Schadendorf D, Algermissen B, Hamann K, Riewald M, Nürnberger F, Czarnetzki B M
Department of Dermatology, Clinical Immunology, and Asthma, Free University Berlin, Germany.
J Am Acad Dermatol. 1993 May;28(5 Pt 2):884-8. doi: 10.1016/0190-9622(93)70125-d.
An 18-year-old man had a 3-week history of malaise, a 1-week history of a papular eruption, and increasingly severe multisystem neurologic symptoms. A diagnosis of acute monoblastic leukemia was made. Immunophenotypic characterization of peripheral blood, bone marrow, and cutaneous infiltrates revealed a predominant myelomonocytic phenotype with the coexpression of intercellular adhesion molecule type 1, IgE receptor, terminal deoxynucleotidyl transferase, and some T-cell markers. These findings may have important clinical and pathogenetic implications regarding the biologic and pathologic behavior of the myelomonocytic leukemic cells. They also explain in part the impressive presentation of the disease in the skin.
一名18岁男性有3周的全身不适病史、1周的丘疹性皮疹病史以及日益严重的多系统神经症状。诊断为急性单核细胞白血病。对外周血、骨髓和皮肤浸润进行免疫表型特征分析,显示主要为髓单核细胞表型,伴有细胞间黏附分子1型、IgE受体、末端脱氧核苷酸转移酶和一些T细胞标志物的共表达。这些发现可能对髓单核细胞白血病细胞的生物学和病理行为具有重要的临床和发病机制意义。它们也部分解释了该疾病在皮肤中的显著表现。