Marra Diego E, McKee Phillip H, Nghiem Paul
Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
J Am Acad Dermatol. 2004 Oct;51(4):543-6. doi: 10.1016/j.jaad.2004.02.019.
Graft-versus-host disease (GvHD) is a frequent and serious complication of bone-marrow transplantation (BMT), and carries a high morbidity and mortality if not promptly recognized and treated. The rash of acute GvHD is often difficult to distinguish clinically from a drug eruption, and skin biopsies are often performed in an attempt to render a diagnosis. Histologically, eosinophils are classically associated with hypersensitivity reactions, and their presence in inflamed tissue is considered suggestive of a drug-induced dermatitis. We present 3 cases of acute exanthema in BMT recipients in whom the presence of eosinophils on skin biopsy specimen led to an initial diagnosis of drug eruption over GvHD. As a result, these patients experienced delays in the institution of definitive immunosuppressive therapy for GvHD. We review the growing literature suggesting that no single or combined histologic feature, including tissue eosinophils, is useful in differentiating GvHD from drug eruptions in BMT recipients. Indeed, in most cases, the cause of a new-onset blanchable erythematous rash in a BMT recipient is most accurately determined by close examination and follow-up of the clinical features without a skin biopsy.
移植物抗宿主病(GvHD)是骨髓移植(BMT)常见且严重的并发症,若未及时识别和治疗,发病率和死亡率都很高。急性GvHD的皮疹在临床上常难以与药疹区分,因此常进行皮肤活检以作出诊断。从组织学上看,嗜酸性粒细胞通常与超敏反应相关,其在炎症组织中的存在被认为提示药物性皮炎。我们报告了3例BMT受者的急性皮疹病例,其皮肤活检标本中存在嗜酸性粒细胞,最初被诊断为药疹而非GvHD。结果,这些患者在开始针对GvHD的确定性免疫抑制治疗方面出现了延迟。我们回顾了越来越多的文献,这些文献表明,没有单一或综合的组织学特征,包括组织嗜酸性粒细胞,可用于区分BMT受者的GvHD和药疹。事实上,在大多数情况下,通过密切检查和随访临床特征而非皮肤活检,最能准确确定BMT受者新发可褪色红斑皮疹的病因。