Signalment:  
Gross Description:  
Histopathologic Description:
Skin, right hind limb (submitted tissue): Numerous anastamosing lymphatic channels dissect between deep dermal collagen bundles and extend into the subcutis and superficial dermis. The channels are lined by single layers of attenuated to mildly plump endothelial cells that separate variably sized islands of collagen and adipocytes. Individual cells are fusiform to spindloid, contain elongate to irregular hyperchromatic nuclei, and have scant, pale basophilic cytoplasm. Cell borders are variably distinct, and anisocytosis and anisokaryosis are minimal. Mitotic figures are not observed. Mild numbers of lymphocytes and plasma cells often form small discrete aggregates around blood vessels with mild, multifocal infiltration into the surrounding dermis and panniculus. The dermis and subcutis are moderately expanded by clear edema fluid.
Lung, liver, pancreas, gastrointestinal tract (tissues not included on the submitted slide): The lung, liver, pancreas, and gastrointestinal tract contained multiple masses composed of neoplastic epithelial cells consistent with metastatic cholangiocarcinoma.Â
Morphologic Diagnosis:  
Lab Results:  
- Greater than 90% of the cells had strong, nearly diffuse labeling with Factor VIII-related antigen (von Willebrands factor).
- 100% of the cells had strong, diffuse labelling with vimentin (mesenchymal marker).
- Approximately 60-70% of the cells had weak to strong, multifocal labeling with LYVE-1 (lymphatic vessel endothelial receptor 1).Â
Condition:  
Contributor Comment:  
Tissue submitted was from the skin and subcutis of the right hind limb. Histologic lesions in this tissue were consistent with lymphangiomatosis. Lymphangiomatosis is a rare disorder characterized by increased numbers of lymphatic endothelial cells forming irregular, anastomosing, vascular clefts and empty channels.(6) This condition is reported in both cats and dogs, and is grossly characterized by a poorly circumscribed mass or regionally extensive swelling.(6) Tumors of lymphatic origin typically occur in the skin and subcutis with the caudal ventral abdomen and inguinal regions predisposed.(5) Additional reported locations include the head, neck, cranial trunk, axilla, bone, and extremities.(3) Lesions present as intermittent, fluctuant swellings with a variably protracted clinical course and have reportedly affected an entire limb. Lesions often form ulcers and draining tracts with leakage of fluid resulting in cutaneous vesiculation.(6) Smaller discrete lesions should be referred to as lymphangioma, whereas lymphangiomatosis has been described as lymphangioma affecting soft tissues and/or parenchymal organs in a diffuse or multifocal manner.(2,6) Lymphangioma, lymphangiomatosis, and lymphangiosarcoma tend to occur in younger animals; however, lymphangiosarcoma has been reported in dogs ranging from 8 weeks to 13 years of age.(3) A single case of lymphangiosarcoma has been described in a cow and two cases have been described in horses.(8,11,12) Immunohistochemistry may be used to confirm endothelial origin of proliferative lymphatic conditions using factor VIII-related antigen, CD31, vimentin, and LYVE-1.(1,2,6) For this case, the abnormal endothelial cells had strong, nearly diffuse intracytoplasmic immunoreactivity for factor VIII-related antigen and vimentin, and moderate, multifocal immunoreactivity for LYVE-1.Â
If metastatic disease is not present, distinguishing lymphangiosarcoma from lymphangiomatosis based on clinical and histological features may be difficult.(6) It has been suggested that some of the previously described cases of non-metastatic lymphangiosarcomas with well-differentiated endothelial cells may have represented lymphangiomastosis, particularly when these lesions were found in young dogs.(4,13) Lymphangiomatosis, although histologically benign, is often recurrent and progressive.(6) Surgical resection, chemotherapy, and radiotherapy have been used to treat both lymphangiomatosis and lymphangiosarcoma.(6,8)
JPC Diagnosis:  
Conference Comment:  
In humans there is a form of lymphangioma referred to as progressive lymphangioma which occurs in adults, most commonly on the limbs, and is characterized grossly as a red cutaneous macule that enlarges with age.(10) Histologically, there is a proliferation of thin-walled lymphatic channels that dissects between dermal collagen bundles and forms horizontal clefts; lesions may extend into the subcutis. Cutaneous lymphangiomatosis occurs as a diffuse, benign lymphatic proliferation affecting multiple tissue planes over a large area, most commonly in young children;(10) interestingly, the lesion tends to regress when the child stops growing. Lymphangiomatosis is characterized histologically as many variably dilated lymphatic channels which dissect between all normal structures, resulting in islands of normal tissue that appear to be hanging in the air. A distinguishing feature between these two entities is the presence of cutaneous vesicles in lymphangiomatosis, a feature which is lacking in lymphangiomas.(10)
