Treatment of subcutaneous lipomas in the horse

Molly T. Kearney Carlson College of Veterinary Medicine, Oregon State University, Corvallis, OR

Search for other papers by Molly T. Kearney in
Current site
Google Scholar
PubMed
Close
 BVSc, MSc
and
J. Lacy Kamm Carlson College of Veterinary Medicine, Oregon State University, Corvallis, OR

Search for other papers by J. Lacy Kamm in
Current site
Google Scholar
PubMed
Close
 DVM, PhD, DACVS

Abstract

OBJECTIVE

To describe the treatment of subcutaneous lipomas in the horse.

ANIMALS

3 horses.

CLINICAL PRESENTATION

The horses were aged 1 to 2 years old, with lipoma of the abdomen, prepuce, and tarsus.

RESULTS

All cases had surgical removal of the masses under general anesthesia. Recurrence of an invasive abdominal lipoma occurred in case 1 at the exit site of a passive drain. The recurrence was treated unsuccessfully with injectable cisplatin, and a second revision surgery with the use of an active drain resulted in resolution. In case 2, complete resection of an encapsulated lipoma of the lateral prepuce was successful with no recurrence. In case 3, incomplete resection of a tarsal lipoma resulted in a sound horse, with no further growth. Histopathologic analysis revealed that all masses were composed of well-differentiated adipocytes with no evidence of malignancy.

CLINICAL RELEVANCE

Subcutaneous lipomas are relatively rare and affect horses primarily ≤ 2 years of age. They are benign, although their presence can be deleterious due to invasion of local structures or the impact on normal locomotion. The margins of invasive tumors are difficult to identify due to their integration with normal tissue. Incomplete removal may allow for mass recurrence. Active suctions drains are beneficial if dead space is a concern.

Abstract

OBJECTIVE

To describe the treatment of subcutaneous lipomas in the horse.

ANIMALS

3 horses.

CLINICAL PRESENTATION

The horses were aged 1 to 2 years old, with lipoma of the abdomen, prepuce, and tarsus.

RESULTS

All cases had surgical removal of the masses under general anesthesia. Recurrence of an invasive abdominal lipoma occurred in case 1 at the exit site of a passive drain. The recurrence was treated unsuccessfully with injectable cisplatin, and a second revision surgery with the use of an active drain resulted in resolution. In case 2, complete resection of an encapsulated lipoma of the lateral prepuce was successful with no recurrence. In case 3, incomplete resection of a tarsal lipoma resulted in a sound horse, with no further growth. Histopathologic analysis revealed that all masses were composed of well-differentiated adipocytes with no evidence of malignancy.

CLINICAL RELEVANCE

Subcutaneous lipomas are relatively rare and affect horses primarily ≤ 2 years of age. They are benign, although their presence can be deleterious due to invasion of local structures or the impact on normal locomotion. The margins of invasive tumors are difficult to identify due to their integration with normal tissue. Incomplete removal may allow for mass recurrence. Active suctions drains are beneficial if dead space is a concern.

Introduction

Lipomas are neoplastic masses of mesenchymal origin composed of well-differentiated adipocytes. Subcutaneous lipomas are usually solitary, fluctuant to firm, benign masses in all domestic animals.1 Complete excision is the mainstay of treatment.2 Subcutaneous lipomas of the horse can be classified as encapsulated or infiltrative.3,4 Infiltrative lipomas, while less common in horses, can show extensive involvement of the soft tissues, including adjacent subcutaneous adipose, muscle, nerve, and synovium. Subcutaneous lipomas are relatively rare and primarily found most commonly in young horses ≤ 2 years of age, which is in stark contrast to the more common mesenteric lipoma, which is found in older horses.49 Subcutaneous lipomas typically occur on the limbs, thorax, and abdominal wall. Equine lipomas have also been reported in other areas, such as the pericardium, myocardium, meninges, and maxillary sinus.3,1012 While subcutaneous lipomas are undesirable in cosmetic appearance, they are often asymptomatic and clinically unremarkable. However, clinical signs may develop due to their insidious growth and location causing deleterious effects.13,14

