Recurrent adenocarcinoma in a ferret

A 4.5-year-old, neutered male ferret with a history of recurrent adenocarcinoma in the preputial region was given 2 radiation treatment courses designed to control the rapidly growing neoplasm. The tumor regressed completely after the first 3.5-week course of therapy. The ferret remained clinically disease-free for 4 months, at which time small masses were noticed in the inguinal area and the original tumor site. A second course of therapy was administered, which again resulted in complete clinical regression of the neoplasm. However, the duration of remission was brief. Local recurrence and abdominal metastasis were observed within 2 months of the completion of therapy.     

Coccygeal chordoma in a dog.

A 4-cm diameter spherical mass was removed from the region of the second coccygeal vertebra of a 6-year-old female Doberman Pinscher dog. The mass had been present for 7 months and was described as multilobular and smooth. Histologically, the neoplasm consisted of small spindle-shaped cells surrounding lobules of large vacuolated polygonal cells. Mucin was present within most lobules. The large polygonal cells stained positively with antibodies against vimentin, cytokeratin, and S-100 protein. Although the spindle-shaped cells stained positively with antibodies against vimentin, they only occasionally contained cytokeratin. The histology and immunohistochemistry are consistent with that reported for chordoma. Although 4 chordomas have previously been reported in dogs, this is the first case in which immunohistochemistry has been used to support the histological diagnosis. Neither recurrence nor metastasis was reported 10 months after surgical excision.     

Simultaneous hyperplasia, metaplasia, and neoplasia in an 8 year-old boxer dog: a case report

Generalized gingiva hyperplasia and multiple gingival masses were observed in an 8 year-old boxer dog. The masses were removed surgically. Three of them were biopsied. Microscopic examination was reported as fibrous gingival hyperplasia, fibrous epulis with osseous metaplasia, and mast cell tumor. Twenty-two months following surgery, moderate generalized gingival hyperplasia was present, with no clinical evidence of regrowth of the neoplasms.     

A case of coccygeal chondroid chordoma in a cat: morphological and immunohistochemical features

In August 2007, a 4-year-old, intact, female Domestic Shorthair cat was examined for a mass on the tip of the tail. Histological examination performed after apical caudectomy revealed a neoplasm affecting the distal part of the last coccygeal vertebra. The neoplasm consisted of lobules of physaliferous cells surrounding cartilaginous tissue and a central core of trabecular bone. A diagnosis of chondroid chordoma was made based on histomorphological features and immunohistochemical results. Chondroid chordoma has been previously reported in humans, rats, ferrets, and mink. To the authors' knowledge, chondroid chordoma has not been reported in cats. Neither recurrence nor metastasis was reported 7 months after surgery.     

Malignant pilomatrixoma in an old english sheepdog

A tumor of hair follicle origin with histological features characteristic of a benign pilomatrixoma was removed surgically from the tail of a five year old male Old English Sheepdog. The tumor recurred locally two months after surgery, and 14 months later metastatic involvement of the lungs became clinically evident. This aggressive local growth and metastasis indicate that canine pilomatrixoma, although normally considered benign, may have malignant potential which is difficult to predict histologically.     

Pacemaker implantation in a ferret (Mustela putorius furo) with third-degree atrioventricular block.

A 7.5-year-old castrated male ferret (Mustela putorius furo) was diagnosed with third-degree atrioventricular (AV) block. A monopolar epicardial pacemaker system was implanted, resulting in a regular, paced cardiac rhythm with third-degree AV block at 140 beats per minute. Over the next 2 months, the ferret developed anorexia, interstitial pneumonia, intermittent diarrhea, and hind-limb weakness and had a slow and progressive recovery. The ferret developed clinical signs of congestive heart failure 4 months after the surgery, resulting in its death 3 weeks later. Necropsy results attributed the death to cardiac failure due to extensive myocardial mineralization. To the authors' knowledge this is the first published report of surgical report of surgical pacemaker implantation in a ferret.     

RADIOGRAPHIC, COMPUTED TOMOGRAPHIC AND HISTOPATHOLOGIC APPEARANCE OF A PRESUMED SPINAL CHORDOMA IN A DOG

A 4-year-old Labrador Retriever presented for urinary incontinence and constipation of 2 weeks duration. There was a tender abdomen, lumbar pain and conscious proprioceptive deficits in both pelvic limbs. Depressed pelvic limb reflexes were present consistent with a lower motor neuron lesion. In radiographs of the lumbar spine there was narrowing of the intervertebral disc space at L5-L6 with irregular, multifocal areas of mineralized opacities dorsal to the intervertebral disc space, presumably within the vertebral canal. On computed tomography, an intramedullary, partially mineralized mass was identified in the spinal cord at the level of caudal L5 through cranial L6. At necropsy there was a four-centimeter enlarged, irregular segment of spinal cord at the level of L5-L6. When sectioned, the spinal cord bad a mineralized texture. Histologically there were variable sized cells that were stellate in appearance with vacuolated cytoplasm (physaliferous cells) and mucinous background consistent with a chordoma. Chordoma is a rare, skeletal neoplasm that originates from mesoderm-derived notochord and has been reported in humans and animals. Extraskeletal development of a chordoma within the spinal cord is a rare manifestation of this neoplasm. However, based on other reports in dogs, solitary extraskeletal locations of chordomas may be the typical expression of this neoplasm in the dog. Differentiation of similar histologically appearing tumors, such as a parachordoma or myxoid chondrosarcoma, will require immunohistochemical characterization of these tumors in veterinary patients.     

