Male pseudohermaphroditism in a cat

A seven-month-old male pedigree cat was brought to the Norwegian College of Veterinary Medicine for routine castration. Visual examination of the external genitalia revealed a wide genital cleft with non-fused bilaterally located testicular pouches. A large clitoris, which was penis-like with small penile spines, was seen protruding dorsally from the ventral commissure of the genital cleft. During an exploratory coeliotomy, no intra-abdominal genital structures of müllerian origin were found. The skin pouches on either side of the vulvar cleft were incised and grossly normal testicles were removed. Histology of the removed gonads showed no or very sparse spermatogenesis. The chromosomal sex was determined by karyotyping to be a normal male 38XY. Based on these findings, the diagnosis of male pseudohermaphroditism was made. The aetlology of the condition in this cat was not determined.     

Male pseudohermaphroditism in a Labrador Retriever,and a review of mammalian sexual differentiation

CASE HISTORY: An 8-month-old Labrador Retriever was referred with a history of ambiguous external genitalia.

CLINICAL FINDINGS AND TREATMENT: Clitoromegaly within apparent vulval folds, and an adjacent subcutaneous mass were noticed on external examination. An intra-abdominal testicle, with epididymis and suspected vas deferens ducts, was found during exploratory celiotomy. Incision over the subcutaneous mass revealed the accompanying testicle. Clitoridectomy was performed and an os clitoris removed. Normal juvenile testes were diagnosed on histology of the gonads. Chromosomal studies revealed a normal 78, XY male chromosomal constitution. Due to the combination of a male karyotype (78, XY), the presence of testicular tissue in the gonads, and the appearance of the external genitalia, a diagnosis of male pseudohermaphroditism (MPH) was made.

CLINICAL RELEVANCE: This case presents the first report of MPH in a Labrador Retriever, and highlights the diagnostic steps recommended when confronted with a dog with ambiguous external genitalia.     

Male pseudohermaphroditism in a Labrador Retriever, and a review of mammalian sexual differentiation

CASE HISTORY: An 8-month-old Labrador Retriever was referred with a history of ambiguous external genitalia. CLINICAL FINDINGS AND TREATMENT: Clitoromegaly within apparent vulval folds, and an adjacent subcutaneous mass were noticed on external examination. An intra-abdominal testicle, with epididymis and suspected vas deferens ducts, was found during exploratory celiotomy. Incision over the subcutaneous mass revealed the accompanying testicle. Clitoridectomy was performed and an os clitoris removed. Normal juvenile testes were diagnosed on histology of the gonads. Chromosomal studies revealed a normal 78, XY male chromosomal constitution. Due to the combination of a male karyotype (78, XY), the presence of testicular tissue in the gonads, and the appearance of the external genitalia, a diagnosis of male pseudohermaphroditism (MPH) was made. CLINICAL RELEVANCE: This case presents the first report of MPH in a Labrador Retriever, and highlights the diagnostic steps recommended when confronted with a dog with ambiguous external genitalia.     

Bovine viral diarrhea virus type 2-induced meningoencephalitis in a heifer

The brain from a 15-month-old, black female Angus, with a 48-hour history of central nervous system disease, was submitted to the Oklahoma Animal Disease Diagnostic Laboratory. Microscopic findings consisted of acute, multifocal meningoencephalitis, with neuronal degeneration and necrosis and gliosis. Viral isolation yielded noncytopathic bovine viral diarrhea virus (BVDV). Virus genotyping classified the virus as BVDV type 2. Immunohistochemical labeling for BVDV antigens with BVD MAb 3.12F1 clone was prominent in the cytoplasm of neurons, glial cells, ependymal epithelium, perivascular macrophages and spindle cells, smooth muscle cells, and intravascular monocytes of the cerebrum and brain stem. Laboratory results support that tissue alterations occurred as a result of BVDV type 2 infection. In the absence of other clinical signs related to BVDV infection and using the microscopic and laboratory evidence presented, we propose that the BVDV type 2 isolated from this case may represent a neurovirulent strain of the virus. To the best of our knowledge, this is the first report of brain lesions and neuronal viral antigen localization in BVDV genotype 2 viral infection, acquired either congenitally or postnatally.     