There are limited case descriptions and treatments of equine subcutaneous lipomas. Three cases were euthanized prior to or during surgery because of the difficulty or consequences of resecting infiltrative lipomas of the stifle joint, abdominal wall, and caudal antebrachium.57 Three cases resolved without recurrence following surgical resection, including 2 completely resected encapsulated thoracic masses and an incompletely resected infiltrative mass of the dorsal carpus that involved the common digital extensor tendon sheath.5,7 Recurrence was seen postoperatively in 2 cases of infiltrative lipomas, both following resection of thoracic masses; in 1 case recurrence was observed after a second more aggressive surgery, after which the owner decided not to pursue further treatment, while in the other case the second surgical procedure resulted in complete resolution.8,9 Recurrence is also seen in other species, as postoperative recurrence of infiltrative lipomas in dogs and humans is reported as 36% to 50% and 3% to 62%, respectively.15,16 In both species, complete excision of an infiltrative lipoma is often limited by the dimensions of the lipoma, which also appears to be the case in horses. These reports illustrate the difficulty in resecting infiltrative subcutaneous lipomas. Our case series serves to both consolidate the previous literature and to discuss our treatment of both encapsulated and infiltrative lipomas. Further, we illustrate the use of chemotherapeutics and active drains to assist in the treatment of these masses.

Methods

Patient description

Over a 3-year period, 3 cases of subcutaneous lipomas presented to a referral facility for surgical resection because of concern for the masses impacting performance due to restriction of movement; surgical resection of lipomas is considered the treatment of choice. All horses had ultrasonography (MyLab Seven; Esaote SPA) performed prior to surgery to determine the local extent of the masses and aid in surgical planning. An abdominal and linear transducer was used to determine mass consistency and anatomic location within tissues and assist in establishing mass dimensions. Each mass was found in a location with normal adipose tissue and appeared confluent with the adjacent adipose tissue. Lipomas were not biopsied prior to surgery, as the results would not have altered the course of treatment.

Surgical procedure

A complete physical exam was performed prior to surgery. Procaine penicillin (22,000 IU/kg, IM, q 12 h), gentamicin (6.6 mg/kg, IV, q 24 h), and phenylbutazone (2.2 mg/kg, IV, q 12 h) were administered immediately prior to induction for general anesthesia and for the following 24 hours. Surgical resection was performed under general anesthesia maintained under isoflurane inhalant. A linear or elliptical incision was made in the skin depending on the amount of tension at the skin margin to allow primary closure. The mass was bluntly and sharply dissected away from the epidermal layers. A 2- to 3-cm margin was taken from the grossly defined edges of the lipoma, and 1 fascial plane was taken from the deep margin when available. A further description of variation between surgeries is discussed in the Results section. All surgical sites were closed in 2 layers. The subcutaneous tissue was closed with a simple continuous pattern with 2-0 poliglecaprone suture to minimize dead space. The skin was closed with 0 nylon in a simple interrupted suture pattern and, when necessary due to tension, a near-far-far-near suture pattern. All horses recovered from surgery without event. Horses were discharged the day after surgery.

Histopathology

The masses were submitted for histological analysis. Analysis revealed that all masses were composed of well-differentiated adipocytes with no evidence of malignancy. A lipoma with fat necrosis was found in case 1.

Follow-up

The horses were followed for at least 12 months after surgery. In-person examinations were performed at 3 to 6 months following the final procedure. Discussions with the owner or digital images were used as follow-up after 6 months postoperatively. All owners provided explicit verbal consent for the use of their horse’s data for scientific analysis.

Results

Case 1

A yearling Warmblood gelding presented with a large mass on the left flank. No prior treatment had been attempted. Ultrasound was performed and showed that the mass extended from the subcutaneous tissue, infiltrating the external abdominal oblique muscle. The internal abdominal oblique and transversus abdominus muscles were unaffected. The mass was hypoechogenic and of similar echogenicity to the surrounding adipose tissue. The mass was resected by use of a 40-cm-long linear incision with the horse in right lateral recumbency and under general anesthesia. The skin overlying the mass was not removed in its entirety due to the size of the mass and desire to close the site primarily. The epidermis was dissected from the subcutaneous tissue by use of blunt and sharp dissection with Metzenbaum scissors. Differentiation of the mass from the surrounding normal subcutaneous tissue was not possible grossly, as the mass did not appear encapsulated. Upon removal, the mass measured 40 X 20 X 8 cm (Figure 1). A penrose drain was placed and exited the abdomen at the cranioventral border of the incision. The drain was removed 5 days after surgery.

