The anaesthetic management of patients with acromegaly, a rare clinical syndrome, for urgent non pituitary surgery has little documentation in the literature. We report such a case further complicated by dilated cardiomyopathy. The anaethetic challenges in the face of limited resources are highlighted. Keywords: Acromegaly, dilated cardiomyopathy, non-pituitary surgery, emergencyNQJHM Vol. 15 (2) 2005: pp. 103-10
Purpose To reveal the variety of symptoms experienced by patients before acromegaly diagnosis and to...
It is well accepted that mortality in acromegaly is increased because of cardiovascular and respirat...
McCune-Albright Syndrome is a rare disorder affecting the skin, bones and endocrine tissues. It is c...
Abstract Background Acromegaly is a rare syndrome in which there is unregulated hypersecretion of gr...
Acromegaly, a syndrome related to growth hormone/IGF-1 excess, is frequently complicated by cardiova...
The management of acromegaly caused by an uncommon growth hormone-secreting pituitary adenoma can be...
Object. In addition to difficulties with anesthetic and medical management, transsphenoidal operatio...
Acromegaly is a slowly progressive disease characterized by 30% increase of mortality rate for card...
Acromegaly is an insidious disease of the pituitary caused by a growth hormone-secreting adenoma. Ge...
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-C...
No sponsorships or competing interests have been disclosed for this article. Objectives. Patients wi...
Because growth hormone and IGF-1 both have regulatory roles in the cardiovascular system, patients ...
Background: Acromegaly defines as chronic elevations of insulin-like growth factor-1 (IGF-1) and gro...
In a series of 256 patients with acromegaly, 10 had evidence of heart disease for which no explanati...
Cardiovascular involvement is common in acromegaly and can lead to development of acromegalic cardio...
Purpose To reveal the variety of symptoms experienced by patients before acromegaly diagnosis and to...
It is well accepted that mortality in acromegaly is increased because of cardiovascular and respirat...
McCune-Albright Syndrome is a rare disorder affecting the skin, bones and endocrine tissues. It is c...
Abstract Background Acromegaly is a rare syndrome in which there is unregulated hypersecretion of gr...
Acromegaly, a syndrome related to growth hormone/IGF-1 excess, is frequently complicated by cardiova...
The management of acromegaly caused by an uncommon growth hormone-secreting pituitary adenoma can be...
Object. In addition to difficulties with anesthetic and medical management, transsphenoidal operatio...
Acromegaly is a slowly progressive disease characterized by 30% increase of mortality rate for card...
Acromegaly is an insidious disease of the pituitary caused by a growth hormone-secreting adenoma. Ge...
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-C...
No sponsorships or competing interests have been disclosed for this article. Objectives. Patients wi...
Because growth hormone and IGF-1 both have regulatory roles in the cardiovascular system, patients ...
Background: Acromegaly defines as chronic elevations of insulin-like growth factor-1 (IGF-1) and gro...
In a series of 256 patients with acromegaly, 10 had evidence of heart disease for which no explanati...
Cardiovascular involvement is common in acromegaly and can lead to development of acromegalic cardio...
Purpose To reveal the variety of symptoms experienced by patients before acromegaly diagnosis and to...
It is well accepted that mortality in acromegaly is increased because of cardiovascular and respirat...
McCune-Albright Syndrome is a rare disorder affecting the skin, bones and endocrine tissues. It is c...