Myofibroblastoma of the neck in a heifer

A 1.5-year-old Holstein heifer had a subcutaneous tumor mass (20 cm diameter) on the ventral portion of the neck, and the tumor was diagnosed as a locally invasive myofibroblastoma. It consisted of moderately cellular fibrous tissue, and the interlobular septum of the thymus was invaded by tumor cells. The neoplastic cells were positive for alpha smooth muscle actin and vimentin, but not for desmin. Electron microscopy disclosed the presence of moderately developed rough endoplasmic reticulum and microfilaments with focal densities.     

Testicular feminization in a cat

Testicular feminization, caused by an inherited defect of the androgen receptor, was diagnosed in a domestic cat. Individuals affected with this syndrome are genetic males that have testes but fail to undergo masculinization because the internal and external genitalia cannot respond to androgens. The affected cat had the external appearance of a sexually normal female, but during surgery for ovariohysterectomy, only 2 abdominal gonads were found. Müllerian (uterus) or wolffian (epididymides) derivatives were not present. Only testicular tissue was found in histologic sections of the gonad. A normal male chromosome constitution (38,XY) was found in karyotypes prepared from lymphocyte cultures. High affinity binding of dihydrotestosterone was undetectable in fibroblasts cultured from genital skin of the affected cat, indicating that the cytosolic androgen receptor was nonfunctional. Pedigree analysis indicates that this is an X-linked disorder in cats, as it is in other mammals. Accurate diagnosis and genetic counseling are advocated to reduce the prevalence of the disorder.     

Congenital melanoma in a heifer

The clinical, intra-operative and pathological findings taken from a case of melanoma in a 9-month-old female Holstein Friesian heifer are reported here. The tumor, hanging on the right side of the thorax, was present at birth and increased in size with time. Muscular invasion by tumoral tissue was detected during surgery. Histological and cytological data indicated that the neoplasia (melanocytoma) was benign but the prognosis, related to the invasiveness of this neoplasm, was considered reserved. Melanoma is a rare tumor in cattle, often congenital, although already reported in pigs and in horses.     

Autosomal trisomy in a heifer

A malformed Ayrshire heifer had one additional autosome in all the lymphocyte metaphases studied. Chromosome banding techniques showed the karyotype of the calf to be 2n = 61, XX, +24.Slight prognathia of the lower jaw and peculiar abbrevations in the structure of the genitals were the most apparent anomalies, in addition to heart abnormalities, a poorly-closed urachus and slow growth rate.     

Melanosis in a Holstein heifer

A case of Melanosis in a Holstein heifer is described in this report. Many of the visceral organs, diaphragm and skeletal muscles have got dark-brown to black and diffuse pigmentation in different diameters on their surfaces and cuts. Microscopically, brown to black coloured pigment containing cells were detected in the heart, lung, liver, spleen and muscle tissues. After depigmentation process, it was seen that the normal histological structure of the organ disappeared in these pigmented region. There were large, vesicular and macrophage-like cells with small nuclei. In immunohistochemical staining, HMB45 was strongly positive in many tissues.     

Male pseudohermaphroditism, cryptorchism, and Sertoli cell neoplasia in three miniature Schnauzers.

A syndrome of male pseudohermaphroditism, cryptorchidism, and testicular neoplasia was diagnosed in 3 Miniature Schnauzers. The dogs had clinical signs of hyperestrogenism and were either unilateral or bilateral cryptorchids. At surgery, it was discovered that the dogs were male pseudohermaphrodites, having intra-abdominal testes containing Sertoli cell tumors and uteri that had undergone endometrial cystic hyperplasia.