter. Tumor could be either benign or malignant. By 1998, the pathophysiology of NICTH was believed due to over-consumption of glycogen by a huge tumor. Later on, it was confirmed that NICTH caused by overproduction of macro IGFII molecules. Typically, the elevated IGFII levels in NICTH are associated with suppressed the serum levels of insulin, C-peptide, IGFI, and growth hormone. An IGFII: IGFI ratio of >10 is considered to be clinically significant and highly suggestive of NICTH. A complete surgical resection or de-bulking of the tumor whenever possible is the treatment of choice and if successful, usually results in resolution of hypoglycemia. For the inoperable one, high dose glucocorticoid and human growth hormone therapy has been shown to resolve hypoglycemia. In conclusion, TIH or NICTH is caused by overproduction of macro IGFII molecules by a large tumor. A complete surgical resection of the tumor whenever possible is the treatment of choice. For the inoperable one, a high dose or glucocorticoid or human growth hormone therapy has been shown to resolve hypoglycemia. |