Kim Jeong Eun, Oh Eui Hyun, Ro Young Suck, Ko Joo Yeon
Department of Dermatology, Hanyang University College of Medicine, Seoul, Korea.
Ann Dermatol. 2016 Jun;28(3):371-4. doi: 10.5021/ad.2016.28.3.371. Epub 2016 May 25.
Anaplastic large-cell lymphoma (ALCL) is a CD30-positive T-cell/null-cell lymphoma that is clinically classified into either primary cutaneous ALCL or systemic ALCL (S-ALCL) sub-types. Because 90% of childhood S-ALCL cases are anaplastic lymphoma kinase (ALK)-positive, there is a lack of data on ALK-negative S-ALCL cases among pediatric patients. Herein, we report a rare case of ALK-negative S-ALCL in a 9-year-old Korean boy who initially presented with itchy erythematous maculopapules and an erosive nodule on the trunk area. We emphasize the need of high index of suspicion of an underlying malignant disease in the presence of refractory eczematous lesions.
间变性大细胞淋巴瘤(ALCL)是一种CD30阳性的T细胞/裸细胞淋巴瘤,临床上分为原发性皮肤ALCL或系统性ALCL(S-ALCL)亚型。由于90%的儿童S-ALCL病例为间变性淋巴瘤激酶(ALK)阳性,因此缺乏儿科患者中ALK阴性S-ALCL病例的数据。在此,我们报告一例罕见的ALK阴性S-ALCL病例,患者为一名9岁韩国男孩,最初表现为躯干区域瘙痒性红斑丘疹和糜烂性结节。我们强调,在出现难治性湿疹样病变时,需要高度怀疑潜在的恶性疾病。