Martires Kathryn, Callahan Shields, Terushkin Vitaly, Brinster Nooshin, Leger Marie, Soter Nicholas A
Ronald O. Perelman Department of Dermatology, NYU School of Medicine, NYU Langone Medical Center.
Dermatol Online J. 2016 Dec 15;22(12):13030/qt8467m0j9.
We report a 68-year-old woman with chroniclymphocytic leukemia, who developed numerous,pruritic, edematous, and vesicobullous skin lesionsof the face and extremities over the course of severalmonths. The diagnosis of eosinophilic dermatosis ofhematologic malignancy (EDHM) was made basedon the clinical history and histopathologic features.Owing to the possible link between EDHM and amore aggressive underlying CLL, she was startedagain on chemotherapy. This case serves as areminder that, although the precise pathogenesis ofEDHM remains unclear, the paraneoplastic disorderis the result of immune dysregulation. Patientswho develop EDHM should undergo prompthematologic/oncologic evaluation.
我们报告一例68岁慢性淋巴细胞白血病女性患者,在数月病程中面部和四肢出现大量瘙痒性、水肿性及水疱大疱性皮肤损害。基于临床病史和组织病理学特征,诊断为血液系统恶性肿瘤性嗜酸性皮肤病(EDHM)。鉴于EDHM与潜在侵袭性更强的慢性淋巴细胞白血病之间可能存在关联,遂再次对她进行化疗。该病例提醒我们,尽管EDHM的确切发病机制尚不清楚,但这种副肿瘤性疾病是免疫失调的结果。发生EDHM的患者应迅速接受血液学/肿瘤学评估。