de la Rosa García Estela, Bologna Molina Ronell, Vega González Teresa de Jesús
Health Care Department, Universidad Autónoma Metropolitana Xochimilco, México.
Med Oral Patol Oral Cir Bucal. 2006 Nov 1;11(6):E486-92.
Graft versus host disease (GVHD) is a common complication in bone marrow transplant (BMT) patients. It is characterized by systemic and oral cavity alterations. Depending on the timing of lesions, GVHD is classified as acute or chronic. Alterations in the oral cavity are lichenoid reticular lesions, erythema, ulcerations, and xerostomia. Sporadically, mucocele and pyogenic granulomas can be present.
To describe GVHD oral manifestations in eight allogenic BMT patients, and discuss GVHD and drug-immunosuppresion associated lesions diagnosis and treatment.
For a year, we examined the oral mucosa of eight consecutive allogenic BMT patients attending the Dermatology out-patient clinic at the Instituto Nacional de Cancerologia (National Institute of Oncology) in Mexico City, looking for oral mucosa lesions.
Patients were five men and three women, ages 24.8 -/+ 9.7 years. Four had a BMT because of chronic granulocytic, two for acute myeloblastic, one for acute lymphoblastic leukemia, and one for aplastic anemia. Three patients developed acute GVHD, with reticular oral mucosa lesions, erythema and mucositis; and all eight developed chronic GVHD, with reticular oral lesions, erythema, and ulcerations. A Patient had tongue and cheek pyogenic granulomas. Six reported xerostomia. Other oral lesions, associated to drug-immunosuppression, were candidiasis and herpes simplex.
Patients with GVHD frequently develop oral lesions, some of which interfere with normal feeding; timely diagnosis and treatment are therefore essential to improve the quality of life of affected patients. We propose an alternative treatment for pyogenic granulomas.
移植物抗宿主病(GVHD)是骨髓移植(BMT)患者常见的并发症。其特征为全身及口腔改变。根据病变发生时间,GVHD分为急性或慢性。口腔改变包括苔藓样网状病变、红斑、溃疡和口干。偶见黏液囊肿和化脓性肉芽肿。
描述8例异基因BMT患者的GVHD口腔表现,并探讨GVHD及药物免疫抑制相关病变的诊断和治疗。
我们对墨西哥城国家肿瘤研究所皮肤科门诊连续8例异基因BMT患者的口腔黏膜进行了为期一年的检查,以寻找口腔黏膜病变。
患者5男3女,年龄24.8±9.7岁。4例因慢性粒细胞性白血病进行BMT,2例因急性髓细胞性白血病,1例因急性淋巴细胞性白血病,1例因再生障碍性贫血。3例患者发生急性GVHD,表现为口腔黏膜网状病变、红斑和黏膜炎;8例均发生慢性GVHD,表现为口腔网状病变、红斑和溃疡。1例患者有舌部和颊部化脓性肉芽肿。6例报告有口干。其他与药物免疫抑制相关的口腔病变为念珠菌病和单纯疱疹。
GVHD患者常出现口腔病变,其中一些会影响正常进食;因此,及时诊断和治疗对于提高受影响患者的生活质量至关重要。我们提出了一种治疗化脓性肉芽肿的替代方法。