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Peer-reviewed veterinary case report

Dog with Cushing's syndrome caused by adrenal tumor pheochromocytoma

By Sungin Lee et al.·Published in BMC Veterinary Research·2020·Department of Veterinary Clinical Sciences, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, GB·View original on DOAJ

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Original publication title: Ectopic Cushing’s syndrome associated with a pheochromocytoma in a dog: a case report

Species:
dog

Plain-English summary

An 11-year-old male Scottish terrier was brought to the vet with symptoms of Cushing’s syndrome, including a pot belly, excessive thirst and urination, hair loss, and skin infections. After tests, the vet found a tumor on the dog's adrenal gland, which was identified as a pheochromocytoma (a type of tumor that can affect hormone levels). The dog underwent surgery to remove the tumor and was treated with medications before the operation. Following the surgery, the dog's hormone levels returned to normal, and he showed no signs of illness for at least eight months.

People also search for: dog Cushing's syndrome symptoms · Scottish terrier adrenal tumor treatment · pheochromocytoma in dogs

Abstract

Abstract Background Ectopic Cushing’s syndrome (ECS) associated with malignant tumors, such as small cell lung carcinoma, bronchial carcinoids, and pheochromocytoma, has been reported in human medicine. However, ECS related to pheochromocytoma has not been reported in dogs. Case presentation An 11-year-old castrated, male Scottish terrier was diagnosed with a left adrenal mass. Cushing’s syndrome was suspected based on clinical signs, including pot belly, polyuria, polydipsia, bilateral alopecia, recurrent pyoderma, and calcinosis cutis. Cushing’s syndrome was diagnosed on the basis of consistent clinical signs and repeated adrenocorticotropic hormone (ACTH) stimulation tests. In addition, tests for fractionated plasma metanephrine/normetanephrine suggested a pheochromocytoma. Unilateral adrenalectomy was performed after medical management with trilostane and phenoxybenzamine. Histopathology confirmed a diagnosis of pheochromocytoma without cortical lesions. After surgery, fractionated metanephrine/normetanephrine and the findings of low-dose dexamethasone suppression and ACTH stimulation tests were within the normal ranges without any medication. There were no clinical signs or evidence of recurrence and metastasis on thoracic and abdominal X-rays and ultrasonography up to 8 months after surgery. Conclusions Pheochromocytoma should be considered a differential diagnosis for dogs with Cushing’s syndrome with an adrenal tumor. A good prognosis can be expected with prompt diagnosis and surgical intervention.

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Original publication on DOAJ: https://doi.org/10.1186/s12917-020-2244-7