Kwan Michelle, Yang Christopher S, Nguyen Cuong V
Northwestern University Feinberg School of Medicine, 420 E Superior St, Chicago, IL, 60611, USA.
Department of Dermatology, Northwestern University Feinberg School of Medicine, 676 N St. Clair St, Suite 1600, Chicago, IL, 60611, USA.
Arch Dermatol Res. 2025 Apr 1;317(1):660. doi: 10.1007/s00403-025-04103-3.
The systemic associations of adult xanthogranulomas (XGs), the most common subtype of non-Langerhans cell histiocytosis, are poorly understood. In this retrospective cohort analysis, we studied adult patients diagnosed with XGs and investigated the clinical features and systemic associations of adult XGs. Among 138 patients (mean age 43.3 years, 51.4% female, 76.8% white), adult XGs most frequently presented on the trunk (40.6%), differing from the pediatric predilection for the head and neck. Patients presenting with multiple XGs (3.6%) were significantly more likely to have systemic malignancies (p = 0.009), particularly hematologic malignancies (p = 0.001), as well as non-malignant hematologic disorders (p = 0.027). Hyperlipidemia (37%), cardiac disease (51.4%), and endocrine disease (31.2%) were the most prevalent systemic comorbidities. In conclusion, the presentation of multiple XGs in an adult is associated with malignancy (particularly hematologic malignancies) and non-malignant hematologic disorders, suggesting a possible link with immune dysregulation. Molecular testing in one patient with multiple XGs and CMML transformed to AML revealed the same KMT2a deletion in both the XGs and the bone marrow, raising the possibility of clonal relationships in some cases.
成人黄色肉芽肿(XG)是非朗格汉斯细胞组织细胞增多症最常见的亚型,其全身相关性尚不清楚。在这项回顾性队列分析中,我们研究了诊断为XG的成年患者,并调查了成人XG的临床特征和全身相关性。在138例患者中(平均年龄43.3岁,女性占51.4%,白人占76.8%),成人XG最常出现在躯干(40.6%),这与小儿好发于头颈部不同。出现多个XG的患者(3.6%)发生全身恶性肿瘤的可能性显著更高(p = 0.009),尤其是血液系统恶性肿瘤(p = 0.001),以及非恶性血液系统疾病(p = 0.027)。高脂血症(37%)、心脏病(51.4%)和内分泌疾病(31.2%)是最常见的全身合并症。总之,成人出现多个XG与恶性肿瘤(尤其是血液系统恶性肿瘤)和非恶性血液系统疾病相关,提示可能与免疫失调有关。一名患有多个XG且慢性粒单核细胞白血病转化为急性髓系白血病的患者的分子检测显示,XG和骨髓中存在相同的KMT2a缺失,这增加了某些病例中存在克隆关系的可能性。