Figure 1
Figure 1

Gross appearance of the resected mass in case 1.

Citation: Journal of the American Veterinary Medical Association 2024; 10.2460/javma.24.02.0146

Six weeks after surgery, a mass was noted at the exit site of the previously located drain, approximately 10 cm cranioventral to the incision (Figure 2). This mass was treated with 1 mg/cm3 injectable cisplatin mixed with sterile sesame oil on 3 occasions, at 3-week intervals. The lipoma continued to grow in the face of local chemotherapy, and subsequently the horse returned to surgery. The second mass was resected with 3-cm gross margins, at which time an active suction drain (Jackson-Pratt drain with grenade canister) was placed. The removed mass measured 12 X 5 X 2 cm. After the second surgery, the horse returned to normal athleticism as a performance horse. No recurrence was reported at 24 months after surgery.

Figure 2
Figure 2

Gross appearance of the recurrence of the mass in case 1. The area of recurrence is shown with a circle.

Citation: Journal of the American Veterinary Medical Association 2024; 10.2460/javma.24.02.0146

Case 2

A 2-year-old Standardbred gelding presented with a mass of the lateral external prepuce. Ultrasonography showed a capsule present around the mass. The 30 X 25 X 3-cm mass was resected by use of a 35-cm-long incision with the horse in dorsal recumbency and under general anesthesia. Visually upon resection, the mass appeared grossly to be encapsulated, and 3-cm margins in the surrounding adipose tissue were removed. Histological analysis confirmed the presence of a fibrous capsule. An active suction drain (Jackson-Pratt drain with grenade canister) was placed exiting cranial to the prepuce. The drain was removed 5 days after surgery. No recurrence was seen at the surgery site or drain site at 12 months after surgery. The horse had no complications and went on to race.

Case 3

A yearling Thoroughbred filly presented with a mass of the dorsolateral tarsus of the right hindlimb that appeared on ultrasound to be adherent to the joint capsule of the tarsocrural joint (Figure 3). The joint capsule appeared smooth, and the mass did not appear to be invading the synovial space. The mass extended from the level of the joint capsule dorsally and wrapped around the long digital extensor tendon. It did not appear encapsulated on ultrasound. The filly was sound. The mass was incompletely resected by use of a 15-cm-long incision over the dorsal aspect of the joint with the horse in dorsal recumbency and under general anesthesia. The mass measured 15 X 8 X 2 cm. The joint capsule was not resected, and as seen grossly during surgery, there was adipose adhered to the capsule. The priority in this case was for the filly to remain sound and to not compromise the joint capsule and extensor tendon rather than achieve complete resection. In the 24-month follow-up period, the mass did not grow further and the horse remained sound (Figure 4) and was used as a broodmare.

Figure 3
Figure 3

Transverse ultrasonographic image of the mass surrounding the common digital extensor tendon (arrowhead) in case 3.

Citation: Journal of the American Veterinary Medical Association 2024; 10.2460/javma.24.02.0146

Figure 4
Figure 4

Gross appearance of the tarsocrural mass 4 weeks after resection in case 3.

Citation: Journal of the American Veterinary Medical Association 2024; 10.2460/javma.24.02.0146

Discussion

Subcutaneous lipomas occur in young horses, most commonly ≤ 2 years of age, and appear to be hyperplasia of normal adipose tissue, with no tendency to metastasize.17 Despite being classified as histologically benign, subcutaneous lipomas can grow insidiously to large sizes and be invasive to local tissues. Gross identification of tumor margin is extremely difficult in locations with significant subcutaneous adipose.

