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面部原发性皮肤Rosai-Dorfman病的放射治疗:一例对多线治疗耐药的病例报告及文献综述

Radiation Therapy for Primary Cutaneous Rosai-Dorfman Disease of the Face: A Case Report Resistant to Multiple Lines of Treatment and a Literature Review.

作者信息

Lopez Navarro Omar G, Cervera-Ceballos Eduardo E, Poitevin-Chacón Adela, Perez-Lopez Hidralba, Flores-Vazquez Fabiola, Urbalejo-Ceniceros Víctor I, Arriaga-Marroquin Jose A, Aviles-Salas Alejandro, Sanchez-Rodriguez Irving E, Villalvazo Alejandro, Gutierrez-Valencia Enrique, Gonzalez-Espinosa Tomas F

机构信息

Hematology and Medical Oncology, Medica Sur, Mexico City, MEX.

Hematology, Instituto Nacional de Cancerología, Mexico City, MEX.

出版信息

Cureus. 2025 Jul 27;17(7):e88864. doi: 10.7759/cureus.88864. eCollection 2025 Jul.

Abstract

Rosai-Dorfman disease (RDD) is a rare subtype of sinus histiocytosis, with primary cutaneous RDD (PCRDD) being an even rarer form, characterized by cutaneous lesions without systemic involvement. PCRDD presents a significant diagnostic challenge and is often resistant to conventional therapies, including surgical resection, steroids, and chemotherapy. Currently, no established management guidelines exist for this condition. Radiation therapy is emerging as a promising treatment option, especially for refractory cases involving cosmetically sensitive or difficult-to-resect areas. This case report presents a patient with treatment-resistant PCRDD affecting the face, which was refractory to multiple therapeutic approaches, including chemotherapy. The patient achieved durable remission with radiation therapy at an 18-month follow-up, highlighting the efficacy of this modality in managing resistant PCRDD and the importance of a multidisciplinary approach.

摘要

罗萨伊-多夫曼病(RDD)是鼻窦组织细胞增多症的一种罕见亚型,原发性皮肤罗萨伊-多夫曼病(PCRDD)则更为罕见,其特征为皮肤病变且无全身受累。PCRDD带来了重大的诊断挑战,并且通常对包括手术切除、类固醇和化疗在内的传统疗法耐药。目前,针对这种病症尚无既定的管理指南。放射治疗正成为一种有前景的治疗选择,尤其是对于涉及美容敏感或难以切除区域的难治性病例。本病例报告介绍了一名患有面部难治性PCRDD的患者,该患者对包括化疗在内的多种治疗方法均无效。在18个月的随访中,患者通过放射治疗实现了持久缓解,突出了这种治疗方式在管理耐药性PCRDD方面的疗效以及多学科方法的重要性。

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