Pelger-Huët anomaly in two related mixed-breed dogs

• Published in: Journal of veterinary diagnostic investigation 2011-07, Vol.23 (4), p.863-865
• Main Authors: Vale, André M., Tomaz, Loreno R., Sousa, Rejane S., Soto-Blanco, Benito
• Format: Article
• Language: English
• Subjects: Animals; Dog Diseases - genetics; Dog Diseases - pathology; Dogs; Female; Genetic Predisposition to Disease; Male; Pelger-Huet Anomaly - diagnosis; Pelger-Huet Anomaly - veterinary
• ISSN: 1040-6387; 1943-4936
• DOI: 10.1177/1040638711407891

A 6-month-old male mixed-breed dog weighing 12.6 kg weight was presented for evaluation of a subcutaneous nodule on the dorsum. The medical history indicated trimethoprim–sulfamethoxazole treatment 2 months before presentation at the veterinary hospital. The initial complete blood cell count (CBC) results included an apparent left shift. Microscopic examination of a blood smear (Panoptic stain) revealed granulocytes with hyposegmented nuclei, coarse mature chromatin, and a nuclear shape varying from round to bilobed (pince-nez) or slightly indented. Occasional neutrophils and eosinophils had typical segmentation of nuclei. Abnormalities were not present in limited serum biochemical testing. The CBC was repeated 17 and 120 days later, and the results were similar to those observed in the first examination. The parents of the patient were located, and a CBC was performed on both animals. The dam, but not the sire, had nuclear hyposegmentation of granulocytes, confirming the diagnosis of Pelger-Huët anomaly.