A review of veterinary pathology reference texts(5,6,7,14) reveals discordance over the preferred nomenclature for this proliferative lymphatic lesion. Based on descriptions in humans, there are features of both lymphangioma and lymphangiomatosis in the case of this dog. The most recent WHO fascicle for soft tissue tumors of veterinary species only describes lymphangioma, which occurs most commonly in young animals and is believed to represent congenital malformation.(7) The moderator commented that in the cases he has evaluated, the lesions are difficult to fully resect owing to the lack of a mass effect making palpation of the edges of the lesion difficult, resulting in incomplete surgical resection. The lesions are progressive, a feature also described in the reference texts, exhibit characteristic pitting edema, and occur most commonly on the abdomen, ventral neck, inguinal area and prepuce. The moderator further commented that in his experience, lymphangiomatosis involves many parts of the body, is histologically characterized by multiple dilated lymphatics, and contains a myxoid stroma.Â
In the case of this dog, the signalment and clinical history (e.g. older animal with a lesion is located on the limb) and the histologic findings of thin-walled lymphatic channels that dissect dermal collagen with formation of horizontal clefts with extension into the subcutis support a diagnosis of lymphangioma. However, the findings of diffuse lymphatic proliferation affecting multiple tissue planes over a large area and islands of tissue hanging in the air are more consistent with the classification of lymphangiomatosis, demonstrating the complexity of this lesion. One important fact for which the references agree is the progressive nature of both lymphangioma and lymphangiomatosis, a clinical feature that may be more relevant than the histologic classification from a prognostic standpoint.(5,6,7,14)
References:
1. Barnes JC, Taylor SM, Clark EG, Haines DM, Broughton SJ. Disseminated lymphangiosarcoma in a dog. Can Vet J. 1997;38:42-44.
2. Berry WL, Nesbit JW, Pearson J. Lymphangiomatosis of the pelvic limb in a Maltese dog. J Sm Anim Prac. 1996;37:340-343.
3. Diessler ME, Castellano MC, Massone AR, Portiansky EL, Allende MG, Idiart JR. Cutaneous lymphangiosarcoma in a young dog: clinical anatomopathological and lectinhistochemical description. J Vet Med A Physiol Pathol Clin Med. 2003;50:452-456.
4. Fossum TW, Miller MW, Mackie JT. Lymphangiosarcoma in a dog presenting with massive head and neck swelling. J Am Anim Hosp Assoc. 1998;34:301-304.
5. Ginn PE, Mansell JEKL, Rakich PM. Skin and appendages. In: Maxie MG, ed. Jubb, Kennedy and Palmers Pathology of Domestic Animals. Vol. 1, 5th ed. Philadelphia, PA: Elsevier Ltd; 2007:768.
6. Gross TL, Ihrke PJ, Walder EJ. Vascular tumors. In: Skin Diseases of the Dog and Cat. 2nd ed. Ames, IA: Blackwell Science; 2005:748-755.
7. Hendrick MJ, Mahaffery EA, Moore FM, Vos JH, Walder EJ. Histological Classification of Mesenchymal Tumors of Skin and Soft Tissues of Domestic Animals. 2nd Series. Vol. 2. Washington D.C.: Armed Forces Institute of Pathology, American Registry of Pathology; 1998:22-25.
8. Ijzer J, van den Ingh TSGAM. Lymphangiosarcoma in a horse. J Comp Path. 2000;122:312-316.
9. Itoh T, Mikawa K, Mikawa M, Nibe K, Uchida K. Lymphangiosarcoma in a dog treated with surgery and chemotherapy. J Vet Med Sci. 2004;66(2):197-199.
10. Kempson RL, Fletcher CDM, Evans HL, Hendrickson MR, Sibley RK. Vascular tumors. In: Atlas of Tumor Pathology: Tumors of the Soft Tissues. 3rd Series, Fascicle 30. Washington D.C.: Armed Forces Institute of Pathology/American Registry of Pathology; 1998:360-363.
11. Ruggles AJ, Irby NL, Saik JE, Orsini PG. Ocular lymphangiosarcoma in a cow. J Am Vet Med Assoc. 1992;200(12):1987-1988.
12. Sanchez B, Nieto A, Ruiz DE Leon MA, Rodriguez J, Flores J: Metastatic lymphangiosarcoma in a horse. Vet Pathol. 2002;39:266-268.
13. Shiga A, Shirota K, Une Y, Nomura Y: Lymphangiosarcoma in a dog. J Vet Med Sci. 1994;56(6):1199-1202.
14. Van Vleet JF, Ferrans VJ. Cardiovascular system. . In: McGavin MD, Zachary JF, eds. Pathologic Basis of Veterinary Disease. 4th ed. St. Louis, MO: Elsevier; 2007:611.