Aslam Zaheer, Chowdhary Omer, Razik Anjana, Negmeldin Mostafa
Respiratory Medicine, Bedford Hospital NHS Trust, Bedford, GBR.
Respiratory Medicine, Luton and Dunstable University Hospital, Luton, GBR.
Cureus. 2024 Jul 18;16(7):e64825. doi: 10.7759/cureus.64825. eCollection 2024 Jul.
Rosai-Dorfman disease (RDD) is a rare benign condition that presents most commonly with lymphadenopathy and skin lesions and is characterized by infiltration of histiocytes into the skin and soft tissues. We present a case of RDD in an Afro-Caribbean male in his 50s who presented to our chest clinic with shortness of breath, cough, and weight loss of 15 kg over one year. CT scan showed evidence of right pleural effusion, mediastinal and hilar lymphadenopathy, and bony lesions in the spine. Cytology from multiple pleural effusions and endobronchial ultrasound-guided fine needle aspiration from lymph nodes did not show any malignancy. Left axillary excisional biopsy showed a pattern consistent with RDD. The patient was started on interferon therapy by the hematologist and pleurodesis after repeated pleural taps failed to relieve recurrent right pleural effusions. This case emphasizes the importance of tissue diagnosis to avoid misdiagnosis and unnecessary treatment.
罗萨伊-多夫曼病(RDD)是一种罕见的良性疾病,最常见的表现是淋巴结病和皮肤病变,其特征是组织细胞浸润皮肤和软组织。我们报告一例50多岁的非洲加勒比男性RDD病例,该患者因气短、咳嗽以及一年内体重减轻15公斤就诊于我们的胸部诊所。CT扫描显示有右侧胸腔积液、纵隔和肺门淋巴结病以及脊柱骨质病变的证据。多次胸腔积液的细胞学检查以及经支气管超声引导下淋巴结细针穿刺均未发现任何恶性肿瘤迹象。左腋窝切除活检显示的模式与RDD一致。血液科医生开始对该患者进行干扰素治疗,在反复胸腔穿刺未能缓解复发性右侧胸腔积液后进行了胸膜固定术。该病例强调了组织诊断对于避免误诊和不必要治疗的重要性。