| Literature DB >> 30774022 |
Hirokazu Ishino1, Susumu Takekoshi2, Takahiro Teshima3, Kazuyuki Uchida4, Iwao Sakonju1, Yasushi Hara5.
Abstract
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.Entities:
Keywords: corticotroph; dog; ganglioglioma; hyperadrenocorticism; pituitary
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Year: 2019 PMID: 30774022 DOI: 10.1177/0300985819829530
Source DB: PubMed Journal: Vet Pathol ISSN: 0300-9858 Impact factor: 2.221