Sweet Syndrome in a Patient with Acute Leukemia on Azacitidine and Venetoclax Treatment

Maria Gabriela Rezmuves, Marcela Cristina Candea, Raluca Sipos-Craciun, Ligia Ariana Bancu, Agnes Zsuzsanna Szasz, Smaranda Demian
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Abstract

Abstract Introduction Sweet syndrome, also called acute febrile neutrophilic dermatosis, is a rare disorder characterized by skin lesions accompanied by high fever and elevated inflammatory markers. Case Presentation In January 2023, a 73-year-old Caucasian male was diagnosed with acute myeloblastic leukemia and subsequently chemotherapy with azacitidine and venetoclax was initiated. One week after the second round of chemotherapy with azacitidine, the patient developed a fever of 39˚C. Physical examination revealed purple plaques on the skin of the head, neck, and arms associated with pain but not itching. Initially, the plaques appeared at the site of the subcutaneous azacitidine injection (left upper extremity) and then began to spread. The infectious diseases consultation established the diagnosis of multiple abscesses. Antibiotic therapy was initiated with meropenemum and linezolidum, and later colistin was associated, but the skin lesions and the patient’s condition worsened. A dermatology consultation was performed, which established the diagnosis of Sweet syndrome, and subsequently corticosteroid therapy was started. The skin lesions started to improve after 3 days. Conclusions Sweet syndrome is a rare condition that is difficult to diagnose because of the wide spectrum of differential diagnoses.
阿扎胞苷加维妥乐治疗急性白血病甜证1例
Sweet综合征,又称急性发热性中性粒细胞皮肤病,是一种罕见的以皮肤病变伴高热和炎症标志物升高为特征的疾病。2023年1月,一名73岁的白人男性被诊断为急性髓母细胞白血病,随后开始阿扎胞苷和venetoclax化疗。第二轮阿扎胞苷化疗一周后,患者出现39℃的发热。体格检查发现头部、颈部和手臂皮肤有紫色斑块,伴有疼痛但无瘙痒。最初,斑块出现在皮下注射阿扎胞苷的部位(左上肢),然后开始扩散。传染病会诊确定了多发脓肿的诊断。最初使用美罗培明和利奈唑仑进行抗生素治疗,后来使用粘菌素,但皮肤病变和患者病情恶化。进行了皮肤科会诊,确定了Sweet综合征的诊断,随后开始皮质类固醇治疗。3天后皮肤病变开始好转。结论甜综合征是一种罕见的疾病,因其鉴别诊断范围广而难以诊断。
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