Hyperadrenocorticism Caused by a Pituitary Ganglioglioma in a Dog.
Hirokazu IshinoSusumu TakekoshiTakahiro TeshimaKazuyuki UchidaIwao SakonjuYasushi HaraPublished in: Veterinary pathology (2019)
An 11-year-old castrated male Chihuahua dog was presented with complaints of polyuria, polydipsia, abdominal enlargement, and alopecia. Hyperadrenocorticism was diagnosed on the basis of clinical signs, blood tests, adrenocorticotropin-stimulation test results, and an elevated serum adrenocorticotropin concentration. Contrast-enhanced magnetic resonance imaging showed that the pituitary gland was enlarged, compatible with a pituitary macroadenoma. Pituitary-dependent hyperadrenocorticism was suspected, and transsphenoidal hypophysectomy was thus performed for complete resection of the tumor. After surgery, the serum adrenocorticotropin concentration normalized and the hyperadrenocorticism resolved. Histological and immunocytochemical analyses revealed a benign tumor composed of mature neuronal cells and glial cells, suggestive of a ganglioglioma with immunolabeling for adrenocorticotropin. Careful analysis of the resected tumor revealed no pituitary adenoma tissue. The clinical and histopathologic findings indicated that the ganglioglioma was directly responsible for the hyperadrenocorticism. This is the first case of hyperadrenocorticism caused by a ganglioglioma in a dog.
Keyphrases
- magnetic resonance imaging
- contrast enhanced
- induced apoptosis
- growth hormone
- computed tomography
- cell cycle arrest
- magnetic resonance
- diffusion weighted
- endoplasmic reticulum stress
- diffusion weighted imaging
- oxidative stress
- single cell
- cell death
- lymph node
- pulmonary embolism
- cerebral ischemia
- blood brain barrier