The behavior of subcutaneous lipomas in horses differs from those in other species. These tumors are consistently found in younger horses in comparison to humans and dogs, in which they appear later in life.2,18 Further, the tumors appear to stop growing as the horse enters adolescence, as seen following the incomplete resection in case 3 and in previous literature.7 In 2 cases of incomplete surgical removal, including case 3 of this study, the tumors remained but did not continue to grow.7 The pathogenesis for the early occurrence of lipomas in horses and their lack of growth after adolescence is unknown. However, it may be suggested that infiltrative lipomas present at birth or early in life may be congenital in origin, compared to lipomas with a later age of onset such as in humans and dogs, which may represent postdifferentiation genetic aberration of the normal adipocyte’s karyotype.8

Previous literature has described 3 cases in which passive drainage (capillary, fenestrated, and penrose drains) was utilized following the resection of lipomas in horses; in all 3 instances, the lipoma was infiltrative.4,7,9 In 2 of these cases, the infiltrative lipoma was located on the thorax, and in both animals the lipoma recurred.8,9 Passive drainage was also employed in the resection of a lipoma of the carpus that infiltrated the common digital extensor tendon sheath.7 There was no recurrence following excision of the tumor and synovial lining.

The thoracic mass reported in this case series (case 1) was also an infiltrative lipoma. A penrose drain was utilized, and the mass was observed to recur 3 months postoperatively at the location of the exit site of the drain. An active suction drain was used at the time of the second resection, after which no recurrence was observed. Subsequently, an active suction drain was used in the resection of a preputial lipoma (case 2) and no recurrence was noted.

The authors hypothesize that best practice would be to utilize active suction drainage in the resection of large lipomas where dead space is created and cannot otherwise be mitigated. The use of a drain following excision of neoplasia may allow for the passage of abnormal cells to a previously unaffected area of tissue. In the human literature, surgical drain site metastasis is rare but possible, even following cases of microscopically and macroscopically complete excision.19,20 The authors consider the use of an active suction drain best practice when a large amount of dead space is created when compared to the alternative of a seroma forming.

Cisplatin was utilized in case 1, despite which the recurrent mass continued to grow. Local chemotherapy was performed to attempt to decrease the size of the tumor and prevent a subsequent, more aggressive resection. Cisplatin was utilized due to its common use in the treatment of cutaneous tumors in the horse.21 There is no report of the use of cisplatin in the literature to treat lipomas of any species or of other chemotherapeutics used to treat lipomas in horses. In humans, chemotherapeutic agents have not been utilized to treat lipomas to the authors’ knowledge. There is 1 report22 of a dog having partial response to systemic doxorubicin administration within 6 weeks. There is no strong evidence to suggest the use of chemotherapeutics in equine patients that can be extrapolated from other species, likely due to the low mitotic rate of lipomas rendering them ineffective. There is evidence to suggest irradiation (cobalt 60 radiation) can benefit dogs in long-term local tumor control of infiltrative lipomas.15,23 For incompletely removed infiltrative lipomas in the dog, the average time to recurrence is 8 months following surgical excision, which increases to a mean of 46 months when combined with radiation therapy in dogs.15,24 While irradiation has not been described to treat lipomas in equids, radiation therapy has been shown to be a very effective treatment modality for equine tumors, but logistical reasons limit its impact in equine oncology.25

Infiltrative lipomas also pose a further diagnostic dilemma: they are indistinguishable from simple lipomas with either cytology or biopsy, as at a cellular and histological level they are identical. Even with histopathology, an infiltrative lipoma may be erroneously diagnosed as a simple lipoma, unless the tumor cells are appreciated to infiltrate the normal adjacent tissue.15

Imaging modalities can assist in differentiating infiltrative and encapsulated lipomas. Ultrasonography is a commonly used modality to assist in this determination. Infiltrative lipomas have been ultrasonographically described as either having poorly defined borders or simply infiltrative in appearance.69 In contrast, simple lipomas have been described as well-encapsulated masses with hyperechoic margins and hypoechogenicity compared to the surrounding adipose tissue.26 The best modality for imaging lipomas is CT, as it enables the visualization of the interdigitation of the fat attenuation of the mass in comparison to the soft tissue attenuation of muscle and the extension of the lesion through fascial planes.15 Magnetic resonance imaging is more sensitive at detecting microscopic fat in comparison to CT.27 However, both CT and MRI pose limitations for the imaging of abdominal and thoracic masses in juvenile horses due to their disproportionate size in comparison to the gantry diameter but are still useful for the head and limbs. For cases 1 and 2, CT and MRI would not have been possible due to the anatomical locations of the lipomas (flank and prepuce).

