DRESS Syndrome That Resembles Graft-Versus-Host Disease after Chemotherapy in a Pediatric Patient: A Case Report.

IF 0.9 Q4 DERMATOLOGY
Case Reports in Dermatology Pub Date : 2024-10-08 eCollection Date: 2024-01-01 DOI:10.1159/000541046
Marian Rolón, Mateo Barros, Clara Ortiz, Sergio Danilo Cruz Romero, Johanna Álvarez
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Abstract

Introduction: Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a potentially life-threatening, drug-induced adverse reaction characterized by skin eruptions, lymphadenopathy, fever, and a broad range of other bodily manifestations. The spectrum of histopathologic and clinical presentations is wide; therefore, DRESS syndrome can mimic other diseases.

Case presentation: We present a case of a 4-year-old male patient who started chemotherapy with vincristine, cytarabine, and etoposide. The first clinical signs were fever, hemodynamic in-stability, and maculopapular erythema. Biopsies of skin lesions were taken, and hyperkeratosis, focal parakeratosis, acanthosis with slight spongiosis, and intraepithelial dyskeratotic cells were observed. There was a perivascular lymphoid infiltrate with abundant eosinophils in the dermis, and eosinophil permeations to the acrosyringium and epithelium were found.

Conclusion: DRESS syndrome is a drug-induced reaction that shares histopathological findings in skin biopsies with those seen in graft-versus-host disease. Although the histological findings are non-pathognomonic, they were characteristic enough to be of importance in the differential diagnosis.

一名儿科患者化疗后出现类似移植物抗宿主病的 DRESS 综合征:病例报告。
简介:伴有嗜酸性粒细胞增多和全身症状的药物反应(DRESS)综合征是一种可能危及生命的药物诱发不良反应,以皮肤糜烂、淋巴结病、发热和一系列其他身体表现为特征。组织病理学和临床表现的范围很广,因此,DRESS 综合征可能会模仿其他疾病:本病例为一名 4 岁男性患者,开始接受长春新碱、阿糖胞苷和依托泊苷化疗。最初的临床症状是发热、血流动力学不稳定和斑丘疹性红斑。对皮损进行了活检,观察到角化过度、局灶性角化不全、伴有轻微海绵状增生的棘皮症和上皮内角化不良细胞。真皮内有大量嗜酸性粒细胞的血管周围淋巴浸润,并发现嗜酸性粒细胞渗透到棘层和上皮细胞:结论:DRESS 综合征是一种药物诱导的反应,其皮肤活检组织病理学结果与移植物抗宿主病相同。虽然这些组织学发现不具病理特征,但在鉴别诊断中具有重要意义。
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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
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