98%
921
2 minutes
20
An 8-year-old neutered male Miniature Poodle, weighing 6.7 kg, was presented with lethargy, anorexia, and single seizure episode. Neurological examination revealed bilaterally absent menace reflexes and an obtunded mental status. Magnetic resonance imaging showed a papilliform shaped mass measuring 1.2 × 1.4 × 1.3 cm in size, with a volume of 1.17 cm in the third ventricle. 3,4-dihydroxy-6-[F] fluoro-l-phenylalanine (F-FDOPA) positron emission tomography/computed tomography (PET/CT) was performed 53 days after presentation, revealing a hypermetabolic region in the intraventricular mass with mean and maximal standardized uptake values (SUV and SUV) of 1.2 and 1.42, respectively, and a tumor to normal tissue (T/N) ratio of 1.33. The mass lesion measured 1.3 × 1.4 × 1.2 cm in size, with a volume of 1.09 cm on contrast-enhanced CT images. The metabolic tumor volume (MTV) was 1.184 No evidence of brain parenchymal metastases was observed. Therefore, the dog was tentatively diagnosed with a brain tumor, which was suspected to be a choroid plexus papilloma (CPP) and chemotherapy with prednisolone and cyclophosphamide was initiated. As worsening clinical signs were observed, a second F-FDOPA PET/CT scan was performed on day 183. The SUV, SUV, and T/N ratio of the lesion were 1.49, 1.85, and 1.62, respectively. The mass lesion measured 1.0 × 1.0 × 1.3 cm in size, with a volume of 0.68 cm on contrast-enhanced CT images, whereas the MTV was increased to 2.217 cm. The dog died 186 days after the presentation. To the best of our knowledge, this is the first report describing the F-FDOPA PET/CT findings in a dog with an intraventricular brain tumor suspected of having CPP. In the present case, although the lesion size decreased on CT contrast imaging, an increase in the MTV was observed on follow-up F-FDOPA PET/CT after chemotherapy. Thus, an increase in MTV post-chemotherapy combined with the worsening clinical signs and limited survival period in dogs correlates with poor prognosis, as previously reported in a human study. This case offers significant diagnostic insights into canine intraventricular tumors within the field of veterinary medicine.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11979511 | PMC |
http://dx.doi.org/10.3389/fvets.2025.1477063 | DOI Listing |
Cureus
August 2025
Surgery and Anatomy, Hospital das Clinicas da Faculdade de Medicina de Ribeirão Preto - Universidade de São Paulo, Ribeirão Preto, BRA.
The Von Hippel-Lindau disease (VHL) is an autosomal dominant condition characterized by multiple cystic tumors in several organs, including the pancreas. The symptoms are variable, and suspicion must be raised with typical lesions, such as a hemangioblastoma of the central nervous system (CNS) or retina, associated with a renal cell carcinoma, a pheochromocytoma or multiple pancreatic cysts, besides neuroendocrine tumors (NET). The diagnosis in a patient without a family history should be suspected in case of a hemangioblastoma of the CNS and/or retina, which could also be associated with other lesions, such as pancreatic cysts and NETs.
View Article and Find Full Text PDFRadiol Case Rep
November 2025
Department of Clinical and Experimental Medicine, Foggia University School of Medicine, Viale L. Pinto 1, 71122 Foggia, Italy.
We report a rare case of breast and axillary metastases in a 75-year-old man diagnosed with prostate carcinoma. Initially, the patient presented with lower urinary tract symptoms (LUTS) and elevated prostate-specific antigen (PSA) levels. Prostate cancer was confirmed by biopsy and treated with androgen deprivation therapy (ADT) and radiotherapy.
View Article and Find Full Text PDFIndian J Endocrinol Metab
August 2025
Department of Endocrinology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Introduction: Benign adrenal tumours are frequently seen in endocrinology, affecting mostly men in middle aged. But incidentalomas are more common in the elderly. Functional adrenal tumours most commonly secrete cortisol, aldosterone and very rarely, oestrogen.
View Article and Find Full Text PDFClin Nucl Med
September 2025
Departments of Nuclear Medicine.
DOTANOC avidity is a well-known feature of head and neck paragangliomas, detected using 68Ga-DOTANOC PET/CT due to their high somatostatin receptor expression. However, other hyper vascular tumours can also show increased tracer uptake, requiring further evaluation. We present a case of DOTANOC avid soft tissue mass in the right posterior cervical triangle on 68Ga-DOTANOC PET/CT, initially suspected to be a paraganglioma.
View Article and Find Full Text PDFClin J Gastroenterol
September 2025
Department of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka, 541-8567, Japan.
Hepatic reactive lymphoid hyperplasia (RLH), also known as hepatic pseudolymphoma, is a rare benign condition that predominantly affects middle-aged-to-elderly women and is often associated with autoimmune disorders. The imaging features of hepatic RLH frequently mimic those of malignant hepatic tumors, such as hepatocellular carcinoma (HCC), cholangiocarcinoma, or metastatic liver tumors, making its diagnosis based solely on imaging modalities challenging, often leading to unnecessary surgical resection. However, the optimal diagnostic strategy for hepatic RLH remains controversial.
View Article and Find Full Text PDF