Lipomas should be resected with 3-cm gross margins when possible if a capsule is not identified at surgery or with imaging modalities, as infiltrative lipomas may more appropriately be considered an aggressive tumor type, warranting the large excisional margins that are afforded to other aggressive tumor types.9,28 Ultrasonography and gross examination may not be helpful in determining the margin of the mass. If necessary, due to large amounts of dead space, active suction drains should be utilized, as this may aid in the removal of neoplastic cells. Chemotherapy was not beneficial in the single case reported in this case series, and likely the lower rate of mitosis in lipomas would make these cells less amenable to chemotherapy.

Acknowledgments

The authors thank the staff at Veterinary Associates Equine of Auckland, New Zealand, for their care of the animals included in this study.

Disclosures

The authors have nothing to disclose. No AI-assisted technologies were used in the generation of this manuscript.

Funding

The authors have nothing to disclose.

References

  • 1.

    Hendrick MJ. Mesenchymal tumours of the skin and soft tissues. In: Meuten DJ, ed. Tumours In Domestic Animals. John Wiley & Sons; 2017:159.

    • Search Google Scholar
    • Export Citation
  • 2.

    McEntee MC, Thrall DE. Computed tomographic imaging of infiltrative lipoma in 22 dogs. Vet Radiol Ultrasound. 2001;42(3):221-225. doi:10.1111/j.1740-8261.2001.tb00928.x

    • Search Google Scholar
    • Export Citation
  • 3.

    Ludwig EK, Byron CR, Lahmers KK, Santos MP. Frontal and caudal maxillary sinus lipoma in a horse. Can Vet J. 2017;58(5):503-507.

  • 4.

    Olle E, Saunders J, Desmecht D. Infiltrative lipoma on the forearm of a horse. Vlaams Diergen Tijds. 2002;71(2):142-144.

  • 5.

    Bristol DG, Fubini SL. External lipomas in three horses. J Am Vet Med Assoc. 1984;185(7):791-792.

  • 6.

    Lepage OM, Laverty S, Drolet R, Lavoie JP. Infiltrative lipoma in a quarter horse. Cornell Vet. 1993;83(1):57-60.

  • 7.

    Hammer EJ, Chope K, Lemire TD, Reef VB. A lipoma of the extensor tendon sheaths in a horse. Vet Radiol Ultrasound. 2002;43(1):63-65. doi:10.1111/j.1740-8261.2002.tb00445.x

    • Search Google Scholar
    • Export Citation
  • 8.

    Erkert RS, Moll HD, MacAllister CG, Confer AW, Ritchey JW. Infiltrative lipoma in an American Quarter Horse gelding. Equine Vet Educ. 2007;19(7):380-383. doi:10.2746/095777307X216349

    • Search Google Scholar
    • Export Citation
  • 9.

    Rebsamen E, Gygax D, Dennler M, Jud R, Kummer M. External infiltrating lipoma in a two-week-old foal: computed tomographic evaluation for the assessment of the extension and invasiveness of the tumour. Equine Vet Educ. 2010;22(12):602-607. doi:10.1111/j.2042-3292.2010.00137.x

    • Search Google Scholar
    • Export Citation
  • 10.

    Baker D, Kreeger J. Infiltrative lipoma in the heart of a horse. Cornell Vet. 1987;77(3):258-262.

  • 11.

    Anderson WI, King JM. Incidental meningeal lipoma in a horse. Vet Pathol. 1988;25(6):530-531. doi:10.1177/030098588802500623

  • 12.

    Hamir AN, Habecker P, Tulleners E. Equine intrapericardial lipoma. Vet Rec. 1994;135(10):235-236. doi:10.1136/vr.135.10.235

  • 13.

    Case JB, MacPhail CM, Withrow SJ. Anatomic distribution and clinical findings of intermuscular lipomas in 17 dogs (2005-2010). J Am Anim Hosp Assoc. 2012;48(4):245-249. doi:10.5326/JAAHA-MS-5767

    • Search Google Scholar
    • Export Citation
  • 14.

    Lamagna B, Greco A, Guardascione A, et al. Canine lipomas treated with steroid injections: clinical findings. PLoS One. 2012;7(11):e50234. doi:10.1371/journal.pone.0050234

    • Search Google Scholar
    • Export Citation
  • 15.

