An uncommon culprit of neutropenic fever: a case of Sweet syndrome following induction therapy for acute myeloid leukemia.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Archive of clinical cases Pub Date : 2023-11-21 eCollection Date: 2023-01-01 DOI:10.22551/2023.41.1004.10262
Ahmed Alderazi, Alec B Rezigh
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Abstract

Sweet syndrome (SS) is a rare inflammatory disorder characterized by the rapid onset of a characteristically tender rash, fever, and other systemic symptoms. These manifestations are often mistaken for an infection that is not responding to antimicrobials, especially in immunocompromised hosts. We present the case of a 44-year-old woman who developed SS following induction chemotherapy for newly diagnosed acute myeloid leukemia (AML). She exhibited a painful rash on the anterior chest, which spread centrifugally, along with neutropenic fever unresponsive to broad-spectrum antimicrobials. Biopsy of the rash revealed a dense neutrophilic infiltrate within the dermis, confirming the diagnosis of SS. The patient was subsequently treated with systemic steroids with prompt resolution of fevers and improvement of her rash. This case highlights that SS can manifest with a robust neutrophilic infiltrate, even in the context of neutropenia stemming from chemotherapy. SS serves as a crucial consideration in hematologic malignancies, particularly AML, when patients present with fever and cutaneous eruptions. Prompt recognition followed by systemic steroid therapy often leads to symptom resolution.

中性粒细胞减少热的罕见病因:急性髓性白血病诱导治疗后出现Sweet综合征1例。
甜综合征(SS)是一种罕见的炎症性疾病,其特征是迅速出现特征性的软疹、发烧和其他全身症状。这些表现常常被误认为是对抗菌剂无反应的感染,特别是在免疫功能低下的宿主中。我们提出的情况下,44岁的妇女谁发展SS诱导化疗后新诊断急性髓性白血病(AML)。她表现出胸部前部疼痛的皮疹,并离心扩散,同时伴有中性粒细胞减少热,对广谱抗菌素无反应。皮疹活检显示真皮内有致密的中性粒细胞浸润,证实了SS的诊断。患者随后接受全身类固醇治疗,发烧迅速消退,皮疹得到改善。该病例强调SS可以表现为强大的中性粒细胞浸润,即使是在化疗引起的中性粒细胞减少的情况下。当患者出现发热和皮肤疹时,SS是血液系统恶性肿瘤,特别是AML的关键考虑因素。及时识别,然后进行全身类固醇治疗通常会导致症状缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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