Spontaneous remission of acromegaly following subclinical pituitary apoplexy [Subklinik hipofizer apopleksiyi takiben spontan remisyona giren akromegali]

Küçük Resim Yok

Tarih

2011

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Turkiye Klinikleri

Erişim Hakkı

info:eu-repo/semantics/closedAccess

Özet

Pituitary apoplexy is a rare and sometimes underdiagnosed complication of pituitary adenomas. We present here the case of a patient who was referred to our endocrinology outpatient clinic for his acromegalic appearance. Endocrinological evaluation revealed low basal growth hormone and normal insulin-like growth factor 1 levels, secondary hypothyroidism and adrenal insufficiency. A haemorrhagic adenoma was detected on pituitary MRI scan. In the light of clinical and laboratory evidences, probably, our patient had a previous somatotroph pituitary adenoma which caused acromegaly but further developed subclinical pituitary apoplexy which ended up with hypopituitarism.

Açıklama

Anahtar Kelimeler

Acromegaly, Hypopituitarism, Subclinical pituitary apoplexy

Kaynak

Turkish Journal of Endocrinology and Metabolism

WoS Q Değeri

Scopus Q Değeri

Q4

Cilt

15

Sayı

2

Künye