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与利妥昔单抗治疗华氏巨球蛋白血症相关的鼻皮肤坏死的发生及随后的自发缓解。

Development of nasal skin necrosis associated with rituximab treatment for Waldenström's macroglobulinemia and subsequent spontaneous resolution.

作者信息

Pearlman Aaron N, Fechner Frank P, Constantinides Minas

机构信息

Department of Otolaryngology, New York University School of Medicine, New York City 10016, USA.

出版信息

Ear Nose Throat J. 2006 Jul;85(7):431-3.

Abstract

We report the unusual case of a 72-year-old man who developed acute and extensive necrosis of the nasal skin and soft-tissue envelope while undergoing chemotherapy for Waldenström's macroglobulinemia, a lymphoproliferative disorder The patient's treatment involved infusions of rituximab, a chimeric monoclonal antibody that is directed against B cell surface membrane protein CD20. The patient refused surgery to restore the nose, and he was treated conservatively with wet-to-dry dressings and antibiotic ointment. Approximately 5 weeks after admission, the eschar had exfoliated, revealing that the underlying skin was pink and healthy; no significant areas of necrosis remained. Within weeks, the nose had healed completely without scarring. A good aesthetic result was achieved exclusively through healing by secondary intention. We wish to alert the medical community that (1) conservative management of even extensive nasal skin loss should be considered when clinically acceptable, and (2) there may be an association between anti-CD20 antibody therapy for Waldenström's macroglobulinemia and skin necrosis.

摘要

我们报告了一例罕见病例,一名72岁男性在接受华氏巨球蛋白血症(一种淋巴增殖性疾病)化疗时,出现了鼻部皮肤和软组织包膜的急性广泛性坏死。患者的治疗包括输注利妥昔单抗,这是一种针对B细胞表面膜蛋白CD20的嵌合单克隆抗体。患者拒绝进行修复鼻子的手术,而是采用湿-干敷料和抗生素软膏进行保守治疗。入院约5周后,焦痂脱落,显示其下方的皮肤呈粉红色且健康;没有明显的坏死区域残留。几周内,鼻子完全愈合且无瘢痕形成。仅通过二期愈合就取得了良好的美学效果。我们希望提醒医学界:(1)在临床可接受的情况下,即使是广泛的鼻部皮肤缺损也应考虑保守治疗;(2)华氏巨球蛋白血症的抗CD20抗体治疗与皮肤坏死之间可能存在关联。

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