Successful Treatment of Idiopathic Multicentric Castleman Disease With Rash as the Initial Symptom Using a Rituximab-Based Regimen.

IF 1.3 Q4 HEMATOLOGY Journal of hematology Pub Date : 2024-10-01 Epub Date: 2024-10-21 DOI:10.14740/jh1313
Li Zhu, Yi Liu, Fang Yu, Xue Jiao Yin, Qiu Mei Yao, Hai Tao Meng, Liang Shun You, Hong Yan Tong
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Abstract

Idiopathic multicentric Castleman disease (iMCD) is a rare lymphoproliferative disorder characterized by enlarged lymph nodes and systemic inflammation, often involving multiple organ dysfunction. However, cutaneous involvement in iMCD is rare and heterogeneous, and studies on the treatment of iMCD with skin involvement are scarce. Here, we present a rare case of iMCD with prominent facial skin involvement, which showed significant improvement with rituximab-based regimen treatment.

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使用利妥昔单抗方案成功治疗以皮疹为首发症状的特发性多中心卡斯特曼病
特发性多中心卡斯特曼病(iMCD)是一种罕见的淋巴细胞增生性疾病,其特点是淋巴结肿大和全身炎症,常涉及多器官功能障碍。然而,iMCD 的皮肤受累罕见且异质性强,有关治疗皮肤受累的 iMCD 的研究也很少。在此,我们介绍了一例罕见的面部皮肤受累的 iMCD 病例,该病例在接受基于利妥昔单抗的方案治疗后病情明显好转。
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来源期刊
Journal of hematology
Journal of hematology HEMATOLOGY-
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