    McEntee MC, Page RL, Mauldin GN, Thrall DE. Results of irradiation of infiltrative lipoma in 13 dogs. Vet Radiol Ultrasound. 2000;41(6):554-556. doi:10.1111/j.1740-8261.2000.tb01889.x

    • Search Google Scholar
    • Export Citation
  • 16.

    Schellong H, Falcone A, Günther M, Schmidt H. Infiltrating intramuscular lipoma. Article in German. Chirurg. 1997;68(3):279-282. doi:10.1007/s001040050189

    • Search Google Scholar
    • Export Citation
  • 17.

    Hobert MK, Brauer C, Dziallas P, et al. Infiltrative lipoma compressing the spinal cord in 2 large-breed dogs. Can Vet J. 2013;54(1):74-78.

  • 18.

    Dionne GP, Seemayer TA. Infiltrating lipomas and angiolipomas revisited. Cancer. 1974;33(3):732-738. doi:10.1002/1097-0142(197403)33:3<732::aid-cncr2820330319>3.0.co;2-3

    • Search Google Scholar
    • Export Citation
  • 19.

    St Peter SD, Nguyen CC, Mulligan DC, Moss AA. Subcutaneous metastasis at a surgical drain site after the resection of pancreatic cancer. Int J Gastrointest Cancer. 2003;33(2-3):111-115. doi:10.1385/ijgc:33:2-3:111

    • Search Google Scholar
    • Export Citation
  • 20.

    Morelli U, Cirocchi R, Mecarelli V, et al. Gastric adenocarcinoma cutaneous metastasis arising at a previous surgical drain site: a case report. J Med Case Rep. 2009;3(1):65. doi:10.1186/1752-1947-3-65

    • Search Google Scholar
    • Export Citation
  • 21.

    Carr EA. Skin conditions amenable to surgery. In: Auer JA, Stick JA, eds. Equine Surgery. 5th ed. Elsevier Health Sciences; 2018:429.

  • 22.

    Kim HJ, Chang HS, Choi CB, et al. Infiltrative lipoma in cervical bones in a dog. J Vet Med Sci. 2005;67(10):1043-1046. doi:10.1292/jvms.67.1043

    • Search Google Scholar
    • Export Citation
  • 23.

    Feng Y, Kent MS, Théon AP, Hansen KS. Conventionally fractionated radiation therapy is associated with long-term survival in dogs with infiltrative lipomas. J Am Vet Med Assoc. 2023;261(11):1-8. doi:10.2460/javma.23.05.0288

    • Search Google Scholar
    • Export Citation
  • 24.

    Bergman PJ, Withrow SJ, Straw RC, Powers BE. Infiltrative lipoma in dogs: 16 cases (1981-1992). J Am Vet Med Assoc. 1994;205(2):322-324. doi:10.2460/javma.1994.205.02.322

    • Search Google Scholar
    • Export Citation
  • 25.

    Théon AP. Radiation therapy in the horse. Vet Clin North Am Equine Pract. 1998;14(3):673-688, viii. doi:10.1016/S0749-0739(17)30192-X

  • 26.

    Volta A, Bonazzi M, Gnudi G, Gazzola M, Bertoni G. Ultrasonographic features of canine lipomas. Vet Radiol Ultrasound. 2006;47(6):589-591. doi:10.1111/j.1740-8261.2006.00191.x

    • Search Google Scholar
    • Export Citation
  • 27.

    Pereira JM, Sirlin CB, Pinto PS, Casola G. CT and MR imaging of extrahepatic fatty masses of the abdomen and pelvis: techniques, diagnosis, differential diagnosis, and pitfalls. Radiographics. 2005;25(1):69-85. doi:10.1148/rg.251045074

    • Search Google Scholar
    • Export Citation
  • 28.

    Ehrhart N, Culp WT. Principles of surgical oncology. In: Kudnig ST, Séguin B, eds. Veterinary Surgical Oncology. John Wiley & Sons; 2012:9. doi:10.1002/9781118729038.ch1

    • Search Google Scholar
    • Export Citation
All Time Past Year Past 30 Days
Abstract Views 116 116 0
Full Text Views 251 251 81
PDF Downloads 129 129 46
Advertisement