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以颈部淋巴结病为表现的药物超敏反应伴嗜酸性粒细胞增多和全身症状及粒细胞缺乏症。

Drug Reaction with Eosinophilia and Systemic Symptoms and Agranulocytosis Presenting as Cervical Lymphadenopathy.

作者信息

Chen Laura, Chia Clemente, Saha Anik

机构信息

Monash Health, Clayton, VIC, Australia.

出版信息

Hosp Pharm. 2022 Feb;57(1):130-134. doi: 10.1177/0018578721990899. Epub 2021 Jan 27.

Abstract

Drug reaction with eosinophilia and systemic symptoms (DRESS) is a rare cause of cervical lymphadenopathy. It is a potentially life-threatening hypersensitivity reaction, commonly characterized by fever, rash, hematological abnormalities, and multi-organ involvement. Its association with agranulocytosis is even rarer, with fewer than 10 cases describing the coexistence of DRESS with agranulocytosis reported in the English literature. An otherwise well 40-year-old female presented with a sore throat and cervical lymphadenopathy, with investigations revealing DRESS and agranulocytosis secondary to carbamazepine. DRESS and agranulocytosis are serious, potentially life-threatening adverse drug reactions which can initially present as cervical lymphadenopathy. As carbamazepine is considered first-line therapy for certain chronic neuropathic conditions such as trigeminal neuralgia, clinicians should be aware of the varying clinical presentations of both conditions.

摘要

药物超敏反应伴嗜酸性粒细胞增多和全身症状(DRESS)是颈部淋巴结病的罕见病因。它是一种潜在的危及生命的超敏反应,通常表现为发热、皮疹、血液学异常和多器官受累。其与粒细胞缺乏症的关联更为罕见,英文文献中报道的描述DRESS与粒细胞缺乏症共存的病例不到10例。一名原本健康的40岁女性出现咽痛和颈部淋巴结病,检查发现是由卡马西平引起的DRESS和粒细胞缺乏症。DRESS和粒细胞缺乏症是严重的、潜在危及生命的药物不良反应,最初可能表现为颈部淋巴结病。由于卡马西平被认为是某些慢性神经病变如三叉神经痛的一线治疗药物,临床医生应了解这两种病症的不同临床表现。

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