Woods J P, Johnstone I B, Bienzle D, Balson G, Gartley C J
Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Canada.
J Am Anim Hosp Assoc. 1995 Jan-Feb;31(1):70-6. doi: 10.5326/15473317-31-1-70.
Lymphangioma, immune-mediated thrombocytopenia (IMT), and von Willebrand's disease (vWD) were diagnosed by histology, hematology, and a coagulation profile in a 14-month-old, female dachshund. Clinical and laboratory findings included ecchymotic inguinolabial swelling, thrombocytopenia, positive platelet factor-3 assay, prolonged buccal mucosal bleeding time, and subnormal von Willebrand factor antigen concentration and factor VIII activity. The IMT resolved with immunosuppressive glucocorticoid therapy. Histologic examination identified lymphangioma which was too extensive for surgical excision. The history and the clinical and laboratory findings were consistent with congenital vWD, although acquired vWD secondary to lymphangioma could not be ruled out.
一只14个月大的雌性腊肠犬经组织学、血液学和凝血检查确诊患有淋巴管瘤、免疫介导性血小板减少症(IMT)和血管性血友病(vWD)。临床和实验室检查结果包括腹股沟阴唇瘀斑性肿胀、血小板减少、血小板因子3检测阳性、颊黏膜出血时间延长以及血管性血友病因子抗原浓度和因子VIII活性低于正常水平。免疫抑制性糖皮质激素治疗使IMT得到缓解。组织学检查发现淋巴管瘤范围过大,无法进行手术切除。尽管不能排除继发于淋巴管瘤的获得性vWD,但病史以及临床和实验室检查结果与先天性vWD相符。