Smooth muscle hamartoma in a castrated male red deer (Cervus elaphus) in New Zealand.

Abstract

Reports of neoplasia in deer remain rare (Hill and Staples 1999), despite the conviction that as deer farming became more common, a greater number of pathological processes, including tumours, would be recognised in deer (Pérez et al. 1998). Skin tumours are among the most common neoplasms reported in red deer (Cervus elaphus) and are usually papillomavirus-associated dermal fibropapillomas and papillomas (Erdélyi et al. 2009; Vaatstra et al. 2014; Garcês et al. 2020). Additional reports of cutaneous and subcutaneous tumours in red deer include malignant schwannoma and dermal malignant melanoma (Pérez et al. 1998; Scandrett and Wobeser 2004). In related deer species, subcutaneous dermoid cysts have been described in caribou (Rangifer tarandus) (Wobeser et al. 2009) and cutaneous fibromas in predominantly male white-tailed deer (Odocoileus virginianus) (Berry 1925; Friend 1967; Sundberg and Nielsen 1982). A 17-year-old, 187-kg, castrated, male red deer was examined at the Massey University (Palmerston North, NZ) deer unit on 27 January 2022, with a spherical, deep dermal mass about 3 cm in diameter, raised above the surrounding skin level. The mass was identified on the upper left neck about 7 cm below the base of the left ear, at the angle of the mandible (Figure 1a). At re-examination 1 week later, the mass had almost doubled in size. The mass appeared discrete from the underlying tissue, so a decision was made to remove it that day, while the size of the mass was still manageable. The deer had been abandoned by its mother after dystocia and was hand reared. It had been castrated at a very young age and has resided at the deer unit ever since and been in good health. The deer had been paddocked alone most of its life, excluding short periods when it was paddocked with other deer that had undergone surgical or medical procedures and needed to be separated from the main herd. The animal was placed in a Heenan hydraulic crush (Farmquip Ltd., Napier, NZ) and lightly restrained during the surgery. The sides of the crush were manipulated to give good access to the surgery site. The deer was sedated with 0.2 mg/kg of 5% xylazine (Phoenix Pharm Distributors Ltd., Auckland, NZ) given IM into the neck, and a local anaesthetic block using SC 2% lignocaine (Nopaine 2%; Phoenix Pharm Distributors Ltd.) was placed around the mass. The site was surgically scrubbed and prepared while the local anaesthetic block took effect. An elliptical skin incision was made, and the mass was removed via blunt dissection, with a 1-cm margin (Figure 1b). The wound was closed using simple interrupted suture pattern with 4 metric PDS absorbable suture (Ethicon, Somerville, NJ, USA). Bleeding was minimal and there were no complications during the procedure, although the deer lay down once the crush was opened. The sedation was reversed using 0.2 mg/kg yohimbine IV (Reversal Injection; Phoenix Pharm Distributors Ltd.). Post-operative analgesia was administered using 0.5 mg/kg SC meloxicam (Metacam; Boehringer Ingelheim (NZ) Ltd., Auckland, NZ). No antibiotics were given. The excised mass was placed in 10% buffered formalin and submitted for histology to Massey University (Palmerston North, NZ) Pathobiology Department. The deer recovered well from the surgery. There was slight post-surgical swelling on day 5, which rapidly improved, with no swelling evident 2 weeks after surgery. The mass was sectioned into four and fixed in 10% neutral buffered formalin for 48 hours, processed and embedded into paraffin blocks. Routine H&E stains were performed on multiple 5-μm sections of tissue cut from the formalin-fixed, paraffin-embedded blocks. One section of the mass was additionally stained with Masson’s trichrome and phosphotungstic acid haematoxylin (PTAH). Histological examination revealed an unencapsulated but generally well demarcated deep dermal proliferation of muscle bundles below the overlying haired skin. Muscle bundles were generally of small to medium uniform size, well differentiated, and surrounded and separated by an extensive collagen stroma (Figures 2A and B), confirmed by Masson’s trichrome staining (Figures 2C and D). PTAH staining did not reveal the presence of obvious cross-striations