Elkeeb Dena, Hopkins Zachary, Miles Rodney R, Halwani Ahmad, Wada David
University of Chicago Medicine, Section of Dermatology, Chicago, Illinois, USA, University of Utah, Department of Dermatology, Salt Lake City, Utah, USA.
University of Utah, School of Medicine, Salt Lake City, Utah, USA.
Eur J Dermatol. 2018 Dec 1;28(6):809-817. doi: 10.1684/ejd.2018.3463.
Aleukemic leukemia cutis (ALC) is an extremely rare cutaneous manifestation of an aggressive systemic hematological malignancy, associated with dermal infiltration by leukemic cells preceding peripheral blood involvement. This condition is associated with poor outcome, and dermatologists are often responsible for making the initial diagnosis in a timely fashion. To describe a case of ALC and review the literature with an emphasis on the clinical features, summarizing the cutaneous manifestations of this rare systemic disorder. Electronic searches were performed in PubMed and Embase for published studies and case reports in English from 1970 to 2017. The presented case is a 46-year-old male with numerous asymptomatic skin-colored papules, plaques, and subcutaneous nodules with no detectable peripheral blood involvement, who was treated and subsequently relapsed twice with no evidence of peripheral blood or bone marrow involvement. Based on the review, skin nodules were the most common physical exam finding, comprising 27 cases (62.8%). The most common anatomic locations of cutaneous findings were the trunk and extremities, occurring in 23 (53.5%) and 20 (46.5%) cases, respectively. Since the cutaneous presentation of ALC is notably variable, a high degree of clinical suspicion is required. In view of this case and review of the literature, leukemia cutis should be included in the differential diagnosis of evolving, infiltrative cutaneous nodules or plaques, triggering an evaluation of the bone marrow and peripheral blood when the pathologic features raise concern for this disorder.
白细胞不增多性白血病性皮肤浸润(ALC)是侵袭性全身性血液系统恶性肿瘤极为罕见的皮肤表现,与白血病细胞在皮肤浸润先于外周血受累有关。这种情况预后较差,皮肤科医生常负责及时做出初步诊断。描述1例ALC病例并复习文献,重点关注临床特征,总结这种罕见全身性疾病的皮肤表现。在PubMed和Embase中进行电子检索,查找1970年至2017年以英文发表的研究和病例报告。所报告病例为一名46岁男性,有许多无症状的肤色丘疹、斑块和皮下结节,外周血未检测到受累,接受治疗后复发两次,外周血和骨髓均无受累证据。基于文献复习,皮肤结节是最常见的体格检查发现,共27例(62.8%)。皮肤表现最常见的解剖部位是躯干和四肢,分别为23例(53.5%)和20例(46.5%)。由于ALC的皮肤表现差异很大,需要高度的临床怀疑。鉴于该病例及文献复习,白血病性皮肤浸润应纳入不断演变的浸润性皮肤结节或斑块的鉴别诊断,当病理特征引发对该疾病的关注时,应评估骨髓和外周血。