TY - JOUR
T1 - A rare case of hypoglycemia in a patient with elevated right hemidiaphragm.
AU - Rosseel, Liesbeth
AU - De Leu, Nico
AU - Van Hecke, Wim
AU - Unuane, David
PY - 2012/6/28
Y1 - 2012/6/28
N2 - A 57-year-old woman was admitted to the emergency department, presenting with episodes of altered consciousness and behaviour which, upon further examination, were linked to periods of recurrent hypoglycaemia. Imaging revealed a large mass in the right thoracic cavity while blood analysis demonstrated diminished C-peptide, (pro-)insulin, insulin-like growth factor 1 (IGF-I) and IGF binding protein 3 levels. Based on these findings, an IGF-II secreting tumour was suspected. Before the excision of the tumour, euglycaemia could only be achieved by means of intravenous glucose administration and the use of oral corticosteroids. Anatomopathologically the diagnosis of a solitary fibrous tumour (SFT) was confirmed. Immunoblot analysis on the serum revealed elevated 'big'-IGF-II levels, confirming our initial diagnosis of Doege-Potter syndrome in SFT.
AB - A 57-year-old woman was admitted to the emergency department, presenting with episodes of altered consciousness and behaviour which, upon further examination, were linked to periods of recurrent hypoglycaemia. Imaging revealed a large mass in the right thoracic cavity while blood analysis demonstrated diminished C-peptide, (pro-)insulin, insulin-like growth factor 1 (IGF-I) and IGF binding protein 3 levels. Based on these findings, an IGF-II secreting tumour was suspected. Before the excision of the tumour, euglycaemia could only be achieved by means of intravenous glucose administration and the use of oral corticosteroids. Anatomopathologically the diagnosis of a solitary fibrous tumour (SFT) was confirmed. Immunoblot analysis on the serum revealed elevated 'big'-IGF-II levels, confirming our initial diagnosis of Doege-Potter syndrome in SFT.
UR - http://www.scopus.com/inward/record.url?scp=84893387938&partnerID=8YFLogxK
U2 - 10.1136/bcr.03.2012.5972
DO - 10.1136/bcr.03.2012.5972
M3 - Article
C2 - 22744247
AN - SCOPUS:84893387938
SN - 1757-790X
VL - 2012
JO - BMJ Case Reports [E]
JF - BMJ Case Reports [E]
M1 - 2274424
ER -