Rostral maxillectomy and radiation therapy to manage squamous cell carcinoma in a ferret.

A 4-year-old, male, neutered ferret presented with squamous cell carcinoma of the right maxillary region associated with the tissues surrounding the upper canine tooth. A rostral maxillectomy was performed to excise the mass. Histopathologic examination showed questionable margins of tumor removal. Approximately 2 months after surgery, the ferret received a course of radiation therapy and is currently being monitored for tumor regrowth.     

Hyperinsulinism and hypoglycemia associated with pancreatic islet cell tumor in a ferret

Pancreatic islet cell tumor causing hypoglycemia and hyperinsulinism was diagnosed in a ferret with a history of progressive neurologic dysfunction. The diagnosis was suspected by the findings of hypoglycemia when the ferret was not fed, hyperinsulinism, and an amended insulin/glucose ratio approaching infinity. A focal pancreatic mass was removed by partial pancreatectomy, resulting in euglycemia and the resolution of clinical signs. Histologic diagnosis of the pancreatic mass was consistent with islet cell tumor (insulinoma). The ferret remained clinically normal for 8 months, but died after recurring episodes of hyperglycemia and glucosuria. Necropsy revealed no evidence of islet cell neoplasia involving the pancreas or other structures.     

A histomorphologic and immunohistochemical study of chordoma in twenty ferrets (Mustela putorius furo).

The histomorphologic and immunohistochemical features of chordoma in 20 ferrets were evaluated. The mean age was 3.4 years, and, in the cases for which sex was known, females (n = 10) outnumbered males (n = 5) two to one. All 20 tumors occurred on the tip of the tail. Nineteen of 20 tumors (95%) were composed of three tissue components, often arranged concentrically with lobules of physaliferous cells at the periphery, trabecular bone in the center, and cartilage in between. The bone often contained marrow and hematopoietic cells. One tumor lacked chondromatous or osseous tissue. Immunohistochemical results were consistent with previous studies of chordoma. All 20 tumors (100%) were positive for keratin and vimentin intermediate filaments; 15 (75%) were positive for S-100 protein; and 17 (85%) were positive for neuron specific enolase. This neoplasm shares morphologic and immunohistochemical features with "classic," as well as chondroid chordoma, of human beings, making it a potential animal model.     

Thoracic vertebral chordoma in a domestic ferret (Mustela putorius furo).

A castrated adult male 1.0-kg domestic ferret (Mustela putorius furo) was referred for evaluation of a mass of >5 mo duration that was associated with the thoracic spine. The ferret had motor dysfunction and no conscious proprioception or pain perception in either hind limb. Segmental reflexes were present. Survey radiography, myelography, and magnetic resonance imaging showed a mass involving the ninth and 10 thoracic vertebrae and compressing the spinal cord. Decompressive surgery was performed, but clinical signs persisted. A diagnosis of chordoma was made using histopathology and immunohistochemistry. This is the first reported case of a chordoma involving the thoracic vertebrae in a domestic ferret.     

Chordoma in a cat

A chordoma within the deep musculature adjacent to C3 and C4 was excised from a 14-year-old castrated domestic cat. Metastatic chordoma developed in a prescapular lymph node 10 months later. At necropsy 11 months after complete excision of the primary tumor, metastases were found in both retropharyngeal lymph nodes.     

Malignant seminoma with gross metastases in a dog

A 10-year-old male crossbred dog developed a non-painful unilateral testicular swelling; the other gonad was reduced in size. Both gonads were removed surgically; the larger contained a diffuse seminoma, the smaller atrophic testis contained an interstitial cell adenoma and several intratubular seminomas. Six months after being castrated the dog developed palpable intraabdominal masses. Necropsy revealed gross metastatic malignant seminoma in para-aortic lymph nodes. No histological features were identified to correlate with the malignant behaviour of this usually benign tumour.     

Adjuvant Electrochemotherapy Increases Local Control in a Recurring Equine Anal Melanoma

A 25-year-old gelding sport horse was referred for the treatment of recurring bilateral anal amelanotic melanoma. On physical examination, the horse presented bilateral poorly delimited perianal masses that recurred 2 months after surgical excision. The owner elected the lesions to be treated with surgery combined with electrochemotherapy using the drug cisplatin. The two masses were removed, and the surgical bed was treated with electrochemotherapy. A second session was performed 3 weeks later. The horse remained disease-free for 5 months and then experienced a marginal recurrence in one side. The nodule was re-treated, and the horse remained disease-free for 2 additional months, when it died of abdominal metastases. Electrochemotherapy can be added to the current strategies to palliate recurrent melanomas in horses.     

