中国麻风皮肤病杂志 ›› 2026, Vol. 42 ›› Issue (8): 586-589.doi: 10.12144/zgmfskin202608586

• 病例报告 • 上一篇    下一篇

多中心网状组织细胞增生症一例

邓向芬,王惠芬,周小芳,王娟   

  1. 陆军军医大学第一附属医院(西南医院)皮肤科,重庆市卫生健康委免疫性皮肤病重点实验室,重庆,400038
  • 出版日期:2026-08-15 发布日期:2026-08-03

Multicentric reticulohistiocytosis: a case report

DENG Xiangfen, WANG Huifen, ZHOU Xiaofang, WANG Juan   

  1. Department of Dermatology, The First Affiliated Hospital (Southwest Hospital) of Army Medical University; Chongqing Municipal Health Commission Key Laboratory of Immunological Skin Diseases, Chongqing 400038, China
  • Online:2026-08-15 Published:2026-08-03

摘要: 多中心网状组织细胞增生症(multicentric reticulohistiocytosis,MRH)是一种罕见的累及多系统的非感染性肉芽肿性疾病。本文报道一例MRH患者。患者,女,44岁,手部、面部、前胸红斑、丘疹伴多发关节痛4个月。彩超示右侧肘关节滑膜炎,伴轻度活动性炎症。组织病理示真皮密集的组织细胞及多核巨细胞浸润,胞浆丰富,毛玻璃样改变。免疫组化:CD68、CD163阳性,S-100个别阳性。诊断:多中心网状组织细胞增生症。予以泼尼松30 mg/d口服治疗,1个月后皮疹及关节疼痛明显好转,后用甲氨蝶呤5 mg, 2次/周维持治疗,随访6个月,病情稳定。

关键词: 多中心网状组织细胞增生症, 串珠样丘疹, 关节疼痛

Abstract: Multicentric reticulohistiocytosis (MRH) is a rare non-infectious granulomatous disease involving multiple systems. Herein we report one case of MRH. The patient was a 44-year-old female presenting with erythema and papules on the hands, face and precordium accompanied by multiple arthralgia for 4 months. Color doppler ultrasonography revealed synovitis of the right elbow joint with mild active inflammation.Histopathological analysis indicated a dense infitration of histiocytes and multinucleated giant cells in the dermis, characterized by abundant cytoplasm and ground glassy changes. Immunohistochemical staining showed positive results for CD68 and CD163, individual positivity for S100. The final diagnosis was MRH. Treatment involved oral prednisone at a dosage of 30 mg once a day, resulting in significant improvement of the rash and joint pain after one month. Subsequently, the patient was maintained on methotrexate at a dose of 5 mg twice a week. The condition is stable followed-up for 6 months.

Key words: multicentric reticulohistiocytosis(MRH), beaded papules, joint pain