Vadeboncoeur Sophie, Provost Nathalie
Division of Dermatology, Université de Montréal, Montreal, QC, Canada
Division of Dermatology, Université de Montréal, Montreal, QC, Canada.
J Cutan Med Surg. 2016 Sep;20(5):474-7. doi: 10.1177/1203475416640795. Epub 2016 Mar 22.
Multiple xanthogranulomas (XGs) in adults are rare, although an increasing number of case reports are being published. The most frequent association is hematologic malignancies, but the majority of cases remain idiopathic, with occasional spontaneous resolution.
The aims of this report are to describe a case of eruptive XG in a woman with a solid neoplasia who was receiving imatinib and to review the literature.
This 33-year-old woman had a gastrointestinal stromal tumor. After undergoing surgical removal and being on imatinib for 1 year, the patient developed multiple slightly erythematous papules with an orange hue on the axillary region, trunk, abdomen, and thighs. A biopsy confirmed the diagnosis of XG.
This is to the investigators' knowledge the first case of eruptive XG in the setting of a solid neoplasia. The possibility of drug-induced XG lesions due to imatinib cannot be excluded. This presentation could be added to the list of associations of adult XG.
成人多发性黄瘤(XG)较为罕见,尽管发表的病例报告数量在不断增加。最常见的关联是血液系统恶性肿瘤,但大多数病例仍为特发性,偶尔会自发消退。
本报告旨在描述一例接受伊马替尼治疗的患有实体瘤的女性发生的发疹性XG病例,并对相关文献进行综述。
这位33岁的女性患有胃肠道间质瘤。在接受手术切除并服用伊马替尼1年后,患者在腋窝、躯干、腹部和大腿出现多个略带红斑的橙色丘疹。活检确诊为XG。
据研究者所知,这是实体瘤背景下发疹性XG的首例病例。不能排除伊马替尼导致药物性XG病变的可能性。这种表现可补充到成人XG的关联列表中。