Chondrosarcoma Associated With the Appendicular Skeleton of 2 Domestic Ferrets

A 5-year-old male neutered ferret (Mustela putorius) and a 2-year-old male neutered ferret were evaluated for fast growing immobile swellings involving the left hock and the right scapula, respectively. In both cases, serum chemistry was unremarkable and a complete blood count demonstrated mild anemia. In case 1, radiographic evaluation demonstrated increased soft tissue density in the region of the distal tibia and fibular tarsal bone. A fine-needle aspirate demonstrated atypical mesenchymal cells, and an incisional biopsy revealed irregular partly mineralized proliferations of cartilage consistent with chondrosarcoma. Computed tomography was performed, demonstrating attachment of the mass to the distolateral tibial epiphysis. A limb-sparing surgery was performed; however, 5 months following resection local reoccurrence was noted. At 18 months, the ferret underwent a left hind limb amputation. No sign of metastatic disease was reported at 27 months. In case 2, radiographic evaluation demonstrated a poorly organized mineralized soft tissue mass extending from the right acromion to the area surrounding the neck of the scapula. Microscopic evaluation of an incisional biopsy revealed a chondrosarcoma. A forequarter amputation was performed. The ferret died 4 years later with no evidence of local recurrence or the development of metastatic disease. These 2 cases represent the first reports of chondrosarcoma in the appendicular skeleton of 2 ferrets. Based on these 2 cases, local recurrence may be expected unless adequate surgical margins are achieved. The metastatic potential of chondrosarcoma in this species appears to be low.     

Surgical treatment of epulides in dogs: 25 cases (1974-1984)

Epulides were diagnosed and surgically removed in 25 dogs. Histologic examination of the epulides indicated that 40% (10/25) were acanthomatous, 32% (8/25) were ossifying, and 28% (7/25) were fibromatous. Recurrence of the tumor directly resulted in the death of 2 dogs. One of these dogs died of malnutrition 13 months after removal of an ossifying epulis, and regrowth of an acanthomatous epulis that was not resected completely resulted in malnutrition and death in another dog 6 months after surgery. Malignant transformation was observed in a third dog 6 months after removal of an ossifying epulis when an osteosarcoma developed where the epulis had been removed. The range of survival was 6 to 134 months, mean survival time was 43.1 months, median survival time was 49 months, and 1-year survival rate was 92%. Satisfactory long-term tumor control was achieved by aggressive surgical treatment of epulides.     

Adenocarcinoma of the gland of the third eyelid in seven dogs

Adenocarcinoma of the gland of the third eyelid developed as a smooth, pink nodule on the bulbar aspect of the third eyelid of seven 10- to 16-year-old dogs. Tumors recurred in 4 dogs. One dog, which initially had the most infiltrative-appearing tumor among those studied, was euthanatized 7 months after the first excision, because of extensive local recurrence and suspected metastasis. Tumors did not recur after removal of the entire third eyelid as the initial or follow-up procedure. We recommend removal of the entire third eyelid to prevent local recurrence of the tumor.     

Canine ocular gliomas: a retrospective study

Objective The purpose of this paper is to classify glial tumors observed in the canine retina and optic nerve, describe the histopathological features and provide prognostic information on these neoplasms. Methods The database of the Comparative Ocular Pathology Laboratory of Wisconsin (COPLOW) was searched to collect canine glioma cases. Clinical and follow-up information was gathered from submission forms and an extensive follow-up survey. Slides were reviewed to describe the histopathological characteristics of the neoplasm and classify them. Immunohistochemistry for Glial Fibrillary Acidic Protein (GFAP) was performed in all cases. Results 18 canine glioma cases were found in the COPLOW database. There was no breed or gender predilection. The mean age was 9.33 ± 3.67 years. Follow-up information was available for 12 dogs, 8 of which were dead at the time of most recent contact, with a survival time ranging from 0 days (globes received after euthanasia) up to 20 months post-enucleation. In 6 of the 8 dogs that had died during this stud), tumor extended to the margin where the optic nerve had been sectioned. Light microscopic examination of the optic nerve of the affected eyes of four dogs that were still alive during this study revealed no tumor at this surgical margin. One neoplasm was classified as low-grade astrocytoma, 5 tumors as medium-grade astrocytoma, 11 tumors as high grade-astrocytoma and 1 tumor as oligodendroglioma. GFAP was positive in all but two tumors. Conclusion Retinal and optic nerve gliomas may be considered as differential diagnoses of intraocular and orbital masses. The metastatic potential appears to be low, but ascending invasion into the ventral aspect of the brain is possible.